Pediatric Hospital Care:

ETHIOPIA

POCKET BOOK

Guidelines for the Management of

Common Illnesses in Hospitals

(Second Edition, 2016)

I
 Table of Contents

Table of Contents ............................................................................. II

Acknowledgements .......................................................................VIII
Abbrevations.................................................................................... X
CHAPTER 1-TRIAGE AND EMERGENCY CONDITIONS ........................ 12
1.1 Triage……………………………………………………………………………….12
1.2 Airway and Breathing ...................................................... 18
1.3 Circulation ...................................................................... 31
1.4 Dehydration .................................................................... 42
1.5 Cardiopulmonary Resuscitation (CPR) ............................... 42
1.6 Pediatric Trauma ............................................................. 45
1.7 Burn Injury ...................................................................... 47
1.8 Common Childhood Poisoning .......................................... 48
CHAPTER 2 - DIAGNOSTIC APPROACHES TO THE SICK CHILD ............ 61
2.1 Relationship to the IMNCI approach ................................. 61
2.2 Taking history.................................................................. 61
2.3 Approach to the sick child and clinical examination ........... 62
2.4 Laboratory investigations ................................................. 63
2.5 Differential diagnoses ...................................................... 64
CHAPTER 3 - PROBLEMS OF THE NEWBORN AND THE YOUNG
INFANT .................................................................................... 65
3.1 Routine care of the newborn at delivery ........................... 65
3.2 Neonatal resuscitation ................................................... 71

II
 3.3 Prevention of neonatal infections .................................... 75
3.4 Management of infants with hypoxic ischaemic
encephalopathy .................................................................... 76
3.5 Danger signs in newborns and young infants .................... 77
3.6 Convulsions ................................................................... 79
3.7 Serious bacterial infection ................................................ 80
3.8 Neonatal Meningitis ........................................................ 81
3.9 Supportive care for sick neonates ..................................... 82
3.10 Preterm and low-birth-weight infants ............................. 88
3.11 Kangaroo Mother Care (KMC) ......................................... 91
3.12 Common problems of low-birth-weight infants ............... 95
3.13 Discharge and follow-up of low-birth-weight infants ....... 98
3.14 Other common neonatal problems................................. 99
3.15 Babies of mothers with infections ................................. 121
CHAPTER- 4 - COUGH OR DIFFICULT BREATHING ........................... 129
4.1 Child presenting with cough ........................................... 129
4.2 Pneumonia ................................................................... 134
4.3 Complications of pneumonia .......................................... 143
4.4 Cough or cold ................................................................ 146
4.5 Conditions presenting with wheeze ............................... 148
4.6 Conditions presenting with stridor .................................. 161
4.7 Conditions presenting with chronic cough ....................... 170
4.8 Heart failure .................................................................. 185
CHAPTER 5 – DIARRHOEA ............................................................. 188

III
 5.1 Child presenting with diarrhoea...................................... 189
5.2 Acute Diarrhoea ............................................................ 191
5.3 Persistent diarrhoea ...................................................... 202
5.4 Dysentery ..................................................................... 209
CHAPTER 6 – FEVER ...................................................................... 214
6.1 Child presenting with fever ............................................ 214
6.2 Malaria……………………………………………………..223
6.3 Meningitis ..................................................................... 235
6.4 Measles…………………………………………………….244
6.5 Septicaemia .................................................................. 249
6.6 Typhoid fever ................................................................ 252
6.7 Ear infections ................................................................ 254
6.8 Urinary tract infection.................................................... 257
6.9 Relapsing Fever ............................................................. 259
6.10 Acute Tonsillopharyngitis ........................................... 260
6.11 Primary herpetic gingivostomatiitis............................... 261
6.12 Septic Arthritis and Acute Osteomyelitis ....................... 262
6.13 Rheumatic fever ......................................................... 264
6.14 Dengue ....................................................................... 268
CHAPTER 7 - SEVERE ACUTE MALNUTRITION................................. 276
7.1 Diagnosis ...................................................................... 276
7.2 Initial assessment of the severely malnourished child ...... 277
7.3 Admission criteria .......................................................... 281

IV
 7.4 Organization of Care ...................................................... 283
7.5 Treatment Approach...................................................... 284
7.6 Treatment of medical complications ............................... 284
7.7 Routine Medicines ......................................................... 296
7.8 Dietary Treatment ......................................................... 300
7.9 Failure to respond......................................................... 311
7.10 Discharge Criteria........................................................ 313
CHAPTER 8 - CHILDREN WITH HIV/AIDS ........................................ 318
8.1 HIV/AIDS....................................................................... 318
8.2 Sick child with suspected or confirmed HIV infection ....... 318
8.3 Antiretroviral therapy .................................................... 329
8.4 Supportive care for HIV-positive children ........................ 339
8.5 Management of HIV-related conditions........................... 342
8.6 Prevention of mother-to-child HIV transmission, and infant
feeding…………………………………………………………348
8.7 Follow-up ...................................................................... 351
8.8 Palliative and end-of-life care ......................................... 352
CHAPTER 9 - COMMON SURGICAL PROBLEMS............................... 355
9.1 Care before, during and after surgery.............................. 355
9.2 Congenital anomalies..................................................... 363
9.3 Injuries……………………………………………………..370
9.4 Abdominal problems ..................................................... 381
9.5 Bowel obstruction beyond the newborn period ............... 384
9.6 Infections requiring surgery............................................ 389

V
CHAPTER 10 - SUPPORTIVE CARE .................................................. 393
10.1 Nutritional management .............................................. 393
10.2 Supporting breastfeeding ............................................. 393
10.3 Fluid management ....................................................... 410
10.4 Management of fever .................................................. 411
10.5 Pain control ................................................................. 413
10.6 Management of anaemia ............................................. 423
10.7 Oxygen therapy ........................................................... 429
10.8 Toys and Play Therapy.................................................. 433
CHAPTER 11 - MONITORING THE CHILD’S PROGRESS..................... 437
11.1 Monitoring procedures ................................................ 437
11.2 Monitoring chart ......................................................... 438
CHAPTER 12 - COUNSELING AND DISCHARGE FROM HOSPITAL ..... 441
12.1 Timing of discharge from hospital ................................. 441
12.2 Counseling .................................................................. 442
12.3 Nutrition counseling ................................................... 443
12.4 Home treatment ........................................................ 445
12.5 Checking the mother’s health ....................................... 446
12.6 Checking immunization status ...................................... 446
12.7 Communicating with the first-level health worker ......... 447
12.8 Providing follow-up care .............................................. 448
ANNEX 1: Practical Procedures ............................................. 450
ANNEX 2: Drug dosages and regimens .................................. 469

VI
ANNEX 3: Eguipment Sizes ................................................... 490
ANNEX 4: Intravenous fluids ................................................ 491
ANNEX 5: Assessing nutritional status .................................. 493
ANNEX 6: BP Levels for Boys and Girls .................................. 517
Inderx…………………………………………………………..521

VII
 Acknowledgements
This second edition of the Pocket Book of Pediatric Hospital Care for
Ethiopia was developed by adaptation of the Who Pocket Book of Hospital
Care for Children (2013) through the technical and financial assistance of
WHO-Ethiopia and with the support and input of many experts in the field.
Great effort has been made to harmonize all treatment recommendations
with the currently existing national care and treatment guidelines. It is our
strong belief that this guideline will contribute significantly to the efforts
being made to improve quality of hospital care services for children
especially emergency triage and treatment at referral sites.
The FMOH of Ethiopia is very grateful for the all rounded support of
WHO/Ethiopia and the commitment and devotion shown by the Child
Health Team of the country office for the accomplishment of this work.
We would like to sincerely acknowledge the remarkable contribution of Dr
Damte Shimelis, Dr Etsegenet Gedlu, Dr Berhanu Gudetta and Prof. Bogale
Worku who served as consultants in the adaptation of the generic WHO
guideline.
Special thanks to Rebecca Zewdie and Hana Siyoum for their assistance in
typing and formatting of the material.
The FMOH gratefully acknowledges the technical contribution of all
professionals who were involved in the development of this national
pediatric hospital care guideline particularly for the following experts: -

Name of participant Organization

Dr. Dagnew Muluneh -FMOH/WHO

Dr. Mahlet Abayneh -UOG (Gondar)
Dr. Birkneh Tilahun -Hawassa University
Dr. Mulugeta Naizgi -Mekelle University
Dr. Zelalem Addis -Bahir Dar University
Dr. Lamesginew Mossie -Hosana
Dr. Netsanet Workneh -Jimma University

VIII
 Dr. Gezahegn Nekatibeb -Debre Berhan
Dr. Lisanu Tadesse -FMOH
Dr. Tesfalem Hagos -Mekelle University
Dr. Wegen Shiferaw -WHO Ethiopia Child
Health Team

Finally the Federal Ministry of Health would like to recognize the Ethiopian
Pediatrics Society for coordination and finalization of this pocket book.

Abraham Endeshaw (MD)

Director, Medical Services Directorate
Federal Ministry of Health, Ethiopia

IX
Abbrevations

ACT Artemisinin Combination Therapy

AIDS acquired immunodeficiency syndrome
AVPU Alert, responding to Voice, responding to Pain,
Unconscious)
BP blood pressure
CMV cytomegalovirus
CSF cerebrospinal fluid
DPT diphtheria, pertussis, tetanus
EPI expanded programme of immunization
FG French gauge
G6PD glucose 6-phosphate dehydrogenase
HIV human immunodeficiency virus
HUS haemolytic uraemic syndrome
IM intramuscular injection
IMCI Integrated Management of Childhood Illness
IV intravenous injection
JVP jugular venous pressure
LIP lymphoid interstitial pneumonitis
LP lumbar puncture
NG nasogastric
OPV oral polio vaccine
ORS oral rehydration salts
ORT oral rehydration therapy
PCP Pneumocystis carinii pneumonia

X
PCV packed cell volume
PPD purified protein derivative (used in a test for tuberculosis)
ReSoMal rehydration solution for malnutrition
RDA recommended daily allowance
RUTF Ready to Use Therapeutic Food
SAM Severe Acute Malnutrition
SD standard deviation
STI sexually transmitted infection
TB tuberculosis
TMP trimethoprim
TPHA treponema pallidum haemogglutination assay
SMX sulfamethoxazole
UTI urinary tract infection
VDRL veneral disease research laboratories
WBC white blood cell count
WHO World Health Organization
°C degrees Celsius
°F degrees Fahrenheit

XI
CHAPTER 1-TRIAGE AND EMERGENCY CONDITIONS

1.1 Triage
TRIAGE is the sorting of patients into priority groups according to their
need and the resources available.

Many deaths in hospital occur within 24 hours of admission. Some of these

deaths can be prevented if very sick children are quickly identified on their
arrival and treatment is started without delay.

Categories after Triage Action required

EMERGENCY CASES Need immediate emergency
treatment
PRIORITY CASES Need assessment and rapid
attention
QUEUE CASES Can wait their turn in the queue

The ABCDO concept

Triage of patients involves looking for signs of serious illness or injury.
These emergency signs related to the Airway-Breathing-
Circulation/Consciousness-Dehydration/Disability, and Other Emergencies
are easily remembered as “ABCDO”.

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Each letter refers to an emergency sign which, when positive, should alert
you to a patient who is seriously ill and needs immediate assessment and
treatment.
Emergency signs include:
 obstructed or absent breathing
 severe respiratory distress
 central cyanosis
 signs of shock (cold hands, capillary refill time longer than or
equal to 3 seconds, weak and fast pulse)
 coma (or seriously reduced level of consciousness)
 convulsions
 signs of severe dehydration in a child with diarrhoea
 Disabilities like motor deficit (paraplegia/paresis,
hemiplegia/paresis, facial palsy…)
 Other emergency signs (bleeding child, immediate poisoning,
Major Trauma)

Bleeding child:
 Bleeding due to trauma
 Spontaneous bleeding (epistaxis, hematemesis, rectal
bleeding, umbilical bleeding…)
Immediate poisoning:
 Acute eye or skin poisoning
 Ingested poison within one hour
Major trauma:
 Compound (open) fracture
Priority signs
These children need prompt assessment (no waiting in the queue). These
signs can be remembered with the mnemonic 3 TPR - MOB:
 Tiny baby: any sick child aged less than two months
 Temperature: child is very hot or very cold
 Trauma or other urgent surgical condition
 Pallor (severe)
 Poisoning (other than those that require emergency care)
 Pain (severe)
 Respiratory distress

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  Restless, continuously irritable, or lethargic
 Referral (urgent)
 Malnutrition: Visible severe wasting
 Oedema of both feet
 Burns
The triaging process should be short (average of 20 seconds) and a
continious processes with frequent assessment. One of the following can
be used to differentiate the groups:

-Stamp method or
-Colored sticker (Red, Yellow, Green)

14
15
Table 1.1: Emergency management of triaged children

16
17
When a child with emergency signs is identified, start the appropriate
emergency treatments immediately. Do not proceed to the next step
before treatment is begun for a positive sign. If the child has no emergency
signs, check for priority signs.
General Treatment for Priority Signs
While waiting, supportive treatments should be given. For example, a child
who is febrile should receive antipyretic such as paracetamol. Similarly, a
child with a burn may have severe pain and the pain should be controlled
while waiting for definitive treatment.
1.2 Airway and Breathing
The letters A and B in “ABCDO” represent “Airway and Breathing”. If there
is no problem with the airway or breathing, you should look for signs in the
areas represented by C.
Assessment and management of the Airway and Breathing
 Is the child breathing?
 Is the airway obstructed?
 If the child is not breathing, or if the child has severe respiratory
distress, is there an obstruction to the flow of air?

Table 1.2: Assessment and treatment of airway and breathing

AB  Not breathing  Manage
AIRWAY  Central cyanosis, airway
AND or Any Sign  Give oxygen
BREATHING  Severe respiratory Positive  Make sure the
distress child is warm
 If yes, is the
breathing
obstructed
Check for head/neck trauma before treating the child; do not move neck if
cervical spine injury is possible.

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 Assessment of an
obstructed Airway
 LOOK
Is the chest moving?
 LISTEN
Listen for any breath
sounds. Are they normal?
 FEEL

Figure 1.1: Look, Listen, Feel

Can you feel the movement of air through nose or mouth of the child?

The following signs suggest that the upper airway is obstructed

 Increased inspiratory effort with retraction
 Abnormal respiratory sounds (e.g. stridor)
 Lack of breath sounds despite respiratory effort (i.e. complete
airway obstruction)
If the child is not breathing or if the airway appears obstructed, you must
first open the airway.

Management to open the airway

If the upper airway is obstructed, use the following techniques:

Simple techniques to open the airway

1. Open the airway with head tilt–chin lift for non-trauma patients
or jaw trust for trauma or suspected trauma patients
2. Clear the airway by suctioning the mouth and nose
3. Perform techniques to remove foreign body obstructing the
airway
4. Use airway adjuncts (e.g. oral airway)
5. Avoid unnecessary agitation which worsens the
obstruction

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Maneuvers to open the airway
Manage anatomic obstruction (hypo-pharyngeal tissue blocking the
airway). If a patient is not properly positioned, there will be anatomic
obstruction of the airway by the hypo-pharyngeal tissue as you can see in
Figures 1.2 and 1.3.

Figure 1.2: Anatomic Figure 1.3: Releiving

Obstruction Anatomic obstruction

Chin lift and head tilt

Place your hand on the child’s forehead and apply a little pressure to
achieve the tilt. The fingers of the other hand are used to gently lift the
chin. The drawings illustrate two different positions. Figure 1.4 shows the
position for infants, the nose pointing upwards. Figure 1.5 shows the
position for children, the chin pointing up. Use it only for patients without
trauma or suspected trauma.

Figure 1.4: Neutral position Figure 1.5: Sniffing position to

to open the airway in an open the airway in an older child
infant (“chin-up”)

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Jaw trust
To open and manage the airway when trauma is suspected, a jaw
thrust is used, as illustrated in Figure 1.6.

Figure 1.6: Jaw thrust technique to

open the airway
This is a way of opening the airway without moving the head. It is safe to
use in cases of trauma for children of all ages. The Jaw thrust is achieved by
placing two or three fingers under the angle of the jaw on both sides, and
lifting the jaw upwards. If a child has trauma you must avoid further injury
during assessment or treatment. This child may have a spinal injury,
which could be made worse by moving him. Therefore, stabilization of the
head and neck should be performed for all patients with suspected trauma
of the head and neck. (See Figure 1.7)
To check for head or neck trauma:
 Ask if the child has had trauma to the head or neck or a fall which
could have damaged the spine
 Look for bruises or other signs of head or neck trauma
To stabilize the neck:
Keep the child lying on his/her back
 Prevent the neck from moving by supporting the child’s head with
a cervical collar or using other materials (e.g. liter bags of IV fluid
on each side)
 Tape the child’s forehead to the sides of a firm board to secure
this position
 Place a strap over the chin

21
If the child is vomiting, turn them on their side, keeping the head in line
with the body (log roll maneuver, See Figure 1.8). If the child is restless, ask
an attendant to stabilize the neck without upsetting the child more.

Figure 1.7: Stabilizing the neck

when trauma is suspected

Log roll
This maneuver is used when a patient’s body needs to be moved while still
providing stability to the neck. Move a patient with a suspected cervical
spine injury carefully. Avoid rotation and extremes of flexion and
extension. One person, usually the most senior attendant, should assume
responsibility for the neck. He or she should stand at the head of the bed,
hold the patient’s head, place their fingers under the angle of the mandible
with the palm over the ears and parietal region, and maintain gentle
traction to keep the neck straight and in line with the body (see Figure 1.8).
When the patient is not being moved, a sandbag placed on each
side or a cervical collar can splint the neck.

Figure 1.8: Log roll: stabilizing the neck of the patient while moving the body

22
Additional methods for maintaining anatomic airway
The occiput is prominent in neonates and in young infants and during
supine flexion of the neck, partial obstruction of the airway may occur.
Putting a small towel roll placed under the shoulder could help infants to
open the airway. Similarly putting towel under the neck and head for older
children helps to open the airway.
Clearing the airway
Besides manual opening of the airway, suction of secretions, mucus, or
blood from the mouth may be necessary to re-establish airway patency. It
aids in the clearance of liquid and particulate material. An example of a
common suction device is seen in Figure 1.9.
Appropriate size catheter is required. Excessively deep suctioning of any
patient should be avoided to minimize the risk of vomiting, aspiration,
laryngospasm, or bradycardia.

Figure 1.9: Yankauer catheter (A) and suction catheter (B) for
clearing secretions from the airway

If vomiting occurs, the child's head is first

turned to one side, and suctioning is
continued until the emesis is cleared. This
procedure is done once we are sure that the
child is not having cervical cord injury which
may be aggravated by the movement.

Insertion of an Oropharyngeal (Guedel) Airway

The oropharyngeal airway can be used in an unconscious patient to
improve airway opening. It may not be tolerated in a patient who is awake
and may induce choking or vomiting. Guedel airways come in different
sizes (see Figure 1.10). An appropriate sized airway goes from the centre of
the teeth (incisors) to the angle of the jaw (see Figure 1.11).

23
Figure 1.10: Guedel tubes of
different sizes and types

Infant:
 Select an appropriate sized airway
 Position the child to open the airway, taking care not to move
the neck if trauma suspected
 Using a tongue depressor, insert the oropharyngeal airway, the
convex side up (Fig 1.12)
 Re-check airway opening
 Use a different sized airway or reposition if necessary
 Give oxygen

Figure 1.11: Selecting the right

size of an oropharyngeal airway

Figure 1.12: Inserting an

oropharyngeal airway in an
infant: convex side up

24
Child
 Select an appropriate sized oropharyngeal airway.
 Open the child’s airway, taking care not to move the neck if
trauma suspected.
 Using a tongue depressor, insert the airway “upside down”
(concave side up) until the tip reaches the soft palate.
o
 Rotate through 180 and slide back over the tongue.
(Figure 1.13)
 Recheck airway opening.
 Use a different sized airway or re-position if necessary.
 Give oxygen.

Figure 1.13: Inserting an oropharyngeal airway in an older child;

concave side up and turning it around

Management of foreign body aspiration (a choking child)

Ask the child’s caretaker explicitly for a history of choking. Techniques to

remove foreign bodies are based on support of forced expiration rather
than a blind finger sweep of the mouth or mechanical removal of the
object. A blind finger sweep in infants and children should not be done, as
it might cause serious bleeding. Attempts to force the foreign body out of

25
the airway should be done immediately, because airflow may be halted
completely and sudden death could be imminent.

A child with a history of aspiration of a foreign body who shows increasing

respiratory distress is in immediate danger of choking. Attempts to remove
the foreign body should be made instantly. Do not hesitate. If a foreign
body is causing the obstruction, the treatment depends on the age of the
child.

Management of young infant with foreign body aspiration

 Lay the infant on your arm or thigh in a head down position

 Give 5 blows to the infant’s back with heel of hand.
 If obstruction persists, turn infant over and give 5 chest thrusts
with 2 fingers, one finger breadth below nipple level in midline.
 If obstruction persists, check infant’s mouth for any obstruction
which can be removed
 If necessary, repeat sequence with back slaps again.

Figure 1.14: Management of young infant with foreign body

aspiration

26
Management of a child with foreign body aspiration
 Give 5 blows to the child’s back with heel of hand with child sitting,
kneeling or lying
 If the obstruction persists, go behind the child and pass your arms
around the child’s body; form a fist with one hand immediately
below the child’s sternum; place the other hand over the fist and
pull upwards into the abdomen; repeat this Heimlich maneuver 5
times
 If the obstruction persists, check the child’s mouth for any
obstruction which can be removed.
 If necessary, repeat this sequence with back slaps again.
After you have performed this procedure, you should check inside the
mouth for any foreign body. Obvious foreign bodies should be removed.
The breathing should be checked again. If these maneuvers are
unsuccessful or if the child becomes unconscious, start bag and mask
ventilation. If available, laryngoscopy with direct visualization can remove
the foreign body with a forceps.

27
Figure 1.15: Management of child with foreign body aspiration

Advanced Intervention

This is done in a setting where experts are available

1. Endotracheal intubation
2. Removal of foreign body with direct visualization by laryngoscope
3. Application of positive airway pressure (CPAP)
4. Cricothyroidotomy
If the airway obstruction is due to anaphylaxis (patients with urticaria,
swelling of the lips and face, change of voice, cough, wheeze and dyspnea)
manage airway, give adrenaline and other management for anaphylaxis.

Management of breathing problem

1. Bag and mask ventilation

2. Give oxygen by different ways depending on the child’s condition

3. Thoracentesis and or tube thoracostomy

28
Proper Technique for Bag-Mask Ventilation

 It is important for the mask to be the correct size for the child
 The correct size and position are shown in the illustration (see
Figure 1.16).
 The mask should also be placed correctly over the face in order to
prevent leakage. The mask should cover both the entire mouth as
well as both nostrils.
 To ensure a proper seal around the mask, use the C-E technique.
This involves making a C-shape using your thumb and index finger
around the base of the mask and press down onto the face. At the
rd th
same time, use your 3 -5 digits and place them along the edge of
the jaw in the shape of inverted E and elevate the mandible
anteriorly. (see Figure 1.17 & 1.18)
 If oxygen is available, connect it to the bag-mask
 When providing bag-mask ventilation, ensure for chest rise or
auscultation of breath sounds
 Ventilate the child with a rate of 40-60/min for neonate, 20/min for
infant and 12-15 breath per minute for child
 Do not hyperventilate and avoid pressure over the mask
 If chest rise is not visible, common problems include poor mask seal
around the face, airway obstruction due to improper airway
positioning, or excessive secretions requiring suctioning

Figure 1.16: Choosing the right mask size

29
 Figure 1.17: One person bag Figure 1.18: Two person bag
mask demonstrating C-E mask technique
techniques

Give Oxygen to treat hypoxemia

There are two possible sources of oxygen: oxygen concentrators and

oxygen-filled cylinders (see Figure 1.19 and 1.20)

Figure 1.19: Oxygen concentrator Figure 1.20: Oxygen Cylinder

Oxygen Delivery
Two methods are recommended for the delivery of oxygen in an
emergency setting: nasal prongs and nasal catheter. Nasal prongs are best
for delivering oxygen to young infants and children with severe croup or
pertussis; do not use nasal catheters as they provoke paroxysms of
coughing. Set a flow rate of 0.5-1 liters/min in infants and 1-2 litres/min if

30
 older in order to deliver 30-35% oxygen concentration in the inspired air.
Face Mask: an alternative method in emergency settings is the use of a
face mask, which requires higher flow rates (6-10 liters/ minute). It is
therefore not suitable for permanent oxygen delivery, and is reserved for
serious emergency.

1.3 Circulation
The letter C in “ABCDO” stands for assessment and management of
Circulation, Coma and Convulsions.

Assess the circulation

To assess if a child has a circulation problem you should know:

 Does the child have warm hands?

 If not, is the capillary refill time ≥ 3 seconds?
 And is the pulse weak and fast?

Table 1.3: Assessment and treatment of circulation

C Cold hands  Stop any bleeding
CIRCULATION with:  Give oxygen
 Capillary Signs  Make sure the child is warm
refill ≥ 3 IF NO SEVERE MALNUTRITION:
Positive
seconds,  Insert IV and begin giving fluids
and rapidly
 If not able to insert peripheral IV,
 Weak insert an intra- osseous line or
Check for severe
and malnutrition external jugular
fast IF SEVERE MALNUTRITION:
pulse  Give IV glucose
 Proceed immediately to
full assessment and treatment
Check for head/neck trauma before treating the child; do not move the neck if cervical spine
injury is possible.

31
Is the Pulse Weak and Fast?

Figure 1.21: Feeling the brachial pulse

in an infant

Shock
The most common cause of shock in children is loss of fluid from
circulation, either through loss from the body as in severe diarrhea or
when the child is bleeding, or through capillary leak in a disease such as
severe sepsis or burn. In all cases, it is important to replace this fluid
quickly (as shown in Chart 5).

If the child has severe malnutrition, you must use a different fluid and a
different rate of administration and monitor the child very closely.

Treatment of Shock

The following actions need to be started simultaneously:

 If the child has any bleeding, apply pressure to stop the bleeding
 Give oxygen
 Make sure the child is warm
 Select an appropriate site for administration of fluids
 Establish IV or interosseous access
 Take blood samples for emergency laboratory tests
 Begin giving fluids for shock.

Stop any bleeding

32
The best and safest way to stop bleeding is to apply firm and direct
pressure to the point that is bleeding with a gloved hand. Do not use a
tourniquet.

Give oxygen
All children who are in shock require oxygen. It can be given in any of the
ways discussed in the previous section.

Figure 1.22: Controlling

external bleeding

33
Make sure the child is warm

This should be done by ensuring that the child is dry and covered with
blankets or warm clothing.

Select an appropriate site for administration of fluids

The most appropriate route for administration is intravenous and a

peripheral vein is preferable but not always accessible. Alternatives are
interosseous (IO) infusion or a central vein catheter.

Give Intravenous Fluids

First assess the child for severe malnutrition before selecting treatment as
shown on Chart 5 (refer chapter 7 for assessment of malnutrition). The
severely malnourished child is considered to have shock if he/she is
lethargic or unconscious and has cold hands plus either:

 Slow capillary refill (≥ 3 seconds), or

 Weak, fast or absent radial or femoral pulses and
 Absence of signs of heart failure in an edematous child
Table 1.4: Treatment of shock
If the child has NO severe Acute Malnutrition If the child HAS Severe Acute Malnutrition
 Insert an intravenous line (and draw  Weigh the child.
blood for emergency laboratory  IV Fluid (15ml/kg over 1hr)
investigations).  Fix the cannula and immobilize the
 Fix the cannula and immobilize the extremity with a splint.
extremity with a splint.  Give normal saline or Ringer lactate
 Attach Ringer’s lactate or normal saline with 5% glucose at 15 ml/kg given over
- make sure the infusion is running well. 1 hour (if available use half strength
 Infuse 20 ml/kg as rapidly as possible. Darow’s solution with 5% glucose)
 The circulation should be reassessed as  Stay with the child and check the pulse
described before. and breathing rate every 5-10 minutes.
 Improvement: warmer hands, pulse  Discontinue the intravenous infusion if
slows and capillary refill faster. either of these increases (pulse by 15,
 If there is NO improvement: respiratory rate by 5/ min).
 Give another 20 ml/kg of Ringer’s  If the child improved, change the IV
lactate or normal saline as quickly as fluid with oral intake/ Resomal after 2
possible. Reassess the circulation again, hrs
and if there is still no improvement, If there IS improvement:
 Give another 20 ml/kg of Ringer’s (pulse and breathing rate fall)
lactate or normal saline, as quickly as  Repeat 15ml/kg over 1 hour.
possible. The circulation should be If there is NO improvement:
assessed again.  Call senior health worker.
 If there is still NO improvement:  Give maintenance IV fluid 4ml/kg/hour
 Consider Blood Transfusion unless there while waiting for blood.
is profuse watery diarrhoea. In this  Transfuse fresh whole blood at 10ml/kg
case, repeat Ringer's lactate. slowly over 3 hours (use packed cells if
 The circulation should be assessed in cardiac failure).
again.  Follow National Guideline for
 If there is still NO improvement: Management of SAM
 See inpatient treatment guidelines for
underlying condition

Assessment and management of Coma and Convulsion

To assess the child’s neurological status you need to know:

 Is the child in coma?

 Is the child convulsing?

35
 Table 1.5: Assessment and treatment of coma and convulsion
Cm Coma  Manage the
COMA or airway
Cn Convulsing  Give oxygen
CONVULSION (now) If coma or  If convulsing, give
convulsing diazepam rectally
 Position the child
(if head or neck
trauma is
suspected,
stabilize the neck
first)
 Give IV glucose

Consciousness level of a child should be assessed using a simple AVPU

scale.

A Is the child Alert? If not,

V Is the child responding to Voice? If not,

P Is the child responding to Pain?

U The child who is Unresponsive to Voice (or being shaken) and to pain is
Unconscious.

Initial assessment of level of consciousness should be done by AVPU. Using

Glasgow Coma Scale (GSC) is time taking for the initial assessment but can
be used for follow up of the child’s progress.

36
Table 1.6: Glasgow Coma Scale
Child Infant
Eye Opening Spontaneous 4 Spontaneous
(E) To speech 3 To speech
To pain 2 To pain
None 1 None

Verbal (V) Oriented 5 NoneCoos/Babbles

Confused 4 Irritable Cry
Inappropriate 3 Cries/Pain
Incomprehensible 2 Moans
None 1 None

Motor (M) Obeys commands 6 Spontaneous

Purposeful 5 Withdraws(touch)
Withdrawals(pain) 4 Withdraws (pain)
Flexion(pain) 3 Abnormal flexion
Extension(pain) 2 Abnormal Extension
None 1 NoneSpontaneous

Treatment of coma and convulsion

Treatment of coma and convulsions has some similarities and will be

described together.

Table 1.7: Treatment of coma and convulsion

COMA CONVULSION
If the child is unconscious you should: If the child is convulsing now
 Manage the airway you should:
 Position the child (if there is a history  Manage the airway
of  Position the child
trauma, stabilize neck first)  Check the blood sugar
 Check blood sugar  Give IV glucose
 Give IV glucose  Give anticonvulsant

37
Position the Child
Coma
Any unconscious child who is breathing and keeping the airway open
should be placed in the recovery postion. This position helps to reduce the
risk of vomit entering the child’s lungs (see Figure 1.23). It should only be
used in children who have not been subjected to trauma.

Figure 1.23: Positioning the unconscious child

(recovery position)

If neck trauma is not suspected:

 Turn the child on the side to reduce risk of aspiration

 Keep the neck slightly extended and stabilize by placing the cheek on
one hand
 Bend one leg to stabilize the body position
If trauma is suspected:
 Stabilize neck and turn the child to the side using log roll method.
If the child is having a convulsion, do not attempt to hold him/her down or
put anything in the child’s mouth. If the child vomits turn the child on
his/her side to avoid aspiration. If the convulsion has stopped and the
airway is clear, the child can be placed in the recovery position (see Figure
1:23).

38
Check the Blood Sugar
Coma and convulsion
Hypoglycemia is present if the measured blood glucose level is low <2.5
mmol/l (45 mg/dl) in a well nourished or <3 mmol/liter (54 mg/dl) in a
severely malnourished child.
When the blood glucose cannot be measured, hypoglycaemia should be
assumed to be present in all children in coma or having a convulsion and
should be treated.
Give IV Glucose
Coma and convulsion
 Insert an IV line and draw blood for emergency laboratory
investigations.
 Give 5 ml/kg of 10% glucose solution rapidly by IV infusion
 Recheck the blood glucose in 30 minutes. If it is still low, repeat 5
ml/kg of 10% glucose solution.
 Feed the child as soon as conscious.

If the child is not able to feed and there is a danger of aspiration, give:

 Milk or sugar solution via nasogastric tube.

 Maintenance IV fluid containing 5-10% glucose (dextrose)
 To make sugar solution, dissolve four level teaspoons of sugar (20
grams) in a 200-ml cup of clean water.

39
Table 1.8: Amount of glucose to give by age
Age/weight Volume of 10% To make up 10% glucose using
glucose 40% glucose solution
solution to be Volume of 40% Volume of
given as glucose normal saline
bolus (5 ml/kg)
Less than 2 months (<4 15 ml 4 ml 11ml
kg) 25 ml 6 ml 19ml
2 - <4 months (4 - <6 kg) 40 ml 10 ml 30ml
4 - <12 months (6 - <10 60 ml 15 ml 45ml
kg) 80 ml 20 ml 60ml
1 - <3 years (10 - <14 kg)
3 - <5 years (14 - <19 kg)
Note: If you have a 50% glucose solution; to make it 10% use 1 part 50% to 4
parts of normal saline or sterile water. 10% solution can also be prepared from
85% of 5% DW and 15% of 40% DW of the calculated volume.

Give an Anticonvulsant
Diazepam is the first drug to use if the child is convulsing in front of you. No
drug should be given if the convulsion has stopped. Diazepam can be given
by the rectal or intravenous route. Rectal diazepam acts within 2 to 4
minutes. In an emergency, it is easier and quicker to give it rectally than
intravenously, unless an intravenous line is already running. The dose is
0.5mg/kg (0.1 ml/kg) rectally or 0.25mg/kg (0.05 ml/kg) intravenously.
Estimated doses of rectal diazepam, lorazepam and midazolam are shown
in Table 1.9 below.

Draw up the dose from an ampoule of diazepam into a tuberculin (1 ml)

syringe. Then remove the needle. Insert the syringe 4 to 5 cm (about the
length of your little finger) into the rectum and inject the diazepam
solution. Hold the buttocks together for a few minutes. If you already have
intravenous access, you can give the correct volume of drug directly, but
slowly, in at least one full minute. Reassess the child after 10 minutes.

If still convulsing, give a second dose of diazepam, rectally or, even better,
give lorazepam (or diazepam intravenously slowly over 1 minute if an IV
infusion is running). If the convulsion continues in spite of this second dose,
consider giving phenytoin 20mg/kg IV/IO over 20 min (1mg/kg/min)

40
 monitor heart rate for arrhythmia. Alternatively phenobarbital 15-20 mg
/kg IV or intraousues can be used if phenoytoin not available

Table 1.9: Diazepam, lorazepam and midazolam dosages by weight/ age for the treatment of
convulsions
Weight/Age Diazepam Lorazepam Midazolam
Diazepam Diazepam IV/ Buccal IV Buccal
given given IV (4mg/ml (5mg/5ml (5mg/1ml)0.
rectally (10 mg/2ml ampoule) ampoule) 5mg/kg
(10 mg/2ml solution) 0.1mg/kg 0.25mg/kg Volume=0.2
solution) Dose (0.025ml/kg) (0.25ml/kg) 5ml/kg
Dose 0.05ml/kg
0.1ml/kg
4 kg ( <2 mon) 0.4ml 2ml 0.1ml 1ml 0.2ml
6 kg (2-6mon) 0.6ml 0.3ml 0.15ml 1.5ml 0.3ml
8 kg (6-8mon) 0.8ml 0.4ml 0.2ml 2ml 0.4ml
10 kg (8-10 mon) 1ml 0.5ml 0.25ml 2.5ml 0.5ml
12 kg (10-12 mo) 1.2ml 0.6ml 0.3ml 3ml 0.6ml
14 kg (1-3yrs) 1.4ml 0.7ml 0.35ml 3.5ml 0.7ml
16 kg (4-5yrs) 1.6ml 0.8ml 0.4ml 4ml 0.8ml
18 kg (5-6yrs) 1.8ml 0.9ml 0.45ml 4.5ml 0.9ml
20 kg (6-7yrs) 2ml 1ml 0.5ml 5ml 1ml

Diazepam and phenobarbital can affect the child’s breathing; it is

important to reassess the airway and breathing regularly and a bag and
mask should be ready.

Table 1.10: Dose of phenobarbital for young infants (phenobarbital 200mg/ml

solution)
Weight of infant 2 kg or less 2-3 kg
Loading dose of phenobarbital, 20mg/kg, 0.2 ml 0.3 ml
Reload if convulsions continue with 10mg/kg 0.1 ml 0.15 ml

If there is high fever:

 Sponge the child with room-temperature water to reduce the

fever.
 Do not give oral medication until the convulsion has been
controlled (danger of aspiration).

41
1.4 Dehydration
The letter D in the ABCDO stands for Dehydration. These assessments can
take place if those for A, B, and C were all normal, or if emergency
treatments have been given for any problem encountered. If there are no
signs of dehydration, you can move on to look for other emergency signs
and then for priority signs (for assessment and management of
dehydration refer to chapter 5).

1.5 Cardiopulmonary Resuscitation (CPR)

The most important action of preventing death due to cardiac arrest is
anticipation and prevention of the occurrence of cardiac arrest by
intervening when a child manifests in respiratory distress or early stages of
shock.
Step 1: Check patient responsiveness
 Attempt to rouse the patient with verbal or painful stimuli
 If no response, assume that the brain is no longer receiving
adequate oxygen and continue down management pathway for
cardiac arrest
Step 2: Assessment and management of airway
 To assess for a patent airway, use the look/listen/feel approach:
Step 3: Giving rescue breaths

If the airway is patent and spontaneous respiration is not observed or

the child is not breathing adequately, then artificial ventilation should
be initiated.
 Using a bag mask device, give 2 breaths in quick succession and
observe for chest rise (Figure 1.24).
 If bag mask is not available, perform mouth-to-barrier using a
plastic barrier device (Figure 1.25).

 You should be able to observe chest rise with these breaths. If no

chest rise is seen, reposition the head and re-attempt breaths.

42
 Figure 1.25: Mouth to barrier
Figure 1.24: Bag mask technique
device to give rescue breath

 After two breaths are delivered, assess for a pulse.

 In an infant or small child, the pulse should be palpated in the
brachial artery. In an older child, the carotid or radial artery may
be assessed.
 If no pulse is felt after 10 seconds, chest compressions should be
initiated.

Step 4: Chest compressions

 To find the correct hand position in an older child, palpate the

xiphoid process and place hands directly above this area on the
sternum.
 In older children, place one hand on top of the other and push
down onto the chest, making sure to keep your shoulders directly
over your hands and elbows remain locked (Fig 1.26).
 In younger children (<8 years old), hand position is the same as an
older child although only 1 hand is needed for compressions
(Figure 1.27).
 In infants, use 2 fingers in the center of the chest just below the
nipples in one rescuer (Figure 1.28). In the presence of two
rescuers, incircling method is preferable (Figure 1.29).
 The basic principle behind high-quality CPR is that adequate chest
compressions are performed.

43
  The key to adequate compressions is as follows:
o Push fast (rate of 100/min)
o Push hard (about 1/3 to 1/2 of antro-posterior chest
diameter)
o Allow for full chest recoil in between compression and
minimize interruptions
o Rotate rescuers ever 2 minutes or sooner when tired (see
the algorithm for the basic principle of CPR).
Deciding to Terminate Resuscitative Efforts
In the majority of situations, prolonged resuscitative efforts for children are
unlikely to be successful and can be discontinued if there is no return of
spontaneous breathing after 20 minutes of proper CPR.

Figure 1.26: Hand placement Figure 1.27: Hand placement in a

in an older child younger child

44
 Figure 1.28: Hand Figure 1.29: Incircling
placement in an infant method (two rescuers)
(one rescuer)

Neonatal resuscitation
Most babies require basic essential newborn care at and after delivery.
Only few need extra support and resuscitation (see chapter 3).

Common Respiratory Emergencies in Children

Common respiratory emergencies include pneumonia, croup, asthma,
foreign body aspiration and retropharyngeal abscess (refere to chapter 4
for assessment and management of specific conditions)

1.6 Pediatric Trauma

Evaluation of trauma patients

In evaluating trauma patients, a standardized systemic approach reduces

morbidity and mortality. The steps are as follows:

 Primary survey (rapid primary evaluation) and resuscitation of vital

functions; this is usually done simultaneously.
 Utilization of adjuncts to the primary survey and resuscitation
 Secondary survey (detailed history and head to toe examination)
 Transition to definitive care

45
Primary survey

Identify and treat immediate life threatening conditions. This should be

performed in a stepwise approach as follows:

A Airway maintenance with cervical spine protection

B Breathing and ventilation
C Circulation with hemorrhage control
Ds Disability (evaluation of neurologic status)
O/E Exposure and environmental control

Adjuncts to primary survey:

 Consider laboratory studies that need to be done – Hct/Hgb, blood

group and Rh, random blood sugar, urinalysis to look for hematuria,
and liver enzymes (raised liver enzymes may indicate intrabdominal
liver injury)
 Urinary catheter should be placed to monitor urine output as well as
an NG tube (children's stomachs should be assumed to be full)
 If bedside ultrasound is available, consider performing FAST
(Focused Assessment with Sonography for Trauma) exam to assess
for conditions such as intrabdominal bleeding or cardiac tamponade
Secondary survey

Should include a complete head to toe evaluation including:

 history
 complete examination
 laboratory studies
 radiographic studies
 problem identification
Use the mnemonic ‘AMPLE’ to assist in taking history in trauma patients

A Allergies
M Medications
P Past medical and surgical history
L Time of the child's last meal
E Events preceding the accident

46
For further assessment and management of specific trauma, refere to
chapter 9.

1.7 Burn Injury

Burn injury is one of the common injuries in children accompanied by high
risk of mortality and morbidity. The morbidity includes: acute life-
threatening complications (fluid loss, blood loss, airway obstruction, renal
failure, and superinfection) and chronic complications (significant
disfigurement, disability and psychological trauma).

Emergency treatment of burn injury

 Cool the burn area with cold tap water within 30 min for 20 min this
stops the heat as well as decreases the progression of burn, but avoid
it for large area burn as it increases the risk of hypothermia. Use of ice
should also be avoided.
 Similarly don’t use grease (e.g. butter, oil) since it predisposes for
infection and doesn’t disperse heat. If the burn is caused by hot tar,
use mineral oil to remove the tar.
 Remove all clothing and jewelry – especially rings.
Airway & Breathing

 Manage as trauma patient. Since the airway swelling increases in the

next 24 hours, there is a need of early advanced airway management
(intubation or tracheotomy).
 Administer 100% oxygen to displace carbon monoxide during
inhalational burn
Circulation

 Shock is common in children with burns that involve more than 10% to
12% of the total body surface area.
 Secure urgently an IV line for burns of ≥10% of Body Surface Area
(BSA), for all inhalation and electric burns. If possible, IV line should be
on the intact skin but access through burned areas may be secured. If
IV couldn’t be found, use intra-osseous route.

47
 Don’t put adhesive plaster circumferentially to the body as it can cause
circulatory insufficiency.
 For children with severe burn (≥ 20% TBSA) give 20 mL per kg of
crystalloids till assessment of the extent of the burns and calculation of
the rest of the fluid of the 24 hours is completed.
 For most children the Parkland formula is an appropriate starting
guideline for fluid resuscitation (4 mL lactated Ringer/kg/% BSA
burned) in addition to the patient's calculated maintenance fluids after
the 1st bolus is subtracted. Half of the fluid is given in the first 8 hours
of the resuscitation and the remaining half over the next 16 hours.
 Children younger than 5 yrs of age require the addition of 5% dextrose
in the first 24 hr of resuscitation
 Additional fluids may also be necessary when burns are associated
with an inhalation injury, fractures or other traumatic lesions causing
blood loss.
 If patients are not alert and oriented, consider: associated injuries such
as : carbon monoxide (CO) poisoning, inhalation injury, hypoxia and
preexisting medical condition

Indication for Hospital Admission

 burn is >10% of their body

 Burns over Face ,neck ,hands ,feet ,perineum ,or joint ,
 Circumferential burns
 inhalational and high tension electric burns
 suspected child abuse
See chaper 9 for further assessment and subsequent management.

1.8 Common Childhood Poisoning

Suspect poisoning in any unexplained illness in a previously healthy child.

If the child arrives within 1 hour of ingestion of poisons, he/she will be

managed as an emergency because this needs urgent treatment.

48
Primary survey: Assess ABCDO with additional consideration of the
poisoning agent

Airway: Remove excessive secretions; look for any inhalational injury that
might potentially worsen with time. Check for signs of burns in or around
the mouth or of stridor (upper airway/laryngeal damage) suggesting
ingestion of corrosives. Consider consultation for early intubation, if the
patient has severe airway compromise.

Breathing: Look for signs of respiratory distress and give oxygen if

indicated

Circulation: Check the pulse, capillary refill and skin color. If there is shock
treat accordingly

Coma: check the AVPU and pupillary response

 Determine blood sugar and give Dextrose if hypoglycemic or if the

child has reduced level of consciousness, treat as if hypoglycemic.

Dehydration: Assess hydration status (dry tongue, buccal mucosa and

sunken eyeball)

Exposure: Remove all clothing and wash with soap and water and check
body temperature

Secondary survey: more specific evaluation with history and physical

examination and laboratory to identify the exact cause and extent with
simultaneous detoxification of the patient.

History and physical examination

History
 Find out full details of the poisoning agent
 Attempt to identify the exact agent involved requesting to see the
container, where relevant
 Try to find the best estimate of the agent dose or amount (keep in
mind one pill can kill)
 The route of exposure (inhalation, injection, ingestion, contact)

49
  The time of ingestion to presentation (important for the
management of the child)
 Check that no other children were involved

Physical exam
Do detailed examination which help to identify the causes: breath odor,
temperature, eye sign (dilated vs constricted pupil), skin (hot flushed, dry)
and bowel sound.

General Principles of Management

Management of a child with acute poisoning includes four principles:

 Decontamination (GI, skin, eye)

 Enhancing elimination
 Giving antidote and
 Supportive care
Gastrointestinal decontamination

This is most effective if done within one hour of ingestion, and after this
time there is usually little benefit, except with agents that delay gastric
emptying, sustained release preparations and massive pill ingestions.

Methods of gastrointestinal tract (GIT) decontamination includes ipecac

induced vomiting, use of cathartics, gastric lavage, activated charcoal and
whole bowel irrigation (WBI)

Syrup of ipecac and cathartics are not recommended to manage children

with acute poisoning.

Gastric emptying with lavage

Gastric lavage is useful only if it is done within one hour of ingestion of

poisons (especially liquid).

During the procedure:

 Make sure a suction apparatus is available in case the child vomits.

 Place the child in the left lateral/ head down position.

50
  Measure the length of tube to be inserted.
 Pass a 24–28 French gauge tube through the mouth into the
stomach ( as a smaller size nasogastric tube is not sufficient to let
particles such as tablets pass)
 Ensure the tube is in the stomach by aspiration
 Perform lavage with 15 ml/kg/cycle body weight of normal saline
(0.9%) maximum 200 to 400ml
 The volume of lavage fluid returned should approximate to the
amount of fluid given
 Lavage should be continued until the recovered lavage solution is
clear of particulate matter.

Contraindications to gastric lavage are:

 Ingestion of corrosives or petroleum products

 unconscious child with unprotected airway
Activated Charcoal

 It is more effective if used with in 1 hour but may be given as late

as 4 hours if the toxic agent causes delayed intestinal movement
 The usual dose of activated charcoal is 1 g per kg; adolescents
should receive maximum of 50 g
 The amount of water is 8-10 times the amount of the charcoal,
e.g. 5 g in 40 ml of water
 If possible, give the whole amount at once; if the child has
difficulty in tolerating it, the charcoal dose can be divided.
 It can be mixed with caffeine free diet cola or juice to improve the
child’s intake
 Don’t force the child, you can insert NG tube to facilitate intake
Toxins poorly or not adsorbed by charcoal are:

 Caustics (alkali and acids)

 hydrocarbons
 alcohol
 heavy metals (lead)
 iron and lithium

51
Whole Bowel Irrigation (WBI)

 WBI is administration of large volume of polyethylene glycol

solution with balanced electrolyte.
 Usually given by NGT
 Effective after ingestion of slowly absorbed substances, substances
poorly adsorbed to activated charcoal (lithium, iron) and pills
 For children 35ml/kg/hr can be given and adolescents can take 1-2
lts per hour
Skin Decontamination
 Remove all clothing and personal effects and thoroughly clean all
exposed areas with copious amounts of tepid water.
 Use soap and water for oily substances.
 Attending staff should take care to protect themselves from
secondary contamination by wearing gloves and apron.
 Removed clothing and personal effects should be stored safely in a
see through plastic bag that can be sealed, for later cleansing or
disposal.
Eye Decontamination
 Rinse the eye for 10–15 minutes with clean running water or saline,
taking care that the run-off does not enter the other eye by lying on
the side and running into the inner canthus and out of the outer
canthus.
 Evert the eyelids and ensure that all surfaces are rinsed.
 Where possible, the eye should be thoroughly examined under
fluorescein staining for signs of corneal damage.
 If there is significant conjunctival or corneal damage, the child
should be seen urgently by an ophthalmologist.

Decontamination for Inhaled Poisons

 Remove from the source of exposure.
 Urgently call for help
 Administer supplemental oxygen, if there is respiratory distress or
cyanosis or oxygen saturation ≤90%
 Inhalation of poisonous gases may cause swelling and upper airway
obstruction, bronchospasm and delayed pneumonitis

52
Multiple-Dose Activated Charcoal
 This method enhances poison elimination by interfering with
enterohepatic recirculation GI dialysis
 Give 0.25 to 0.5 g/kg every 3 to 4 hour until the patient’s
condition improves
 Considered in drug poising including phenobarbital,
carbamazepine, phenytoin, digoxin, salicylates, and theophylline
Further Management of the Poisoned Child

 Give specific antidote if this is available and indicated

 Keep the child under observation for 4–24 hours depending on the
poison swallowed
 Keep unconscious children in the recovery position.
 Refer the child to the next level health facility, only when
appropriate and where this can be done safely
 If the child is unconscious or has deteriorating conscious level, has
burns to mouth and throat, is in severe respiratory distress, is
cyanosed or is in heart failure, stabilize him/her before referral
Specific poisons
1. Corrosive compounds

 Acid and alkali corrosives are common household agents which

cause immediate severe burning of exposed surfaces, usually with
intense difficulty of feeding. Eg. sodium hydroxide, potassium
hydroxide, acids, bleaches or disinfectants
 Do not induce vomiting or use activated charcoal or gastric lavage
when corrosives have been ingested as this may cause further
damage to the mouth, throat, airway, lungs, esophagus and
stomach.

 Give milk or water within 30 minutes to dilute the corrosive agent.

This is only recommended as first aid in mildly symptomatic
children.

53
  In the event of esophageal injury or perforation, fluids may
extravasate from the esophagus to the mediastinum.
 Don’t try to neutralize with acid/alkaline as this may cause
exothermic reaction may occur that also can worsen esophageal
injury
 Secure IV line. Do not give anything by mouth and arrange referal
for surgical evaluation.

2. Hydrocarbons
These are highly volatile substances which can cause chemical pneumonitis
even after ingestion of small volume

E.g. Kerosene, turpentine substitutes, petrol, benzene

Do not induce vomiting or give activated charcoal or gastric lavage as this

increases aspiration.

Specific treatment includes oxygen therapy if in respiratory distress, do

chest X-ray on presentation and after 6 hours as the first could be normal.
If clinically stable after 6 hours consider discharge.

Don’t give steroid or prophylactic antibiotic unless the patient develops

signs of infections.

3. Organophosphate and carbamate poisoning

 These are commonly used insecticides and herbicides
 Eg. organophosphorus (malathion, parathion, TEPP,
mevinphos/Phosdrin and carbamates (methiocarb and carbaryl)
 These compounds can be absorbed through the skin, ingested or
inhaled.
 The child may have central nervous system symptoms (dizziness,
headache, ataxia, convulsions, and coma)
 Muscarinic effects of these poisons can be memorized with
mnemonic "DUMBBELS"
o Diarrhea
o Urination
o Miosis

54
 o Bradycardia
o Bronchorhea
o Emesis
o Lacrimation
o Salivation
Management
 Remove poison by irrigating eye or washing skin (if in eye or on
skin)
 Give activated charcoal within 1 hours of ingestion, however it
could be given up to 4 hours after ingestion of the poison.
 In a serious ingestion where activated charcoal cannot be given,
consider careful aspiration, do gastric lavage (the airway should be
protected).
 After decontamination, antidotal therapy begins with
administration of atropine sulfate
 Give a dose of 0.05 to 0.1 mg per kg to children and 2 to 5 mg for
adolescents IV or IM. This dose should be repeated every 10 to 30
minutes or as needed until chest secretions and pulmonary rales
cleared.
 Therapy is continued until all absorbed organophosphate has been
metabolized and may require 2 mg to more than 2,000 mg of
atropine for a few hours to several days.
 If muscle weakness develops after atropinization, give pralidoxime
(cholinesterase reactivator) 25–50mg/kg diluted with 15 ml water
by IV infusion over 30 minutes repeated once or twice, or followed
by an intravenous infusion of 10 to 20 mg/kg/hour, as necessary.
4. Paracetamol

Paracetamol is administered about 15-20mg/kg/dose and ingestion of 150-

200mg/kg will cause toxicity in children

 Give activated charcoal within 4 hours of ingestion

 Decide if antidote is required to prevent liver damage: ingestions of
150 mg/kg or more or toxic 4 hour paracetamol level where this is
available.

55
  Antidote is more often required for older children who deliberately
ingest paracetamol or when parents overdose children by mistake.
 If within 8 hours of ingestion give oral methionine or IV
acetylcysteine.
 Methionine can be used if the child is conscious and not vomiting
(<6 years: 1 gram every 4 hours for 4 doses; 6 years or older: 2.5
grams every 4 hours for 4 doses).
 If more than 8 hours after ingestion, or the child cannot take oral
treatment, give IV acetylcysteine.
 For children <20 kg give the loading dose of 150 mg/kg in 3 ml/kg of
5% glucose over 15 minutes, followed by 50 mg/kg in 7 ml/kg of 5%
glucose over 4 hours, then 100 mg/kg IV in 14 ml/kg of 5% glucose
over 16 hours. The volume of glucose can be scaled up for larger
children.
 Continue infusion of acetyl cysteine beyond 20 hours if late
presentation or evidence of liver toxicity.
 If liver enzymes can be measured and are elevated, continue IV
infusion until enzyme levels are falling.
5. Phenobarbital Poisoning

 Phenobarbital is primarily used as anticonvulsant

 Its overdose results in central nervous system depression with
respiratory distress and suppression of skeletal, cardiac and smooth
muscles.
 Poisoned child may present with respiratory depression and
deranged vital signs (hypotension, bradycardia and hypothermia)
 Pupils may constrict early but dilate later

Management

 Initial management of phenobarbital poisoning is supportive and

stabilization of ABCs. Check blood glucose and treat if hypoglycemic
 Give activated charcoal in a dose of 1g/kg for a child (for
adolescents give 50g).
 For patients who have a compromised airway, endotracheal
intubation is advised prior to giving charcoal.

56
  With very large overdoses, antecedent gastric lavage may be
considered.
 The therapeutic range for phenobarbital is generally considered 15
to 40 μg/ mL.
 Since Phenobarbital undergoes enterohepatic circulation, multiple
dose activated charcoal (MDAC) should be given to decrease the
half life of the drug and increase its clearance.
6. Carbon Monoxide Poisoning

 Remove patient from the source

 Give 100% oxygen to accelerate removal of carbon monoxide
(note patient can look pink but still be hypoxemic) until signs of
hypoxia disappear.
7. Snake Bite

Snake bite should be considered in any severe pain or swelling of a limb or

in any unexplained illness presenting with bleeding or abnormal
neurological signs.

The child may present with local signs or systemic signs

 Local signs include pain, swelling, fang marks, tender lymph node
enlargement and local bleeding.
 Initial systemic signs include nausea, vomiting, abdominal pain and
headache.
 Specific signs depend on the venom and its effects. These include:
o Shock, tachycardia, hypotension
o Signs of neurotoxcity: respiratory difficulty or paralysis, ptosis,
bulbar palsy (difficulty swallowing or talking), limb weakness
o Signs of muscle breakdown: coagulopathy-epistaxis, gum
bleeding, bleeding from venipuncture sites, echymosis,
bruising, hemoptysis

 Check hemoglobin and if possible, blood clotting should be

assessed.

57
Management

First aid

 Assess and manage the ABCDO of life (includes treatment for shock
and respiratory arrest)
 Splint the limb below the level of the heart to reduce movement
and absorption of venom
 Apply a firm bandage to affected limb from fingers or toes to
proximal of site of bite
 Irrigate and dress the wound
 Avoid cutting the wound or applying tourniquet
 Paralysis of respiratory muscles can last for days and requires
intubation and mechanical ventilation or manual ventilation (with a
mask or endotracheal tube or tracheostomy ag-valve system) by
relays of staff and/or relatives until respiratory function returns.
Antivenom
 If there are systemic signs or severe local signs (swelling of more
than half of the limb or severe necrosis), refer the child to hospital
where anti-venom is available.
 Prepare IM epinephrine (adrenaline) 10 micrograms/Kg IM (i.e
0.1ml/kg of 1 in 10,000 IM) and IV chlorpheniramine, be ready if
allergic reaction occurs
 Give polyvalent anti-venom if the species is not known
 Follow the directions given on the anti-venom preparation
 The dose for children is the same as for adults
 Dilute the anti-venom in 2–3 volumes of 0.9% saline and give
intravenously over 1 hour
 Give more slowly initially and monitor closely for anaphylaxis or
other serious adverse reactions
 Before you give the anti-venom, perform skin test with 0.02 to 0.03
ml in 1:10 dilution
 If itching/urticarial rash, restlessness, fever, cough or difficult
breathing develop, then stop anti-venom and give epinephrine
(adrenaline) 10 micrograms/kg

58
  More anti-venom should be given after 1–2 hr if the patient is
continuing to bleed briskly or has deteriorating neurologic or
cardiovascular signs.
 Start giving the anti-venom with a minimal dose of 22-40 ml for
mild cases and give a maximum of 200-400 ml for severe cases.
 Response of abnormal neurological signs to anti-venom is more
variable and depends on type of venom
Surgical Management
 Seek surgical opinion if there is severe swelling in a limb, it is
pulseless or painful or there is local necrosis
 Surgical care includes:
o Excision of dead tissue
o Incision of fascial membranes to relieve pressure in limb
compartments, if necessary
o Skin grafting, if extensive necrosis
o Tracheostomy (or endotracheal intubation) if paralysis of
muscle involved in swallowing occurs
Supportive care
 Give fluids orally or by NG tube according to daily requirements
 Keep a close record of fluid intake and output.
 Provide adequate pain relief
 Elevate limb if swollen
 Give prophylaxis for tetanus
 Antibiotic treatment is not required unless there is tissue necrosis
at wound site
 Avoid intramuscular injections
 Monitor very closely immediately after admission, then hourly for
at least 24 hours as envenoming can develop
Drowning
 Initial treatment should be geared towards ensuring adequate
airway, breathing, circulation and consciousness (ABCs).
 Check if there are any injuries especially following diving or an
accidental fall.
 Facial, head and cervical spine injuries are common.
 Give oxygen and ensure adequate oxygenation

59
 Remove all wet clothes
 Use nasogastric tube to remove swallowed water and debris from
the stomach
 Bronchoscopy for removal of foreign material, such as aspirated
debris or vomitus plugs from the airway where necessary
0
 Warm the child externally if core temperature is > 32 C by using
radiant heaters or warmed dry blankets
0 0
 If core temperature is < 32 C use warmed IV fluid (39 C) or do
gastric/ lavage with warmed 0.9% saline
 Check for hypoglycemia and electrolyte abnormalities especially
hyponatremia - this will increase the risk of cerebral edema
 Give antibiotics for possible infection if there are pulmonary signs

60
CHAPTER 2 - DIAGNOSTIC APPROACHES TO THE SICK CHILD

2.1 Relationship to the IMNCI approach

The pocket book is symptom-based in its approach, with the symptoms
following the sequence of the IMNCI guidelines: cough, diarrhea, fever. The
diagnoses also closely match the IMNCI classifications, except that the
expertise and investigative capabilities that are available in a hospital setting
allow classifications like “very severe disease” or “very severe febrile
disease” to be defined more precisely making possible such diagnosis as
severe pneumonia, severe malaria, septicemia and meningitis.
Classifications for conditions such as pneumonia and dehydration follow the
same principles as the IMNCI. Young infants (up to 2 months) and severely
malnourished children are considered separately (as in the IMNCI approach)
because these children require special attention and treatment to reduce
the high mortality in the group.
Any critically sick child must be stabilized after brief history and physical
examination. In hospital, the stages of management for any child are:

 Emergency triage
 Emergency treatment (if required)
 Taking history
 Physical examination
 laboratory investigations (if required)
 making diagnosis or differential diagnosis
 treatment
 supportive care
 monitoring
 planning discharge
 Follow-up
2.2 Taking history
Taking a history generally starts with understanding the presenting
complaint: “Why did you bring the child?” It progresses to the history of
the present illness. The symptom-specific chapters give some guidance on

61
 questions that should be asked about symptoms, which help in a
differential diagnosis of the illness.

These include personal, vaccination, and family, social and environmental

histories. They might lead to important counselling messages, such as
sleeping under a bed net for a child with malaria, breastfeeding or sanitary
practices for a child with diarrhoea, or reducing exposure to indoor air
pollution for a child with pneumonia. In younger infants, the history of
pregnancy and birth is important. The feeding history of infants and
younger children is essential, as this is often when malnutrition begins. For
older children, information on development milestones is important.

Whereas the history is obtained from a parent or caretaker for younger

children, older children can contribute important information. You must
establish a rapport with the child and the parent before starting the
examination. In general, children between the ages of 8 months and 5
years require the most flexible approach.

2.3 Approach to the sick child and clinical examination

All children must be examined fully and systematically so that no important
sign will be missed. Leave the child in the arms of the mother or care taker.
Do not upset the child unnecessarily. Observe as many signs as possible
before touching the child; these include:
 Is the child alert, interested and looking about?
 Is the child irritable
 Does the child appear drowsy?
 Is the child convulsing?
 Is the child vomiting?
 Is the child able to suck or breastfeed?
 Is the child cyanosed or pale?
 Are there signs of respiratory distress?
 Does the child appear to breath fast?
 Is there lower chest wall in-drawing?
 Does the child use auxiliary muscles?

62
  Count the respiratory rate*
Examination recommended checking last:
 Checking for pallor in the palm and finger nails
 Capillary filling in finger nails or sole of foot
 Skin turgor
 Throat examination
 Otoscope examination of the ear
 Auscultation of chest and heart
 Blood pressure measurements
*Ask the mother or caretaker to cautiously reveal part of the chest to look for
lower chest wall in-drawing to count the respiratory rate and at the same time
observe if there is use of auxiliary muscles. If a child is disturbed or crying, it
might need to be left for a brief time with its mother in order to settle, or the
mother could be asked to breastfeed, before key signs such as respiratory rate
can be measured.

2.4 Laboratory investigations

Laboratory investigations have to be targeted based on the history and
physical findings and aimed to narrow the differential diagnosis. The
following basic laboratory investigations should be available in all small
hospitals which provide pediatric care in Ethiopia:
 CBC (Hct, WBC with differential, platelets and RBC indices)
 Blood smear for malaria parasites
 Blood glucose
 Urine analysis including microscopy
 Stool microscopy
 CSF analysis and microscopy
 Blood grouping and cross-matching
 HIV counseling and testing.
In the care of sick newborns (under 1 week old), blood bilirubin (total
and direct) is also an essential investigation.
Other investigations, such as pulse oximetry, chest X-ray, culture and
sensitivity tests (blood, urine, stool, CSF) can help in complicated cases.

63
Indications for these tests are outlined in the appropriate sections of this
pocket book.

2.5 Differential diagnoses

After the assessment has been completed, consider the various conditions
that could cause the child’s illness and make a list of possible differential
diagnoses. This helps to ensure that wrong assumptions are not made, a
wrong diagnosis is not chosen, and rare problems are not missed. Remember
that a sick child might have more than one diagnosis or clinical problem
requiring treatment.
After the main diagnosis and any secondary diagnoses or problems have been
determined, treatment should be planned and started. Once again, if there is
more than one diagnosis or problem, the treatment recommendations for all
of them may have to be taken together. It is necessary to review the list of
differential diagnoses again at a later stage after observing the response to
treatment, or in the light of new clinical findings. The diagnosis might be
revised at this stage, or additional diagnoses included in the considerations.

64
CHAPTER 3 - PROBLEMS OF THE NEWBORN AND THE YOUNG
INFANT

This chapter provides guidance for the management of problems in

newborns and young infants from birth to 2 months of age. This includes
neonatal resuscitation, the recognition and management of neonatal sepsis
and other bacterial infections, and the management of low and very low
birth weight (VLBW) infants and other common neonatal problems. Drug
tables for commonly used drugs in neonates and young infants are
included at the end of this chapter, also providing dosages for low birth
weight and premature babies.

3.1 Routine care of the newborn at delivery

Most of the newborns require only simple supportive care at and after
delivery

Standardized procedures in Essential Newborn Care (ENC)

Step 1: Dry and stimulate

 Deliver the newborn on the abdomen of the mother

 Immediately dry the whole body including the head and limbs, if no
meconium
 If there is meconium, thick mucus, or blood, suction the mouth and
nose before proceeding to drying
 Stimulate by rubbing the back or tapping or flicking the soles of the
feet
 Don’t let the baby remain wet, as this will cool the baby and make it
hypothermic

65
 Remove the wet towel and change with another dry and clean towel.
Don’t let the baby remain wet, as this will cool the baby and make it
hypothermic
 Let the baby stay in skin-to-skin contact on the abdomen and the
whole body of the baby (including the head) should be covered with
the second clean and dry towel
Step 2: Evaluate Breathing
 Check if the baby is crying while drying it. If the baby does not cry, see
if the baby is breathing properly
 If the baby is crying or breathing well, continue routine essential
newborn care
 If the baby is not breathing and/or is gasping, clear the airways warm
and stimulate by rubbing the back or tapping or flicking the soles of
the feet. Provide routine care if the baby starts to breath
spontaneously after this first maneuver.
 If the baby is still not breathing and/or is gasping after initial
maneuver, cut the cord rapidly and take the baby to the newborn
corner to start bag and mask ventilation within the first golden minute.
 If the baby breathes well, after the bag and mask ventilation, continue
routine essential newborn care but monitor the baby after placing him
with the mother.
 Do not do suction of the mouth and nose as a routine. Do it only if
there is meconium, thick mucus, or blood.

66
Normal breathing

Normal breathing rate in a newborn baby is 30 to 60 breaths per

minute. The baby should not have any chest in-drawing or grunting.
Small babies (less than 2.5 kg at birth or born before 37 weeks
gestation) may have some mild chest in-drawing and may periodically
stop breathing for a few seconds.

Do not do suction of the mouth and nose as a routine. Do it only if there

is meconium, thick mucus, or blood.

Step 3: Cord Care

Optimal cord care consists of the following:

 Clamping/tying the cord: If the baby does not need bag and mask
ventilation, wait for cord pulsations to cease or approximately 1-3
minutes after birth, whichever comes first, and then place one single
use clamp /cord tie 2 centimeters from the baby’s abdomen and the
second single use clamp/cord tie another 2 centimeters from the first
single use clamp/cord tie.

 Cutting the cord soon after birth can decrease the amount of blood
that is transfused to the baby from the placenta and, in preterm
babies, it is likely to result in subsequent anemia and increased
chances of needing a blood transfusion

 Cutting the cord: Cut the cord in between the two clamps/ties with
sterile scissors or surgical blade, under a piece of gauze in order to
avoid splashing of blood. At every delivery, a clean separate pair of
scissors or blade should be designated for this purpose.

67
Counseling on cord care
 Check for bleeding/oozing and retie if necessary.
 The cord may be tied by using sterile cotton ties, elastic bands, or pre -
sterilized disposable cord tie.
 Advise the mother not to cover the cord with the diaper
 Don’t use bandages as it may delay healing and introduce infection
 Don’t use alcohol for cleansing as it may delay healing.
 Don’t apply traditional remedies to the cord as it may cause tetanus or
other infections
 Apply 4% chlorhexidine gel immediately after cutting the cord and
continue applying once daily for 7 days to prevent infection
Watch out for:
 Purulent discharge or bleeding from the cord stump
 Redness around the cord especially if there is swelling
 Fever or feels hot/cold or other signs of infection.
Step 4: Keep the newborn warm (prevent hypothermia)
 Keep the baby warm by placing it in skin-to-skin contact on the
mother’s chest.
 Cover the baby’s body and head with clean cloth. If the room is cool
0
(<25 C), use heater to warm the room or use a blanket to cover the
baby over the mother.
Step 5: Initiate breastfeeding in the first one hour
Check for the readiness of the baby to breast feed
 Eyes open
 The baby’s head slightly back
 Tongue down and forward
 Mouth open
 Licking movements

68
Skin-to-skin contact and early breastfeeding are the best ways to keep an
infant warm and prevent hypoglycaemia. Term and low-birth-weight
neonates weighing <2000g should be put in prolonged skin-to-skin contact
with the mother soon after birth after they have been dried thoroughly to
establish faster stabilization and to prevent hypothermia.
 Early breastfeeding means breastfeeding within the first hour,
with counseling for correct positioning and attachment.
 Early breastfeeding reduces the risk of postpartum hemorrhage
for the mother.
 Colostrum (the “first milk”) has many benefits for the baby,
especially anti-infective properties.
 Breastfeeding delays the mother's return to fertility because of
lactation.
Breast feeding provides the best possible nutrition for the baby. Feed day
and night, at least 8 times in 24 hours, allowing on-demand sucking by the
baby.

 If the baby is small (<2,500 grams), wake the baby to feed every 2
hours
 If the baby is not feeding well, seek help
 Successful breastfeeding requires support for the mother from the
family and health institutions
 There is no need for extra water for normal babies, even in hot
climates
 Avoid use of bottles or pacifiers

69
Step 6: Administer eye drops/eye ointment
 Wash your hands with soap and water
 Clean eyes immediately after birth with swab soaked in sterile
water, using separate swab for each eye.
 Clean from medial to lateral side.
 Apply tetracycline eye ointment/drops within 1 hour of birth
usually after initiating breast feeding.
 Advise the mother not to put anything else in baby's eyes as it can
cause infection and towatch out for discharge from the eyes,
especially with redness and swelling around the eyes.
Step 7: Administer vitamin K Intramuscularly (IM) to all newborns
Vitamin K protects babies from serious bleeding that may result in death or
brain damage. Every newborn should be given vitamin K
 1 mg for babies with gestational age of 34 weeks or above
 0.5 mg for premature babies less than 34 weeks gestation
Step 8: Place the newborn’s identification bands on the wrist and ankle
 Put identification bands with the names of the mother, the father,
and the date and time of birth on the hands and/or ankle.
Step 9: Weigh the newborn when it is stable and warm
 Place the naked baby on the paper/linen. If the linen is large,
cover the baby with the cloth.
 Never leave the baby unattended on the scale.
 Inform the mother the weight of newborn

70
Step 10: Record all observations, weight and treatment provided in the
registers/appropriate chart/cards
Note:
 Defer the bath for at least 24 hours.
 Clean the newborn of an HIV-infected mother as recommended
 Organize transport if necessary
 Give immunization per the national EPI schedule
 A complete examination should be performed within 90 minutes
of birth or whenever the baby appears unwell.
3.2 Neonatal resuscitation
For some babies the need for resuscitation may be anticipated: those born
to mothers with chronic illness, where the mother had a previous fetal or
neonatal death, a mother with pre-eclampsia, in multiple pregnancies, in
preterm delivery, in abnormal presentation of the fetus, with a prolapsed
cord, or where there is prolonged labor or rupture of membranes, or
meconium-stained liquor. However, for many babies the need for
resuscitation cannot be anticipated before delivery.

71
Chart 3.1.A: Neonatal resuscitation

Therefore, be prepared for resuscitation at every delivery.

Follow the assessment steps of chart 3.1A (Essential Newborn Care)

72
Chart 3.1.B: Neonatal resuscitation Steps and process

73
Chart 3.1.C: Neonatal resuscitation

74
Post Resuscitation Care
Infants who require resuscitation are at risk for deterioration after their
vital signs have returned to normal. Once adequate ventilation and
circulation has been established:
 Stop ventilation
 Return to mother for skin-to-skin contact as soon as possible
 Closely monitor breathing difficulties, signs of asphyxia and
anticipate need for further care.
Cessation of resuscitation
It is appropriate to consider discontinuing after effective resuscitation
efforts if:
Infant is not breathing and heartbeat is not detectable beyond 10 min, stop
resuscitation.
If no spontaneous breathing and heart rate remains below 60/min after 20
min of effective resuscitation, and where advanced care is not available,
discontinue active resuscitation
Record the event and explain to the mother or parents that the infant has
died. Give them the infant to hold if they wish so.

3.3 Prevention of neonatal infections

Many early neonatal infections can be prevented by:
 Avoid unnecessary separation of the newborn from the mother,
e.g. baby unit
 Hand-washing before delivering and handling the infant
 Good basic hygiene and cleanliness during delivery Appropriate
umbilical cord care

75
Give prophylactic antibiotics only to neonates with documented risk factors
for infection:
 Membranes ruptured > 18 hr before delivery
o
 Mother had fever > 38 C before delivery or during labor
 Amniotic fluid was foul smelling or purulent.
 Give IM or IV ampicillin and gentamicin for at least 2 days and
reassess; continue treatment only if there were signs of sepsis (or
a positive blood culture).
Many late neonatal infections are acquired in hospitals. These can be
prevented by:
 Exclusive breastfeeding
 Strict procedures for hand-washing or alcohol hand rubs for all
staff and for families before and after handling infants
 Using Kangaroo mother care and avoiding routine use of
incubators for preterm infants. If an incubator is used, do not use
water for humidification (where Pseudomonas will easily colonize)
and ensure that it was thoroughly cleaned with an antiseptic.
 Strict sterility for all procedures
 Clean injection practices
 Removing intravenous drips when they are no longer necessary
3.4 Management of infants with hypoxic ischaemic encephalopathy
Hypoxic ischaemic encephalopathy can result from lack of oxygen to vital
organs before, during or immediately after birth. The initial treatment is
effective resuscitation as above.
Problems during the days after birth:

76
  Convulsions: Treat with Phenobarbital; ensure hypoglycaemia is
not present (check blood glucose).
 Apnoea: common after severe birth asphyxia; sometimes
associated with convulsions. Resuscitate with bag and mask, and
manage with oxygen by nasal prongs.
 Inability to suck: Feed with expressed breast milk via a nasogastric
tube or cup. Avoid delayed emptying of the stomach, which may
lead to regurgitation of feeds.
 Poor motor tone: Floppy or with limb stiffening (spasticity):
physiotherapy
Prognosis can be predicted by recovery of motor function and sucking
ability. An infant who is normally active will usually do well. An infant who,
within a week of birth, is still floppy or spastic, unresponsive and cannot
suck has a severe brain injury and will do poorly. The prognosis is less grim
for infants who have recovered some motor function and are beginning to
suck. The situation should be sensitively discussed with parents throughout
the time the infant is in hospital.
3.5 Danger signs in newborns and young infants
Neonates and young infants often present with non-specific symptoms and
signs that indicate severe illness. These signs might be present at or after
delivery or in a newborn presenting to hospital or develop during hospital
stay. The aim of initial management of a neonate presenting with these
signs is stabilization and preventing deterioration. The signs include:
 not feeding well
 convulsions
 drowsy or unconscious

77
  movement only when stimulated or no movement at all
 fast breathing (>60 breaths per min)
 grunting
 severe chest indrawing
 raised temperature, > 38 °C
 hypothermia, < 35.5 °C
 central cyanosis
 severe jaundice
 severe abdominal distension

Emergency management of danger signs

 Open and maintain airway. Give oxygen by nasal prongs if the
young infant is cyanosed or in severe respiratory distress or
hypoxaemic (oxygen saturation ≤ 90%).
 Give bag and mask ventilation with oxygen (or room air if oxygen
is not available) if there is apnoea, gasping or respiratory rate too
slow (< 20).
 Insert venous cannula.

Give ampicillin (or penicillin) and gentamicin (see below)

If drowsy, unconscious or convulsing, check blood glucose. If glucose < 2.2
mmol/l (< 40 mg/100 ml), give 10% glucose at 2 ml/kg IV push. Then give a
sustained IV infusion of 5 ml/kg per hour of 10% glucose while oral feeds
are built up and glucose level normalizes.
If you cannot check blood glucose quickly, assume hypoglycaemia and give
glucose IV. If you cannot insert an IV drip, give expressed breast milk or
10% glucose 2 ml/kg push and then 5 ml/kg per hour through a nasogastric
tube.

78
  Give phenobarbital if convulsing.
 Admit.
 Give vitamin K (if not given before).
 Monitor the infant frequently (see below).
3.6 Convulsions
The commonest causes of neonatal convulsions include:
 hypoxic ischaemic encephalopathy (as a result of perinatal
asphyxia)
 central nervous system infection
 hypoglycaemia
 hypocalcaemia

Treatment
Management of the neonate or young infant who is having a fit:
 Manage the airway and breathing.
 Ensure circulatory access.
 If hypoglycaemic, give glucose IV or via NG tube (2 ml/kg of 10%
glucose). If blood glucose cannot be measured, give empirical
treatment with glucose.
Treat convulsions with phenobarbital (loading dose 20 mg/kg IV). If
convulsions persist, give further doses of phenobarbital 10 mg/kg up to a
maximum of 40 mg/kg. Watch for apnoea. Always have a bag-mask
available. If needed, continue phenobarbital at a maintenance dose of 5
mg/kg per day. If hypocalcaemic, symptoms may settle if the infant is given
2 ml/kg of 10% calcium gluconate? Preparation and dosage/monitoring as a
slow IV infusion, and continue with oral supplementation.
 Rule out central nervous system infection. Treat if present (see
below).

79
3.7 Serious bacterial infection
Newborns with documented risk factors are more likely to develop serious
bacterial infection. All of the danger signs listed in section 3.5 are signs of
serious bacterial infection, but there are others.
Localizing signs of infection are:
 signs of pneumonia
 many or severe skin pustules
 umbilical redness extending to the peri-umbilical skin
 umbilicus draining pus
 bulging fontanelle (see below)
 painful joints, joint swelling, reduced movement and irritability if
these parts are handled
Treatment
Antibiotic therapy

 Empirical antibiotics should be given to a newborn with suspected

neonatal sepsis.
 Admit to hospital.
 When possible, do a lumbar puncture and obtain blood cultures
before starting antibiotics.
For newborns with any signs of serious bacterial infection or sepsis, give
ampicillin (or penicillin) and gentamicin as first-line antibiotic treatment
(for dosages, see Table 3:14 below)
 If at greater risk of staphylococcus infection (extensive skin
pustules, abscess or omphalitis in addition to signs of sepsis), give
IV cloxacillin and gentamicin.
 The most serious bacterial infections in newborns should be
treated with antibiotics for at least 7–10 days.
 If an infant is not improving within 2–3 days, change the antibiotic
treatment or refer the infant for further management

80
Other treatment
 If the infant is drowsy or unconscious, ensure that hypoglycaemia
is not present if it is, give 2 ml/kg 10% glucose IV.
 Treat convulsions with phenobarbital
 For management of pus draining from eyes,
 If the child is from a malarious area and has fever, take a blood fi
lm to check for malaria. Neonatal malaria is very rare. If
confirmed, treat with artesunate or quinine
 For supportive care

3.8 Neonatal Meningitis

Clinical signs
Suspect meningitis if signs of serious bacterial infection are present,
particularly if any one of the following is present:
The infant is:
 Drowsy, lethargic or unconscious
 Convulsing
 Has a bulging fontanelle
 Irritable
 Has a high-pitched cry.
It is important to attempt lumbar puncture once the infant has been
stabilized, ideally within 2 hours of initiating antibiotic treatment, because
it serves to confirm the diagnosis.

81
 Normal fontanelle Bulging fontanelle

Figure 3.1: Bulging fontanelle – sign of meningitis in young infants

with an open fontanelle

Treatment
 The first-line antibiotics are ampicillin and gentamicin for 3 weeks
 Alternatively, give a third-generation cephalosporin, such as
ceftriaxone (50 mg/kg every 12 hr) or cefotaxime (50 mg/kg every
12 hour if < 7 days or every 6–8 hourr if > 7 days of age), and
gentamicin for 3 weeks.
 If there are signs of hypoxaemia, give oxygen
 If the infant is drowsy or unconscious, ensure that hypoglycaemia
is not present if it is, give 2ml/kg 10% glucose IV.Treat convulsions
(after ensuring they are not due to hypoglycaemia or hypoxaemia)
with phenobarbital Make regular checks for hypoglycaemia.
3.9 Supportive care for sick neonates
Neonatal Thermoregulation
Hypothermia
0 0
The normal body temperature is between 36.5 C -37.5 C.
0
Hypothermia is defined as skin (axillary) temperature less than 36.5 C.

82
Newborns are at risk of hypothermia because of their large surface area
for small body mass.
Prevention
Before delivery:
 Warm the delivery room
 Organize newborn corner with adequate heat source
At delivery:
 Dry the baby thoroughly immediately after birth and remove wet
clothes.
 Use cap to prevent significant heat loss through the scalp
 Keep the newborn in skin to skin contact with the mother
 Keep the newborn under pre-heated radiant warmer–if
resuscitation is needed
 Cover weighing scales with warm towel
 Initiate early breast feeding

Subsequent care
 Arrange appropriate transportation if needed
 Postpone bathing (bath after 24 hours)
 Warm hands and stethoscope before touching the baby
 Do examination/resuscitation of the infant under the radiant
warmer
 Practice rooming in wards/post natal rooms
 Keep the newborn away from windows and drafts
 Continue breast feeding

83
General management
 Identify and treat cause of hypothermia (disease process and
environmental conditions)
 Put hypothermic infants on KMC, in incubators or under radiant
warmer.
 Warm the new born slowly (see management of severe
hypothermia)
 Monitor axillary temperature every 30 minutes till newborn
temperature becomes stable
Monitor environmental temperature
Management of newborns with severe hypothermia
 Warm the baby using a pre-warmed radiant warmer.
 Remove cold or wet cloths.
 Cover the baby with warm clothes and hat.
 Treat for sepsis ,if present
 Measure blood glucose and treat if hypoglycemic.
 Keep IV line under the radiant warmer to warm the fluid.
 Measure the baby’s temperature every hour.
 If the baby’s temperature is increasing at least 0.5 °C per hour in
st
the 1 three hours, re-warming is successful.
 Then measure the baby’s temperature every two hours.
If the baby’s temperature does not rise or is rising more slowly than 0.5°C
per hour, check and reset temperature of the warmer.
Once the baby’s temperature is normal, measure the temperature every
three hours for 12 hours and then 12 hourly.
 Monitor for complications and manage accordingly

84
 o Look for respiratory problems
o Monitor vital signs
o Monitor urine output
o Monitor blood sugars
o Look for signs multi organ failure
 Dangers of warmers
 Hyperthermia
 Dehydration
 Mask serious infections
o
Fever: is considered when axillary temperature is above 37.5 C.
The most common cause of high temperature (fever) in newborns and
young infants is environmental temperature; however infection has to be
ruled out. Do not use antipyretic agents such as paracetamol for controlling
fever in young infants. Control the environment. If necessary, undress the
child and investigate for possible bacterial infection.

Signs of high temprature

 The newborn will be tachypnic
 Excessive sweating
 Flushed, bright and pink skin
Management
 Initiate early and frequent breast feeding
 Keep the baby away from source of excessive heat
 Remove extra cloths
 Look for possible causes including infections and treat accordingly.

85
Fluid management
 Encourage the mother to breastfeed frequently to prevent
hypoglycaemia. If the infant is unable to feed, give expressed
breast milk by nasogastric tube or cup.
 Withhold oral feeding if there is bowel obstruction, necrotizing
enterocolitis, or the feeds are not tolerated, indicated e.g. by
increasing abdominal distension or vomiting everything.
 Withhold oral feeding in the acute phase in infants who are
lethargic, unconscious or having frequent convulsions.
If IV fluids are given, reduce the rate as the volume of oral or gastric milk
feeds increases. IV fluids should ideally be given with an in-line burette to
ensure the exact doses of fluids prescribed.

Increase the amount of fluid given over the first 3–5 days (total amount,
oral plus IV).

 Day one 60 ml/kg per day

 Day two 90 ml/kg per day
 Day three 120 ml/kg per day
Then increase to 150 ml/kg per day

When the infant tolerates oral feeds well, the amount of fluid might be
increased to 180 ml/kg per day after some days. Be careful in giving
parenteral IV fluids, which can quickly overhydrate a child. Do not exceed
100 ml/kg per day of IV fluids, unless the infant is dehydrated or under
phototherapy or a radiant heater. (You can add 10% extra fluid during such
circumstances)

This amount is the total fluid intake an infant needs, and oral intake must
be taken into account when calculating IV rates.

86
  Give more fluid if the infant is under a radiant heater (1.2–1.5
times).
 During the first 2 days of life give 10% glucose infusion IV. Do not
use IV glucose without sodium after the first 2 days of life. Suitable
alternative IV fl uids after the fi rst 2 days are half normal saline
and 5% dextrose.
Monitor the IV infusion very carefully (ideally through an in-line burette).

 Use a monitoring sheet.

 Calculate the drip rate.
 Check the drip rate and volume infused every hour.
 Weigh the infant daily.
 Watch for facial swelling: if this occurs, reduce the IV fl uid to a
minimum or take out the IV line. Introduce breastfeeding or milk
feeding by orogastric or nasogastric tube as soon as it is safe to do
so
Oxygen therapy
Give oxygen to neonates or young infants with any of the following:
 central cyanosis or gasping
 grunting with every breath
 difficulty in feeding due to respiratory distress
 severe lower chest wall indrawing, head nodding (i.e. a nodding
movement of the head, synchronous with the respiration
indicating severe respiratory distress)
Use a pulse oximeter to guide oxygen therapy. Oxygen should be given if
the oxygen saturation is ≤ 90%, and the oxygen flow should be regulated to
maintain saturation of > 90%. Oxygen can be discontinued once the infant

87
can maintain saturation> 90% in room air. Nasal prongs are the preferred
method for delivering oxygen to this age group, with a flow rate of 0.5–1
litre/min, increased to 2 litres/min in severe respiratory distress to achieve
oxygen saturation > 90%.

Thick secretions should be cleared from the throat by intermittent suction

under direct observation, if they are obstructing the airway and the infant
is too weak to clear them. Oxygen should be stopped when the infant’s
general condition improves and the above signs are no longer present.
3.10 Preterm and low-birth-weight infants
3.10.1 Infants with a birth weight of 2.0–2.5 kg (35–36 weeks’ gestation)
These infants are usually strong enough to breastfeed and maintain their
body temperature. Start feeds within 1 hour of delivery. Their mothers
usually need additional support for exclusive breastfeeding. They should be
kept warm at all times. All low-birth-weight infants are at risk of infection
and should be closely observed for infection control.

3.10.2 Infants with a birth weight < 2.0 kg (< 35 weeks’ gestation)
All infants with a gestation < 35 weeks or a birth weight < 2.0 kg should be
admitted to a special care unit. These infants are at risk of hypothermia,
feeding problems, apnoea, respiratory distress syndrome and necrotizing
enterocolitis. The smaller the infant, the higher the risk. The risks
associated with keeping the child in hospital (e.g. hospital-acquired
infections) should be balanced against the potential benefit of better care.

See the infants at least twice a day to assess feeding ability, fluid intake or
the presence of any danger signs or signs of serious bacterial infection. If
any of these signs is present, it should be closely monitored. Management
of common problems is discussed below.

Feeding
Many low-birth-weight infants will be able to suckle at the breast. Infants
who can suckle should be breastfed. Those who cannot breastfeed should
be given expressed breast milk with a cup and spoon. When the infant is

88
sucking well at the breast and gaining weight, reduce the cup feeds. Infants
unable to feed from a cup and spoon should be given intermittent bolus
feeds through a gastric tube.

Feed the infant only the mother’s own milk. In exceptional situations, when
this is not possible, donated human milk should be given, if safe milk-
banking facilities are available. Formula should be given only if neither of
the above is possible.

Special feeding considerations for infants weighing < 1.5 kg at birth

These infants are at the highest risk of feeding problems and necrotizing
enterocolitis. The smaller the infant, the higher the risk.
Starting on the first day, give 10 ml/kg per day of enteral feeds, preferably
expressed breast milk, with the remaining fluid requirement at 50 ml/kg
per day met by IV fluids. If the infant is well and active and not receiving IV
fluids, give 2–4 ml of expressed breast milk every 2 hr through a
nasogastric tube, depending on the weight of the infant.

If the infant cannot tolerate enteral feeds, give IV fluids at 60 ml/kg per day
for the first day of life. It is best to use a paediatric (100 ml) intravenous
burette; 60 drops=1 ml, therefore one drop per minute = 1 ml/hr.

Check blood sugar every 6 hr until enteral feeds are established, especially
if the infant is apnoeic, lethargic or convulsing. Very low-birth-weight
infants may need a 10% glucose solution.

Start enteral feeding when the condition of the infant is stable and there is
no abdominal distension or tenderness, bowel sounds are present,
meconium passed and no apnoea.

 Calculate exact amounts for feeding and the timing of feeds.

 Use a prescription chart.
 Increase daily if well tolerated.

89
When commencing milk feeds, start with 2–4 ml every 1–2 hours by
orogastric or nasogastric tube. Some active very-low-birth-weight infants
can be fed with a cup and spoon or an eyedropper, which must be
sterilized before each feed. Use only expressed breast milk if possible. If a
2–4-ml volume is tolerated with no vomiting, abdominal distension or
gastric aspirates of more than half the feed, the volume can be increased
by 1–2 ml per feed each day. Reduce or withhold feeds if there are signs of
poor tolerance.
Aim to establish feeding within the fi rst 5–7 days so that the IV drip can be
removed, to avoid infection.
The feeds may be increased during the fi rst 2 weeks of life to 150–180 ml/
kg per day (3-hourly feeds of 19–23 ml for a 1-kg infant and 28–34 ml for a
1.5-kg infant). As the infant grows, recalculate the feed volume on the basis
of the higher weight.
Give daily supplements when the infant is accepting full enteral feeds:
 Vitamin D at 400 IU
 Calcium at 120–140 mg/kg
 Phosphorus at 60–90 mg/kg.
 Start iron supplements at 2 weeks of age at a dosage of 2–4 mg/kg
per day Until 6 months of age.
Preventing hypothermia
Low-birth-weight neonates (weighing <2000 g) should be given Kangaroo
mother care starting soon after birth and ensured at all times, day and
night. (See section on Kangaroo mother care)
If the mother is unable to provide Kangaroo mother care, a clean incubator
can be used. Incubators should be washed with disinfectant between

90
infants and should be of a basic design that can be used appropriately by
the staff available.
3.11 Kangaroo Mother Care (KMC)
“Let nature do the nurturing”. The common problems of small
babies–hypothermia, hypoglycaemia, and hypoxia-are alleviated, if

Figure 3.2: KMC

not cured, by a common solution: kangaroo mother care (KMC). ALL

facilities with maternity services SHOULD implement KMC as routine
practice.

What is KMC?
Kangaroo mother care consists of skin-to-skin care of babies (usually low
birth weight or very low birth weight). KMC also promotes early and
exclusive breastfeeding, but may be used even when babies are formula
fed.

What are the cornerstones of KMC?

Kangaroo Position
Dress the baby in a nappy and cap and place in an upright position against
the mother’s bare chest, between her breasts and inside her blouse. One
may use a special garment, or one can tuck the mother’s blouse under the

91
baby or into her waistband. Cover both mother and baby with a Gabi,
blanket or jacket if it is cold. You too can be innovative.
Steps in positioning the baby for KMC:
1. Dress the baby in socks, a nappy, and a cap.
2. Place the baby between the mother’s breasts.
3. Secure the baby on to the mother’s chest with a cloth
4. Put a blanket or a shawl on top for additional warmth.
5. Instruct the mother to put on a front-opened top: a top that opens at the
front to allow the face, chest, abdomen, arms and legs of the baby to
remain in continuous skin-to-skin contact with the mother’s chest and
abdomen.
 Instruct the mother to keep the baby upright when walking or
sitting.
 Advise the mother to have the baby in continuous skin-to-skin
contact 24 hours a day (or less in the case of intermittent KMC).
 Advise the mother to sleep in a half sitting position in order to
maintain the baby in a vertical position.

Figure 3.3: KMC Position

92
Securely wrap the baby with a cloth tied around the mother. (Illustration
adapted from Home Based Life Saving Skills - Baby Information. Buffington,
Sibley, Beck and Armbruster, 2004. American College of Nurse-Midwives,
ISBN 0-914324-09-8.)
Kangaroo Nutrition
Babies who are unable to suckle should be fed expressed breast milk via a
nasogastric tube or cup if they can swallow. Keep babies in the KMC
position whilst being tube fed. Allow them to try to suckle during the tube
feed.
In the KMC position, babies will declare themselves ready to suckle, as their
rooting and suckling reflexes become manifest. Once the baby is able to
suckle, allow the baby to breast feed on demand but at least every 2-3
hours.
Kangaroo Support
It is very important to explain and demonstrate to the mother until she is
motivated and confident to try the kangaroo position. Assist the mother
with positioning and feeding, and give emotional support. The concept
should be explained to other family members (especially the maternal
grandmother), and they can also practice KMC (especially the father).
When do we start KMC?
Intermittent KMC can be practiced while the baby is still in NICU. It is
possible even with babies on oxygen and IV therapy. Frequency is
determined by how stable baby is. A common sense approach is best.
 Continuous KMC can be instituted once the baby is stable, suckling
well and needs no additional care. The baby can then be transferred to

93
 an adjoining KMC ward. Smaller babies may be able to go onto
continuous KMC if they are stable and do not require oxygen.

What is the daily routine of a KMC Ward?

Monitoring
Babies should be weighed daily, and feeds adjusted according to weight
gain. If not yet breastfeeding on demand, they should receive
175ml/kg/day, in 8 feeds 3 hourly.
Babies on oxygen should have their oxygen saturation monitored 3 hourly.
The Basic Neonatal Nursing Observation chart can be used.
When to discharge from the hospital
Discharge:
 when the baby has a sustained weight gain of at least 15 grams
/kg /day for three consecutive days
 when the baby can maintain temperature in a normal range for
three days
 when the baby is able to suck breast adequately
 if the mother is confident and able to give KMC at home
Bring the baby back for follow up in the next few days to ensure that baby
is well and growing. It is advised practice to follow up KMC babies in a
designated place.
Where do we do continuous KMC?
The KMC ward should be in close proximity to the Neonatal Unit and under
the supervision of the neonatal staff, with 24 hour nursing coverage. The
ward should be comfortable, homely and warm but not heated. There
should be no cribs.

94
Discharge from KMC position
Discharge from the kangaroo positions is usually determined by the babies
themselves. When babies are about 40 weeks post menstrual or when their
weight is about 2500 grams (whichever comes first), babies will not be
comfortable in kangaroo position and move a lot to indicate that they no
more need the position. Then the health worker or the mother needs to
discharge the baby from the kangaroo position.

3.12 Common problems of low-birth-weight infants

Respiratory distress syndrome
Preterm infants are at risk for respiratory distress syndrome due to
surfactant deficiency. This can be reduced if pregnant mothers at risk for
premature delivery (e. g. premature contractions or premature rupture of
membranes) are given dexamethasone at two doses of 12 mg 24 h apart.
Respiratory distress usually occurs in a preterm infant during the fi rst 3
days of life. It is a self-limiting condition, because birth triggers an increase
in surfactant production.
The challenge is to support the infant for the fi rst few days of life until such
time as the deficiency resolves.
The key clinical features usually become obvious within 4 h of birth and
include:
 tachypnoea
 an expiratory ‘grunt’
 intercostal and/or subcostal recession and cyanosis.
Treatment
The principles of treatment are:
 minimal handling of the infant

95
  supplementary oxygen if needed to keep the oxygen saturation >
90% but < 95% to avoid eye damage
 initially no oral feeding
 IV fl uids (see above)
 maintenance of a normal temperature range
 IV antibiotics for neonatal sepsis, as it is diffi cult to exclude
pneumonia as a cause of respiratory distress
Continuous positive airway pressure (CPAP) is used, even in expiration, to
prevent airway collapse, improve oxygenation and reduce breathing
fatigue.
If there is persistent respiratory distress or hypoxaemia, do chest X-ray to
check for pneumothorax.
Apnea
It is a disorder of respiratory control characterized by absence of air flow
for ≥20 seconds or less than that if it is accompanied by bradycardia (heart
rate <100/min) or cyanosis. It is classified in to three types:
1. Central – no airflow, no respiratory efforts
2. Obstructive – no airflow, despite respiratory efforts

3. Mixed – often begins as central and later becomes obstructive

It commonly occurs in premature newborns due to immaturity of brain
functions and generally begins 1 or 2 days after birth. In term newborns, it
occurs in association with serious identifiable causes.
Etiology
 Prematurity, infection, metabolic abnormalities
 Hypoxemia, anemia, hypo or hyperthermia
 Gastroesophageal reflux
 Upper airway malformations (TEF)

96
Preventing apnoea
 Maintain normal hematocrit, electrolytes and PaO2
 Avoid neck flexion and abdominal distension
 Kangaroo Mother Care (KMC)
Management
Methylxanthines
Aminophylline
 Loading dose 8mg/kg IV infusion over 30 minutes
 Maintenance – 1.5 to 3mg/kg IV every 8 to 12 hours.
Caffeine – loading dose 20 to 25mg/kg IV slow push every 24 hours
CPAP
Kangaroo mother care
Maintain normal hematocrit, electrolytes and PaO 2
Avoid neck flexion and abdominal distension
Treat underlying etiology
Necrotizing enterocolitis (NEC)
Necrotizing enterocolitis (a bowel infection) may occur in low-birth-weight
infants, especially after enteral feeds are started. The condition is
commoner in low-birth-weight infants fed artificial formulae but may occur
in breastfed infants.
Common signs of necrotizing enterocolitis are:
 abdominal distension or tenderness
 intolerance to feeding
 bile-stained vomit or bile-stained fl uid up the nasogastric tube
 blood in the stools
 Other signs of systemic illness may present including

97
  apnoea
 drowsiness or unconsciousness
 fever or hypothermia
Treatment
 Stop enteral feeding.
 Pass a nasogastric tube and leave it on free drainage.
 Start an IV infusion of glucose–saline.
 Start antibiotics: give ampicillin (or penicillin) plus gentamicin plus
metronidazole for 10 days.
 If the infant has apnoea or other danger signs, give oxygen by
nasal catheter. If apnoea continues, give aminophylline or caffeine
IV.
 If the infant is pale, check the Hb, and transfuse if Hb < 10 g/dl.
 Take a supine and lateral decubitus abdominal X-ray. If there is gas
in the abdominal cavity outside the bowel, there may be bowel
perforation. Ask a surgeon to see the infant urgently.
 Examine the infant carefully each day. Reintroduce expressed
breast milk feeds by nasogastric tube when the abdomen is soft
and not tender, the infant is passing normal stools with no blood
and is not having bilious vomiting. Start feeds slowly and gradually
increase by 1–2 ml per feed each day.
3.13 Discharge and follow-up of low-birth-weight infants
Low-birth-weight infants can be discharged when:
 They have no danger signs or signs of serious infection
 They are gaining weight on breastfeeding alone

98
  They can maintain their temperature in the normal range (36–37
°C) in an open cot
 The mother is confident and able to care for the infant.
Low-birth-weight infants should be given all the scheduled vaccines at the
time of birth and any second doses that are due by the time of discharge.
Counseling on discharge
Counsel parents before discharge on:
 Exclusive breastfeeding
 Keeping the infant warm
 Danger signs for seeking care
Low-birth-weight infants should be followed up weekly for weighing and
assessment of feeding and general health, until they have reached 3 kg.

3.14 Other common neonatal problems

3.14.1 Neonatal Jaundice
Definition - is a yellowish discoloration of the skin and or sclera due to
bilirubin deposition.
In newborns, jaundice appears when total bilirubin (TB) is more than 7 mg
/dl and more than 50 % healthy full term babies and 80% of preterm babies
have some jaundice. Neonatal jaundice can be classified as either
physiologic or pathologic.

Table 3.1: Features differentiating Physiological jaundice from Pathological

Jaundice

99
No Features Physiologic Jaundice Pathological Jaundice

1 Clinical onset of jaundice >24 hrs <24 hrs

(after birth)

2 Jaundice still clinically Term < 8 days Term ≥8 days

visible (day after birth)
Preterm < 14 days Preterm > 14 days

3 Peak Total Serum Bilirubin Term < 12 mg/dl Term > 12 mg/dl
( TSB)
Preterm < 15 mg/dl Preterm > 15 mg/dl

4 Rise in TSB < 5mg/dl/24 hrs > 5mg/dl/24 hrs

5 Conjugated serum bilirubin <2mg/dl >2mg/dl or 15 % of

level TB

Causes of Jaundice
 Isoimmunization: RH incompatibility, ABO incompatibility, Other
blood group incompatibility
 Infection: Bacterial, viral, protozoal
 Breast milk induced jaundice
 Breastfeeding jaundice
 Sequestered blood: Subgaleal hemorrhage, cephalhematoma,
ecchymosis, hemangioma
Erythrocyte biochemical defect: G6PD deficiency, Hexokinase deficiency
Structural abnormalities of erythrocytes: Hereditary spherocytosis,
elliptocytosis
 Disorder of hepatic uptake: Gilbert syndrome
 Disorder of conjugation: Crigler-Najjar syndrome (absence of UGT
activity)

100
  Hypothyroidism: Disorder of enterohepatic circulation (associated
with breast feeding practice)
 Idiopathic jaundice
Clinical manifestations
 A newborn presents with yellowish discoloration of sclera, skin,
mucus membranes
 Depending on severity and time of presentation a newborn may
present with signs of bilirubin encephalopathy.
The following risk factors aggravate bilirubin encephalopathy:
 Prematurity
 Metabolic acidosis,
 Hypoglycemia,
 Sepsis,
 Temperature instability,
 Significant lethargy
 Low serum albumin
Complications of hyperbilirubinemia
Acute bilirubin encephalopathy is early bilirubin toxicity, which is transient
and reversible. If it is not recognized or untreated, it may progress to
permanent neurologic impairment-Kernicterus.
Acute bilirubin encephalopathy has three phases
 Phase 1 ( first 2 days of age): Poor motor reflex, high pitched cry,
decreased tone, lethargy, poor feeding
 Phase 2 (middle of 1st week of age): Hypertonia, seizure and
depressed sensorium, fever, opisthotonos posturing, paralysis of
upward gazing.

101
  Phase 3 (after 1week of age):Hypertonia decreases, Hearing and
visual abnormality, poor feeding, Athetosis and seizure may also
occur
 Chronic bilirubin encephalopathy (Kernicterus) seen after 1 year
of age and manifests with
o Choreoathetoid cerebral palsy
o Upward gaze palsy
o Sensorineural hearing loss
o The intellect may be spared with severe physical handicap
Investigations
 Total bilirubin
 Direct and indirect bilirubin
 Maternal blood group and RH type
 Neonatal blood group and RH type
 Direct/indirect Coombs test
 Hemoglobin (Hgb) or hematocrit (HCT)
 Peripheral RBC morphology
 Reticulocyte production index(RPI)
 Serum albumin level and albumin to bilirubin ratio
 Liver function test (LFT)
 Septic work up.
 Abdominal ultrasound with indication.
Management of Unconjugated Hyperbilirubinemia
The main goal of treatment is to avoid acute and chronic bilirubin
encephalopathy by reducing serum bilirubin level.

102
Note: Always categorize babies into low, medium or high risk based on the
Bhutani curve as shown below before deciding on the management
options.
Principles of treatment include:
1. Phototherapy
2. Exchange transfusion
3. Other medical managements

 Phototherapy– It is the mainstay of treatment

 It is indicated for excessive unconjugated hyperbilirubinemia (see
Bhutani curve for phototherapy).

 It acts by photoisomerization, structural isomerization, and

photooxidation.
 It is not a substitute for exchange transfusion if exchange
transfusion indicated.
 Intensive phototherapy is preferred if available.
 Infant should get adequate feeding.
 Cover the baby’s eye and put diaper with maximum body surface
area being exposed.
 Make sure that the distance between the light source and the
baby should be less than 40 cm.
 The position should be changed every 2 hours from supine to
prone.
 Measure weight daily and increase fluid intake by 25 % extra over
the usual requirement to compensate the insensible water loss.
 Give a bolus of fluid with Normal saline 20ml/kg if bilirubin
remains high

103
Side effects of phototherapy
 Insensible water loss
 Watery and frequent stool
 Retinal damage
 Erythema and increased blood flow
 Bronze baby syndrome (with increased CB)
 Low calcium level (in preterm)
 Interferes with maternal infant bonding
1. Double Volume Exchange transfusion
See Bhutani curve for indications of Double volume exchange transfusion.
The amount of blood volume to be exchanged is equivalent to 2x the blood
volume of the baby (85ml/kg)
o Example for a newborn weighing 3 kilograms the amount of
blood to be exchanged is calculated as follows= 2 x 85ml/kg
x3kg =510 ml
 Do procedure after umbilical catheterization using aseptic
technique
 Heparinize the catheter (instill heparin to the tube) before starting
the procedure.
 The amount of blood to be removed at a time is 5ml to 20 ml
 Strictly monitor the vital signs during the procedure.
 Determine post transfusion hematocrit 4-6 hours after the
procedure.
 Determine bilirubin 4 hourly after the procedure.
 Monitor RBS every 30-60 minutes during the procedure and 2-4
hourly for the first 24 hours after procedure.

104
  Administer 1ml/kg of Calcium gluconate slowly via a peripheral
vein under strict cardiac monitoring after 100ml of blood is
exchanged.
 If the cord is infected or there is a breach in the aseptic technique,
it is wise to start on prophylactic dose of Cloxacillin 50mg/Kg bid
for 2- 3 days and gentamicin 5mg/kg BID for 2-3 days.
 Keep baby NPO for 4 hours before and after procedurebecause it
can predispose the baby to necrotizing enterocolitis.
Selection of blood to be transfused to the newborn
 If there is Rh hemolytic disease – give blood group compatible to
the baby and RH to the mother.
 If there is ABO hemolytic disease – give blood group of the mother
and Rh compatible to the newborn
Note: O negative blood is the most preferable type for exchange
transfusion.
Complication of exchange transfusion
 Cardiac and respiratory disturbances (arrhythmia, volume
overload, perforation of vessels)
 Shock, due to bleeding disorder (clotting factor deficiency) or
inadequate replacement of blood.
 Infection (strict infection screening to reduced this risk )
 Clot formation (causing occlusion of catheters, impairment of
blood flow to the organs due to thromboembolism)
 Alterations in blood chemistry (high potassium, low calcium, low
glucose, decreased in pH)

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  Rare but severe complications include air embolism, portal
hypertension and necrotizing enterocolitis.
Other treatment modalities
 Phenobarbital 5 mg/kg to stimulate liver enzyme in Crigler-Najjar
syndrome.
 High dose of IV immunoglobulin.
 In case of breast milk jaundice, discontinuation of breast milk for
1-3days usually causes a prompt decline, whereas in jaundice
associated with failure of breast-feeding (breast-feeding jaundice)
increase the amount of feeding.

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Figure 3.4: Bhutani curve: phototherapy indication in
hospitalized infants of 35 or more weeks’ gestation

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Figure 3.5: Bhutani curve: Exchange transfusion in infants
of 35 or more weeks’ gestation

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3.14.2 Neonatal Conjunctivitis
Red and swollen eyes or eyes draining pus may be caused by bacteria (e.g.
gonococcus, chlamydia, and staphylococcus)
A. If there is stickiness of eyelids, swelling and/or redness but no pus
discharge,
 Clean the eyelids using sterile normal saline or clean (boiled and
cooled) water and a clean swab, cleaning from the inside edge of
the Eye to the outside edge;
 Have the mother do this whenever possible; repeat four times
daily until the eye problems have cleared.
 If the problem persists after 4 days of the above measures treat
for Chlamydia:
 Give erythromycin by mouth for 14 days;
 Apply 1% tetracycline ointment to the affected eye(s) four times
daily until the eye(s) is no longer red, swollen, or sticky.

B. If eyes are draining pus (Opthalmia Neonatorum)

a. If the Baby is less than 7 days, treat for gonococcal infection.

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  If possible take a specimen of pus using a sterile cotton swab, and
send it to the laboratory for gram stain and/or culture and
sensitivity, so that treatment will be modified accordingly.
 Give Ceftriaxone 50mg/kg IM stat.
 Clean the eyelids using sterile normal saline or clean (boiled and
cooled) water and a clean swab, cleaning from the inside edge of
the Eye to the outside edge;
 Have the mother do this whenever possible and repeat four times
daily until the eye problems have cleared.
 Treat the mother and her partner for gonorrhoea if not already
treated give:
 Ceftriaxone 250 mg IM as a single dose to the mother;
 Ciprofloxacin 500 mg by mouth as a single dose to her partner.
3.14.3 Common hematologic problems of the neonate
Approach to a neonate with bleeding disorder
Introduction
 Neonates have decreased activity of clotting factors (II, VII, IX, X),
impaired platelet function, and suboptimal defense against clot
formation.
 HDN in well babies and disseminated intravascular coagulations
(DIC) in sick babies are among the commonest problems.
Hemorrhagic disease of the newborn (HDN)
Definition: HDN occurs in the healthy infant due to Vitamin K deficiency.
Disseminated intravascular coagulation (DIC)
Definition: DIC it’s a systemic process producing both thrombosis and
hemorrhage due to activation and dysregulation of the hemostatic system.

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 DIC in newborn is due to infection, cold injury, asphyxia or tissue damage
and necrosis. The baby usually appears sick and may have petechiae,
gastrointestinal bleeding, oozing from vein puncture.
Table 3.2: Classification, risk factors, prevention, treatment and incidence
of HDN according to time of onset
Classification Early onset Classic disease Late onset

Age 0 – 24 hrs 2 – 7 days >1wk – 12 weeks of age

Prevention Vitamin- K 0.5 Vitamin- K 0.5 Vitamin- K 0.5 (Preterm)

(Preterm) – 1 mg (Preterm) – 1 mg – 1 mg (term) IM at
(term) IM at birth. (term) IM at birth. birth.

Treatment Vit- K 1mg - 5mg IV Vit- K 1mg - 5mg IV Vit- K 1mg at arrival then
Fresh frozen plasma at
Fresh frozen plasma 10 - 20 ml/kg in
10 - 20 ml/kg in serious bleeding, 1 wk,
serious bleeding, prematurity, liver
prematurity, liver 4 wks, and 8 wks
disease
disease
Treat shock by blood
Treat shock by blood
transfusion

Laboratory findings
 Decreased platelet count and increased PT and PTT
 Decreased fibrinogen
 Management
 Treat the underlying cause
 Vitamin K 1 mg IV.

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 Platelet and fresh-frozen plasma 10-20ml/kg may be considered for
moderate-to-severe bleeding
If bleeding persists do exchange transfusion and continue to transfuse with
fresh-frozen plasma and platelet.
Polycythemia
Definition: Polycythemia is defined as a peripheral venous blood of HCT >
65 %. Capillary blood sample is higher by 10 - 15 % than venous blood.
Management: Partial exchange transfusion
The procedure should be done under strict aseptic technique after umbilical
catheterization
 Partial exchange transfusion in symptomatic patients if venous HCT is
> 65%.
 Increase fluid intake and repeat HCT in 4 to 6 hrs in asymptomatic
infants with venous HCT between 65% - 70%.
 Partial volume exchange transfusion when the peripheral venous HCT
is >70% even in the absence of symptoms.
 Partial volume exchange transfusion is done by withdrawing blood from
umbilical vein and replacing it with Normal saline using the formula as
shown below.
 The amount of blood to be removed at a time is 5ml to 20 ml depending on
the gestational age, birth weight and of the infant. The lower range is used
for preterm, VLBW, and critically ill infants. The higher amount of aliquot
should be utilized in stable newborns that are term with normal birth
weight.
 Determine post transfusion hematocrit after 4-6 hours after the procedure
 Monitor RBS every 2-4 hours for the first 24 hours after procedure.

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 Keep baby NPO for 4 hours before and after procedure for prevention of
NEC and put him on maintaince fluids.
Volume of exchange in ml =
Blood volume of newborn x (observed HCT-Desired HCT*)
Observed HCT
*Desired HCT=55%
Example: What is the amount exchanged in a newborn weighing 3kg
infant and hematocrit of 75 % the amount of blood to be exchanged is
calculated as follows. Volume of blood for term baby is 85ml/kg and for
a preterm to bring HCT to 55 %.

Volume of exchange in ml = 85ml x 3kg x 75-55

75
= 255X 22
75
= 68 ml blood will be exchanged with equal
amount of normal saline
Anemia in newborns
Definition:- Anemia is defined as a hemoglobin (Hgb) or hematocrit (HCT)
that is more than 2 standard deviation below for the age or less than
normal range for postnatal age and birth weight.( For clinical purpose HCT
st
< 45% in the 1 week of life) .
Causes of neonatal anemia
 Blood loss
 Hemolytic anemia
 Diminished RBC production
Clinical approach to a newborn with anemia
 Detailed obstetric history.

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  Physical examination
 Look for acute blood loss: shock, tachycardia, poor capillary refill
time, poor perfusion and acidosis.
 Chronic blood loss associated with pallor, jaundice,
hepatosplenomegaly, cardiac failure.
 Growing preterm baby may manifest with poor weight gain,
apnea, tachypnea or poor feeding.
Investigations
 Complete blood cell count
 Blood group and RH of the newborn and mother.
 Reticulocye production index
 Blood smear to see the morphology and find evidence for
hemolysis (target cells and burr cells).
 Coombs’ test and bilirubin level.
 Apt test in case of gastro-intestinal bleeding to differentiate
swallowed maternal blood from neonatal bleeding.
 Ultrasound of abdomen and head.
 Screening for infections [(TORCH) toxoplasmosis, rubella,
cytomegalovirus infection, herpes simplex infection] and
septicemia.
 Bone marrow aspiration (rarely used).

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Management

Indications for blood transfusion

- In sever cardiopulmonary disease: Transfuse if HCT <40%
- For moderate respiratory distress: Transfuse if HCT < 30%
- For major surgery: Transfuse if HCT <30%
- Infant with asymptomatic anemia: Transfuse if HCT <21%
- If the newborn is in shock refer to the guideline on management of
shock.

Guideline for packed RBC replacement in high risk neonates:

Volume of Packed red blood cell to be transfused can be calculated as
follows:
Volume of transfusion =
Weight in Kg x blood volume / Kg (desired HCT- observed HCT)
HCT of blood to be given
 Average HCT of packed RBC is in the range 70-80%

 Transfuse over 2-4 hours time

 The average blood volume for term newborn is 85 ml/kg: 95ml/kg

in preterm.

 Preferably transfuse fresh blood (<7 days old) to avoid related

complications (decreased PH (7.4 Vs 6.5), elevated potassium level
(4.2mM Vs 78.5mM) and decreased 2, 3- diphosphoglyserate.)

 Exchange transfusion with packed RBCs may be required for

severely anemic infant if direct transfusion result in circulatory
overload.

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Whole blood transfusion
 If packed RBC is not available give whole blood 15-20 ml/kg over
2-3 hours period
 In case of acute blood loss use whole blood 15-20ml/kg over 1-2
hours period.
 Give Fusemide 1mg/kg pre and post transfusion.
 If Anemia is due to blood loss and newborn is asymptomatic give
Iron drops
3.14.4 Hypoglycemia
Definition: Serum glucose level less than 50mg/dl

Risk factors for hypoglycemia

 Prematurity
 Intrauterine growth retardation
 Infant of diabetic mother
 Delayed initiation of feeding
Common clinical manifestations
 CNS irritability manifested by jitteriness , course tremor, twitching
and convulsion
 Episodes of apnea with cyanosis and tachypnea with irregular
breathing (mainly in preterm)
 Tachycardia and sweating (excess catecholamine secretion)
Management
 Establish IV line , give mini bolus 2ml/kg of 10%glucose iv (4ml/kg
if baby has convulsion)
 Infuse 10% glucose at a rate of 6mg/kg/min

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  Check blood glucose every 15min and if blood glucose is still low
increase the rate with 2mg/kg/min every 15 min to a maximum of
12-14mg/kg/min
 If blood glucose is normal at two consecutive time check every
one hour twice then every two hours twice then every four hours
 Unless there is contraindication start feeding the baby with
expressed breast milk
 When blood glucose level remained normal for 12hours or blood
glucose exceed 100 mg /dl decrease the infusion rate by 2mg/kg
and check blood glucose every 6hrs. Once infusion rate is brought
down to 4mg/kg /min, increase the feed and taper infusion fluid
3.14.5 Congenital malformations (see chapter 9)

 Cleft lip and palate (see chapter 9 section congenital anomalies)

 Bowel obstruction
 Abdominal wall defects
 Meningomyelocele
 Congenital dislocation of the hip
 Talipes equinovarus (club foot)
3.14.6 Large for gestational age (LGA) infants
Definitions
th
Large for Gestational Age (LGA): a baby with a birth weight > 90
percentile for gestational age.
Macrosomia: babies with a birthweight > 4000g.

Causes
 Maternal diabetes
 Genetics: “big parents - big baby”

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  Excessive maternal weight: “fat mother - fat baby”
 Rare genetic disorders e.g. Beckwith-Wiedemann Syndrome
Complications and Risks
 Antenatal and Intrapartum risks
o Increased still birth rate (8x in IDM’s)
o Obstructed labour and shoulder dystocia
o Fetal distress
 Neonatal
o Birth trauma (fractures of clavicle/humerus; brachial plexus
injury)
o hypoxic-ischaemic damage
o Hypoglycemia (in all, but especially in IDM’s)
 In addition, in IDM’s: Immature lungs with RDS, polycythaemia,
Neonatal Jaundice, Cardiac defects, Asymmetrical ventricular
septal hypertrophy with left and/or right HOCM, VSD. Rare: sacral
agenesis; microcolon
 Long-term: increased risk of type I and type II diabetes in baby

Management

 Delivery is high risk: expect and manage complications

 Examine for: Birth trauma , Dysmorphia , Macrosomia ,Plethora
,Cardiac murmurs and RDS
 Manage hypoglycaemia: Feed within 30 minutes of birth (unless
severe RDS or intrapartum hypoxia). Low blood sugar readings on
a glucometer MUST be confirmed by a laboratory test.
 Do blood glucose 1 hr post-delivery:

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  Continue frequent breast feeding 2-3hrly continue 3hrly blood
glucose tests for 24 hours
3.14.7 Respiratory distress
Respiratory distress is an extremely common neonatal problem, with a
limited number of common causes. The cornerstone of management is
oxygen, not forgetting the other basics of warmth, food/glucose, and
infection prevention and management

Definition: Respiratory distress is marked by one or more of the following

signs (listed in increasing severity)

 Respiratory rate > 60/minute (tachypnoea/fast breathing)

 Recession or indrawing of the chest
 Flaring of Ala nasae
 Grunting
 Cyanosis
 Irregular breathing, then apnoea
Assessment of severity

 Mild: Respiratory rate > 60/minute with minimal (< 30%) oxygen
requirements
 Moderate: Respiratory rate > 60/minute, recessing, flaring,
cyanosis (requiring up to 60% oxygen)
 Severe: Respiratory rate > 60/minute, grunting, cyanosis (requiring
> 60% oxygen), irregular respiration (progressing to apnoea).
If oxygen requirements go above 60%, baby may need ventilatory support

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Common causes of respiratory distress in the newborn
Pulmonary causes

 Hyaline membrane disease (HMD)

 Meconium aspiration syndrome
 Wet lung syndrome
 Pneumonia
 Pneumothorax
Extra pulmonary causes
 Congenital heart disease/heart failure
 Hypothermia
Metabolic acidosis
 Anaemia and polycythaemia
 Diaphragmatic hernia
 Upper GIT anomalies (e.g. trache-oesophageal fistula)
Investigations
 Chest X-ray (wait 4-6 hours if hyaline membrane disease or
transient tachypnoea of the newborn (TTN) are suspected)
 Gastric aspirate for a shake test and gram stain
 Full Blood Count, CRP and glucose
 Transilluminate the chest if a pneumothorax is suspected
Management
Oxygen

Give enough oxygen to keep the oxygen saturation between 85 and 93%. If
you do not have a pulse oximeter ensures that the baby’s tongue is pink.
You MUST get one in your nursery FOR THE BABIES. If it is not possible to
keep the infant pink in oxygen then continuous positive pressure (CPAP) via
nasal prongs or endotracheal tube should be given – discuss referring your
patient

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  Monitor oxygen saturation

Supportive Care
 Keep the infant warm in an incubator

If the respiratory distress is mild, do intermittent KMC provided that he/she

maintains oxygen saturation (85-93%) on nasal cannula oxygen
 Keep the neonate NPO per mouth for the first 24 hours
 Observe the RR, saturation, HR hourly, and check the blood
glucose 3 hourly
Complications
It is important to watch out for:

 Anaemia of immaturity: Transfuse preterm babies if their Hb is

less than 9gm%.
 In small babies, check pulses daily, and if they are bounding, listen
for a murmur. Refer to a regional hospital if a PDA is present, and
reduce intake to 120ml/kg/day
 Sepsis Neonatorum: Babies in KMC are less likely to acquire
infections, but they are still at risk. At any sign of infection, fully
and carefully assess baby, and manage accordingly

3.15 Babies of mothers with infections

3.15.1 Congenital syphilis

If the mother is VDRL reactive during ANC and treated with non penicillin
drug, consider congenital syphilis and treat the baby with penicilin for 10-
14 days.

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Clinical signs

 Often low birth weight

 Palms and soles: red rash, grey patches, blisters or skin peeling
 ‘Snuffles’: rhinitis with nasal obstruction which is highly infectious
 Abdominal distension due to big liver and spleen
 Jaundice
 Anaemia
 Some VLBW babies with syphilis have signs of severe sepsis with
lethargy, respiratory distress, skin petechiae or other bleeding
Diagnosis: If you suspect syphilis, do serum and CSF VDRL

Treatment

The diagnosis of neurosyphilis in the newborn with syphilitic infection is

difficult because of the poor sensitivity of the CSF VDRL in this age group
and the lack of CSF abnormalities. In general a positive CSF VDRL in
newborn warrants treatment for neurosyphilis, even though it might reflect
passive transfer of antibodies from serum to CSF. It is now accepted that all
infants with presumptive diagnosis of congenital syphilis should be treated
with regimen effective for neurosyphilis because this cannot be reliably
excluded.

 Prefered treatment is - Benzyl penicillin 50,000 units/kg every 12

hours IM or IV for the first 7 days of life and then every 8 hours for
a further 3 days (total of 10 days), Or
 Procaine penicillin 50,000 units/kg as a single dose daily for 10
days
 Screen and treat parents for syphilis and HIV according to the
national guideline

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 NB: If >1 day of therapy is missed, the entire course should be
started. A complete evaluation (CSF analysis, bone X-ray, CBC) is
not necessary if 10 days of parenteral therapy is administered but
may be useful to support a diagnosis of congenital syphilis.

3.15.2 Baby of a mother with tuberculosis

If the mother has active lung tuberculosis and was treated for less than two
months before birth or was diagnosed with tuberculosis after birth:
 Reassure the mother that it is safe for her to breastfeed her baby;
Investigate the baby for possible congenital tuberculosis& Screen
the mother for HIV infection
 Do not give the tuberculosis vaccine (BCG) at birth; Give
prophylactic isoniazid 5 mg/kg body weight by mouth once daily;
 At the age of six weeks, re-evaluate the baby, noting weight gain and
taking an X- ray of the chest, if possible;
 If there are any findings suggestive of active disease, start full anti-
tuberculosis treatment according to national guidelines;
 If the baby is doing well and tests are negative, continue
prophylactic isoniazid to complete six months of treatment;
 Delay BCG vaccine until two weeks after treatment is completed. If
BCG was already given, repeat BCG two weeks after the end of the
isoniazid treatment.
3.15.3 Baby of a mother with HIV infection (see Chapter 8)
3.15.4 Baby of a mother with hepatitis B virus infection

Perinatal exposure to a HBsAg-positive mother is the most important risk

factor for acquisition of HBV in children. The risk of transmission is greatest
if the mother also is HBeAg positive. Nearly 70–90% of their infants

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become chronically infected if untreated. Transmission can occur
intrauterine but most commonly at delivery. HBsAg has been
demonstrated inconsistently in human milk of infected mothers. However,
breast-feeding of unimmunized infants by infected mothers does not
appear to confer a greater risk of hepatitis on offspring than does formula
feeding

Prevention
 Screen mothers for HBV infection during ANC visit
 Immunize new born at delivery (post exposure. See Table 3.3
below)
 Post vaccination testing for HBsAg and anti-HBs should be at 9–15
mo to know the status of the infant if possible
 Screen partner for HBV and HIV
Table 3.3 Indications and Dosing Schedule for Hepatitis B Vaccine and
Hepatitis B Immune Globulin

Vaccine HBIG
Neonate
Engerix-B Schedule Dose (μL) Schedule
(μg)
Infants of HBsAg- 10 Birth, 1, 6 mo 0.5 Within 12
positive women hr of birth

Infants of HBsAg- 10 Birth, 1–2, None

negative women 6–18 mo
th
Nelson text book of Pediatrics 18 edition

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CHAPTER- 4 - COUGH OR DIFFICULT BREATHING

Cough and difficult breathing are common problems in young children. The
causes range from a mild, self-limited illness to severe, life-threatening
disease. This chapter provides guidelines for managing the most important
conditions that cause cough, difficult breathing, or both in children aged 2
months to 5 years.
The differential diagnosis of these conditions is described in Chapter 1.
Management of these problems in infants less than 2 months of age is
described in chaprter 3 and Management in severely malnourished
children is described in Chapter 7.
Most episodes of cough are due to common cold, with each child having
several episodes a year. The commonest severe illness presenting with
cough or difficult breathing is pneumonia, which should be considered first
as any differential diagnosis.

4.1 Child presenting with cough

History
Pay particular attention to the following:
Cough
• duration in days
• paroxysms with whoops or vomiting or bluish discoloration of lips
(central cyanosis)
• associated symptoms like hoarseness of voice, runny nose, fever,
difficulty of breathing, wheezing, etc
• history of contact with chronic cougher or patient with tuberculosis
in the family
• history of choking or sudden onset of stridor and fast breathing
(respiratory distress)
• Presence of any other danger sign like child not able to drink or
vomits everything, has convulsions or is lethargic or unconscious

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 • known or possible HIV infection
• immunization history: BCG, DPT, measles, Hib and pneumococcus
• personal or family history of asthma or allergy
• Social history (family size, exposure to smoke etc)
Examination
The symptoms and signs listed below are a guide to the clinician to reach a
diagnosis. Not all children will show every symptom or sign.
General
 presence of convulsion
 presence of lethargy or unconsciousness
 central cynosis
 head nodding (a movement of the head synchronous with
inspiration indicating severe respiratory distress)
 apnea, gasping, grunting, fast breathing, nasal flaring,
audible wheezing, stridor
 severe palmar pallor
Vital signs - respiratory rate, pulse rate/AHR, temperature, BP
 RR – make a count for a full minute when the child is calm
Fast breathing: Age <2 months old: ≥ 60 breaths*
Age 2–11 months: ≥ 50 breaths
Age 1–5 years: ≥ 40 breaths
* If the breathing rate is 60 or more repeat counting the
breathing rate in young infants for a full minute
Chest
 lower chest wall indrawing ( it occurs when the lower
chest wall goes in when the child breathes in)
 hyperinflated chest
 visible distended veins on the neck
 apex beat displaced / trachea shifted from midline
 percussion-signs of pleural effusion (stony dullness) or
pneumothorax (hyper-resonance)

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  on auscultation coarse crackles, bronchial breath sounds,
decreased or absent air entry or wheezing

Note: lower chest indrawing is when the lower chest wall goes in when
the child breathes in.
Heart
 raised jugular venous pressure (JVP)
 gallop rhythm / murmur of heart on auscultation
 distant heart sound
Abdomen
 enlarged liver and spleen.
 abdominal masses other than liver or spleen
 sign of fluid in the peritoneum (ascites)
Skin
 sever palmar pallor
 rashes (petechiae, ecchymosis)
Extremity
 clubbing of finger nails
 peripheral edem
Investigations
 pulse oximetry–to guide when to start and stop oxygen
therapy
 full blood count
 chest X-ray: in children with very severe pneumonia, or
severe pneumonia not responding to treatment or with
complications, unclear diagnosis or associated with HIV
 sputum for AFB (for children old enough to expectorate) or
gastric aspirate

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Table 4.1 Differential diagnosis of the child presenting with cough or
difficulty in breathing

Diagnosis In favour
Pneumonia Cough with fast breathing
Fever
Nasal flaring
Grunting
Head nodding
Lower chest wall indrawing
Coarse crackles on auscultation
Malaria Lives in or travelled to a malarious area
Fast breathing in febrile child
In severe malaria: deep (acidotic) breathing / lower chest
wall indrawing
Chest clear on auscultation
Blood smear or positive for malaria parasite, or RDT positive
Severe anaemia Shortness of breath on exertion
Severe palmar pallor
Haemoglobin <6 g/dl
Cardiac failure Fast breathing, feeding interruption, cyanosis
Growth failure
Raised jugular venous pressure
Fine crackles on the bases of the lung fields
Apex beat displaced to the left
Gallop rhythm
Heart murmur (in some cases)
Enlarged palpable liver
Clubbing of finger nails
Edema of extremities
Congenital heart Cyanosis
disease Finger clubbing
(cyanotic) Heart murmur
Signs of cardiac failure (in some cases)
Failure to thrive
Congenital heart Difficulty in feeding or breastfeeding with failure to thrive
disease Sweating of the forehead

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(acyanotic) Heaving precordium
Heart murmur (in some cases)
Signs of cardiac failure
Tuberculosis Chronic cough (more than 2 weeks), history of contact with
chronic cougher or known TB patient
Poor growth / wasting or weight loss
Diagnostic: chest X-ray may show primary complex or
miliary tuberculosis, effusion, cavity
Sputum or gastric aspirate positive for AFB

Pertussis Paroxysms of cough followed by whoop, or vomiting,

cyanosis or apnoea
Well between bouts of cough
No fever
No history of PENTA immunization or incomplete
immunization

Foreign body History of sudden choking

Sudden onset of stridor or respiratory distress
Focal areas of wheeze or reduced breath sounds
Chest X-ray finding
Effusion or Reduced movement on the attected side of chest
empyema Stony dullness to percussion (over the effusion)
Air entry absent (over the effusion)
Chest X-ray finding
Pneumothorax Sudden onset, usually after major chest trauma
Hyper-resonance on percussion on one side of the chest
Shift of mediastinum to opposite side
Chest X-ray finding
Pneumocystis HIV test positive in mother or child
Pneumonia (PCP) 2-6 month old child with central cyanosis
Fast breathing
Hyper-expanded chest
Chest clear on auscultation
Enlarged lymph nodes, liver and spleen
Finger clubbing
Chest X-ray changes

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 Asthma or wheeze Recurrent episodes of shortness of breath or wheez
Night cough or cough and wheeze with exercise
Response to bronchodilators
Known or family history of allergy or asthma

Bronchiolitis Cough
Wheeze and crackles
Age usually < 1 year

Severe Shortness of breath on exertion

Anaemia Severe palmar pallor
Hb < 6 g/dl
Croup Inspiratory stridor
Barking character to cough
Hoarse voice

4.2 Pneumonia
Pneumonia is usually caused by viruses or bacteria. Most serious episodes
are caused by bacteria. It is usually not possible, however, to determine the
specific cause by clinical features or chest X-ray appearance. Pneumonia is
classified as severe or non-severe, based on the clinical features. The
management is based on the classification. Antibiotic therapy is needed in
all cases. Severe pneumonia requires additional treatment, such as oxygen,
to be given in hospital.

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Table 4.2 Classification of the severity of pneumonia

Sign or symptom Classification Treatment

Cough or diffi culty in breathing • Admit to hospital

with: Severe • Give oxygen if
• Oxygen saturation < 90% Pneumonia saturation is < 90%
or central cyanosis • Manage the airway
• Severe respiratory • Give recommended
distress e.g. grunting, antibiotic
severe chest indrawing • Treat high fever if
• Signs of pneumonia with present
• a general danger sign
(inability to breastfeed or
drink, lethargy or reduced
level of consciousness,
convulsions)
• Fast breathing  Home care
≥ 60 breaths/minute in a Child  Give appropriate antibiotic
aged <2 months; for 5 days
≥ 50 breaths/ minute in a child Pneumonia  Soothe the throat and
aged 2–11 months relieve cough with a safe
≥ 40 breaths/minute in a child remedy
aged 1–5 years • Advise the mother when to
OR return immediately
• Chest indrawing • Follow up in 2 days
• Definite chest findings on
auscultation
• No signs of pneumonia or No • Soothe the throat and
severe pneumonia pneumonia: relieve cough with safe
remedy
Cough or cold
• Advise the mother when to
return
• Follow up in 5 days if not
improving
• If coughing for more than
3 weeks, follow chronic
cough instructions

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4.2.1 Severe pneumonia
Diagnosis
Cough or difficult breathing plus at least one of the following:
 Central cyanosis or oxygen saturation < 90 on pulse oxymetry
 Severe respiratory distress (fast bqreathing, nasal flaring, grunting
 Lower chest wall indrawing
 Signs of pneumonia with a general danger sign
In addition, some or all of the other signs of pneumonia may be present
Additional auscultatory findings include:
 Abnormal vocal resonance (decreased over a pleural effusion,
increased over lobar consolidation
 Decreased breath sounds, bronchial breath sounds, crackles, pleural
rub.
Investigation
 Obtain an oxygen saturation measurement in all children suspected
to have severe pneumonia
 If possible, obtain a chest X-ray to identify pleural effusion,
empyema, pneumo thorax, pneumatocoele, interstitial pneumonia
and pericardial effusion.

Treatment
Admit the child to hospital.

Oxygen therapy
 Give oxygen to all children with severe pneumonia
 Where pulse oximetry is available, use this to guide oxygen therapy
(give to children with oxygen saturation less than 90%)
 Use nasal prongs, a nasal catheter, or a nasopharyngeal catheter.
Use of nasal prongs is the best method for delivering oxygen for
young infants
 Face masks or head masks are not recommended.

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Oxygen supplies need to be available continuously at all times. A
comparison of the different methods of oxygen administration and
diagrams showing their use is given in chapter 10.
 Continue with oxygen until the signs of hypoxia (such as severe
lower chest wall indrawing, inability to breast feed or breathing rate
of ≥ 70/minute) are no longer present.
 Where pulse oximetry is available, carry out a trial period without
oxygen each day in stable children. Discontinue oxygen if the
saturation remains stable above 90% (atleast 15 minutes on room
air). There is no value in giving oxygen after this time.
 Nurses should check every 3 hours that the catheter or prongs are
not blocked with mucus and are in the correct place and that all
connections are secure. The two main sources of oxygen are
cylinders and oxygen concentrators. It is important that all
equipment is checked for compatibility and properly maintained,
and that staff are instructed in their correct use.
Antibiotic therapy
 Give ampicillin (50 mg/kg IV/IM every 6 hours) or benzylpenicillin
(50,000 u/kg IV or IM every 6 hours) for 3- 5 days; then, if child
responds well, complete treatment at home or in hospital with oral
amoxicillin (25-50 mg/kg three times a day)
 Use ceftriaxone (80 mg/kg IM or IV once daily) in cases of failure of
first line therapy.
Supportive care
 If the child has fever (≥ 39 ° C) which appears to be causing distress,
give Paracetamol.
 If wheeze is present, give a rapid-acting bronchodilator (nebulized
salbutamol, salbutamol by metered dose inhaler with a spacer
device or subcutaneous epinephrine) and start steroids when
appropriate.
 Remove by gentle suction any thick secretions in the throat, which

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 the child cannot clear.
 Ensure that the child receives daily maintenance fluids appropriate
for the child’s age but avoid overhydration (section 10.2).
 Encourage breastfeeding and oral fluids.
 If the child cannot drink, insert a nasogastric tube and give
maintenance fluids in frequent small amounts. If the child is taking
fluids adequately by mouth, do not use a nasogastric tube as it
increases the risk of aspiration pneumonia and obstructs part of the
nasal airway. If oxygen is given at the same time as nasogastric
fluids, pass both tubes through the same nostril.
 Encourage the child to eat as soon as food can be taken.
Monitoring
The child should be checked by nurses at least every 3 hours and by a
doctor at least twice a day. In the absence of complications, within two
days there should be signs of improvement (breathing slower, less
indrawing of the lower chest wall, less fever, and improved ability to eat
and drink, better oxygen saturation).
Complications or other diagnoses to be considered
If the child has not improved after two days, or if the child’s condition has
worsened, look for complications or other diagnoses. If possible, obtain a
chest X-ray. The commonest other possible diagnoses are:
Staphylococcal pneumonia. This is suggested if there is rapid clinical
deterioration despite treatment, by a pneumatocoele or pneumothorax
with effusion on chest X-ray, numerous Gram-positive cocci in a smear of
sputum, or heavy growth of S. aureus in cultured sputum or empyema
fluid. The presence of septic skin pustules supports the diagnosis.

Treat with cloxacillin (50 mg/kg IM or IV every 6 hours) and gentamicin (7.5
mg/kg IM or IV once a day). When the child improves (after altleast 7 days
of IV or IM antibiotics), continue gentamycin IM daily for a total of 10 days
and cloxacillin orally 4 times a day for a total course of 3 weeks. Note that
cloxacillin can be substituted by another anti-staphylococcal antibiotic such

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as vancomycin, flucloxacillin or dicloxacillin
Empyema: This is suggested by persistent fever, and physical and chest X-
ray signs of pleural effusion.
Tuberculosis: A child with persistent cough and fever for more than 2
weeks and signs of pneumonia should be evaluated for tuberculosis. If
another cause of the fever cannot be found, tuberculosis should be
considered and treatment for tuberculosis, following national guidelines,
may be initiated and response to anti-Tb treatment evaluated.
The HIV status of all children should be confirmed if not known.
HIV infection or exposure to HIV. Some aspects of antibiotic treatment are
different for children who are HIV positive or in whom HIV infection is
suspected.Although pneumonia in many of these children has the same
etiology as that in children without HIV, Pneumocystis pneumonia (PCP),
often at the age of 4–6 months (see chapter 8) is an important cause to be
suspected and treated.
Treat as for severe pneumonia above; give ampicillin plus gentamicin IM or
IV for 10 days.
If the child does not improve within 48 h, switch to ceftriaxone at 80 mg/kg
IV once daily over 30 min. If ceftriaxone is not available, give gentamicin
plus cloxacillin, as above.

For children < 12 months, also give high-dose co-trimoxazole (8 mg/kg

trimethoprim and 40 mg/kg sulfamethoxazole IV every 8 hours or orally
three times a day) for 3 weeks. For a child aged 12–59 months, give this
treatment only if there are clinical signs of PCP
(Such as chest X-ray findings of interstitial pneumonia).

Figure 4.1.A: Normal

Chest X-ray

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 Figure 4.1.B: Lobar pneumonia of
the right lower zone indicated by a
consolidation

For further management of the child, including PCP prophylaxis, see

Chapter 8.
Staphylococcal pneumonia: Typical features include pneumatocoeles on
the right side of the illustration, and an abscess with an air-fluid level on
the left side of the illustration (Fig 4.1.C).

Figure 4.1.C: Staphylococcal pneumonia Fifure 4.1.D: Pneumothorax

Pneumothorax: The right lung is collapsed towards the hilus, leaving a

transparent margin around it without lung structure. In contrast, the right
side demonstrates markings extending to the periphery (Fig 4.1.D).

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Figure 4.1.E: Hyperiflated chest Figure 4.1.F: Miliary TB

Hyperinflated chest: Features are an increased transverse diameter, ribs

running more horizontally, a small contour of the heart, and flattened
diaphragms (Figure 4.1.E).

Appearance of miliary tuberculosis: widespread small patchy infiltrates

throughout both lungs: “snow storm appearance” (Fig 4.1.F).

Discharge
Children with severe pneumonia can be discharged when:
 Respiratory distress has resolved.
 There is no hypoxaemia (oxygen saturation, > 90%).
 They are feeding well.
 They are able to take oral medication or have completed a course
of parenteral antibiotics.
 The parents understand the signs of pneumonia, risk factors and
when to return.
Follow-up
Children with severe pneumonia may cough for several weeks. As they
havebeen very sick, their nutrition is often poor. Give the vaccinations that
are due, and arrange follow-up 2 weeks after discharge, if possible, to
check the child’s. Also address risk factors such as malnutrition, indoor air
pollution and parental smoking.

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4.2.2. Pneumonia (non-severe)
Diagnosis
Cough or difficult breathing plus at least one of the following signs:
 Fast breathing: age 2–11 months, ≥ 50/min
age 1–5 years, ≥ 40/min
In addition, either crackles or pleural rub may be present on chest
auscultation.
Check that there are no signs of severe pneumonia, such as:
 Oxygen saturation < 90% on pulse oximetry or central cyanosis
 Severe respiratory distress (e.g. grunting, very severe chest
indrawing)
 Inability to breastfeed or drink or vomiting everything
 Convulsions, lethargy or reduced level of consciousness
 Auscultatory fi ndings of decreased or bronchial breath sounds
or signs
 Of pleural effusion or empyema.
Treatment
 Treat the child as an outpatient.
 Advise carers to give normal fluid requirements plus extra
breast milk or fluids if there is a fever. Small frequent drinks are
more likely to be taken and less likely to be vomited
 Give the first dose at the clinic and teach the mother how to
give the other doses at home

Antibiotic therapy
 Give oral amoxicillin:
 In settings with high HIV infection rate, give oral amoxicillin at
least 40 mg/kg per dose twice a day for 5 days.
 In areas with low HIV prevalence, give amoxicillin at least 40
mg/kg per dose twice a day for 3 days. Avoid unnecessary
harmful medications such as remedies containing atropine,
codeine derivatives or alcohol

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Follow-up
Encourage the mother to feed the child. Advise her to bring the child back
after 3 days, or earlier if the child becomes sicker or is not able to drink or
breastfeed. When the child returns, check:
 Whether the breathing has improved (slower), there is less
fever, there is no chest indrawing and the child is eating better,
complete the antibiotic treatment.
 If the breathing rate and/or chest indrawing or fever and/or
eating have not improved, exclude a wheeze. If no wheeze,
admit to hospital for investigations to exclude complications or
alternative diagnosis.
 If signs of severe pneumonia are present, admit the child to
hospital and treat as above.
 Address risk factors such as malnutrition, indoor air pollution
and parental smoking.
Pneumonia in children with HIV infection
 Admit to hospital and manage as severe pneumonia (see section
4.2.1)
 For further management of these children, including PCP
prophylaxis (see Chapter 8,).
4.3 Complications of pneumonia
Septicaemia is the most common pneumonia complication and occurs
when the bacteria causing pneumonia spreads into the blood stream
(see chapter 6). The spread of bacteria can lead to septic shock or
metastatic secondary infections like meningitis especially in infants,
peritonitis, and endocarditis especially in patients with valvulvar heart
disease or septic arthritis. Other common complications include pleural
effusion, empyema and lung abscess.

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4.3.1 Pleural effusion and empyema
Diagnosis
A child with severe pneumonia or pneumonia may develop pleural effusion
or empyema.
 On examination, the chest is dull to percussion and breath
sounds are reduced or absent over the affected area.
 A pleural rub may be heard at an early stage before the
effusion is fully developed.
 A chest X-ray shows fluid on one or both sides of the chest.
 When empyema is present, fever persists despite antibiotic
therapy and the pleural fluid is cloudy or frankly purulent.

Treatment
Drainage
Pleural effusions should be drained, unless they are very small. If
effusions are present on both sides of the chest, drain both. It may be
necessary to repeat drainage 2–3 times if fluid returns. (See Appendix
for guidelines on chest drainage). Where possible, pleural fluid should
be analysed for protein and glucose content, cell count and differential,
and examined after Gram and Ziehl-Neelsen staining and bacterial and
Mycobaterium tuberculosis culture.
Antibiotic therapy
 Give ampicillin or cloxacillin (50 mg/kg IM or IV every 6 h)
or vancomycin (20mg/kg IV evry 6 h) and gentamicin (7.5 mg/kg
IM or IV once a day). When the child improves (after at least 7
days of IV or IM antibiotics), continue cloxacillin orally four times a
day for a total course of 3 weeks.

Note: Cloxacillin is preferable if staphylococcal infection is suspected.

Infection with S. aureus is more likely if pneumatocoeles are also present.

Antibiotic treatment depends on the culture and sensitivity result when it is

available

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Failure to improve
If fever and other signs of illness continue, despite adequate chest drainage
and antimicrobial therapy, test for HIV infection and assess for possible
tuberculosis.

 A trial of anti-TB therapy may be required (see chapter 4).

4.3.2 Lung abscess

A lung abscess is a circumscribed, thick-walled cavity in the lung that
contains purulent material resulting from suppuration and necrosis of the
involved lung parenchyma. It frequently develops in an unresolved area of
pneumonia. This could be a result of pulmonary aspiration, diminished
clearance mechanisms, embolic phenomena, or haematogenous spread.

Diagnosis
Common signs and symptoms:
 Fever
 Pleuritic chest pain
 Sputum production or haemoptysis
 Weight loss
 On examination: reduced chest movement, decreased breath
sounds, dullness to percussion, crackles, and bronchial breathing.
 Chest X-ray: solitary, thick-walled cavity in the lung with
or without air-fluid level.
• Ultrasonography and CT scan: to localize the lesion and guide
drainage or needle aspiration.

Treatment
The choice of antibiotic is usually empirical and is based on the underlying
condition of the patient and the presumed etiological agent.
• Give ampicillin or cloxacillin (50 mg/kg IM or IV every 6 h) or

145
 vancomycin (20mg/kg every 6 h) and gentamicin (7.5 mg/kg IM or
IV once a day). Continue treatment as in empyema (see chapter 4)
for up to 3 weeks.
• Surgical management is considered in cases of large lung abscess
especially when associated with haemoptysis or clinical
deterioration despite appropriate antibiotic therapy. Drainage is
usually through percutaneous tube drainage or ultrasound guided
needle aspiration.
4.3.3 Pneumothorax
Pneumothorax is usually secondary to an accumulation of air in the pleural
spaces from alveolar rupture or from infection with gas-producing
microorganisms.
Diagnosis
• Signs and symptoms may vary according to the extent of lung
collapse,degree of intrapleural pressure, and rapidity of onset.
• On examination: chest bulging on the affected side if one side is
involved, shift of cardiac impulse away from the site of the
pneumothorax, decreased breath sounds on the affected side,
grunting, severe respiratory distress and cyanosis may occur late
in the progression of the complication.
• Differential diagnosis include lung cyst, lobar emphysema, bullae,
diaphragmatic hernia
• Chest X-ray is crucial in the confi rmation of diagnosis
Treatment
Insert needle for urgent decompression, before insertion of an intercostal
chest drain. (See Annex for guidelines on chest drainage). Drainage is
usually through percutaneous tube drainage or ultrasound guided needle
aspiration.
4.4 Cough or cold
These are common, self-limited viral infections that require only supportive
care. Antibiotics should not be given. Wheeze or stridor may occur in some

146
children, especially infants. Most episodes end within 14 days. Cough
lasting 14 days or more may be caused by tuberculosis, asthma, pertussis
or symptomatic HIV infection (see Chapter 8).
Diagnosis
Common features:
 cough
 nasal discharge
 breathing
 fever
Thefollowing signs should not be present:
 general danger signs.
 signs of severe pneumonia or pneumonia
 stridor when the child is calm
 wheezing may occur in young children (see below).
Treatment
• Treat the child as an outpatient.
• Soothe the throat and relieve the cough with a safe remedy, such
as a warm, sweet drink, tea with honey, fruit juice, etc.
• Treat high fever (≥ 39 ° C) with paracetamol
• Clear secretions from the child’s nose before feeds using a cloth
soaked in water, which has been twisted to form a pointed wick.
• Give normal fl uid requirements plus extra breast milk or fl uids if
there is fever.Small frequent drinks are more likely to be taken
and less likely to be vomited.
Do not give any of the following:
 an antibiotic (they are not effective and do not prevent
pneumonia)
 remedies containing atropine, codeine or codeine derivatives, or
alcohol (these may be harmful)
 medicated nasal drops.

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Follow-up
Advise the mother to:
• feed the child( increase frequency of breast feeding)
• watch for fast or difficult breathing and return, if either develops
• return if the child becomes more sick, or is not able to drink or
breastfeed.
4.5 Conditions presenting with wheeze
Wheeze is a high-pitched whistling sound near the end of each expiration.
It is caused by spasmodic narrowing of the distal airways. To hear a
wheeze, even in mild cases, place the ear next to the child’s mouth and
listen to the breathing while the child is calm, or use a stethoscope.
In the first 2 years of life, wheezing is mostly caused by acute viral
respiratory infections such as bronchiolitis or coughs and colds. After 2
years of age, most wheezing is due to asthma. Some children with
pneumonia present with wheeze. It is important always to consider
treatment for pneumonia particularly in the first 2 years of life.Children
with wheeze but no fever, chest indrawing or danger signs are unlikely to
have pneumonia and should therefore not be given antibiotics.
Diagnosis
History
 previous episodes of wheeze
 Family history of allergy/atopy or asthma
 response to bronchodilators
 asthma diagnosis or long-term treatment for asthma
 night-time or early morning shortness of breath, cough or
wheeze.
Examination
 Shortness of breath at rest or on exertion
 wheezing on expiration
 prolonged expiration
 resonant percussion note

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  hyperinflated chest
 Lower chest indrawing if severe
 Rhonchi on auscultation
Response to rapid-acting bronchodilator
 If the cause of the wheeze is not clear, or if the child has fast
breathing or chest indrawing in addition to wheeze, give a rapid-
acting bronchodilator and assess after 15 minutes. Response to a
rapid-acting bronchodilator helps to determine the underlying
diagnosis and treatment.
 Give the rapid-acting bronchodilator by one of the following
methods:
o nebulized salbutamol
o salbutamol by a metered dose inhaler with spacer device
( may use locally available plastic bottles)
o if neither of the above methods is available, give a
subcutaneous injection of epinephrine (adrenaline).
 Assess the response after 15 minutes. Signs of
improvement are:
o less respiratory distress (easier breathing)
o less lower chest wall indrawing
o improved air entry.
 Children who still have signs of hypoxia (i.e. central cyanosis,
low oxygen saturation < 90, not able to drink due to
respiratory distress, severe lower chest wall indrawing) or
have fast breathing should be admitted to hospital for further
treatment.

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Table 4.3 Differential diagnosis of the child presenting with wheeze

Diagnosis In favour
Asthma History of recurrent wheeze, some unrelated to coughs
and colds
Hyperinflation of the chest
Prolonged expiration
Reduced air entry (if very severe, airway obstruction)
Good response to bronchodilators
History of atopy / family history of asthma or atopy
First episode of wheeze in a child aged <2 years
Wheeze episode at time of seasonal bronchiolitis
Bronchiolitis Hyperinflation of the chest
Prolonged expiration
Reduced air entry (if very severe, airway obstruction)
Poor/no response to bronchodilators
Wheeze always related to coughs and colds
\No family or personal history of asthma/eczema/hay
Wheeze fever
associated Prolonged expiration
with Reduced air entry (if very severe, airway obstruction)
cough or cold Good response to bronchodilators
Tends to be less severe than wheeze associated with
asthma
History of sudden onset of choking or wheezing
Wheeze may be unilateral
Foreign body Air trapping with hyper-resonance and mediastinal shift
Signs of lung collapse: reduced air entry and impaired
percussion note
No response to bronchodilators
Cough with fast breathing
Pneumonia Lower chest wall indrawing
Fever
Coarse crackles
Nasal flaring
Grunting

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4.5.1 Bronchiolitis
Bronchiolitis is a lower respiratory viral infection, which typically is most
severe in young infants, occurs in annual epidemics, and is characterized by
airways obstruction and wheezing. Respiratory syncytial virus is the most
important cause. Secondary bacterial infection may occur. The
management of bronchiolitis associated with fast breathing or other signs
of respiratory distress is therefore similar to that of pneumonia. Episodes
of wheeze may occur for months after an attack of bronchiolitis, but will
eventually stop.
Diagnosis
Typical features of bronchiolitis, on examination, include:
 wheezing which is not relieved by up to three doses of a rapid-
acting bronchodilator
 hyperinflation of the chest, with increased resonance to percussion
 lower chest wall indrawing
 fine crackles or wheezes on auscultation of the chest
 difficulty in feeding, breastfeeding or drinking owing to respiratory
distress.
 Nasal discharge, which can cause severe nasal obstruction
Treatment
Most children can be treated at home, but those with the following signs of
severe pneumonia should be treated in hospital.
 oxygen saturation < 90% or central cyanosis.
 apnoea or history of apnoea
 inability to breastfeed or drink, or vomiting everything
 convulsions, lethargy or unconsciousness
 gasping and grunting (especially in young infants).
Oxygen
 Give oxygen to all children with severe respiratory distress or
oxygen saturation ≤ 90% (see section 4.2.1). The recommended
method for delivering oxygen is by nasal prongs or a nasal catheter.

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 The nurse should check, every 3 hours, that the catheter or prongs
are in the correct position and not blocked with mucus, and that all
connections are secure.
Antibiotic treatment

 If the infant is treated at home, give amoxicillin (40 mg/kg twice a

day) orally for 5 days only if the child has signs of pneumonia (fast
breathing and lower chest wall indrawing).
 If there are signs of severe pneumonia, give ampicillin at 50 mg/kg
or
 benzylpenicillin at 50 000 U/kg IM or IV every 6 h for at least 5 days
and complete with PO amoxicilline for extra 5 days to complete a
10 day course

Supportive care
 If the child has fever (≥ 39 ° C) which appears to be causing distress,
give paracetamol
 Ensure that the hospitalized child receives daily maintenance fluids
appropriate for the child’s age (see chapter 10), but avoid
overhydration. Encourage breastfeeding and oral fluids.
 Encourage the child to eat as soon as food can be taken. Nasogastric
feeding should be considered in any patient who is unable to
maintain oral intake or hydration (expressed breast milk is the best).
 Gentle nasal suction should be used to clear secretions in infants
where nasal blockage appears to be causing respiratory distress.
Monitoring
A hospitalized child should be assessed by a nurse every 6 hours (or every 3
hours, if there are signs of very severe illness) and by a doctor at least once
a day. Monitor oxygen therapy Watch especially for signs of respiratory
failure, i.e. increasing hypoxia and respiratory distress leading to
exhaustion.

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Complications
If the child fails to respond to oxygen therapy, or the child’s condition
worsens suddenly, obtain a chest X-ray to look for evidence of
pneumothorax.
Tension pneumothorax associated with severe respiratory distress and shift
of the heart requires immediate relief by placing a needle in the affected
area to allow the air that is under pressure to escape (needle
thoracentesis). Following this, continuous air exit should be assured by
inserting a chest tube with an underwater seal until the air leak closes
spontaneously and the lung expands).

Infection control
Bronchiolitis is very infectious and dangerous to other young children in
hospital with other conditions. The following strategies may reduce cross-
infection:
 hand-washing by personnel between patients
 ideally isolate the child, but maintain close observation
 during epidemics, restrict visits to children by parents and siblings
with symptoms of upper respiratory tract infection.
Discharge
An infant with bronchiolitis can be discharged when respiratory distress
and hypoxaemia have resolved, when there is no apnoea and the infant is
feeding well.Infants are at risk for recurrent bronchiolitis if they live in
families where adults smoke or if they are not breastfed. So, advise the
parents against smoking.
Follow-up
Infants with bronchiolitis may have cough and wheeze for up to 3 weeks. As
long as they are well with no respiratory distress, fever or apnoea and are
feeding well they do not need antibiotics.

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4.5.2 Asthma
Asthma is a chronic inflammatory condition with reversible airways
obstruction. It is characterized by recurrent episodes of wheezing, often
with cough, which respond to treatment with bronchodilators and anti-
inflammatory drugs. Antibiotics should be given only when there are signs
of pneumonia.

Diagnosis
History - recurrent episodes of wheezing, often with cough. diffi culty in
breathing and tightness in the chest, particularly if these are frequent and
recurrent or are worse at night and in the early morning. Findings on
examination may include:
 Fast breathing
 Hypoxia (oxygen saturation < 90%)
 absence of fever
 lower chest wall indrawing
 use of accessory muscles for breathing (best noted by looking
at the muscles of the neck)
 prolonged expiration with audible wheeze
 reduced or no air entery when obstruction is life threatening
 hyperinflation of the chest
 usually good response to treatment with a bronchodilator.
If the diagnosis is uncertain, give a dose of a rapid-acting bronchodilator
(see adrenaline/epinephrine and salbutamol. A child with asthma will
usually improve rapidly, showing signs such as a decrease in the respiratory
rate and in chest wall indrawing and less respiratory distress. A child with
severe asthma may require several doses before a response is seen.

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Table 4.4 Asthma Treatment Algorithm
Mild Asthma Moderate Asthma Severe Asthma (life
threatening)
Normal mental state Normal to agitated Agitated or confused
Talks in sentences mental state mental state
Little or no accessory Talks in phrases Talk in single word or
muscle use Mild to moderate unable to talk
SPO2>95% accessory muscle Significant accessory
Wheeze + normal use muscle use
breath sounds SPO2 90-95% SPO2<90%
Wheeze + reduced Wheeze
breath sounds +significantly reduce
breath sounds
Note: If patient has sign or symptoms from two different categories,
always treat according to the most sever feature
Treatment
 A child with the first episode of wheezing and no respiratory
distress can usually be managed at home with supportive care and
with a bronchodilator.
 If the child is in respiratory distress (acute severe asthma) or has
recurrent wheezing, give salbutamol by nebulizer or metered-dose
inhaler. If salbutamol is not available, give subcutaneous
epinephrine. Reassess the child after 15 minutes to determine
subsequent treatment:
 If respiratory distress has resolved, and the child does not have
fast breathing, advise the mother on home care with inhaled
salbutamol from a metered dose and spacer devise (which can be
made locally from plastic bottles).or, when this is not available,
oral salbutamol syrup or tablets.
 If respiratory distress persists, admit to hospital and treat with
oxygen, rapid-acting bronchodilators and other drugs, as described
below.
Severe life-threatening asthma
 If the child has life-threatening acute asthma, is in severe

155
 respiratory distress with central cyanosis or reduced oxygen
saturation ≤ 90%, has poor air entry(silent chest), is unable to
drink or speak or is exhausted and confused, admit to hospital
and treat with oxygen, rapid-acting bronchodilators and other
drugs, as described below.
 In children admitted to hospital, promptly give oxygen, a rapid-
acting bronchodilator and a first dose of steroids.
Oxygen
 Give oxygen to keep oxygen saturation > 95% in all children with
asthma who are cyanosed (oxygen saturation ≤ 90%) or whose
difficulty in breathing interferes with talking, eating or
breastfeeding.
 A positive response (less respiratory distress, better air entry on
auscultation) should be seen in 15 minutes. If this does not occur,
give the rapid-acting bronchodilator at up to 1-hourly intervals.
 If there is no response after 3 doses of rapid-acting
bronchodilator, add IV aminophylline.
Rapid-acting bronchodilators
Give the child one of the three rapid-acting bronchodilators, nebulized
salbutamol, salbutamol by metered-dose inhaler with a spacer device, or
subcutaneous epinephrine (adrenaline), as described below.
1. Nebulized salbutamol
The driving source for the nebulizer must deliver at least 6–9 litres/minute.
Recommended methods are an air compressor or oxygen cylinder. If
neither is available, use a durable and easy-to-operate foot-pump,
although this is less effective.
Place the bronchodilator solution and 2–4 ml of sterile saline in the
nebulizer compartment and treat the child until the liquid is almost all used
up. The dose of salbutamol is 2.5 mg (i.e. 0.5 ml of the 5 mg/ml nebulizer
solution). This can be given 4-hourly, reducing to 6–8 hourly once the
child’s condition improves. If necessary in severe cases, it can be given
hourly.

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 2. Salbutamol by metered-dose inhaler with a spacer device
Spacer devices with a volume of 750 ml are commercially available.
Introduce two puffs (200 micrograms) into the spacer chamber. Then place
the child’s mouth over the opening in the spacer and allow normal
breathing for 3–5 breaths. This can be repeated in rapid succession until six
puffs of the drug have been given to a child < 5 years, 12 puffs for > 5 years
of age.

After 6 or 12 puffs, depending on age, assess the response and repeat

regularly until the child’s condition improves. In severe cases, 6 or 12 puffs
can begiven several times an hour for a short period.This can be reduced to
6–8 hourly after the child’s condition improves.
Some infants and young children cooperate better when a face mask is
attached to the spacer instead of the mouthpiece.
If commercial devices are not available, a spacer device can be made from
a plastic cup or a 1-litre plastic bottle. These require 3–4 puffs of
salbutamol and the child should breathe from the device for up to 30
seconds.
Subcutaneous epinephrine (adrenaline)
If the above two methods of delivering salbutamol are not available, give a
subcutaneous injection of epinephrine (adrenaline) - 0.01 ml/kg of 1:1000
solution (up to a maximum of 0.3 ml), measured accurately with a 1 ml
syringe. If there is no improvement after 15 minutes, repeat the dose once.

Figure 4.2: Use of spacer device

and face mask to give
bronchodilator treatment. A
spacer can be made locally
from a plastic soft-drink bottle.

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Steroids
If a child has a severe or life-threatening acute attack of wheezing (asthma),
give oral prednisolone, 1 mg/kg, for 3–5 days (maximum, 60 mg) or 20 mg
for children aged 2–5 years. If the child remains very sick, continue the
treatment until improvement is seen.
Repeat the dose of prednisolone for children who vomit, and consider IV
steroids if the child is unable to retain orally ingested medication.
Treatment for up to 3 days is usually suffi cient, but the duration should be
tailored to bring about recovery. Tapering of short courses (7–14 days) of
steroids is not necessary.
IV hydrocortisone (4 mg/kg repeated every 4 h) provides no benefit and
should be considered only for children who are unable to retain oral
medication.
Magnesium sulfate
Intravenous magnesium sulfate may provide additional benefit in children
with severe asthma treated with bronchodilators and corticosteroids.
Magnesium sulfate has a better safety profile in the management of acute
severe asthma than aminophylline. As it is more widely available, it can be
used in children who are not responsive to the medications described
above.
 Give 50% magnesium sulfate as a bolus of 0.1 ml/kg (50
mg/kg) IV over 20 minutes.
Oral bronchodilators
• Once the child has improved sufficiently to be discharged home, if
there is no inhaled salbutamol available or affordable, then oral
salbutamol (in syrup or tablets) can be given. The dose is: 0.075-0.1
mg/kg 3-4 times a day.
Aminophylline
Aminophylline is not recommended in children with mild-to-moderate
acute asthma. It is reserved for children who do not improve after several
doses of a rapid-acting bronchodilator given at short intervals plus oral
prednisolone.

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If indicated in these circumstances:
 Admit the child ideally to a high-care or intensive-care unit, if
available, for continuous monitoring.
 Weigh the child carefully and then give IV aminophylline at an initial
loading dose of 5–6 mg/kg (up to a maximum of 300 mg) over at
least 20 min but preferably over 1 h, followed by a maintenance
dose of 5 mg/kg every 6 h.

IV aminophylline can be dangerous at an overdose or when given

too rapidly.Omit the initial dose if the child has already received any
form of aminophylline or caffeine in the previous 24 h.Stop giving it
immediately if the child starts to vomit, has a pulse rate >180/min,
develops a headache, or has a convulsion.
Oral bronchodilators
Use of oral salbutamol (in syrup or tablets) is not recommended in the
treatment of severe or persistent wheeze. It should be used only when
inhaled salbutamol is not available for a child who has improved suffi
ciently to be discharged home.
Dosage:

 Age 1 month to 2 years: 100 μg/kg (maximum, 2 mg) up to four

times daily
 Age 2–6 years: 1–2 mg up to four times daily
Antibiotics
Antibiotics should not be given routinely for asthma or to a child with
asthma who has fast breathing without fever. Antimicrobial treatment is
indicated, however, when there is persistent fever and other signs of
pneumonia.
Supportive care
Ensure that the child receives daily maintenance fluids appropriate for
his/her age. Encourage breastfeeding and oral fluids. Encourage adequate
complementary feeding for the young child, as soon as food can be taken.
Monitoring
A hospitalized child should be assessed by a nurse every 3 hours, or every 6

159
hours as the child shows improvement (i.e. decreased breathing rate, less
lower chest wall indrawing, and less respiratory distress), and by a doctor
at least once a day.
Record the respiratory rate and watch especially for signs of respiratory
failure—increasing hypoxia and respiratory distress leading to exhaustion.
If the response to treatment is poor, give salbutamol more frequently, up
to once every 60 minutes. If this is ineffective, monitor oxygen therapy as
described on Section 10.7.
Complications
If the child fails to respond to the above therapy, or the child’s condition
worsens suddenly, obtain a chest X-ray to look for evidence of
complications like pneumothorax.
Follow-up care
Asthma is a chronic and recurrent condition.
 Once the child has improved sufficiently to be discharged home,
inhaled salbutamol through a metered dose inhaler should be
prescribed with a suitable (not necessarily commercial) spacer and
the mother instructed on how to use it.
 A long-term treatment plan should be made based on the
frequency and severity of symptoms. This may include
intermittent or regular treatment with bronchodilators, and
intermittent courses of steroids. See standard paediatric textbooks
for more information.
4.5.3 Wheeze with cough or cold
Most first episodes of wheezing in children aged <2 years are associated
with cough and cold. These children are not likely to have a family history
of atopy (e.g. hay fever, eczema, and allergic rhinitis) and their wheezing
episodes become less frequent as they grow older. The wheezing, if
troublesome, might respond to salbutamol treatment at home.

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4.6 Conditions presenting with stridor
Stridor is a harsh noise during inspiration, which is due to narrowing of the
air passage in the oropharynx, subglottis or trachea. If the obstruction is
severe, stridor may also occur during expiration.
The major causes of severe stridor are viral croup (caused by parainfluenza
virus, RST measles etc), foreign body, retropharyngeal abscess, diphtheria
congenital abnormalities or trauma to the larynx

Diagnosis
History
Depends on the cause of stridor
 first episode or recurrent episode of stridor
 history of choking
 stridor present soon after birth
 fever
 symptoms of common cold ( runny nose, sneezing)

Examination
 audible stridor
 hoarseness of the voice
 barking type of cough
 Other findings specific to the cause (bull neck appearance and
grey pharyngeal membrane in diphtheria, maculopapular skin
rashes in measles etc).
 decreased or absent air entry, cyanosis, signs of respiratory
distress in severe cases

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 Table 4.5 Differential diagnosis of the child presenting with stridor

Diagnosis In favour
Viral croup Barking cough
Respiratory distress
Hoarse voice
If due to measles, signs of measles (see section 6.4)

Retropharyngeal Soft tissue swelling

abscess Difficulty in swallowing
Fever

Foreign body Sudden history of choking

Respiratory distress
Diphtheria Bull neck appearance due to enlarged cervical nodes
and oedema
Red throat
Grey pharyngeal membrane
Blood-stained nasal discharge
No evidence of DTP vaccination
Congenital Stridor present since birth
anomaly laryngotracheomalacia

Soft stridor
Epiglottitis ‘Septic’ child
Little or no cough
Drooling of saliva
Inability to drink
Anaphylaxis History of allergen exposure
Wheeze
Shock
Urticaria and oedema of lips and face
Burns Swollen lips
Smoke inhalation

4.6.1 Viral croup

Croup causes obstruction in the upper airway which, when severe, can be
life-threatening. Most severe episodes occur in infants. This section deals
with croup caused by various respiratory viruses. For croup associated with
measles, see chapter 6.

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Diagnosis
Mild croup is characterized by:
 fever
 a hoarse voice
 a barking or hacking cough
 stridor that is heard only when the child is agitated
Severe croup is characterized by:
 stridor when the child is quiet
 rapid breathing and indrawing of the lower chest wall
 decreased or absent air entry on auscultation
 cyanosis

Table 4.6 Croup Scoring

0 1 2 3
Stridor None Mild Moderate at Severe on Inspiration
rest and Expiration
None or markedly
Reduced air entry
Retraction None Mild Moderate Severe and marked use
of accessory muscles
Air Entry Normal Mildly Moderately Markedly decreased
decreased decreased
Color Normal Normal Normal Cyanosed
Level of Normal Restless Anxious Lethargic
Consciousness When Agitated Depressed
disturbed Restless

Score:
1. Scores 1-5 = mild 2. Scores 6-7 = mild to moderate 3. Scores 7-8
= moderate mostly admitted 4. 8 and above or any of the severe
category needs admission for tracheostomy
Treatment
Mild croup can be managed at home with supportive care, including
encouraging oral fluids, breastfeeding or feeding, inhalation of steam at
home as appropriate

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A child with moderate and severe croup should be admitted to hospital for
treatment
Non drug therapy
 Mist therapy: giving humidified air using croup tent for
moderate croup. Oxygen should be given, if there is incipient
airway obstruction and a tracheotomy is deemed necessary
and is to be performed (Note that the use of nasal prongs or a
nasal or nasopharyngeal catheter can upset the child and
precipitate obstruction of the airway).
 Steroid treatment: Give one dose of dexamethasone (0.6
mg/kg IM), or equivalent dose of some other steroid like
prednisolone. If available, use nebulized budesonide at 2 mg.
Start the steroids as soon as possible. It is preferable to dissolve
the tablet in a spoonful of water for children unable to swallow
tablets. Repeat the dose of steroid for children who vomit.
 Antibiotics: These are not effective and should not be given.
 Adrenaline. As a trial, give the child nebulized adrenaline (2 ml
of 1:1000 solution). If this is effective, repeat as often as every
hour, with careful monitoring. While this treatment can lead to
improvement within 30 min in some children, it is often
temporary and may last only about 2 hours.
 Intubation and tracheotomy
 If there are signs of incipient airway obstruction, such as
severe indrawing of the lower chest wall and restlessness,
intubate the child immediately.
 If this is not possible, transfer the child urgently to a hospital
where intubation or emergency tracheotomy can be done.
 If this is not possible, monitor the child closely and ensure that
facilities for an emergency tracheotomy are immediately
available, as airway obstruction can occur suddenly.
Tracheotomy should only be done by experienced staff or a pediatric

164
surgeon.
Supportive care
 Don’t disturb the child
 If the child has fever (≥ 39 ° C or ≥ 102.2 ° F) which appears to be
causing distress, give paracetamol.
 Encourage breastfeeding and oral fluids.
 Children on croup tent should be on iv fluid till they are out of it
 Encourage the child to eat as soon as food can be taken.
Monitoring - The child’s condition, especially respiratory status, should be
assessed by nurses every 3 hours and by doctors twice a day. The child
should occupy a bed close to the nursing station, so that any sign of
incipient airway obstruction can be detected as soon as it develops.

4.6.2 Diphtheria
Diphtheria is a bacterial infection caused by Corynebacterium diphtheria
and it can be prevented by immunization. Infection in the upper airway or
nasopharynx produces a grey membrane which, when present in the larynx
or trachea, can cause stridor and obstruction. Nasal involvement produces
a bloody discharge. Diphtheria toxin causes muscular paralysis and
myocarditis, which is associated with increased mortality.
Diagnosis
Carefully examine the child’s nose and throat and look for a grey, adherent
membrane, which cannot be wiped off with a swab. Great care is needed
when examining the throat, as this may precipitate complete obstruction of
the airway. A child with pharyngeal diphtheria may have an obviously
swollen neck, termed a ‘bull neck’.

Figure 4.3: Pharyngeal membrane of

diphtheria; Note: the membrane
extends beyond the tonsils and covers
the adjacent pharyngeal wall.

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 Figure 4.4: Bull neck: a sign of
diphtheria due to enlarged
lymph nodes in the neck

Treatment
Antitoxin
• Give 40 000 units of diphtheria antitoxin (IM or IV) immediately,
because delay can lead to increased mortality.
 As there is a small risk of a serious allergic reaction to the horse
serum in the antitoxin, an initial intradermal test to detect
hypersensitivity should be carried out, as described in the
instructions and treatment for anaphylaxis be made available.
Antibiotics
Any child with suspected diphtheria should be given procaine penicillin
(50, 000 units/kg IM) daily for 7 days.
Oxygen
 Avoid using oxygen unless there is incipient airway obstruction.
Signs such as severe indrawing of the lower chest wall and
restlessness are more likely to indicate the need for
tracheostomy (or intubation) than oxygen. Moreover, the use of
nasal prongs or a nasal or nasopharyngeal catheter can upset
the child and precipitate obstruction of the airway.
 However, oxygen should be given, if there is incipient airway
obstruction and a tracheotomy is deemed necessary and is to be
performed.

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Tracheotomy/intubation
 Tracheotomy should be performed only by experienced staff or
surgeon, if there are signs of incipient airway obstruction, such
as severe lower chest wall indrawing and restlessness. If
obstruction occurs, an emergency tracheostomy should be
carried out. Orotracheal intubation is an alternative, but may
dislodge the membrane and fail to relieve the obstruction.
Supportive care
 If the child has fever (≥ 39°C or ≥ 102.2°F) which appears to be
causing distress, give paracetamol.
 Encourage the child to eat and drink. If there is difficulty in
swallowing, nasogastric feeding is required.
 Avoid frequent examinations or disturbing the child unnecessarily.
Monitoring
The child’s condition, especially respiratory status, should be assessed by
nurses every 3 hours and by doctors twice a day. The child should occupy a
bed close to the nursing station, so that any sign of incipient airway
obstruction can be detected as soon as it develops.
Complications
Myocarditis and paralysis may occur 2–7 weeks after the onset of illness.
Signs of myocarditis include a weak, irregular pulse and evidence of heart
failure. Refer to standard paediatric textbooks for details of the diagnosis
and management of myocarditis.
Public health measures
 Nurse the child in a separate room by staffs that are fully
immunized against diphtheria.
 Give all immunized household contacts a diphtheria toxoid
booster.
 Give all unimmunized household contacts one IM dose of
benzathine penicillin (600,000 units to those aged ≤ 5 years;
1,200,000 units to those aged >5 years). Immunize them with

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 diphtheria toxoid and check daily for 5 days for any signs of
diphtheria.

4.6.3 Epiglottitis
Epiglottitis is a medical emergency that may result in death if not treated
quickly. It is mainly caused by the bacteria H. infl uenzae type b but may
also be caused by other bacteria or viruses associated with upper
respiratory infections.
Epiglottitis usually begins as an infl ammation and swelling between the
base of the tongue and the epiglottis. The swelling may obstruct the
airway.
Diagnosis
 sore throat with diffi culty in speaking
 diffi culty in breathing
 soft stridor
 fever
 drooling of saliva
 difficulty in swallowing or inability to drink.
Treatment
Treatment of patients with epiglottitis is directed to relieving the airway
obstruction and eradicating the infectious agent.
 Keep the child calm, and provide humidified oxygen, with close
monitoring.
 Avoid examining the throat if the signs are typical, to avoid
precipitating
obstruction.
 Call for help and secure the airway as an emergency because of
the danger
of sudden, unpredictable airway obstruction. Elective intubation is
the best treatment if there is severe obstruction but may be very
difficult; consider the need for surgical intervention to ensure
airway patency.
 Give IV antibiotics when the airway is safe: ceftriaxone at 80
mg/kg once daily for 5 days.

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4.6.4 Anaphylaxis
Anaphylaxis is a severe allergic reaction, which may cause upper airway
obstruction with stridor, lower airway obstruction with wheezing or shock
or all three. Common causes include allergic reactions to antibiotics, to
vaccines, to blood transfusion and to certain foods, especially nuts.
Consider the diagnosis if any of the following symptoms is present and
there is a history of previous severe reaction, rapid progression or a history
of asthma, eczema or atopy.
This situation is potentially life-threatening and may result in a change in
level of consciousness, collapse, or respiratory or cardiac arrest.
 Assess the airways, breathing and circulation.
 If the child is not breathing, give five rescue breaths with a bag-
valve mask and 100% oxygen and assess circulation.
 If no pulse, start basic life support

Table 4.7 classification of the severity of anaphylaxis

Treatment
 Remove the allergen as appropriate.
 For mild cases (just rash and itching), give oral antihistamine and oral
prednisolone at 1 mg/kg.
 For moderate cases with stridor and obstruction or wheeze:
o Give adrenaline at 0.15 ml of 1:1000 IM into the thigh (or
subcutaneous); the dose may be repeated every 5–15

169
 min.
 For severe anaphylactic shock:
o Give adrenaline at 0.15 ml of 1:1000 IM and repeat every
5–15 min.
o Give 100% oxygen.
 Ensure stabilization of the airway, breathing, circulation and secure
IV access.
 If the obstruction is severe, consider intubation or call a
anaesthetist and surgeon to intubate or create a surgical airway.
 Administer 20 ml/kg normal saline 0.9% or Ringer’s lactate solution
IV asrapidlyas possible. If IV access is not possible, insert an
intraosseous line.
4.7 Conditions presenting with chronic cough
Chronic cough is one that lasts for more than 2 weeks.
History
Ask for
 duration of coughing
 nocturnal cough
 paroxysmal cough or associated severe bouts ending with
vomiting or whooping
 weight loss (check growth chart, if available), night sweats
 persistent fever
 close contact with a known case of Tb patients or with pertussis
 history of attacks of wheeze and a family history of allergy or
asthma
 history of choking or inhalation of a foreign body
 child suspected or known to be HIV-infected
 treatment given and response
Examination
 fever
 lymphadenopathy (generalized and localized, e.g. in the neck)
 wasting
 wheeze / prolonged expiration

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  apnoeic episodes
 subconjunctival haemorrhages
 signs associated with foreign body aspiration:
o unilateral wheeze
o area of decreased breath sounds which is either dull or
hyper-resonant on percussion
o deviation of the trachea or apex beat.
 signs associated with HIV infection.
 clubbing , cyanosis
 cardiac findings (murmur)
Table 4.8 Differential diagnosis of the child presenting with
chronic cough
Diagnosis In favour

Tuberculosis Weight loss or failure to thrive

Anorexia, night sweats
Enlarged liver and spleen
Chronic or intermittent fever
History of contact with chronic cougher
Signs of fluid in chest (dull to percussion/reduced breath
sounds)
Asthma History of recurrent wheeze, often unrelated to coughs and
colds
History of asthma/atopy in the family
Hyperinflation of the chest
Prolonged expiration
Reduced air entry (in very severe airway obstruction)
Good response to bronchodilators
Foreign body Sudden onset of choking or stridor ,wheezing or hyperinflation
Unilateral chest signs
Recurrent lobar consolidation
Poor response to medical treatment
Pertussis Paroxysms of cough followed by whoop, vomiting, cyanosis or
apnoea
Subconjunctival haemorrhages
No history of DPT immunization
Afebrile

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 HIV Known or suspected maternal or sibling HIV infection
History of blood transfusion
Failure to thrive
Oral thrush
Chronic parotitis
Skin infection with herpes zoster (past or present)
Generalized lymphadenopathy
Chronic fever
Persistent diarrhoea
Finger clubbing
Bronchiectasis History of tuberculosis or aspirated foreign body
Poor weight gain
Purulent sputum, bad breath
Finger clubbing
Localized signs on X-ray
Lung abscess Reduced breath sounds over abscess
Poor weight gain / chronically ill child
Cystic or cavitating lesion on chest X-ray

4.7.1 Pertussis
Caused by a bacteria Bordetella pertussis .It is most severe in young infants
who have not yet been immunized. After an incubation period of 7–10
days, the child develops fever, usually with a cough and nasal discharge
which clinically are indistinguishable from a common cold and cough. In the
second week, there is paroxysmal coughing which can be recognized as
pertussis. The episodes of coughing can continue for 3 months or longer.
The child is infectious for a period of 2 weeks up to 3 months after the
onset of illness.
Diagnosis
Suspect pertussis if a child has been having a severe cough for more than
two weeks, especially if the disease is known to be occurring locally. The
most useful diagnostic signs are:
 Paroxysmal coughing followed by a whoop when breathing
in, often with vomiting
 Subconjunctival haemorrhages
 Child not immunized against pertussis.

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  Young infants may not whoop; instead, the cough may be
followed by cessation of breathing (apnoea) or cyanosis, or
apnoea may occur without coughing.
 Also, examine the child for signs of pneumonia and ask
about convulsions.

Figure 4.5: Subconjunctival

haemorrhages prominent on
the white sclera

Treatment
Treat mild cases in children aged ≥ 6 months at home with supportive care.
Admit infants aged under 6 months to hospital; also admit any child with
pneumonia, convulsions, dehydration, severe malnutrition, or prolonged
apnoea or cyanosis after coughing.
Antibiotics
 Give oral erythromycin (12.5 mg/kg four times a day) for 10
days. This does not shorten the illness but reduces the period of
infectiousness.
 Alternatively, if available, give azithromycin at 10 mg/kg
(maximum, 500 mg) on the first day, then 5 mg/kg (maximum,
250 mg) once a day for 4 days.
 If there is fever, if erythromycin or azithromycin is not available,
or if there are signs of pneumonia, treat with amoxicillin as
possible secondary pneumonia.
 Follow the other guidelines for severe pneumonia

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Oxygen
 Give oxygen to children who have spells of apnoea or cyanosis, or
severe paroxysms of coughing or low oxygen saturation < 90% on a
pulse oxymeter
 Use nasal prongs, not a nasopharyngeal catheter or nasal catheter
which can provoke coughing. Place the prongs just inside the nostrils
and secure with a piece of tape just above the upper lip. Care should
be taken to keep the nostrils clear of mucus since this blocks the
flow of oxygen. Set a flow rate of 1–2 litres/min (0.5 litre/min in
young infants). Humidification is not required with nasal prongs.
 Continue oxygen therapy until the above signs are no longer
present, after which there is no value in continuing with oxygen.
 The nurse should check, every 3 hours, that the prongs or catheter
are in the correct place and not blocked with mucus, and that all
connections are secure.
Airway management
 During paroxysms of coughing, place the child head down and
prone, or on the side, to prevent any inhaling of vomitus and to
aid expectoration of secretions.
 If the child has cyanotic episodes, clear secretions from the nose
and throat with brief, gentle suction.
 If apnoea occurs, clear the airway immediately with gentle
suction, give manual respiratory stimulation or bag ventilation,
and administer oxygen.
Supportive care
 Avoid, as far as possible, any procedure that could trigger
coughing, such as application of suction, throat examination,
and use of a nasogastric tube.
 Do not give cough suppressants, sedatives, mucolytic agents or
anti histamines.
 If the child has fever (≥ 39 ° C) which appears to be causing

174
 distress, give paracetamol.
 Encourage breastfeeding or oral fluids. If the child cannot drink,
pass a nasogastric tube and give small, frequent amounts of fluid
to meet the child’s maintenance needs (see chapter 10). If there
is respiratory distress, give maintenance fluids IV to avoid the
risk of aspiration and reduce triggering of coughing. Ensure
adequate nutrition by giving smaller, more frequent feeds. If
there is continued weight loss despite these measures, feed the
child by nasogastric tube.
Monitoring
The child should be assessed by nurses every 3 hours and by the doctor
once a day. To facilitate observation for early detection and treatment of
apnoeic or cyanotic spells, or severe episodes of coughing, the child should
occupy a bed in a place close to the nursing station where oxygen is
available. Also, teach the child’s mother to recognize apnoeic spells and to
alert the nurse if these occur.
Complications
Pneumonia: is the most common complication of pertussis caused by
secondary bacterial infection or inhalation of vomited material.
 Signs suggesting pneumonia include fast breathing between
coughing episodes, fever, and the rapid onset of respiratory
distress.
 Treat pneumonia in children with pertussis as follows:
o Give parenteral ampicillin (or benzylpenicillin) for 5
days,or alternatively give azithromycin for 5 days.
o Give oxygen as described for the treatment of severe
pneumonia
Convulsions: These may result from anoxia associated with an
apnoeic or cyanotic episode, or toxin-mediated encephalopathy.
 If a convulsion does not stop within two minutes, give an
anticonvulsant (diazepam or paraldehyde)

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Malnutrition: Children with pertussis may become malnourished as a result
of reduced food intake and frequent vomiting.
 Prevent malnutrition by ensuring adequate feeding, as
described above, under “supportive care”.
Haemorrhage and hernias: Subconjunctival haemorrhage and epistaxis are
common during pertussis.
 No specific treatment is needed.
 Umbilical or inguinal hernias may be caused by violent
coughing.
 Do not treat them unless there are signs of bowel obstruction,
but refer the child for surgical evaluation after the acute phase.
Public health measures
 Give DPT immunization to any child in the family who is not fully
immunized and to the child with pertussis.
 Give a DPT booster to previously immunized children.
 Give erythromycin estolate orally (12.5 mg/kg 4 times a day)
for 14 days should be given promptly to all household and
other close contacts such as day care regardless of age, history
of immunization or symptoms.

4.7.2 Tuberculosis
Most children infected with Mycobacterium tuberculosis do not develop
tuberculosis disease. The only evidence of infection may be a positive skin
test. The development of tuberculosis disease depends on the competence
of the immune system to resist multiplication of the M. tuberculosis
infection. This competence varies with age, being least in the very young.
HIV and severe malnutrition lower the body’s defences, and measles and
whooping cough temporarily impair the strength of the immune system. In
the presence of any of these conditions, tuberculosis disease can develop
more easily. Any organ including cervical lymph nodes, bones, joints,
abdomen, ear, eye, and skin may be affected by M.tuberculosis.
But it is most often severe when the disease is located in the lungs,
meninges or kidney. Many children present only with failure to grow

176
normally, weight loss or prolonged fever. Chronic cough can also be a
presenting sign; in children, however, sputum-positive pulmonary
tuberculosis is rarely diagnosed.
Diagnosis
The risk of tuberculosis is increased when there is an active case
(infectious, smear-positive pulmonary tuberculosis) in the same house, or
when the child is malnourished, has HIV/AIDS, or has had measles in the
past few months. Consider tuberculosis in any child with the following:
History:
 unexplained weight loss or failure to grow normally;
 unexplained fever, especially when it continues for more than
2 weeks;
 chronic cough (i.e. cough for more than 3 weeks)
 exposure to an adult with probable or definite pulmonary
tuberculosis.
Examination:
 enlarged non-tender lymph nodes or a lymph node abscess,
especially in the neck
 crackles, bronchial breath sound , etc
 signs of fluid in the chest
 signs of meningitis, especially when these develop over several
days and the spinal fluid contains mostly lymphocytes and
elevated protein;
 abdominal swelling, with or without palpable lumps; ascites
 progressive swelling or deformity in the bone or a joint,
including the spine.
Investigations
 Try to obtain specimens for microscopic examination of acid-fast
bacilli (Ziehl-Neelsen stain) and for culture of tubercle bacilli.
Possible specimens include three consecutive early morning
fasting gastric aspirates, sputum, CSF (if clinically indicated), and

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 pleural fluid and ascites fluid. Owing to low detection rates by
these methods, a positive result would confirm tuberculosis, but
a negative result does not exclude the disease.
 Obtain a chest X-ray. A diagnosis of tuberculosis is supported
when a chest X-ray shows a miliary pattern of infiltrates or a
persistent area of infiltrate or consolidation, often with pleural
effusion, or a primary complex.
 Perform a PPD skin test: The test is usually positive in children
with tuberculosis (reactions of >10 mm are suggestive of
tuberculosis; <10 mm in a child, previously immunized with BCG,
is equivocal). However, the PPD test may be negative in children
with tuberculosis who have HIV/AIDS or when there is miliary
disease, severe malnutrition or recent measles.
 Xpert MTB/RIF should be used as the initial diagnostic test in
children suspected of having multidrug-resistant TB (MDR-TB) or
HIV-associated TB.
 Routine HIV testing should be offered to all children suspected
of TB.
Treatment
The lesions of primary tuberculosis have a smaller number of M.
tuberculosis organisms than those of secondary (reactivated) pulmonary
tuberculosis. Thus, treatment failure, relapse, and development of
secondary resistance are less common among children. Children with
pulmonary TB usually have low bacterial load, as cavitating disease is
relatively rare. On the other hand, children more often develop extra-
pulmonary TB (EPTB). Very severe and disseminated TB (e.g. miliary TB and
TB meningitis) is commonly found in the young (<3 years old) child.
Because tuberculosis in infants and children younger than 4 years of age is
more likely to disseminate, treatment should be started as soon as the
diagnosis is made.

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Children and adolescents with adult-type pulmonary tuberculosis should be
treated with the initiation of four-drug regimen. Three times a week
therapy is not recommended for children. Pyridoxine is recommended for
infants, children, and adolescents who are being treated with INH and who
have nutritional deficiencies, symptomatic HIV infection, or who are
breastfeeding. DOT should be used for all children with tuberculosis. Even
when drugs are given under DOT, tolerance of the medications must be
monitored closely. DOTS treatment must be directly supervised by health
professionals. In general, extra-pulmonary tuberculosis in children can be
treated with the same regimens as pulmonary disease. Exceptions are
disseminated TB disease, and meningitis, for which the recommended
duration is 9 to 12 months.

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Table 4.9 Anti-TB regimens for children

(FMOHE, GUIDELINES FOR CLINICAL AND PROGRAMMATIC MANAGEMENT OF TB,

LEPROSY AND TB/HIV IN ETHIOPIA, APRIL, 2012)
NOTE: 1. Children with suspected or confirmed Tuberculous meningitis,
genitor-urinary and osteo-articular TB should be treated with a
four-drug regimen (HRZE) for 2 months, followed by a two-drug

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 regimen (HR) for 10 months; the total duration of treatment
being 12 months. The recommended treatment dosages are the
same as those described for pulmonary tuberculosis.
2. All Anti-TB drugs should be administered daily and intermittent
therapy is not recommended.
Table 4.9.1 Recommended doses of paediatric treatment:
Recommended dose

Daily
Drug
Dose and range Maximum
mg/Kg body (mg)
weight)
Isoniazid 10 (10-15) 300

Rifampicin 15 (15-20) 600

Pyrazinamide 25 (20- 30) -

Ethambutol 20 (20- 30) -

(FMOHE, Tuberculosis, Leprosy and Tb/HIV prevention and Control

Program, Manual 4th edition, 2008)
The recommended dose of Ethambutol is higher in children (20 mg/Kg)
than in adults (15 mg/Kg), because the pharmacokinetics is different.
Although ethambutol was frequently omitted from treatment regimens for
children in the past, due in part to concerns about the difficulty of
monitoring for toxicity (particularly for optic neuritis) in young children, a
literature review indicates that it is safe in children at a dose of 20 mg/Kg
[range 15-25 mg/Kg/daily].
Streptomycin should be avoided when possible in children because the
injections are painful and irreversible auditory nerve damage may occur.

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Multidrug-resistant TB
In cases of MDR TB, treat children with proven or suspected pulmonary TB
or tuberculous meningitis with a fl uoroquinolone or other second-line TB
drug. An appropriate MDR TB treatment regimen in the context of a
wellfunctioning MDR TB control programme should be used. The decision
to treat should be taken by a clinician experienced in managing paediatric
TB. For detailed information refer the national MDR TB guideline.
Monitoring
Confirm that the medication is being taken as instructed, by direct
observation of each dose. Monitor the child’s weight gain (daily) and
temperature (twice daily) in order to check for resolution of the fever.
These are signs of the response to therapy. When treatment is given for
suspected tuberculosis, improvement should be seen within one month. If
this does not happen, review the patient, check compliance and reconsider
the diagnosis.
Public health measures
 Notify the case to the responsible district health authorities.
Ensure that treatment monitoring is carried out, as recommended
by the national tuberculosis programme. Check all household
members of the child (and, if necessary, school contacts) for
undetected cases of tuberculosis and arrange treatment for any
who are found.
 Children < 5 years of age who are household or close contacts of
people with TB and who, after an appropriate clinical evaluation,
are found not to have active TB should be given 6 months of
isoniazid preventive therapy (10 mg/ kg/day, range 7–15 mg/kg,
maximum dose 300 mg/day).
Follow-up
A programme of ‘active’ follow-up, in which a health worker visits the child
and his or her family at home, can reduce default from TB treatment.
During follow-up at home or in hospital, health workers can:
 Check whether medications for TB are being taken regularly.

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 Remind the family and the treatment supporter about the
importance of taking medications regularly, even if the child is
well, for the full duration of treatment.
 Screen family contacts, including other children in the family, by
inquiring about cough, and start these children on isoniazid
preventive therapy.
 Suggest how the family’s home environment might be made
healthier for children, such as eliminating smoking inside the
house, good ventilation and hand-washing.
 Discuss with the parents the importance of nutrition in recovery
from TB and any problems in providing good nutrition for their
children.
 Check the child for growth, nutritional state and signs of TB and
other treatable conditions. If problems are found, the health
worker should recommend how these can be treated or refer the
family to a paediatrician.
 Check the child’s health record, and tell the parents when and
where they should bring the child for doses of vaccine.
 Ask the parents if they have any questions or concerns, and
answer or discuss these, or refer the family to a paediatrician.
 Record their observations on the TB treatment card.
4.7.3 Foreign body aspiration
Nuts, seeds or other small objects may be inhaled, most often by children
under 4 years of age. The foreign body usually lodges in a bronchus (more
often in the right) and can cause collapse or consolidation of the portion of
lung distal to the site of blockage. Choking is a frequent initial symptom.
This may be followed by a symptom-free interval of days or weeks before
the child presents with persistent wheeze, chronic cough or pneumonia,
which fails to respond to treatment. Small sharp objects can lodge in the
larynx causing stridor or wheeze. Rarely, a large object lodging in the larynx
could cause sudden death from asphyxia, unless an emergency

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tracheostomy is done.
Diagnosis
Inhalation of a foreign body should be considered in a child with the
following signs:
 sudden onset of choking, coughing or wheezing; or
 segmental or lobar pneumonia which fails to respond to
antibiotic therapy (note also differential diagnosis of
tuberculosis.
Examine the child for:
 unilateral wheeze;
 an area of decreased breath sounds which is either dull or
hyper-resonant on percussion;
 deviation of the trachea or apex beat.
Obtain a chest X-ray at full expiration to detect an area of hyper-inflation or
collapse, mediastinal shift (away from the affected side), or a foreign body
if it is radio-opaque.
Treatment
Emergency first aid for the choking child is mandatory. Attempt to dislodge
and expel the foreign body. The maneuver depends on the age of the child.
For infants:
 Lay the infant on one arm or on the thigh in a head-down
position.
 Strike the infant’s back five times with the heel of the hand.
 If the obstruction persists, turn the infant over and give five
chest thrusts with two fingers, one finger’s breadth below the
nipple level in the midline.
 If the obstruction persists, check the infant’s mouth for any
obstruction which can be removed.
 If necessary, repeat this sequence with back slaps again.
For older children:
 While the child is sitting, kneeling or lying, strike the child’s back five

184
 times with the heel of the hand.
 If the obstruction persists, go behind the child and pass your arms
around the child’s body; form a fist with one hand immediately
below the sternum; place the other hand over the fist and thrust
sharply upwards into the abdomen. Repeat this up to five times.
 If the obstruction persists, check the child’s mouth for any
obstruction which can be removed.
 If necessary, repeat the sequence with back slaps again.
 Once this has been done, it is important to check the patency of
the airway by:
o looking for chest movements
o listening for breath sounds, and
o feeling for breath.
If further management of the airway is required after the obstruction is
removed see chapter 4. This describes actions which will keep the child’s
airway open and prevent the tongue from falling back to obstruct the
pharynx while the child recovers.
 If not sure of foreign body or suspected refer the child to a
hospital where diagnosis is possible and the object can be
‘removed’ by bronchoscopy. If there is evidence of pneumonia,
begin treatment with ampicillin and gentamicin, as for severe
pneumonia.

4.8 Heart failure

Heart failure in infants and young child may be manifested by fast
breathing and respiratory distress. Underlying causes include congenital
heart disease (usually in the first few months of life), acute rheumatic
fever, myocarditis, pericarditis with or without constriction, infective
endocarditis, acute glomerulonephritis, severe anaemia, and severe
malnutrition. Heart failure can be precipitated or worsened by fluid
overload, especially when giving salt-containing IV fluids.

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Table 4.10 Normal pulse rate for age

Age Lower limits of Average Upper limits of

normal normal
Newborn 70/mn 125/mn 190/mn
1-11 mo 80 120 160
2 yr 80 110 130
4 yr 80 100 120
6 yr 75 100 115
8 yr 70 90 110
10 yr 70 90 110
th
Nelson Text book of Pediatrics 19 edition

Diagnosis
The most common signs of heart failure, on examination, are:
 Fast breathing or interruption of feeding wit diaphoresis
 Tachycardia (heart rate >160/minute in a child under 12 months
old; >120/minute in a child aged 12 months to 5 years).
 Basal crackles on chest exam
 Gallop rhythm on auscultation with or without murmurs.
 Enlarged, tender liver.
 In older children: oedema of the feet, hands or face, or raised JVP
 Severe palmar pallor may be present if severe anaemia is the
cause of the heart failure.
 If the diagnosis is in doubt, a chest X-ray can be taken and will
show an enlarged heart.
 Measure blood pressure if possible. If raised consider acute
glomerulonephritis or coarctation of the aorta (see standard
paediatric textbook for treatment)
Treatment
 Oxygen: Give oxygen if the child has a respiratory rate of ≥

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 70/min, shows signs of respiratory distress, or has central
cyanosis. (Section 10.7).
 Diuretics: Give furosemide (frusemide): a dose of 1 mg/kg
should cause increased urine flow within 2 hours. For faster
action, give the drug IV. If the initial dose is not effective, give 2
mg/kg and repeat in 12 hours, if necessary. Thereafter, a single
daily dose of 1–2 mg/kg orally..
 Supplemental potassium: if frusemide is given for more than 5
days, give spironolactone if not available add oral potassium
(3–5 mmol/kg/day).
 Digoxin: after evaluation by a cardiologist.
Supportive care
 Avoid the use of IV fluids, where possible.
 Support the child in a semi-seated position with head and
shoulders elevated and lower limbs dependent.
 Relieve any fever with paracetamol to reduce the cardiac
workload.
 Avoid unnecessary movement and transportation
 Consider transfusion if severe anemia is present
Monitoring
The child should be checked by nurses every hour and by doctors once a
day. Monitor daily both respiratory and pulse rates, liver size, and body
weight to assess the response to treatment. Continue treatment until the
respiratory and pulse rates are normal and the liver is no longer enlarged.
 Consult cardiologist

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CHAPTER 5 – DIARRHOEA

This chapter gives treatment guidelines on the management of acute

diarrhoea (with severe, some or no dehydration), persistent diarrhoea, and
dysentery in children 2 months to 5 years. Assessment and management of
diarrhea in severely malnourished children is described in another section.
The 3 essential elements in the management of all children with diarrhoea
are rehydration therapy, zinc supplementation and counseling for
continued feeding and prevention.

During diarrhea there is an increased loss of water and electrolytes

(sodium, potassium, bicarbonate and zinc) in the liquid stool. Dehydration
occurs when these losses are not adequately replaced and a deficit of
water and electrolytes develops. The degree of dehydration is graded
according to symptoms and signs that reflect the amount of fluid. The
rehydration regimen is selected according to the degree of dehydration.
Zinc is an important micronutrient for a child’s overall health and
development. Zinc is lost in greater quantity during diarrhoea. Replacing
the lost zinc is important to help the child recover and to keep the child
healthy in the coming months. For these reasons, all patients with
diarrhoea should be given zinc supplements as soon as possible after the
diarrhoea has started.
During diarrhoea, a decrease in food intake and nutrient absorption and
increased nutrient requirements often combine to cause weight loss and
failure to grow. In turn, malnutrition can make the diarrhoea more severe,
more prolonged and more frequent, compared with diarrhoea in non-
malnourished children. This vicious circle can be broken by giving nutrient-
rich foods during the diarrhoea and when the child is well.
Antibiotics should not be used routinely. “Anti diarrhoeal” drugs and anti-
emetics should not be given to young children with acute or persistent
diarrhoea or dysentery; they do not prevent dehydration or improve

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nutritional status and some have dangerous, sometimes fatal, side-effects.

5.1 Child presenting with diarrhoea

History
A careful feeding history is essential in the management of a child with
diarrhoea. Also, inquire into the following:
 Diarrhea
o Frequency of stools
o Duration of diarrhea
o Presence of blood in stools
 Local reports of cholera outbreak
 Recent antibiotic or other drug treatment
 Attacks of crying with pallor in an infant
 Condition of feeding
 Presence of danger signs
 Last voiding (urine)

Physical Examination
Check for vital signs: also helps for follow up
Look for:
 Signs of dehydration:
o Restlessness or irritability
o Lethargy/reduced level of consciousness
o Sunken eyes
o Skin pinch returns slowly or very slowly
o Thirsty/drinks eagerly, or drinking poorly or not able
to drink
 Signs of shock
o Capillary refill

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 o Mental status
 Blood in stool
 Signs of severe malnutrition
 Abdominal mass
 Abdominal distension
Investigation:
The following investigations directed to diarrhea can be done in hospitals
 Stool examination (microscopy)
 Stool Culture & Sensitivity test
 Investigations directed to complications
There is no need for routine stool microscopy or culture in children except
with bloody and persistent diarrhea.

Table 5.1 Differential diagnosis of the child presenting with diarrhea

Diagnosis In favour
Acute (watery) diarrhea More than 3 stools per day
No blood in stools
Cholera Diarrhoea with severe dehydration during
cholera outbreak
Positive stool culture for V. cholerae O1 or O139
Dysentery Blood in stool (seen or reported)
Persistent diarrhea Diarrhoea lasting 14 days or longer
Diarrhoea with severe Any diarrhoea with signs of severe malnutrition
malnutrition
Diarrhoea associated Recent course of broad-spectrum antibiotics
with recent antibiotic
use
Intussusceptions Blood in stool
Abdominal mass (check with rectal examination)
Attacks of crying with pallor in infant

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5.2 Acute Diarrhoea
Table 5.2: Classification of the severity of dehydration in children with
diarrhea

Classification Signs or symptoms Treatment

Severe Two or more of the  Give fluid for severe dehydration
dehydration following signs:  (see Diarrhoea Treatment Plan C
 Lethargy/unconsci in in section 5.2.1
ousness
 Sunken eyes
 Unable to drink or
drinks poorly
 Skin pinch goes
back very slowly
( ≥ 2 seconds )
Some Two or more of the  Give fluid and food for some
dehydration following dehydration - Treatment Plan B
signs:dehydration (see sec 5.2.2
Diarrhoea  After rehydration, advise mother
 Restlessness, on home treatment and when
irritability to return immediately
 Sunken eyes  Follow up in 5 days if not
 Drinks eagerly, improving
thirsty, may not be
reliable sign for
young infants
 Skin pinch goes
back slowly
No  Not enough signs to  Give fluid and food to treat
dehydration classify assome or diarrhoea at home (see
severe dehydration DiarrhoeaTreatment Plan A,
Section 5.2.3)
 Advise mother on when to return
immediately (see Section 5.2.3)
 Follow up in 5 days if not
improving.

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Assessing dehydration
For all children with diarrhoea, hydration status should be assessed and
classified as severe dehydration, some dehydration or no dehydration and
appropriate treatment given.
5.2.1 Severe Dehydration
Children with severe dehydration require rapid IV rehydration with close
monitoring, which is followed by oral rehydration once the child starts to
improve sufficiently.

Diagnosis
If any two of the following signs are present in a child with diarrhoea,
severe dehydration should be diagnosed:
 Lethargy or unconsciousness
 Sunken eyes
 Skin pinch goes back very slowly (2 seconds or more)
 Not able to drink or drinks poorly.

Figure 5.1 Sunken eyes

Treatment
• Start IV fluids immediately. While the drip is being set up, give
ORS solution if the child can drink.

Note: The best IV fluid solutions for rehydration are isotonic solutions:

192
Ringer’s lactate or normal saline (0.9% NaCl). Do not use 5% glucose
(dextrose) solution as they increase the risk for hyponatraemia, which can
cause cerebral oedema.

When the full amount of IV fluid has been given, reassess the child’s
hydration status fully. Persistent severe dehydration after IV rehydration is
unusual; it usually occurs only in children who pass large watery stools
frequently during the rehydration period. If the child is improving but still
shows signs of some dehydration, discontinue IV treatment and give ORS
solution for 4 hours.
Chart 5.1 Diarrhea Treatment Plan C: Treat severe dehydration quickly

193
Cholera - Suspect cholera in children over 2 years old who have acute
watery diarrhoea and signs of severe dehydration, if cholera is occurring in
the area.
 Assess and treat dehydration as for other acute diarrhoea.
 Give an oral antibiotic to which strains of Vibrio cholerae in the area are
known to be sensitive. Possible choices are: tetracycline: 12.5mg/kg 4
times a day for 3 days or erythromycin 4 times a day for 3 days.
 Prescribe zinc supplementation as soon as vomiting stops

Figure 5.2 pinching the child’s abdomen to test for decreased skin turgor

Figure 5.3 Very slow return of skin pinch in severe dehydration

Monitoring
Reassess the child every 15–30 min until a strong radial pulse is present.
Thereafter, reassess the child by checking skin pinch, level of consciousness
and ability to drinkat least every hour, in order to confirm that hydration is
improving. Sunken eyes recover more slowly than other signs and are less

194
useful for monitoring.
When the full amount of IV fluid has been given, reassess the child’s
hydration statusfully.
 If signs of severe dehydration are still present, repeat the IV fluid
infusion outlined earlier. Persistent severe dehydration after IV
rehydration is unusual; it usually occurs only in children who pass
large watery stools frequently during the rehydration period.
 If the child is improving but still shows signs of some dehydration,
discontinue IV treatment and give ORS solution for 4 h (see section
5.2.2 and treatment plan B). If the child is usually breastfed,
encourage the mother tocontinue breastfeeding frequently.
 If there are no signs of dehydration, follow the guidelines in section
5.1.3 and treatment plan A, when appropriate, encourage the
mother tocontinue breastfeeding frequently. Observe the child for
at least 6 h beforedischarge, to confirm that the mother is able to
maintain the child’s hydrationby giving ORS solution.

All children should start to receive some ORS solution (about 5 ml/kg per h)
by cup when they can drink without difficulty (usually within 3–4 h for
infants and 1–2 h for older children). ORS provides additional base and
potassium, which may not be adequately supplied by IV fluid. When severe
dehydration is corrected, prescribe zinc.
5.2.2 Some Dehydration
In general, children with some dehydration should be given ORS solution,
for the first 4 hours at a clinic while the child is monitored and the mother
is taught how to prepare and give ORS solution.

195
Diagnosis
If the child has two or more of the following signs, the child has some
dehydration:
 Restlessness/irritability
 Thirsty and drinks eagerly
 Sunken eyes
 Skin pinch goes back slowly.

Note that if a child has only one of the above signs and one of the signs of
severe dehydration (e.g. restless/irritable and drinking poorly), then that
child also has some dehydration.
Treatment
 In the first 4 hours, give the child the approximate amounts of
ORS solution, according to the child’s weight (or age if the
weight is not known). However, if the child wants more to
drink, give more.
 Replace the ongoing loss (10ml/kg/bowel motion or vomiting)
 Show the mother how to give the child ORS solution, a
teaspoonful every 1–2 minutes if the child is under 2 years;
frequent sips from a cup for an older child.
 Check regularly to see if there are problems.
o If the child vomits, wait 10 minutes; then, resume giving
ORS solution more slowly (e.g. a spoonful every 2–3
minutes).
o If the child’s eyelids become puffy, stop ORS solution reduce
the fluid intake and continue with breast milk. Weigh the

196
 child, and monitor urine out put.
o Check blood glucose or electrolytes if possible in a child who
is restless or irritable and convulsing, in case hypoglycaemia
or hypernatraemia is present. Manage the child accordingly;
if blood glucose measurement is not possible, give IV
glucose or oral sugar.
o If the mother cannot stay for 4 h, show her how to prepare
ORS solution and give her enough ORS packets to complete
rehydration at home plus enough for 2 more days.
o Reassess the child after 4 h, checking for signs of
dehydration listed earlier.

Note: Reassess the child before 4 h if he or she is not taking the ORS
solution or seems to be getting worse.
 If there is no dehydration, teach the mother the four rules of
home treatment:
(i) Give extra fluid.
(ii) Give zinc supplements for 10 – 14 days.
(iii) Continue feeding (see Chapter 10).
(iv) Return if the child develops any of the following signs:
o Drinking poorly or unable to drink or breastfeed
o Develops a general danger sign
o Becomes sicker
o Develops a fever
o Has blood mixed with the stools or more than a few
drops on theoutside of the stool
 If the child still has some dehydration, repeat treatment with

197
 ORS solution for another 4 h, as above, and start to offer food,
milk or juice and breastfeed frequently.
 If there are signs of severe dehydration, see section 5.2.1 for
treatment.
Give zinc supplements. Give zinc and advise the mother how much to give:
≤ 6 months: half tablet (10 mg) per day for 10–14 days
≥ 6 months: one tablet (20 mg) per day for 10–14 days

Feeding
Continuation of nutritious feeding is an important element in the
managementof diarrhoea.
 In the initial 4-h rehydration period, do not give any food except
breast milk. Breastfed children should continue to breastfeed
frequently throughout the episode of diarrhoea. If they cannot suck
from the breast, consider giving expressed breast milk either orally
from a cup or by nasogastric tube.
 After 4 h, if the child still has some dehydration and ORS continues to
be given, give food every 3–4 h.
 All children > 6 months should be given some food before being sent
home.
If the child is not normally breastfed, explore the feasibility of relactation
(i.e. restarting breastfeeding after it was stopped, see chapter 7) or give the
usual breast milk substitute. If the child is ≥ 6 months or already taking
solid food, give freshly prepared foods – cooked, mashed or ground. The
following are recommended:
o Cereal or another starchy food mixed with pulses, vegetables
and meat or fish, if possible, with 1–2 teaspoons of vegetable
oil added to each serving

198
 o Local complementary foods recommended by the IMCI in that
area (see chapter 10
o Fresh fruit juice or mashed banana to provide potassium.
o Encourage the child to eat by offering food at least six times a
day. Give the same foods after the diarrhoea stops, and give
an extra meal a day for 2weeks.

Chart 5.2 Diarrhoea Treatment Plan B: Treat some dehydration with ORS
RECOMMENDED AMOUNT OF ORS IN CLINIC OVER 4-HOUR PERIOD

1. Give extra fluid

2. Give zinc supplements See Diarhoea treatment plan A (Chart 5.3)
3. Continue feeding and Mothers card (section 12.2)
4. When to return

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5.2.3 No dehydration

Children with diarrhoea but no dehydration should receive extra fluids at

home to prevent dehydration. They should continue to receive an
appropriate diet for their age, including continued breastfeeding.

Diagnosis - Diarrhoea with no dehydration should be diagnosed if the child

does not qualify for some or severe dehydration:
Treatment
 Treat the child as an outpatient. See Treatment plan A
 Counsel the mother on the 4 rules of home treatment (chart
5.3).
 Give extra fluid, as follows and as much as the child will take:
o If the child is being breastfed, advise the mother to
breastfeed frequently and for longer duration at each feed.
o If the child is exclusively breastfed, give ORS solution or clean
water in addition to breast milk.
o After the diarrhoea stops, for infants less than 6 months of
age exclusive breastfeeding should be resumed, if
appropriate to the child’s age.
 In non-exclusively breastfed children, give one or more of the
following:
o ORS solution
o Food-based fluids (such as soup, rice water and yoghurt
drinks)
o Clean water
 Tell the mother to give small sips from a cup. If the child vomits,
wait 10 minutes and then give more slowly. She should

200
 continue giving extra fluid until the diarrhoea stops.
 Teach the mother how to mix and give ORS solution and give her
two packets of ORS to take home.
 Give zinc supplements and show the mother how to give it
 Continue feeding
 Advise the mother on when to return—see above.

Chart 5.3 Diarrhoea Treatment Plan A: Treat diarrhoea at home

COUNSEL THE MOTHER ON THE 4 RULES OF HOME TREATMENT:GIVE

EXTRA FLUID, CONTINUE FEEDING, WHEN TO RETURN, GIVE ZINC
SUPPLEMENTS

1. GIVE EXTRA FLUID (AS MUCH AS THE CHILD WILLTAKE)

➤TELL THE MOTHER:
– Breastfeed frequently and for longer at each feed.
– If the child is exclusively breastfed, give ORS or clean water in
addition to breastmilk.
– If the child is not exclusively breastfed, give one or more of the
following: ORS solution, food-based fluids (such as soup, rice
water, and yoghurt drinks), or clean water.
It is especially important to give ORS at home when:
– the child has been treated with Plan B or Plan C during this visit.
– the child cannot return to a clinic if the diarrhoea gets worse.
➤TEACH THE MOTHER HOW TO MIX AND GIVE
ORS. GIVE THE MOTHER 2 PACKETS OF ORS TO USE AT HOME.

➤SHOW THE MOTHER HOW MUCH FLUID TO GIVE

IN ADDITION TO THE USUALFLUID INTAKE:
• Up to 2 years - 50 to 100 ml after each loose stool
• 2 years or more - 100 to 200 ml after each loose stool

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 Tell the mother to:
– Give frequent small sips from a cup.
– If the child vomits, wait 10 minutes. Then continue, but more
slowly.
– Continue giving extra fluid until the diarrhoea stops.
2. GIVE ZINC SUPPLEMENTS
➤TELL THE MOTHER HOW MUCH ZINC TO GIVE:
• Up to 6 months 1/2 tablet (10 mg) per day for 10 days
• 6 months and more 1 tablet (20 mg) per day for 10 days

➤SHOW THE MOTHER HOW TO GIVE THE ZINC

SUPPLEMENTS:
– Infants, dissolve the tablet in a small amount of clean water,
expressed milk or ORS in a small cup or spoon.
– Older children, tablet can be chewed or dissolved in a small
amount of clean water in a cup or spoon.
➤REMIND THE MOTHER TO GIVE THE ZINC FOR THE FULL
10 DAYS.

3. CONTINUE FEEDING
See Mother’s card
4. WHEN TO RETURN

5.3 Persistent diarrhoea

Persistent diarrhoea is diarrhoea, with or without blood, which begins
acutely and lasts for 14 days or longer. When there is some or severe
dehydration, persistent diarrhoea is classified as “severe”.

The following guidelines are for children with persistent diarrhoea who are
not severely malnourished. Suspect and screen for HIV.

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5.3.1 Severe persistent diarrhoea
Diagnosis
 Infants or children with diarrhoea lasting ≥ 14 days, with signs of
dehydration have severe persistent diarrhoea and require
hospital treatment.
Treatment
 Assess the child for signs of dehydration and give fluids according
to Treatment Plans B or C, as appropriate.
ORS solution is effective for most children with persistent diarrhoea. In a
few, however, glucose absorption is impaired and ORS solution is not
effective.

Routine treatment of persistent diarrhoea with antibiotics is not effective

and should not be given. Some children, however, have non-intestinal or
intestinal infections that require specific antibiotic therapy.
 Examine every child with persistent diarrhoea for non-intestinal
infections such as pneumonia, sepsis, urinary tract infection, oral
thrush, and otitis media and treat appropriately.
 Give micronutrients and vitamins.
 Treat persistent diarrhoea with blood in the stool with an oral
antibiotic effective for Shigella (section 5.4)
 Give treatment for amoebiasis (oral metronidazole: 30-50 mg/kg, 3
times a day, for 10 days or tinidazole 50-60mg/kg per day for 3
days) only if:
o Microscopic examination of fresh feces carried out in a
reliable laboratory reveals trophozoites of
Entamoebahistolytica within red blood cells; OR

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 o Antibiotic, which is usually effective for Shigella locally,
have been given without clinical improvement.
 Give treatment for giardiasis (metronidazole: 15 mg/kg, 3 times
a day, for 5 days or Tinidazole 50-75mg/kg po stat) if cysts or
trophozoites of Giardia lamblia are seen in the feces.
Feeding
Careful attention to feeding is essential for all children with persistent
diarrhoea.
Breastfeeding should be continued for as often and as long as the child
wants. Other food should be withheld for 4–6 hours—only for children with
dehydration who are being rehydrated following Treatment Plans B or C.
Hospital diets
Children treated in hospital require special diets until their diarrhoea
lessens and they are gaining weight. The goal is to give a daily intake of at
least 110 calories/kg.

Infants aged under 6 months

 Encourage exclusive breastfeeding. Help mothers who are not
breastfeeding exclusively to do so. But beware of the increased risk
of MTCT through breast milk during relactation.
 If the child is not breastfeeding, give a breast milk substitute that is
low in lactose, such as yoghurt, or is lactose-free. Use a spoon or
cup, do not use a feeding bottle. Once the child improves, help the
mother to re-establish lactation (caution: see above, MTCT).
 For feeding of infants born to HIV positive mothers she should receive
appropriate counseling about the correct use of breast milk
substitutes.

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Children aged 6 months or older
Feeding should be restarted as soon as the child can eat. Food should be
given 3 times a day for those who are on breast or replacement milk or 5
times a day for those not on breast or replacement milk to achieve a total
intake of at least 110 calories/kg/day. Many children will eat poorly,
however, until any serious infection has been treated for 24–48 hours.
Such children may require nasogastric feeding initially. Give the same foods
after the diarrhoea stops and give an extra meal a day for 2 weeks after the
diarrhoea stops for fast recovery.

Two recommended diets

Given below (Tables 5.4 and 5.5) are two diets recommended for children
and infants aged >6 months with severe persistent diarrhoea. If there are
signs of dietary failure (see below) or if the child is not improving after 7
days of treatment, the first diet should be stopped and the second diet
given for 7 days.
Successful treatment with either diet is characterized by:

 Adequate food intake

 Weight gain
 Fewer diarrhoeal stools
 Absence of fever.

The most important criterion is weight gain. There should be at least three
successive days of increasing weight before one can conclude that weight
gain is occurring.

Give additional fresh fruit and well cooked vegetables to children who are
responding well. After 7 days of treatment with the effective diet, they
should resume an appropriate diet for their age, including milk, which

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provides at least 110 calories/kg/day. Children may then return home, but
follow them up regularly to ensure continued weight gain and compliance
with feeding advice.
Dietary failure is shown by:
 An increase in stool frequency (usually to >10 watery stools a
day), often with a return of signs of dehydration (this usually
occurs shortly after a new diet is begun), OR
 A failure to establish daily weight gain within 7 days.
Table 5.4 Diet for persistent diarrhoea, first diet: A starch-based, reduced
milk concentration (low lactose) diet

Food Component Amount (g)

full-fat dried milk (or whole liquid milk: 85 ml) 11
Rice 15
vegetable oil 3.5

cane sugar 3
water to make 200ml

Table 5.5 Diet for persistent diarrhoea, second diet: A no-milk (lactose-
free) diet with reduced cereal (starch)

Food Component Amount (g)

Whole egg 64
Rice 3
Vegetable oil 4
Glucose 3
Water to make 200 ml
Finely ground, cooked chicken (12 g) can be used in place of egg to
give a diet providing 70 calories/100 g.

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Monitoring
Nurses should check the following daily:
 Body weight
 Temperature
 Food taken
 Frequency of diarrhoea.
5.3.2 Persistent diarrhoea (non-severe)
These children do not require hospital treatment but need special feeding
and extra fluids at home.

Diagnosis - Children with diarrhoea lasting 14 days or longer who have no

signs of dehydration and no severe malnutrition

Treatment
 Treat the child as an outpatient.
 Give micronutrients and vitamins according to box (Table 5.6)
Prevent dehydration
 Give fluids according to Treatment Plan A, ORS solution is effective
for most children with persistent diarrhoea. Identify and treat
specific infections
 Do stool exam. Do not routinely treat with antibiotics as they are
not effective. However, give antibiotic treatment to children with
specific non-intestinal or intestinal infections. Until these infections
are treated correctly, persistent diarrhoea will not improve.
 Non-intestinal infections. Examine every child with persistent
diarrhoea for non-intestinal infections, such as pneumonia, sepsis,
urinary tract infection, oral thrush and otitis media. Treat with
antibiotics following the guidelines in this manual.

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  Intestinal infections. Treat persistent diarrhoea with blood in the
stool as per the result of stool exam.

Feeding
Careful attention to feeding is essential for all children with persistent
diarrhoea. These children may have difficulty in digesting animal milk other
than breast milk.
 Advise the mother to reduce the amount of animal milk in the
child’s diet temporarily.
 Continue breastfeeding and give appropriate complementary
foods.
o If still breastfeeding, give more frequent, longer breastfeeds,
by day and night.
o If taking other animal milk, explore the feasibility of replacing
animal milk with fermented milk products (e.g. yoghurt),
which contain less lactose and are better tolerated.
o If replacement of animal milk is not possible, limit animal milk
to 50 ml/kg/day. Mix the milk with the child’s cereal, but do
not dilute it.
o Give other foods appropriate for the child’s age to ensure an
adequate caloric intake. Infants aged >6months whose only
food has been animal milk should begin to take solid foods.
o Give frequent small meals, at least 3 or 5 times a day (see
above).
o Supplementary micronutrients, including zinc (Table 5.6)

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Follow-up
 Tell the mother to bring the child back for reassessment after five
days, or earlier if the diarrhoea worsens or other problems develop.
 Fully reassess children who have not gained weight or whose
diarrhoea has not improved in order to identify any problems, such as
dehydration or infection, which need immediate attention or
admission to hospital.

 Those who have gained weight and who have less than three loose
stools per day may resume a normal diet for their age.
5.4 Dysentery
Dysentery is diarrhoea presenting with loose frequent stools containing
blood. Most episodes are due to Shigella and nearly all require antibiotic
treatment.
Diagnosis
The diagnostic signs of dysentery are frequent loose stools with visible
blood.
Other findings on examination may include:
 Abdominal pain
 Fever
 Convulsions
 Lethargy
 Dehydration (section 5.2)
 Rectal prolapse.
Laboratory
 Stool exam microscopy, stool culture and sensitivity
 WBC and Differential

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Treatment
Children with severe malnutrition and dysentery, and young infants (<2
months old) with dysentery should be admitted to hospital. In addition
children who are toxic, lethargic, have abdominal distension and
tenderness or convulsions are at high risk of sepsis and should be
hospitalized. Others can be treated at home.
 Give an oral antibiotic, to which most strains of Shigella locally
are sensitive:
 First line: Amoxicillin 30-50 mg/kg, 3 times a day for 10 days or
tetracycline
 If child is septic and needs admission: ceftraixone (see dose
above) IV. Prescribe a zinc supplement as done for children with
watery diarrhoea without dehydration.
Note: There is widespread Shigella resistance to ampicillin, co-trimoxazole,
chloramphenicol, nalidixic acid, tetracycline, gentamicin and first- and
second generation cephalosporins, which are no longer effective. There is
also already reported resistance to ciprofloxacin in some countries.
Follow-up
Follow-up children after two days, look for signs of improvement such as
no fever, fewer stools with less blood, improved appetite.
 If there is no improvement after two days,
o Check for other conditions (see Chapter 2),
o Stop the first antibiotic, and
o Give the child a second-line antibiotic which is known to be
effective against Shigella
 If the two antibiotics, which are usually effective for Shigella, have

210
 each been given for 2 days and produced no signs of clinical
improvement,
o Repeat stool exam and treat as an outpatient if there is
amoebiasis
o Check for other conditions (refer to a standard paediatric
textbook).
o Admit the child if there is another condition requiring hospital
treatment.

Infants and young children

Consider surgical causes of blood in the stools (for example,
intussusception; and refer to a surgeon if appropriate. Dysentery is unusual
in neonates and young infants; therefore, consider life-threatening
bacterial sepsis.
 For suspected sepsis give IM or IV ceftriaxone at 100 mg/kg once
daily for 7-10 days.

Supportive care
Supportive care includes the prevention or correction of dehydration and
continued feeding.
Never give drugs for symptomatic relief of abdominal pain and rectal pain,
or to reduce the frequency of stools, as they can increase the severity of
the illness.
Treatment of dehydration
Assess the child for signs of dehydration and give fluids according to
Treatment Plan A, B or C as appropriate.

211
Nutritional management
Ensuring a good diet is very important as dysentery has a marked adverse
effect on nutritional status. However, feeding is often difficult because of
lack of appetite. Return of appetite is an important sign of improvement.
 Breastfeeding should be continued throughout the course of the
illness, more frequently than normal, if possible, because the infant
may not take the usual amount per feed.
 Children aged 6 months or more should receive their normal foods.
Encourage the child to eat more.

Complications
 Dehydration: Assess and mange for dehydration. Give fluids according
to treatment plan A, B or C, as appropriate.
 Potassium depletion: This can be prevented by giving ORS solution
(when indicated) or potassium-rich foods such as bananas or dark
green leafy vegetables.
 High fever: If the child has high fever (≥ 39 ° C), consider systemic
infection.
 Rectal prolapse: Gently push back the rectal prolapse using a surgical
glove or a wet cloth. Alternatively, prepare a warm solution of
saturated magnesium sulphate and apply compresses with this
solution to reduce the prolapse by decreasing the oedema
 Convulsions: give diazepam but avoid rectal diazepam.
 Haemolytic-uraemic syndrome: Where laboratory tests are not
possible, suspect haemolytic-uraemic syndrome (HUS) in patients
with easy bruising, pallor, altered consciousness, and low or no urine
output and Refer immediately

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 Toxic megacolon: Toxic megacolon usually presents with fever,
abdominal distension, pain and tenderness with loss of bowel sounds,
tachycardia and dehydration. Give IV fluids for dehydration, pass a
nasogastric tube,and start antibiotics. Consult surgeon or refer.
 Treat hypoglycemia

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CHAPTER 6 – FEVER

6.1 Child presenting with fever

6.1.1 Fever lasting 7 days or less
History
 Duration and pattern of fever
 Residence in or recent travel to a malaria endemic area
 Recent contact with a person with an infectious disease and/or
similar diseases in the vicinity
 Pain on swallowing,
 Skin rash
 Headache
 Stiff neck or neck pain
 Change of sensorium
 Convulsion
 Pain (crying) on passing urine, change in urine color ( turbid),
smelly urine
 Respiratory symptoms like cough
 Ear pain/ discharge
 GI symptoms
 Vomiting
 Jaundice
 history of vaccination

Examination
General condition: level of consciousness, pallor, signs of respiratory
distress, cyanosis

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Vital sign: temperature, pulse rate, respiratory rate, blood pressure, oxygen
saturation

Head and neck: icteric sclera , bulged fontanel , stiff neck, red swollen
tonsils, follicles, mouth ulcer, discharge from ear, swelling and tenderness
behind ear and red ear-drum on otoscopy,

Chest: fast breathing, retraction, crepitation

Abdomen: hepatosplenomegaly

Limbs: joint swelling, limitation of movement of joints.

Skin examination :
 Pallor: anemia
 Rash
 Pustules, or signs of infection: red, hot, swollen, tender
(staphylococcal infection)
 Haemorrhagic rash: purpura, petechiae (meningococcal infection)
 Maculopapular rash (measles, other viral infections)
Meningeal signs

Laboratory investigations
 Blood smear
 Urine microscopy and culture
 Complete blood count
 Lumbar puncture if indicated ( sign suggest or not sure)
 Blood culture
Differential Diagnoses
There are four major categories of children presenting with fever:
 Fever due to infection with out-localized signs (no rash)
 Fever due to infection with localized signs (no rash)
 Fever with rash
 Fever lasting more than 7 days

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Table 6.1 Differential diagnosis of fever without localizing signs

Diagnosis of fever In favour

Malaria Living in endemic area

Travel history
Anaemia
Enlarged spleen
Blood film positive, RDT
Septicaemia Seriously and obviously ill with no apparent cause
Purpura, petechiae
Shock or hypothermia in young infant or severely
malnourished child
Urinary tract infection Abdominal pain
Loin or suprapubic tenderness
Crying on passing urine
Passing urine more frequently than usual
Incontinence in previously continent child
White blood cells and/or bacteria in urine on
microscopy, or positive dipstick
Fever associated with Signs of HIV infection (see Chapter 8)
HIV infection
Typhoid Seriously and obviously ill with no apparent cause

Abdominal tenderness

Shock, confusion

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 Table 6.2 Differential diagnosis of fever with localized signs

Diagnosis of fever In favor

Meningitis Convulsion
Altered level of consciousness
Bulging fontanels in infant
Stiff neck
Petechiae or purpura
CSF analysis positive
Acute Otitis media Ear pain
Pus draining from ear
Red immobile ear-drum on Otoscopy
Mastoiditis Tender swelling above or behind ear
Osteomyelitis Refusal to move the affected limb
Refusal to bear weight on leg
Local tenderness
Septic arthritis Swollen hot, tender joint
Skin and soft tissue Cellulitis
infection Boils
Skin pustules
Pyomyositis ( purulent infection of muscle)
Pneumonia Fever ,Cough, Grunting
(see section 4.1) nasal flaring, lower chest wall indrawing
Coarse crackles
Bronchial breath sound
Bronchopneumonic infiltrations
Lobar consolidation
Pleural effusion
Viral upper respiratory Runny nose , symptoms of cough / cold

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tract infection No systemic upset

Retropharyngeal abscess History of recent sore throat in older child

Difficulty in swallowing/drooling of saliva
Tender cervical node

Sinusitis Tender cervical nodes facial tenderness over

affected sinus
Foul nasal discharge
Urinary tract infection Crying on passing urine

Passing urine more frequently than usual

Incontinence in previously continent child

Costo-vertebral angle or suprapubic tenderness

White blood cells and/or bacteria in urine on

microscopy, or positive dipstick

Hepatitis Severe anorexia

Abdominal pain
Jaundice
Dark urine

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Table 6.3 Differential diagnosis of fever with rash

Diagnosis of fever In favour

Measles Recent exposure to a measles case

No documented measles immunization
Cough, runny nose, red eyes
Maculopapular rash
Mouth ulcers
Corneal clouding

Viral infections Cough or cold

Mild systemic upset
Transient non-specific rash
Meningococcal infection Petechial or purpuric rash
Bruising
Shock
Stiff neck (if meningitis)
Relapsing fever Poor living condition/overcrowding, homeless
Petechial rash / skin haemorrhages
Jaundice
Tender enlarged liver and spleen
History of relapsing fever
Positive blood smear for Borrelia
Typhus Epidemic of typhus in region
Characteristic macular rash
Muscle pain
Dengue haemorrhagic Bleeding from nose or gums or in vomitus
fever Bleeding in stools or black stools
Skin petaechiae or purpura
Abdominal tenderness
Enlarged liver and spleen
Shock

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6.1.2 Fever lasting longer than seven days
History: take history as fever … see section 6.1.1

Examination

Fully undress the child, and examine the whole body and look for the
following signs:

 Inflamed throat and mucous membranes (throat infection)

 Red, painful ear with immobile ear-drum (otitis media)
 Fast breathing or chest indrawing (pneumonia, empyema )
 Stiff neck or bulging fontanel (meningitis, subdural abscess)
 Petechial or purpuric rash (meningococcal disease or dengue)
 Maculopapular rash (viral infection or drug reaction)
 Jaundice or anaemia (malaria, hepatitis, leptospirosis or
septicaemia)
 Painful spine, hips or other joints (septic arthritis)
 Tender abdomen (suprapubic or loin in urinary tract infection)
 Malar rash , pallor ,(Autoimmune diseases such as SLE)
 Lymphadenopathy, pallor, petechial rash (Malignancy)
 Pallor, splenomegaly, petechiae ( visceral leishmaniasis)
 Other causes of persistent fever with no localizing signs such as
septicemia, Salmonella infections, miliary TB, HIV infection or
urinary tract infection.

Laboratory investigations

 Blood films or rapid diagnostic test for malaria parasites (a positive

test in an endemic area does not exclude other, co-existing causes
of fever)

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  Complete blood count, including platelet count, and examination
of a thin film for cell morphology
 Urinalysis, including microscopy
 Mantoux test, if available (Note:often negative in a child who has
miliary TB, severe malnutrition or HIV infection)
 Chest X-ray
 Blood culture
 lumbar puncture (to exclude meningitis if there are supportive
signs)
 HIV testing
 Widal (rising titer)
 Weil Felix
 Splenic/bone marrow aspiration
6.1.3 Differential Diagnosis
Review all the condition listed in Table 6.1-6.4

Table 6.4 Additional differential diagnosis of fever lasting longer than 7

days

Diagnosis In favour

Abscess Fever with no obvious focus of infection (deep

abscess)
Local tenderness or pain
Tender or fluctuant mass
Specific signs depend on site—sub phrenic,
psoas, liver abscess
Salmonella infection Child with sickle-cell disease
(non-typhoidal) Osteomyelitis or arthritis in infant

221
Infective Known cardiac lesion/Heart murmur
endocarditis Fever
Weight loss
Pallor
Petaechiae
Splinter haemorrhages in nail beds
Finger clubbing
Enlarged spleen
Normocytic normochromic anaemia
Microscopic haematuria
Rheumatic fever Recent known streptococcal infection
Migratory poly arthritis/arthralgia
Carditis
Fast pulse rate not proportional to the degree
of fever
Pericardial friction rub
Chorea
Mitral and /or aortic regurgitation murmur
Positive ASO titer
Miliary tuberculosis Cough
Weight loss
Anorexia, night sweats
Contact to TB patient
Enlarged liver and/or spleen
Fine miliary pattern on chest X-ray
Brucellosis Chronic relapsing or persistent fever, malaise
Musculoskeletal pain
Lower backache or hip pain
Enlarged spleen, anaemia, history of drinking
unboiled milk

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6.2 Malaria
6.2.1 Severe malaria
Severe malaria, which is commonly due to Plasmodium falciparum, is
serious enough to be an immediate threat to life.

Diagnosis
History
A child who has fever or history of fever and lives in malaria-endemic
areas or has a history of travel within the last 30 days to malaria-endemic
areas and positive for asexual parasitaemia and presence of one or more of
the following clinical or laboratory features is considered to have severe
malaria:

 Prostration: inability to sit unassisted in a child who is normally

able to do or inability to feed in young children not yet started to
sit
 Multiple convulsion more than two episodes in 24 hrs.
 Impaired consciousness : Blantyre Coma Scale < 3 in infants,
Glasgow Coma Scale < 11 in older children and adolescent
 Respiratory distress or in-drawing of chest wall
 Frothy blood tinged sputum
 Circulatory collapse or shock
 Bleeding tendency/abnormal bleeding
 Jaundice
 Severe pallor
 Dark cola colored urine
th
 systolic blood pressure lower than 5 centile for age and sex
Laboratory findings
 Hypoglycemia (<2.2 mmol/L or < 40 mg/dL)

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  Parasitic load (2% in low intensity transmission and >20% in high
transmission area )
 Severe anemia (hemoglobin <5g/dl, haematocrit< 15%)
 Acidosis (bicarbonate <15 mmol/L)
 Hyperlactatemia : >5mmol/l
 Renal impairment: Urine output <1ml/kg/hr for infants and 0.5
ml/kg/hr for children; or creatinine level above age related normal
range
 Haemoglobinuria: Dark red or black urine, dipstick positive for
hemoglobin/myoglobin, no microscopic hematuria
 Cerebrospinal fluid analysis to rule out meningitis is mandatory if
no contraindication to do LP in children with altered
consciousness
Treatment
Emergency measures—to be taken within the first hour:
 In unconscious patient keep the air way open, insert NG tube and
remove the gastric contents, and place in recovery position
 Check for hypoglycemia and correct accordingly. If blood glucose
can’t be determine give glucose
 Treat convulsions with I.V or rectal diazepam (Chapter 2, chart 9).
Do not give prophylactic anticonvulsants.
 Treat high grade fever with paracetamol or ibuprofen to reduce
temperature below 390c.
 Check for dehydration and treat appropriately.
 Correct the anemia.
 Institute regular observation of vital and neurologic signs.

224
  Start treatment with an effective antimalarial.
Antimalarial Treatment

 If blood smear confirmation of malaria is likely to take more than

one hour, start antimalarial treatment immediately before the
diagnosis is confirmed.
 In severe malaria treatment has to be given always parenteral
route (IV, IM) until the child tolerate P0 medication. Even if the
child tolerates PO medication earlier, give the parenteral
medication for at least 24 hrs.
 If severe malaria is suspected on clinical findings and the blood
nd
smear is negative, repeat the blood smear. If the 2 test is
negative, malaria is unlikely and look for alternative diagnosis.
The first line treatment of severe malaria

 Artesunate 2.4 mg/kg IV or IM given on admission (time = 0),

then at 12 h and 24 h, then once a day for 6 days or until the
child tolerates PO medication. If the patient tolerates after 24 h,
the medication can be changed to PO Artesunate-Lumefantrine
for the next three days.

 The injectable artesunate (Guilin Pharmaceutical Co, Guanxi,

China) contains 60 mg powder within a 7 ml glass vial that must
first be reconstituted by mixing with a 1 ml glass ampoule of 5%
sodium bicarbonate solution (provided) prior to administration
and then shaken 2-3 minutes for better dissolution.

 To prepare an IV infusion of artesunate (10 mg/ml), next add 5 ml

of 5% glucose (D5W) or Normal Saline to the just-reconstituted 7
ml vial, then infuse slowly intravenously (i.e. 3-4 ml per minute IV).

225
  To prepare artesunate for IM injection, add 2 ml of 5% glucose
(D5W) or Normal Saline to the reconstituted 7 ml vial to make 3
ml of artesunate (20 mg/ml) for IM injection.

Table 6.5 Reconstituted Artesunate dosage for treatment of severe

malaria

Weight (kg) (approximate) IV 10 mg/ml IM 20 mg/ml

0-8 1 ml 0.5 ml
9 to 12 2 ml 1 ml
13-16 3 ml 1.5 ml
17-18 4 ml 2 ml
19-21 5 ml 2.5 ml
22-25 6 ml 3 ml
26-29* 7 ml 3.5 ml
30-33* 8 ml 4 ml
34-37* 9 ml 4.5 ml
38-41* 10 ml 5 ml
42-46* 11 ml 5.5 ml
47+* 12 ml 6 ml
*Note that for persons weighing more than 25 kg, a second artesunate vial
must be completely reconstituted as above for each dose, and then each
dose administered determined by the chart.

If Artesunate not available, give quinine

Quinine Dosage:

 Loading dose: 20 mg/kg of quinine dihydrochloride salt in 5-10

ml/kg of IV fluid preferably 5% glucose over a period of 4 hours.
Then continue with 10 mg/kg quinine salt in IV fluid over 4 hours
TID (8 hrly) until the child is able to take oral treatment.

226
  Wherever IV administration of quinine is not possible: give
Quinine dihydrochloride 20 mg salt per kg loading dose
intramuscularly (divided in to two sites, anterior thigh) the quinine
should be diluted in sterile normal saline to a concentration of
60mg/ml. Then continue with quinine dihydrochloride 10 mg salt
per kg IM every 8 hours until patient can swallow. Diluted
parenteral solution is better absorbed and less painful.

 If the child tolerate oral medication continue with PO Artemether-

lumefantrine (AL) (table 6.6) unless contraindicated or Quinine 10
mg/kg PO every 8 h to complete for 7 days of treatment.

 If Artesunate and quinine not available then give Artemether at

the dose of 3.2 mg/kg IM on admission, then 1.6 mg/kg daily until
the child can take oral medication. Use a 1-ml tuberculin syringe
to give the small injection volume

Table 6.6 Dose of Tablet containing 20 mg Artemether plus 120 mg

Lumefantrine in a fixed dose combination

Number of tablets per dose -Twice daily for 3 days

Weight Age
(Years) Day1 Day2 Day3
(kg)
Morni Evenin Morning Eveni Mornin Eveni
ng g ng g ng

5 – 14 3 Months 1 1 1 1 1 1
– 2 years
15 – 24 3–7 2 2 2 2 2 2
years

25 – 34 8 – 10 3 3 3 3 3 3
years

35+ >10 Years 4 4 4 4 4 4

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Supportive care
 Provide meticulous nursing care, especially for unconscious
patients.
 Correct hypoglycaemia and control fever using antipyretics such as
paracetamol.
 Monitor the daily input and output and hydration status and
provide daily fluid requirements accordingly
 Feed children unable to feed for more than 1–2 days by
nasogastric tube, which is preferable to prolonged IV fluids.
 Avoid giving any harmful drugs like corticosteroids, low-molecular-
mass dextran and other anti-inflammatory drugs
For unconscious child:

 Maintain a clear airway

 Protect eyes, mucosae, skin.
 Nurse the child on the side to avoid aspiration of fluids.
 Turn the patient every 2 hours.
 Do not allow the child to lie in a wet bed.
 Pay attention to pressure points.
 Asses hydration status
 If there is sign of dehydration treat accordingly
 If after careful rehydration, the urine output over 6 hours is less
than 0.5ml/kg/hr, give IV furosemide, initially at 2mg/kg body
weight. If there is no response, double the dose at hourly intervals
to a maximum of 8 mg/kg body weight given over 15 minutes
 Look for signs of overload such as enlarged liver, gallop rhythm,
fine crackles at lung base, engorged neck veins, eye lid edema

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Management of some of the Complications
Coma (cerebral Malaria)
 Assess the level of consciousness according to Blantyre coma scale
(Table 6.7) for children and Glasgow coma scale for older children and
adolescents. Monitor temperature respiratory rate, heart rate, blood
pressure and urine output.
 Provide meticulous nursing care and pay careful attention to the
airway, eyes, mucosae, skin and fluid requirements.
 Exclude other treatable causes of coma (e.g. hypoglycaemia, bacterial
meningitis) and/or treat accordingly
 Manage convulsion if present
Table 6.7 Blantyre coma scale for young children
Score
Eye movements:
Directed (followed mother/caretakers face) 1
Not directed 0
Verbal response:
Appropriate for age (cry) 2
Moan or inappropriate for age (cry) 1
Gasp/none 0
Best motor response:
Localizes painful stimulus (rub your knuckles firmly on the patients 2
sternum) 1
Withdraws limb from pain (press firmly on patients thumbnail bed
with the side of a horizontal pencil) 0
None specific or absent response
Total 1-5

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Convulsions: are common before and after the onset of coma. Can be
manifested as subtle such as nystagmus, twitching of corner of the mouth
or irregular breathing pattern or typical tonic clonic seizure.

Treatment
Anticonvulsant: give rectal diazepam or IV injection (chapter 1 chart 9)

 Correct any possible contributing cause such as hypoglycaemia, or

very high fever give paracetamol.
 If there are repeated convulsions, give Phenobarbital.
(Appendix.2)
Shock
Shock manifested with cold extremities (clammy skin), weak rapid pulse,
and capillary refill ≥ 3 seconds and low blood pressure. The cause can be
hypovolemia or sepsis.

Treatment

 Correct hypovolaemia as appropriate.

 Take blood for culture.
 Do urinalysis.
 Give both antimalarial and antibiotic treatment for septicaemia (see
section 6.5,).
Severe anaemia (see chapter 10)
Give a blood transfusion as soon as possible :

 All children with a hematocrit of <12% or Hb of < 4 g/dL

 Less severely anemic children (Hct 12-15%; Hb 4- 5 g/dl) with very
high parasitaemia (>20% of red cells parasitized),
 Repeat the transfusion if Hb remains low.
 Initiate a daily iron syrup or tablet and monitor after 14 days for
the response and continue for three months.

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  Note that other causes of anemia must be looked for before
patient is discharged and treated accordingly.
Hypoglycaemia
 Hypoglycaemia: (blood glucose: <2.5 mmol/l or <45 mg/dl) is
particularly common in children under 3 years old, in children with
convulsions or hyperparasitaemia, and in comatose patients. It is
easily overlooked because clinical signs may mimic cerebral
malaria.

 Give 5ml/kg 10% dextrose solution IV rapidly followed by

continuous infusion of 6-8mg/kg/min adjusting the rate to
maintain the blood glucose level in the normal range. Recheck the
blood glucose level in 30 minutes.

 1 ml/kg of 50% dextrose diluted with an equal volume of normal

saline IV slowly over several minutes OR

 5 ml/kg of 10% dextrose by slow IV infusion

 In unconscious child prevent further hypoglycemia by initiating NG

feeding once the child is fully conscious. Start feeding with PO.
Continue to monitor the blood glucose level, and treat accordingly
if found to be <2.5 mmol/l or <45 mg/dl.

Acidosis
The child presents with deep, laboured breathing while the chest is clear—
often accompanied by lower chest wall indrawing.

Treatment
 Give intranasal oxygen
 Correct reversible causes of acidosis, especially dehydration and
severe anaemia.

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  If child is not severely anemic (Hb is ≥ 5 g/dl), give 20 ml/kg of
normal saline or an isotonic glucose-electrolyte solution IV over 30
minutes.
 If child is severely anemic (Hb is <5 g/dl), give whole blood (10
ml/kg) over 30 minutes, and a further 10 ml/kg over 1–2 hours
without diuretics. Check the respiratory rate and pulse rate every
15 minutes. If either of these shows any rise, transfuse more
slowly to avoid precipitating pulmonary oedema.
 Monitor response: clinical observation, pulse oximetry, Hct, blood
glucose
Aspiration pneumonia
 Place the child on his or her side or at least 30° head-up.

 Give oxygen, if there is cyanosis, severe lower chest wall indrawing

or increased respiratory rate for the age. SaO 2 is <90%,

 Ampicillin and gentamicin IV for seven days

Monitoring for severe Malaria

 The child should be checked by nurses hourly and by a doctor at
least (every six hr.) Monitor and report immediately any change in
the level of consciousness, convulsions, or changes in the child’s
behavior.
 Monitor the temperature, pulse rate, respiratory rate (and, if
possible, blood pressure) hourly at least for the first 48 hours.
 Monitor the blood glucose level every 3 hours until the child is
fully conscious.
 Check the rate of IV infusion regularly.
 Keep a careful record of fluid intake (including IV) and output.

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6.2.2 Uncomplicated malaria
Diagnosis - The child has:
 Fever (temperature ≥ 37.5 ° C or history of fever, and
 A positive blood smear for malaria, no signs of severe malaria
Note: If a child is from malarious area and has fever with no obvious cause
and it is not possible to confirm malaria on a blood film, treat the child as
case of malaria.

Treatment depends on the plasmodium species.

P. Falciparum: The first-line treatment of Falciparum malaria is Artemether-
lumefantrine (combined tablets containing 20 mg of Artemether and 120
mg of Lumefantrine):

Dosage for combined tablet:

 Child weighing 5 – < 15 kg: one tablet twice a day for 3 days
 Child weighing 15–24 kg: 2 tablets twice a day for 3 days
 Child > 25 kg: 3 tablets twice a day for 3 days
 Child weight less than five kilogram administer oral quinine 8.3
mg/kg base or 10 mg/kg quinine sulfate salt THREE times a day for
7 days
 P.vivax, P. malariae, P. ovale: the first-line drug of choice is
chloroquine 10 mg base/kg PO immediately (Day 1), followed by
10 mg base/kg PO at 24 hours (Day 2), and 5mg base/kg PO at 48
hours (Day 3) for a total dose of 25 mg chloroquine base/kg over
three days.
 If the child is from malaria free area and the compliance is
guaranteed administer primaquine daily for 14 days to eradicate
the hypnozoite form from the liver after completing the
chloroquine dose.

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  Multi-species RDT is positive for P. falciparum and P. vivax (mixed
infection): The recommended first-line treatment for mixed
infection is AL. Note: do not treat a patient with confirmed mixed
infection with both AL and chloroquine
 AL May be used to treat P.vivax infection when chloroquine is
unavailable. If AL is not available for P. falciparum or mixed
malaria infections, use oral quinine. If both chloroquine and AL are
not available for P.vivax infection, use quinine
 Severe malaria due to vivax (although not common) has to be
treated as severe malaria caused by P. falciparum.
Table 6.8 Dose of Chloroquine

Weight Age (years) Day 1 Day 2 Day 3

(kg)

5–6 <4 months

Tablets 1/2 1/4 1/4
Syrup 5 ml 5 ml 2.5 ml
7 – 10 4 – 11months
Tablets 1/2 1/2 1/2
Syrup 7.5 ml 7.5 ml 5 ml
11 – 14 1 – 2 years
Tablets 1 1 1/2
Syrup 12.5 ml 12.5 ml 7.5 ml
15 – 18 3 – 4 years
Tablets 1 1 1
Syrup 15 ml 15 ml 15 ml
19 – 24 5 – 7 years
Tablets 1 1/2 1 1/2 1
Syrup 20 ml 20 ml 15 ml
25 – 35 8 – 10 years 2½ 2½ 1
Tablets
36 – 50 11 – 13 years
Tablets 3 3 2
50+ 14+ years
Tablets 4 4 2

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Complications
Anaemia
 If the Hb is 5–9.3 g/dl (Hct 15–27%) it indicates moderate anemia.
Begin treatment with iron and folate immediately after
completion of antimalarial treatment or on discharge. Give a daily
iron–folate tablet or iron syrup for 14 days (Evaluate the response
and continue the treatment for 3 months.

 Deworming with mebendazole. If the child is > 1 year and has not
received Mebendazole in the previous six month.
 Advise the mother about good feeding practice.
Follow-up
 Tell the mother to return if the fever persists for two days after
starting treatment or sooner if the child’s condition gets worse.
She should also return if the fever comes back.
 Check if the child actually took full treatment and repeat a blood
smear.
 If the treatment was not taken repeat the same medication and
dose.
 Blood smear is still positive despite full treatment, treat with a
second-line antimalarial (see above) and reassess the child to
exclude the possibility of other causes of fever.
 If the fever persists after two days of treatment with the second-
line antimalarial, ask the mother to return with the child and
reassess for other causes of fever.

6.3 Meningitis
6.3.1 Bacterial meningitis

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Early diagnosis is essential for effective treatment.
Diagnosis
History:
 Vomiting
 Fever
 Irritability
 Inability to drink or breastfeed
 A headache or pain in back of neck
 Convulsions
 Similar problems in the vicinity (usually with meningococcal
infection)
 Recent head injury.
Examination:

 Altered level of consciousness ( irritability , lethargy, coma)

 V/S: temperature, PR,BP
 bulged fontanelle
 Stiff neck and other meningeal irritation signs
 Petechial rash or purpura
 Evidence of head trauma suggesting possibility of a recent skull
fracture
 Also, look for any of the following signs of raised intracranial
pressure:
 Unequal pupils
 Rigid posture or posturing and focal paralysis in any of the limbs
or trunk

236
  Irregular breathing

Figure 6.1: Looking and feeling for stiff neck in a child

Figure 6.2: Dilated pupil and opisthotonus

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Laboratory investigations
 Confirm the diagnosis with examination of the CSF. If the CSF is
cloudy, assume meningitis and start treatment while waiting for
laboratory confirmation.

 Microscopy should indicate the presence of meningitis in the

majority of cases with the increased white cell count (WBC > 5 cells
predominately polymorphs). Confirmatory information can be
gained from the CSF glucose (a ratio of CSF to serum glucose of ≤
0.4), CSF protein (high: 400 mg/dl), and positive Gram staining and
culture of the CSF, where possible.

 LP is contraindicated If there are signs of increased intracranial

pressure (unequal pupils, rigid posture, lateralizing sign, irregular
breathing), sever cardiorespiratory distress, and infection at the site
of LP.

 Do Blood culture if available

Treatment
If there is any suspicion, treat immediately with antibiotics before the
results of laboratory CSF examination are available. If the child has signs of
meningitis and a lumbar puncture is not possible, treat immediately.

Antibiotic treatment
Give antibiotic treatment as soon as possible. Choose one of the following
two regimens:
First line

 Crystalline penicillin loading dose of 250,000 IU/ kg IV. stat

followed by 500,000 IU/kg/24 hours IV divided in 8 doses (Q3
hourly) PLUS
 Chloramphenicol, 50 mg/kg IV stat followed by 100mg/kg/day IV
Q6 hourly

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  Haemophilus Influenza B: Chloramphenicol, 100mg/kg/day I.V Q
6hourly for 10 days
 Pneumococcus : penicillin G 500,000IU /kg/day I.V Q 3 hourly for
14 days
 Meningococcus: penicillin G 500,000IU /kg/day i.v. Q 3hourly for 7
days
OR

Second line antibiotic

 Ceftriaxone, 100mg/kg IV, in two divided doses for 10 days for all
cases.

Steroid treatment
The recommended dexamethasone dose in bacterial meningitis is 0.15
mg/kg every 6 h for 48 h. Steroids should be given within 10–20 min before
or during administration of antibiotics.

Do not use steroids in:

 Suspected cerebral malaria
 Suspected viral encephalitis
Poor response for treatment
Complication such as subdural effusion, cerebral abscess (persistant fever,
focal neurologic signs or altered consciousness). If these complications are
suspected, refer the child to hospital with specialized facilities for further
diagnostics and treatment.

 look for other sites of infection such as cellulitis , arthritis, or

osteomyelitis
 check for the possibilities of
 Tuberculous meningitis

239
  Cryptococcal meningitis
 Cerebral malaria
 Viral encephalitis
 Repeat the LP after 3-5 days if fever still present and/or the child's
overall condition is not improving.
6.3.2 Meningococcal epidemics
During a confirmed epidemic of meningococcal meningitis:

 For children aged 0–23 months, treatment should be adapted

according to the patient’s age, and an effort should be made to
exclude any other cause of meningitis.

 For children aged ≥ 2–5 years, Neisseria meningitides is the most

likely pathogen and presumptive treatment is justified. Give
ceftriaxone at 100 mg/kg/day IM or IV once daily for 5 days, and for
infants aged 0-2 months treat for 7 days.

Or
 Give oily chloramphenicol *(100 mg/kg IM as a single dose up to a
maximum of 3 g). If no improvement after 24 h, give a second dose of
100 mg/kg, or change to ceftriaxone as above

* The oily chloramphenicol suspension is thick and may be difficult to push

through the needle. If this problem is encountered, the dose can be divided
into two and an injection given IM.

6.3.3 Tuberculous meningitis

Tuberculous meningitis may have an acute or chronic presentation, with
the duration of presenting symptoms varying from 1 day to 9 months. It
may present with cranial nerve deficits, or it may have a more indolent
course involving headache, meningismus and altered mental status.

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  The initial symptoms are usually nonspecific, including headache,
vomiting, photophobia and fever.
 Consider tuberculous meningitis if any of the following is present:
 Fever has persisted for 14 days.
 Fever has persisted for > 7 days and the child has close contact
with person diagnosed to have tuberculosis
 A chest X-ray suggests TB.
 The patient is unconscious and remains so despite treatment for
bacterial meningitis.

 The patient is known to have HIV infection or is exposed to HIV.

 The CSF has a moderately high white blood cell count (typically 10-
500 white cells per ml, mostly lymphocytes), elevated protein
(0.8–4 g/l) and low glucose (< 1.5 mmol/l),
 GeneXpert positive
 CSF profile persists despite adequate treatment for bacterial
meningitis.
 Occasionally, when the diagnosis is not clear, a trial of treatment
for tuberculous meningitis is added to treatment for bacterial
meningitis
Treatment
The optimal treatment regimen comprises:

 Four-drug regimen (HRZE) for 2 months, followed by a two-drug

regimen (HR) for 10 months, the total duration of treatment being
12 months. Dose ( see section 4.7.2)

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  Prednisolone 2mg/kg/day divided dose for 4 weeks, reducing the
dose over a further 2–3 weeks) should be given in all cases of
tuberculous meningitis.
 Children with proven or suspected tuberculous meningitis caused
by MDR bacilli can be treated with a fluoroquinolone and other
second-line drugs in the context of a well-functioning MDR TB
control programme and within an appropriate MDR TB regimen.
The decision to treat should be taken by a clinician experienced in
managing paediatric TB.
Note: Streptomycin is not advised for children as it may cause otoxicity and
nephrotoxicity, and the injections are painful.

Cryptococcal meningitis
 Consider cryptococcal meningitis in older children known or
suspected to be HIV-positive with immunosuppression. Children
will present with meningitis with altered mental status.
 Perform a lumbar puncture. The opening pressure may be
elevated, but CSF cell count, glucose and protein may be virtually
normal.
 Analyze CSF with India ink preparation, or, if available, do a rapid
CSF Cryptococcal antigen latex agglutination test.

Treatment: A combination of amphotericin and fluconazole (section 8.4.4)

Supportive care
 Examine all children with convulsions for hyperpyrexia and
hypoglycaemia. Treat the hypoglycemia. Control high fever (≥ 39 °
C) with paracetamol.
 In an unconscious child:

242
  Maintain a clear airway.
 Nurse the child on the side to avoid aspiration of fluids.
 Turn the patient every 2 hours.
 Do not allow the child to lie in a wet bed.
 Pay attention to pressure points.
Oxygen treatment
 Give oxygen if the child has convulsions or associated severe
pneumonia with hypoxia (<90% saturation), cyanosis, signs of
respiratory distress

Fluid and nutritional management

 Give two third of the daily fluid requirement. Monitor IV fluids
very carefully and examine frequently for signs of fluid overload.
Fluid restriction is not appropriate in the presence of systemic
hypotension because reduced blood pressure may result in
reduced cerebral perfusion and CNS ischemia.

 Give due attention to acute nutritional support and nutritional

rehabilitation. Feed the child as soon as it is safe. Breastfeed every
3 hours, if possible, or give milk feeds as tolerated. If there is a risk
of aspiration, give fluid diet through nasogastric tube. Continue to
monitor the blood glucose level and treat accordingly.

Monitoring
 Monitor vital signs, the child's state of consciousness, pupils' size,
respiratory pattern and rate, every 2 hour during the first 24 h
then after 4-6 hrs depending on the condition of the child, input
and output and weight daily.

 On discharge, assess all children for neurological problems,

especially hearing loss. Measure and record the head
circumference of infants. If there is neurological damage, refer the
child to neurologist and consider physiotherapy.

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Complications
 Acute complication
 Convulsions
 Hypoglycaemia
 Hyponatremia
 Shock
 Subdural effusion
Long term complications
 Sensory hearing loss
 Motor deficit
 Developmental delay
 Epilepsy
Follow-up
 Sensorineural deafness is common after meningitis. Arrange a
hearing assessment on all children one month after discharge
from hospital.

Public health measures

 In meningococcal meningitis epidemics, advise families of the
possibility of secondary cases within the household so that they
report for treatment promptly.
 Give chemoprophylaxis for close household contacts with
Ciprofloxacin for the index child and close household contacts on
discharge.
 A case of meningococcal meningitis must be reported to local
authorities.
6.4 Measles
Measles is a highly contagious viral disease with serious complications) and
high mortality. It is rare in infants under 3 months of age.

Diagnosis
Diagnose measles if the child has:

244
  Fever
 A generalized maculopapular rash; and
 One of the following: cough, runny nose, or red eyes.
 In children with HIV infection, these signs may not be present and
the diagnosis of measles may be difficult.

Distribution of
measles: rash. This shows the
This shows the later rash
early rash covering the
covering the whole body.
head and upper
part of the trunk

Figure 6.3: Distribution of measles rash

Figure 6.4 Corneal clouding—sign of xerophthalamia in vitamin A deficient

child shown in comparison to the normal eye (right side)

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6.4.1 Severe complicated measles
Diagnosis
In a child with evidence of measles any one of the following symptoms and
signs indicate the presence of severe complicated measles:

 Inability to drink or breastfeed vomits everything

 Convulsions
 On examination, look for signs of complications such as lethargy or
unconsciousness
 Corneal clouding
 Deep or extensive mouth ulcers.
 Pneumonia
 Dehydration
 Stridor due to measles croup
 Severe malnutrition
 Bloody diarrhoea

Treatment
Children with severe complicated measles require treatment in hospital.

 Vitamin A therapy: Give oral vitamin A to all children with measles

unless the child has already had adequate vitamin A treatment for
this illness as an out patient. Give oral vitamin A 50,000 IU (for a
child aged <6 months), 100,000 IU (6–11 months) or 200,000 IU
(12 months up to 5 years) for 2 days.

 If the child shows any eye signs of vitamin A deficiency or is

severely malnourished, a third dose must be given 2–4 weeks after
the second dose on follow up.

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Supportive care
Fever
 If the temperature is ≥ 39 ° C give paracetamol.
Nutritional support (chapter 10)
 Assess the nutritional status
 Encourage continued breast feeding and /or frequent small feeds
 Check for mouth ulcers and treat
Complications
Follow the guidelines given in other sections of this manual for the
management of the following complications:

 Pneumonia
 Otitis media
 Diarrhoea
 Measles croup
 Acute malnutrition
 Tuberculosis
Eye problems: Conjunctivitis and corneal and retinal damage may occur due
to infection, vitamin A deficiency, or harmful local remedies. In addition to
giving vitamin A), treat any infection that is present. If there is a clear
watery discharge, no treatment is needed. If there is pusy discharge, clean
the eyes using cotton wool boiled in water, or a clean cloth dipped in clean
water. Apply tetracycline eye ointment, 3 times a day for 7 days. Never use
steroid ointment. Use a protective eye pad to prevent other infections. If
there is no improvement, refer to an eye specialist.

Mouth ulcers: If the child is able to drink and eat, clean the mouth with
clean, salted water (a pinch of salt in a cup of water) at least 4 times a day.

 Apply 0.25% gentian violet to the sores in the mouth after

cleaning.

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  If the mouth ulcers are severe and/or smelly, give IM/IV benzyl
penicillin (50,000 units/kg every 6 hours) and oral metronidazole
(7.5 mg/kg 3 times a day) for 5 days.

 If the mouth sores result in decreased intake of food or fluids, the

child may require feeding via a nasogastric tube.

Neurological complications: Convulsions, excessive sleepiness, drowsiness

or coma may be a symptom of encephalitis or severe dehydration.

Severe acute malnutrition (Chapter 7)

Monitoring
Take the child’s vital signs twice a day and check for the presence of the
above complications.

Follow-up
Recovery following acute measles is often delayed for many weeks and
even months, especially in children who are malnourished. Arrange for the
child to receive the third dose of vitamin A before discharge, if this has not
already been given.

Public health measures

If possible, isolate children admitted to hospital with measles for at least 4
days after the onset of the rash. Ideally, they should be kept in a separate
ward from other children. In malnourished and immunocompromised
children, the isolation should be continued throughout the duration of the
illness.

When there are measles cases in the hospital, immunize all other children
above the age of 6 months (including those seen in outpatients, children
admitted in the week following a measles case, and HIV-positive children).
If infants aged 6–9 months receive measles vaccine, it is essential for the
second dose to be given as soon as possible after 9 months of age.

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6.4.2 Non-severe measles
Diagnosis
Diagnose non-severe measles in a child whose mother clearly reports that
the child has had a measles rash, or if the child has:
 Fever
 A generalized rash; and
 One of the following—cough, runny nose or red eyes; but
 None of the features of severe measles

Treatment
Treat as an outpatient.

Vitamin A therapy: Check whether the child has already been given
adequate vitamin A for this illness. If not, give 50,000 IU (if aged <6
months), 100,000 IU (6–11 months) or 200,000 IU (12 months to 5 years)
for 2 days.

Supportive care
Fever: If the child’s temperature is ≥ 39 °C give paracetamol.

Nutritional support: Assess the nutritional status by measuring the mid

upper arm circumference. If malnourished, treatment has to be given (see
chapter 7). Encourage mother to continue breast feeding, give frequent
small meals depending the age of the child. Check for mouth ulcer and
treat as above.

Eye and mouth care

Follow-up
Ask the mother to return with the child in two days.
6.5 Septicaemia
Consider septicaemia in a child with acute fever who is severely ill, when no
cause can be found after a careful thorough physical examination. Usually

249
child presents with fever, inability to drink or breast feed, lethargy,
vomiting of everything, convulsion.

It can occur as a complication of meningitis, pneumonia, UTI etc.

The common causative agents include Streptococcus, Haemophilus

influenza and in children with severe malnutrition entericGram-negative
bacilli-Escherichia coli and Klebsiella are the common causative agents.
Wherever meningococcal disease is common, presence of petechiae or
purpura (haemorrhagic skin lesions) indicates meningococcal septicaemia.
In malarious area non-typhoidal Salmonella is a common cause of
septicemia.

Diagnosis
History: Fever, inability to drink or breast feed, lethargy, vomits everything,
convulsion.

Physical examination: fever with no evidence of obvious local infection is

usual manifestation. The presence of fast, weak pulse volume, delayed
capillary refill, hypotension, altered mental status and presence of purpura
indicates severe disease with septic shock.

Investigation:
 The investigations will depend on presentation but may include:
 Blood film : Hemoparasite ( malaria , Relapsing fever)
 CSF analysis to exclude meningitis
 Full blood count
 Urinalysis (including urine culture)
 Blood culture
 Chest X-rays.

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Treatment
I. Antibiotic:
 Give ampicillin (50 mg/kg IV 6-hourly) plus gentamicin (7.5 mg/kg
IM once per day) or,
 Alternatively Ceftriaxone (80 mg/kg IV, once daily over 30–60
minutes) for 7-10 days.
 If Staphylococcus infection strongly suspected give Cloxacillin (50
mg/kg 6 hourly) plus gentamicin (7.5 mg/kg once per day).
*Specimen for culture has to be taken before antibiotic administration as
soon as possible

In child with septic shock:

 Administer oxygen
 Secure IV line and treat shock: fluid administration with Ringer
Lactate or Normal Saline 20 ml/kg fast and if no response repeat
the dose up to 60ml/kg
 Blood transfusion with 20 ml/kg fresh whole blood or 10 ml /kg
packed cells if the patient not responding for fluid administration
 If shock is refractory start with adrenalin or dopamine (refer
standard text book of paediatrics for dosage).
Complications
Common complications of septicaemia include convulsions, confusion or
coma, dehydration, shock, cardiac failure, disseminated intravascular
coagulation (with bleeding episodes), pneumonia, anaemia, renal failure,
etc. Septic shock with multi organ failure is common cause of death.

Monitoring
A child with septic shock needs continuous monitoring of vital signs and for
response of treatment and presence of complications.

251
Child without septic shock has to be checked/assessed by the nurse and
physician
6.6 Typhoid fever
Consider typhoid fever if a child presents with fever persisted for seven or
more days, plus any of the following: diarrhea or constipation, vomiting,
abdominal pain, headache, cough, after malaria has been excluded.

Diagnosis
On examination, key diagnostic features of typhoid are:
 Fever with no obvious focus of infection
 No stiff neck or other specific signs of meningitis or ruled out by
investigation (note: children with typhoid can occasionally have a
stiff neck)
 Signs of systemic upset, e.g. inability to drink or breastfeed,
convulsions, lethargy, disorientation/confusion, or vomiting
everything
 Rose spots on the abdominal wall in light-skinned children
 Hepato-splenomegaly, tense and distended abdomen.

Typhoid fever can present atypically in young infants as an acute febrile

illness with shock and hypothermia. In areas where typhus is common, it
may be very difficult to distinguish between typhoid fever and typhus by
clinical examination alone (see standard paediatrics textbook for diagnosis
of typhus).

Lab test
 Blood culture and sensitivity test,
 WBC and differential
 Widal test – rising titer

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Treatment
 Ciprofloxacin 15mg /kg twice daily for 7-10 days.
 Ceftriaxone: (50 mg/kg IM, once daily) for 7days
 In admitted cases, IV drugs must be instituted.
Supportive care
 If the child has high fever ≥ 39 ° C), give paracetamol.
 Monitor haemoglobin or haematocrit levels and consider
transfusion when there is severe anemia.
Monitoring
The child should be checked for vital signs and complication by nurses and
physicians
Complications
 CNS: convulsions, confusion or coma
 Hematologic: Anemia,
 Gastrointestinal: acute gastrointestinal perforation with
haemorrhage and peritonitis can occur, usually presenting with
severe abdominal pain, vomiting, and abdominal tenderness,
severe pallor and shock. Abdominal examination may show an
abdominal mass due to abscess formation, an enlarged liver
and/or spleen. If there is a sign of gastrointestinal perforation,

open an IV line and give appropriate fluid and insert

nasogastric tube, consult surgeon as soon as possible.
 Miscellaneous: cardiac failure, pneumonia, osteomyelitis
and in young infants, shock and hypothermia can occur.

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6.7 Ear infections
6.7.1 Mastoiditis

Mastoiditis is a bacterial infection of the mastoid bone behind the ear.

Without treatment it can lead to meningitis and brain abscess.

Figure 6.5 Mastoiditis—a tender swelling behind the ear which

pushes the ear forward

Diagnosis
Key diagnostic features are:
 High fever
 Tender swelling behind the ear
Treatment (WHO)
 Give IM or IV cloxacillin 50mg/kg every 6 h or ceftriaxone 50 mg
/kg for total of ten days
 If there is no response to treatment within 48 hours or the child’s
condition deteriorates, consult surgical specialist to consider
incision and drainage of mastoid abscesses or mastoidectomy.
 If there are signs of meningitis, give antibiotic treatment as in
bacterial meningitis
 If brain abscess suspected start antibiotic and consult surgical
specialist immediately

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Supportive care
 If high fever (≥ 39 ° C) is causing distress or discomfort to the child,
give paracetamol.
Monitoring
 The child should be monitored frequently. If the child responds
poorly to treatment, consider the possibility of meningitis or brain
abscess
6.7.2 Acute Otitis Media
Diagnosis
 Opaque, or perforated tympanic membrane with discharge

Figure 6.6 Acute otitis media—bulging red eardrum (compared

to normal appearance of eardrum on left)
Treatment
 Treat the child as an outpatient.
 Give oral antibiotics in one of the following regimens:
 First choice: Oral amoxicillin at 40 mg/kg twice a day for at least 5
days
 If sensitivity for co-trimoxazole is known, give co-trimoxazole
(trimethoprim 4mg/kg and sulfamethaoxazole 20 mg/kg twice
daily for five days).

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  If pus is draining from the ear, show the mother how to wick the
ear three times daily until there is no more pus.
 Tell the mother not to place anything in the ear between
treatments. Do not allow the child to go swimming or get water in
the ear.
 If the child has ear pain or high fever (≥39 °c ), give paracetamol
Follow up
Ask the mother to return after five days.

If pain and or discharge persist, treat for five more days with the same
antibiotic and continue wicking and follow up in five days. If no
improvement refer to ENT.

Figure 6.7: wicking the child’s ear

dry in chronic otitis media

6.7.3 Chronic Otitis Media

If pus has been draining from the ear for 2 weeks or longer, the child has a
chronic ear infection.
Diagnosis
This is based on a history of pus draining from the ear for more than 2
weeks. On examination, confirm chronic otitis media) by otoscopy.
Treatment
 Keep the ear dry by wicking
 Instill topical antibiotic (with or without steroids) once daily for 2
weeks.

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  Drops containing quinolones (norfloxacin, ciprofloxacin) are more
effective than other antibiotic drops and can be applied for 14
days.
Follow-up
 Ask the mother to return after 5 days.
 If the ear discharge persists, check that the mother is continuing
to wick the ear.
 If the ear discharge persists, encourage the mother to continue to
wick the ear dry and refer for ENT evaluation.
6.8 Urinary tract infection
Urinary tract infection (UTI) is common in boys during infancy because of
posterior urethral valve. Beyond infancy females are more affected. As
bacterial culture is usually not available in developing countries, the
diagnosis is usually based on clinical signs and urine microscopy.

Diagnosis
 In infants and young children UTI presents as nonspecific
symptoms
 Fever >38 degree for at least 24 hrs without obvious cause
 Vomiting or poor feeding
 Irritability, lethargy, failure to thrive
 Abdominal pain
 Jaundice (neonate)
 In older children, specific symptoms such as increased frequency,
pain during micturition, abdominal ( loin ) pain may be observed
Investigation
 Examine a clean , fresh, uncentrifuged specimen of urine under
microscopy

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  WBC > 5 white cells/HPF; dipstick positive result for leukocyte;
nitrate positive
 Microscopy : bacteria
 Culture: obtain a “clean catch” urine sample for culture. In sick
infants, supra-pubic aspiration or catheterization is required. And
6
colony count > 10 .
Treatment
Outpatient treatment: Give oral Co-trimoxazole (4 mg trimethoprim/20 mg
sulfamethaoxazole per kg every 12 hours) for 7-10 days. Alternatives
include ampicillin, amoxicillin and cephalexin.

Admission and parenteral treatment indicated if:

 Infant
 Systemic upset such as high grade fever, vomiting, inability to feed
or drink
 Signs of pyelonephritis (loin pain or tenderness)
 If there is a poor response to the first-line antibiotic or the child’s
condition deteriorates, admit the patient and give gentamicin (7.5
mg/kg IM once daily) plus ampicillin (50 mg/kg IM/IV every 6
hours) or a parenteral cephalosporin for seven day.
 Treat young infants aged < 2 months with gentamicin at 7.5 mg/kg
IM or IV once daily until the fever has subsided; then review, look
for signs of systemic infection, and, if absent, continue with oral
treatment, as described above.

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Supportive care
 The child should be encouraged to drink or breastfeed regularly in
order to maintain a good fluid intake, which will assist in clearing
the infection and prevent dehydration.
 Regular voiding habit and complete emptying of bladder has to be
encouraged.
Follow-up
All children less than five years of age with febrile UTI have to be
investigated with US of the kidney and bladder, and voiding
cystourethrography (VCUG).

6.9 Relapsing Fever

Relapsing fever is a louse-borne disease that is caused by the spirochaetes,
Borrelia recurrentis. The disease is common among the homeless and in
those living in overcrowded living conditions.

Diagnosis
 Fever of relapsing pattern
 Petechial rash / skin haemorrhages
 Jaundice
 Tender enlarged liver and spleen
Investigation: Positive blood smear for Borrelia
Treatment
Delousing
 Remove all clothing and wash the body with the antiseptic /soap.
 Shave the hair.
II. Drug Treatment
 Secure IV line with ringer lactate
 Control the temperature with paracetamol

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  Administer Procaine penicillin: 50,000/kg max 400,000 units IM
stat.
 For newborns Crystalline penicillin 10,000 IU/Kg IM stat
 Continuous monitoring of vital sign temperature, pulse RR, blood
pressure in the first three hours is mandatory

 Check blood film after 12 hours of treatment. If negative,

chloramphenicol 25mg/kg every 6 h for 3 days

Complications
 Jarisch-Herxheimer reaction and is believed to be due to a rapid
clearance of the spirochetes and usually develops 60-90 minutes
after the antibiotic is given.

 In the initial phase the heart rate, respiratory rate and

temperature rise quickly to higher level and patient becomes
distressed and anxious followed by vasodilatation and progressive
fall of blood pressure.

 In order to mitigate this complication administer the ringer lactate

fast and control the fever with rectal/IV paracetamol. Respiratory
and cardiovascular support needed as indicated.

6.10 Acute Tonsillopharyngitis

Common upper respiratory tract infection caused mainly by viruses and
sometimes by bacteria commonly Group A beta hemolytic streptococcus.

Diagnosis: mainly clinical:

 Fever, vomiting , difficulty of swallowing

 Hyperemic enlarged tonsils with follicle or exudates
 Tender enlarged anterior cervical lymph nodes

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Treatment
 Benzathine penicillin 600,000IU IM stat for children <27 kgs of
weight; 1.2 million IU for child > 27 kg OR
 Amoxicillin 50 mg/Kg/day po in three divided doses for 10 days
 For patients allergic to penicillin , Erythromycin 40 mg/kg/day in
four divided doses for 10 days
 Follow up in two days if no improvement
6.11 Primary herpetic gingivostomatiitis
It is the most common cause of stomatitis in children 1–3 yr of age.

Clinical manifestation
o
 Abrupt onset of fever as high as 40 c and irritability 1-2 days prior
to the oral lesion.
 Pain in the mouth, salivation, fetor oris, refusal to eat
 Small (2-10mm in diameter) multiple ulcers on the buccal
mucosa, tongue and in some cases the tonsillar regions are
involved and may appear exudative, mimiking acute tonsillitis of
bacterial origin.
 Submandibular lymphadenitis is common.
 Acute phase lasts 4–9 days and is self-limited

Diagnosis is mainly clinical.

Treatment

 Oral acyclovir (15mg/kg/dose five times a day with a maximum

dose of 1g/24 hr for 7 days) started within 72 hr of onset of
lesions.

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  Supportive care: mouth washes with saline, GV (0.25%) paint of
the mucosal lesion, ice-cold fluids, or semisolids are often
accepted when other food is refused.
6.12 Septic Arthritis and Acute Osteomyelitis
Acute infection of the bone or joint is usually caused by spread of bacteria
through the blood. However some bone or joint infections results from an
adjacent focus of infection or from a penetrating injury. Occasionally
several bones and joints might be involved. The commonest causative
agents for pyogenic infection depend on the age of the patient.

In children older than three years, Staphylococcus aureus is the commonest

agent. In younger children H. influenzaetype b, Streptococcus pneumoniae,
or S. pyogenes (group A strept) are responsible. Salmonella is a common
cause in young children living in malarious area and children with sickle-cell
disease.

Diagnosis
 History and physical examination:
 Fever
 Refusal to use the affected limb or joint or bear weight on the
affected leg
 Swelling over the bone and tenderness (osteomyelitis)
 Hot, swollen, tender joint or joints with reduced range of
movement (septic arthritis)

Laboratory investigations
 Leukocytosis
 Raised ESR

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  X-rays are not helpful in diagnosis of acute osteomyelitis in the
early stages of the disease. After 2-3 weeks elevated periosteum
may be visible.
 In septic arthritis soft tissue swelling widening of joint space may
be visible

 Arthrocentesis and synovial fluid analysis: aspiration of fluid from

affected joint space: under strictly aseptic condition after proper
immobilization of the joint and application of adequate local
analgesics using 1% lidocaine, aspirate using needle large enough
to aspirate thick fluid/pus. Send the synovial fluid for analysis: cell
count, gram stain and culture (section 9.5.3).

Treatment
 Antibiotic: choice depends on the age of the patient.
 Child <3 yrs. : ceftriaxone IV for four to six weeks depending on
the response of the patient
 Child > 3 yrs : Cloxacillin 50mg/kg every 6 hrs if not available, give
chloramphenicol
 Clindamycin or second- or third-generation cephalosporin may be
given.
 Once the child’s temperature returns to normal and ESR is
decreasing, change to equivalent oral treatment with the same
antibiotics, and continue for a total of 3 weeks for septic arthritis
and 5 weeks for osteomyelitis.
 Septic Arthritis: Pus has to be removed by aspirating the joint.
Open surgical drainage is indicated in case involving shoulder and
hip joints (Section 9.5.3)

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Supportive care

 The affected limb or joint should be rested and weight bearing not
allowed until the pain subsides.
 Pain management according to severity ( chapter 10)
 Control fever with paracetamol
Chronic osteomyelitis

 The child usually appears less ill and the clinical signs are less
marked local signs and may not have fever. Usually may have
chronic draining sinuses over the affected bone.
 X- Ray may show elevated periosteum, sequestrum (collection of
dead bone)
 Treatment: surgical removal of dead bone (sequestrectomy) and
IV antibiotic for one week and then change to PO for 4-6 weeks
depending on ESR
 Consider tuberculous osteomyelitis when the illness is slow onset
of swelling and chronic course, discharging sinuses and not
responding for above treatment or if the patient has other signs of
tuberculosis.
 Treatment is according to national TB control programme
guideline (section 4.7.2) and surgical treatment is not indicated.
6.13 Rheumatic fever
Rheumatic fever is non-suppurative complications of Group A
streptococcal pharyngitis due to a delayed immune response
affecting joints, central nervous system, integumentary system, and
heart. The symptoms usually appears two to four weeks after the

264
throat infection with beta hemolytic streptococcus .The diagnosis of
acute rheumatic fever is mainly clinical based on modified Jones criteria.
 Two major or one major and two minor manifestations plus
evidence of previous group A streptococcal infection is diagnostic
to rheumatic fever.
Major manifestations are:

 Carditis
 Polyarthritis
 Erythema marginatum
 Subcutaneous nodules
 Chorea.
Minor criteria
 Fever
 Arthralgia in absence of polyarthritis
 Elevated acute phase reactants (erythrocyte sedimentation rate or
leukocyte count)
 PR prolongation, in absence of carditis
 Recent evidence of streptococcal infection
 Elevated or rising anti-streptolysin-O or other streptococcal
antibody
 Rapid antigen test for group A streptococci
 A positive throat culture for streptococci
 Recent scarlet fever

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Table 6.9 WHO criteria for the diagnosis of rheumatic fever and rheumatic
heart disease

Diagnostic categories Criteria

Primary episode of RF Two major or one major and two minor

manifestations plus evidence of a
preceding group A streptococcal
infection

Recurrent attack of RF in a Two major or one major and two minor

patient without established manifestations plus evidence of
rheumatic heart disease preceding group A streptococcal
infection

Recurrent attack of RF in a Preceding group A streptococcal

patient with established infection
rheumatic heart disease

Rheumatic chorea Evidence of Group A streptococcal

infection not required
Insidious onset rheumatic
carditis.

Chronic valve lesions of RHD Diagnosed as having rheumatic heart

(patients Presenting for the first disease
time with pure mitral stenosis or
mixed mitral valve disease.
And/or aortic valve disease

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Treatment
I. Eradication of beta hemolytic streptococcal infection
Benzathine penicillin 300,000-1.2 million IU stat dose depending on the age
II. Suppression of inflammatory response
 Rheumatic Fever without carditis: Aspirin 100 mg/kg/day divided
in four doses for two weeks and decrease to 75 mg /kg divided
doses for two more weeks
 Rheumatic fever with carditis: Prednisolone 2mg/kg in four
divided doses for two weeks
 Tapper the prednisolone in the next two weeks
 While tapering, add Aspirin 75 mg /kg in four divided doses for
the next four weeks
III. Treatment of heart failure
 Bed rest
 Salt free diet
 Oxygen
 Diuretics: furosemide 1-2 mg/kg divided in two doses and
spironolactone 3mg/kg/day once daily. If not available add
potassium chloride 1-2mg/kg PO daily
 Consult cardiologist or refer the child for better evaluation and
management
Complications
 Recurrence of rheumatic fever
 Chronic rheumatic valvular heart disease
 Infective endocarditis
 Arrhythmia

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  Stroke ( Thromboembolic )
 Heart failure
Follow up
 Secondary prophylaxis with Benzathine penicillin 300,000-1.2 mu
every 4 weeks im to prevent recurrence
 Review every 1-3 months at cardiac follow up clinic depending on
clinical condition of the patient
 Referral for possible surgical treatment after cardiology
consultation in case of chronic valvular heart disease
Prevention
Primary prophylaxis: Treatment of bacterial tonsilopharyngitis
Secondary prophylaxis: Monthly Benzathine penicillin for five years for
those with RF without carditis and for life for those with carditis.
In children with chronic valvular heart disease administer antibiotics one
hour before dental, gastrointestinal, and genitourinary procedures to
prevent bacterial endocarditis.

6.14 Dengue
Dengue is caused by an arbovirus transmitted by Aedes mosquitoes

Diagnosis

 Suspect dengue fever in an area of risk for dengue. If the child has:
 Fever lasting > 2 days
 Headache, pain behind the eyes
 Joint and muscle pain
 Abdominal pain, vomiting
 Rash may occur but is not always present.

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  It can be difficult to distinguish dengue from other common
childhood infections.
Treatment
Most children can be managed at home, provided the parents have good
access to a hospital.
Counsel the parents to bring the child back for daily follow-up and to return
immediately if any of the following occur:
 Severe abdominal pain, persistent vomiting,
 Cold, clammy extremities,
 lethargy or restlessness,
 Bleeding, e.g. black stools or coffee-ground vomit.
 Encourage oral fluid intake with clean water or ORS solution to
replace losses during fever and vomiting.
 Give paracetamol for high fever if the child is uncomfortable. Do
not give aspirin or NSAIDs such as ibuprofen, as these drugs may
aggravate bleeding.
 Follow-up the child daily until the temperature is normal.
 Check the hematocrit daily if possible.
 Check for signs of severe disease.
 Admit any child with signs of severe disease
 Mucosal or severe skin bleeding
 Shock, altered mental status
 Convulsions
 Jaundice
 Rapid or marked rise of hematocrit

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6.14.1 Severe dengue
Severe dengue is defined by one or more of the following:
 Suspect severe dengue in an area of risk for dengue if the child has
fever lasting > 2 days, and any of the following features:
 Evidence of plasma leakage
 High or progressively rising hematocrit
 Pleural effusions or ascites
 Circulatory compromise or shock
 Cold, clammy extremities
 Prolonged capillary refill time (> 3 s)
 Weak pulse (fast pulse may be absent even with significant
volume depletion)
 Narrow pulse pressure < 20mmHg
 Spontaneous bleeding
 From the nose or gums
 Black stools or coffee-ground vomit
 Skin bruising or extensive petaechiae
 Altered level of consciousness
 Lethargy or restlessness
 Coma
 Convulsions
 Severe gastrointestinal involvement
 Persistent vomiting
 Increasing abdominal pain with tenderness in the right upper
quadrant
 Jaundice

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Diagnosis
Clinical with high grade fever and any of the above mentioned features.
Treatment
Admit all patients with severe dengue.
Fluid management: patients without shock (pulse pressure > 20 mm Hg)

 Give IV fluids for repeated vomiting or a high or rapidly rising HCT.

Give only isotonic solutions such as normal saline and Ringer’s
lactate or 5% glucose in Ringer’s lactate.
 Start with 6 ml/kg per h for 2 h, and then reduce to 2–3 ml/kg per
h as soon as possible, depending on the clinical response.
 Give the minimum volume required to maintain good perfusion
and urine output. IV fluids are usually needed only for 24–48 h, as
the capillary leak resolves spontaneously after that time.
Fluid management: patients in shock (pulse pressure ≤20 mm Hg)

 Treat as an emergency. Give 10–20 ml/kg of an isotonic crystalloid

solution such as Ringer’s lactate or normal saline over 1 h. If the
child responds (capillary refill and peripheral perfusion start to
improve, pulse pressure widens), reduce to 10 ml/kg for 1 h and
then gradually to 2–3 ml/kg per h over the next 6–8 h.

If the child does not respond (continuing signs of shock), give a further 20
ml/kg of the crystalloid over 1 h, or consider giving 10 ml/kg of a colloid
solution if available such as 6% dextran (molecular mass, 200,000) over 1 h.
Revert to the crystalloid schedule described above as soon as possible.
Frther small boluses of extra fluid (5–10 ml/kg over 1 h) may be required
during the next 24-48 h.

 Decide on fluid treatment on the basis of clinical response.

 Review vital signs hourly ( pulse and blood pressure)

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  Hematocrit
 Monitor urine output.
A rising Hematocrit with unstable vital signs (particularly narrowing of the
pulse pressure) indicates the need for a further bolus of fluid, but extra
fluid is not needed if the vital signs are stable, even if the hematocrit is very
high (50–55%).
The Hematocrit is likely to start falling within the next 24 h as the
absorptive phase of the disease begins.
In most cases, IV fluids can be stopped after 36–48 h. Remember that too
much fluid can result in death due to fluid overload.
Treatment of haemorrhagic complications
 Minor bleeding: Manifested as mucosal bleeding due to low
platelet count. It is usually self-limiting and resolve within two
weeks.
3
 In children with low platelet (less than 20,000/mm ) order strict
bed rest, protect from trauma, and avoid IM injections. Platelet
concentrate not indicated for thrombocytopenia without bleeding.

 Major bleeding: gastrointestinal tract bleeding with tarry (black)

stool is the usual manifestation.

 Consider the possibility of GI bleeding in child with shock who fail

to improve clinically with fluid treatment particularly if appears
very pale, hematocrit is falling or abdomen become distended and
tender.

 Transfusion rarely necessary; if indicated give 5-10ml/kg fresh

whole blood or 10 ml/kg packed cells over 2-4 hrs. Repeat if there
is response and significant bleeding is confirmed.

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Treatment of fluid overload
Fluid overload is an important complication of treatment for shock. It can
develop due to:

 Excess or too rapid IV fluids

 Incorrect use of hypotonic rather than isotonic crystalloid
solutions
 Continuation of IV fluids for too long (once plasma leakage has
resolved)
 Use of large volumes of IV fluid in children with severe capillary
leakage
o Early signs: peri-orbital or soft tissue oedema, fast breathing,
chest indrawing, large pleural effusions, ascites
o Late signs: cyanosis, pulmonary oedema, irreversible shock
(often a combination of ongoing hypovolaemia and cardiac
failure)
The management of fluid overload varies depending on whether the child
is in or out of shock:
 Children who remain in shock and show signs of severe fluid
overload:
 Repeated small boluses of a colloid solution may help with
inotropic agents to support the circulation (see standard
textbooks of paediatrics). Avoid diuretics, as they will cause
further intravascular fluid depletion.
 Aspiration of large pleural effusions or ascites may be needed to
relieve respiratory symptoms, but there is the risk of bleeding

during the procedure.

273
  Continuous positive pressure ventilation before pulmonary
oedema develops if it is available
 If shock has resolved but the child has fast or difficult breathing
and large effusions, give oral or IV furosemide at 1 mg/kg once or
twice a day for 24 h and oxygen therapy.
 If shock has resolved and the child is stable, stop IV fluids and keep
the child on strict bed rest for 24–48 h. Excess fluid will be
reabsorbed and lost through urinary diuresis.
Supportive care
 Treat high fever with paracetamol if the child is uncomfortable. Do
not give aspirin or NSAIDs such as ibuprofen, as they aggravate the
bleeding.
 Do not give steroids.
 Treat Convulsions ( Chart 9)
 If the child is unconscious, follow the guidelines in section 1.5.3.
 Children in shock or with respiratory distress should receive
oxygen, if possible with nasal continuous positive airway pressure
(see above).
 Treat Hypoglycaemia
 If the child has severe hepatic involvement, see standard
paediatric textbook for guidelines.
Monitoring
Child with severe disease

Monitor the vital signs continuously if monitor available, otherwise hourly

particularly the pulse pressure until the patient is stable.

 Monitor input and output hourly

274
  Check the Hematocrit four times a day.
 A doctor should review the patient at least four times a day and
prescribe IV fluids for a maximum of 6 h at a time.
Child without shock
 A nurse should check the child’s vital signs (temperature, pulse
and blood pressure) at least four times a day
 Hematocrit once daily and platelet count daily
 A doctor should review the patient at least once daily.
 Keep a detailed record of all fluid intake and output.

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CHAPTER 7 - SEVERE ACUTE MALNUTRITION
Severe malnutrition is one of the most common causes of morbidity and
mortality among children under the age of 5 years worldwide. With
appropriate case management in hospitals and follow-up care, the lives of
many children can be saved, and the facility case fatality rates can be
reduced significantly, a mortality rate has been reduced from over 30% to
less than 5%.

Severe malnutrition is both a medical and a social disorder. Successful

management of the severely malnourished patients requires that both
medical and social problems be recognized and corrected.

7.1 Diagnosis
Key diagnostic features of severe acute malnutrition are:

 Infants less than six months:

o Weight –for- Length (W/L) less than 70% of NCHS median,
OR
o Presence of pitting Oedema of both feet, OR
o Visible Severe Wasting if it is difficult to determine W/L
 Children 6 months to 5 years:
o Weight for Height (W/H) or Weight –for- Length (W/L) less than
70 % of NCHS median, OR
o Presence of pitting Oedema of both feet, OR
o MUAC<11.5 cm for a child with a length greater than 65 cm if
W/L or W/H is difficult to measure
If weight-for-height or weight-for-length cannot be measured, use the
clinical signs for visible severe wasting (see Figure below, the child with
Mararsmus). A child with visible severe wasting appears very thin and has
no fat. There is severe wasting of the shoulders, arms, buttocks and thighs,

276
with visible rib outlines.
Note: No distinction has been made between the clinical conditions of
kwashiorkor, marasmus, and marasmic kwashiorkor because the approach
to their treatment is similar.

Figure 7.1 A Child with Figure 7.2 B Child with

visible severe wasting edematous malnutrition

7.2 Initial assessment of the severely malnourished child

Take a history concerning:
 Recent intake of food and fluids
 Usual diet (before the current illness)
 Breastfeeding
 Duration and frequency of diarrhoea and vomiting, if there is
recent sunkening of eyes

277
  Type of diarrhoea (watery/bloody)
 Loss of appetite
 Family circumstances (to understand the child’s social
background)
 Cough over 2 weeks
 Contact with an adult with tuberculosis
 Recent contact with measles cases
 Known or suspected HIV infection/exposure.

Do physical examination:
 Look general appearance: lethargy, abnormal gaze
 Take vital signs: temperature, respiratory rate, pulse, BP
 Do growth assessment: weight, height/length, HC, weight-for-
height/length
 Signs of shock and dehydration (cold hands, slow capillary refill,
weak and rapid pulse)
 Conjunctival pallor, sunken eye ball, eye signs of vitamin A
deficiency (dry conjunctiva or cornea, Bitot’s spots, corneal
ulceration, keratomalacia)
 mouth ulcers, oral thrush, signs of local infection( including ear
and throat infections)
 Findings suggestive of pneumonia
 Skin changes of kwashiorkor
o Hypo- or hyperpigmentation
o Desquamation
o Ulceration (spreading over limbs, thighs, genitalia, groin, and
behind the ears)
o Exudative lesions (resembling severe burns) often with
secondary infection (including Candida)
 Severe palmar pallor,

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  Pitting edema of both feet

Figure 7.1 A: Pitting edema




 Bitot’s spot (conjunctival xerosis)—sign of xerophthalmia in a
vitamin A deficient child

Figure 7.1 B: Bitot’s spots

Note: Children with vitamin A deficiency are likely to be photophobic and

will keep their eyes closed. It is important to examine the eyes very gently
to prevent corneal rupture.
 Do appetite test procedure if the child has no serious medical complications
(see section 7.6 for medical complications; Refer Nutrition Guideline for
Appetite test procedures)

Investigation

Do the following investigations depending on the patients’ condition:

CBC, U/A, urine culture, stool exam, chest X-ray, TSP, blood culture, and
HIV test

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Table 7.1 Asses and classify an infant age under 6 months for Severe Acute
Malnutrition (SAM)

280
Table 7.2 Assess and Classify a child age 6 months to 5 years for Severe
Acute malnutrition

7.3 Admission criteria

281
All infants less than 6 months with Severe Acute Malnutrition should be
admitted for inpatient care of the therapeutic feeding program (TFP).
Children 6 months to 5 years with severe acute malnutrition and any one of
the following should be admitted for in-patient care of the TFP:
 Any of the following serious medical complications:
o Severe vomiting/ intractable vomiting
o Hypothermia: axillary’s temperature <35°C or rectal
o
temperature < 35.5 C
o Fever>39°C
o Number of breaths per minute:
– 60 resps/ min for under 2 months
– 50 resps/ minute from 2 to 12 months
– 40 resps/minute from 1 to 5 years OR
– Any chest in-drawing
 Extensive skin lesions(+++ dermatosis)/ infection
 Very weak, lethargic, unconscious
 Fitting/convulsions
 Severe dehydration based on history & clinical signs
 Shock or any condition that requires an infusion or NG tube
feeding.
 Very pale (severe anaemia): Hgb< 4 g/dl
 Hypoglycemia
 Jaundice
 Bleeding tendencies
 Other general signs the clinician thinks warrants transfer to the
in-patent facility for assessment

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 OR
 Failed appetite test,
OR
 If there is no out patient treatment sites in the place where
the child is living
OR
 If the parent chooses to be treated as in-patient despite the
advise of the health worker.
7.4 Organization of Care
On admission, the child with severe malnutrition should be separated from
infectious children and kept in a warm area (25–30 ° C, with no draughts),
and constantly monitored. These patients should be admitted directly to
the TFU/SC and not treated in an emergency ward or casualty department
for the first 24-48 hours, unless the staff of the emergency ward have had
specific training in the management of the complications seen in SAM
patients. Treatment should be performed in a dedicated room. Washing
should be kept to a minimum, after which the child should be dried
immediately.

Facilities and sufficient staff should be available to ensure correct

preparation of appropriate feeds, and to carry out regular feeding during
the day and night. Accurate weighing machines are needed, and records
like the Therapeutic Treatment In-patient Multi-Chart (Multi-chart) should
be kept of the feeds given and the child’s weight so that progress can be
monitored.

All children with SAM should be given first feed of F-75 or 50 ml of sugar
solution (1 rounded teaspoon of sugar in 3and half tablespoons of water)

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orally while waiting for admission.
7.5 Treatment Approach
 Treatment of complications
 Routine medicines
 Dietary Treatment
o Phase I
o Transition phase
o Phase II
In the initial phase, a cautious approach is required because of the child’s
fragile physiological state.
7.6 Treatment of medical complications

7.6.1 Dehydration
Dehydration tends to be over diagnosed and its severity overestimated in
severely malnourished children because it is difficult to estimate
hydration status accurately in SAM children using clinical signs alone.

Diagnosis
Diagnosis of dehydration should mainly be based on the history rather
than on patient examination alone. Ask the mother if the child has had
watery diarrhoea or vomiting, recent change in the child’s appearance and
recent sunkening of eyes.

Consider the diagnosis of dehydration in non-edematous child if there

are:
 Definite history of significant recent fluid loss (diarrhoea
looking like water, not just ‘loose’ stools, appearing with
sudden onset in the last hours or days)
 Clear history of a recent change in the child's appearance
 If the eyes are sunken, then the mother must say that the eyes
have changed to become sunken since the diarrhea or

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 vomiting started.

Edematous children are over-hydrated, but they are frequently

hypovolemic due to dilation of blood vessels with low cardiac output. If the
child with edema has definite watery diarrhoea and is deteriorating
clinically, diagnose dehydration.

For the diagnosis of shock in SAM children see section 7.6.2

Treatment
Do not use the IV route for rehydration except in cases of shock. Give
special rehydration solution for malnutrition, ReSoMal (Table 7.3).
Treat a child with no oedema having signs of dehydration but not in shock
as follows:
 Start with 5ml/kg every 30 minutes for the first two hours orally
or by naso-gastric tube and then adjust according to the weight
changes observed. If there is continued weight loss then increase
the rate of administration of ReSoMal by 10ml/kg/hour. If there is
no weight gain, Increase the rate of administration of ReSoMal by
5ml/kg/hour. Weigh the child each hour and assess his/her liver
size, respiration rate and pulse.
 If there is weight gain and deterioration of the child’s condition
with the re-hydration therapy, the diagnosis of dehydration was
definitely wrong and rehydration should be stopped (a common
circumstance). Normally much less ReSoMal is sufficient to restore
adequate hydration in malnourished than normally nourished
children (e.g. a total of 50ml per kg body weight - 5% body weight).
 After rehydration usually no further treatment is given; however,
for malnourished children from 6 to 24 months, 30ml of ReSoMal
can be given for each watery stool that is lost.
Treat an oedematous child having signs of dehydration but not in shock.
Replace fluid loss at rate of 30 ml of ReSoMal per watery stool. A child
who is in shock (both for oedmatous and non-oedematous) should be

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treated with intravenous fluids. See the management under shock
(section 7.6.2)

Figure 7.2 Summary of treatment of dehydratrion

286
 Figure 7.3 Monitoring a child who is on treatment for dehydration

Table 7.3 Recipe for ReSoMal

Ingredient Amount
Water 2 liters
WHO ORS One 1 liter packet
Sugar 50gms
Electrolyte/Mineral 40ml
solution*

*45 ml of KCL solution can be used if electrolyte/mineral solution is not

available

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7.6.2 Shock
Diagnosis
The severely malnourished child is considered to have shock if he/she is
lethargic or unconscious and has cold hands plus either:

 Slow capillary refill (longer than 3 seconds), or

 Weak ,fast or absent radial or femoral pulses and
 Absence of signs of heart failure in an edematous child
Treatment
 Give oxygen
 Keep the child warm

Treat with intravenous fluids :

 Check the starting respiratory and pulse rates and record them on
the Multi-chart and also on the shock follow up chart. Also record
the starting time.
 Infuse IV fluid at 15ml/kg over 1 hour. Use one of the following
solutions, listed in order of preference:
o Ringer’s lactate solution with 5% glucose*
o 0.9 % normal Saline with 5% glucose* (add 125 ml of 40 % or
100 ml of 50% glucose to 1 litre of 0.9% saline to make this
fluid)

*If either of these is used, add sterile potassium chloride (20 mmol/l) if
possible.
 Observe the child and check respiratory and pulse rates every 10
minutes (see the shock follow up chart below). Follow the liver
size too.
 If the respiratory rate and pulse rate increase and child is gaining
weight, stop the IV rehydration and assume septic or cardiogenic
shock.

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  If respiratory rate and pulse rate are slower after 1 hour, the
child is improving. Repeat the same amount of IV fluids for
another hour. Continue to check respiratory and pulse rates
every 10 minutes.
 After 2 hours of IV fluids, switch to oral or nasogastric
rehydration with ReSoMal. Give 5-10 ml/kg ReSoMal in
alternate hours with F-75 for up to 10 hours or until fully
rehydrated.
Septic (or toxic) shock: Assume that the child has septic shock if a child with
shock fails to improve after the first hour of IV fluids. Treat as follows:
 Give maintenance IV fluids (4 ml/kg/hour) while waiting for
blood. When blood is available, stop all oral intake and IV
fluids, give a diuretic to make room for the blood, and then
transfuse whole fresh blood at 10 ml/kg slowly over 3 hours.
If there are signs of heart failure, give packed cells instead of
whole blood as these have a smaller volume.
 Give broad-spectrum antibiotics (Second line and first line
antibiotics together, Keep warm to prevent or treat
hypothermia, sugar-water by mouth or naso-gastric tube,
minimize disturbance including washing and transportation.
Table 7.4: Shock follow up chart

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7.6.3 Heart failure

Diagnosis: it should be considered when there are conditions like:

 Clinical deterioration with a gain in weight
 A sudden increase in liver size
 An increase in respiration rate
 Crepitations or rales in the lungs
 Prominent superficial and neck veins, etc.

Treatment
Stop all intakes of oral or IV fluids till it improves (Small amounts of sugar-
water can be given orally to prevent hypoglycemia). Give furosemide
SINGLE dose (1mg/kg),

If heart failure is associated with severe anaemia, treat as in section 7.6.5

7.6.4 Hypothermia
Diagnosis
Severely malnourished patients are highly susceptible to hypothermia. The
o
child has hypothermia if axillary temperature is below 35 C).
Treatment
 Feed the child immediately with F-75 and every 2-3 hours,
 Use the “kangaroo technique” for children with a caretaker ,
Put a hat on the child and wrap mother and child together, Give
hot drinks to the mother so her skin gets warmer (plain water,
tea or any other hot drink),
 The room should be kept warm, especially at night (between
o o
28 C and 32 C): a maximum- minimum thermometer should be
on the wall of Phase 1 room to monitor the temperature. Treat
for hypoglycemia and give second-line antibiotic treatment.
Prevent hypothermia through feeding the child 3-hourly including at night,
and keeping the child warm: change wet nappies, and clothes and

290
bedding, avoid exposing the child to cold (e.g. after bathing, or during
medical examinations) and let the child sleep with the mother for warmth
in the night.
 Give appropriate IV or IM antibiotics.

7.6.5 Severe Anemia (haemoglobin <4 g/dl)

Diagnosis: If the haemoglobin concentration is less than 4g/dl or the

packed –cell volume is less than 12% in the first 48 hours after admission,
the child has severe anaemia.

Treatment
Transfuse the child as follows if the child has severe anemia in the first 48
hours:

 Stop all oral intake and IV fluids during the transfusion.

 Look for signs of congestive heart failure such as fast breathing,
respiratory distress, rapid pulse, engorgement of the jugular vein,
cold hands and feet, cyanosis of the fingertips and under the
tongue.
 Give Furosemide 1 mg/kg, given by IV.
 If there are no signs of congestive heart failure, transfuse whole
fresh blood at 10 ml/kg slowly over 3 hours. If there are signs of
heart failure, give 10 ml/kg packed cells over 3 hours instead of
whole blood.
 Monitor the pulse and breathing rate every 15 minutes during the
transfusion. If either increases (RR by 5 breaths/min or PR by 25
beats/min), transfuse more slowly.

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  As malnutrition is usually not the cause of severe anaemia, it is
important to investigate other possible causes such as malaria and
intestinal parasites (for example, hookworm) and treat
accordingly.
Note:
 If the Hgb remains low after the transfusion, don’t repeat it with in
4 days.
 Most heart failure between 2-14 days is not due to severe anemia.
Please consider other diagnosis before deciding to transfuse.

Figure 7.4: Flow chart for treatment of anemia

292
7.6.6 Hypoglycemia

All severely malnourished children are at risk of hypoglycaemia and,

immediately on admission, should be given a feed or 10% glucose or
sucrose.

Diagnosis: it is diagnosed if blood glucose is <3 mmol/l (<54 mg/dl). If the

blood glucose cannot be measured, it should be assumed that all children
with severe malnutrition have hypoglycaemia.
 If the child can drink, give 50 ml bolus of 10% glucose or 10%
sucrose orally. If the child is alert but not drinking, give the 50 ml
by NG tube.
 If the child is lethargic, unconscious, or convulsing, give 5 ml/kg
body weight of sterile 10% glucose by IV, followed by 50 ml of 10%
glucose or sucrose by NG tube.* If the IV dose cannot be given
immediately, give first dose through NG tube.

* If the child will be given IV fluids for shock, there is no need to

follow the 10% IV glucose with an NG bolus, as the child will
continue to receive glucose in the IV fluids.

 Start feeding F-75 half an hour after giving glucose and give it every
half-hour during the first 2 hours. For a hypoglycaemic child, the
amount to give every half-hour is ¼ of the 3-hourly amount shown
on the F-75 Reference Card.
 Take another blood sample after 2 hours and check the child’s
blood glucose again.
o If blood glucose is 54 mg/dl (3mmol/l) or higher, change to 3-
hourly feeds (8 feeds per day) of F-75.

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 o If it is still low, make sure antibiotics and F-75 have been given.
Keep giving F-75 every half-hour and Treat with second-line
antibiotics.

Prevent hypoglycemia by feeding 2-3 hourly, starting immediately and

throughout the night and preventing hypothermia as explained in section
7.6.4
7.6.7 Eye Problems

If the child has any eye signs of vitamin A deficiency,

 Give vitamin A orally on days 1, 2 and 14 (aged <6 months, 50 000
IU; aged 6–12 months, 100 000 IU; older children, 200 000 IU). If the
first dose was given in the referring centre, treat on days 1 and 14
only.

If the eyes show signs of corneal clouding or ulceration, give

additional care to the affected eye(s) to prevent corneal rupture and
extrusion of the lens:
 Instil chloramphenicol or tetracycline eye drops, 4 times daily as
required for 7–10 days,
 Instil atropine eye drops, 1 drop 3 times daily for 3–5 days,
 Cover with saline-soaked eye pads, and bandage the eye(s).If the
child falls asleep with his eyes open, close them gently to protect
them.
7.6.8 Dermatosis

Dermatosis is more common in children who have oedema than in wasted

children. When the skin is raw and weeping, this risk of infection is very
high. The extent of dermatosis can be described as follows:

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 + Mild: discoloration or a few rough patches of skin
+ + Moderate: multiple patches on arms and/or legs
+ + + Severe: flaking skin, raw skin, fissures (openings in the skin)

Treatment
Use regular soap for bathing if the child does have mild or moderate
dermatosis.
Treat the child with severe (+++) dermatosis as follows:
 Bathe for 10-15 min/day in 1% potassium permanganate solution. To
make a 1% solution, dissolve a crystal in enough water so that the
colour is slightly purple and still transparent. Sponge the solution
onto affected areas while the child is sitting in a basin. This dries the
lesions, helps to prevent loss of serum and inhibits infection. If
potassium permanganate solution is not available, affected areas
may be dabbed with gentian violet. If the child has severe
dermatosis but is too sick to be bathed, dab 1% potassium
permanganate solution on the bad spots, and dress oozing areas
with gauze to keep them clean.
 Apply barrier cream to raw areas. Useful ointments are zinc and
castor oil ointment, petroleum jelly, or paraffin gauze dressing.
These help to relieve pain and prevent infection.
 If the diaper area becomes colonised with candida, use nystatin
ointment or cream after bathing. (Candidiasis is also treated with
oral Nystatin)
 Leave off diapers (nappies) so the affected area can dry. Be sure to
dry the child well after a bath and wrap the child warmly.

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7.7 Routine Medicines
Children with SAM should be provided the following routine drugs.
7.7.1 Vitamin A

 On the day of admission (day 1), give vitamin A for all children
except those with oedema or those who received vitamin A in the
past 6 months.
 Give vitamin A to every patient on the day of discharge (in-patient
care) or at the 4th week of the treatment for those in out-patient
care.
 Dose: <6 months: 50,000IU PO at admission; 6-11 months:
100,000IU; ≥12 months: 200,000IU

7.7.2 Folic Acid

 On the day of admission, one single dose of folic acid (5mg for 6
moths to 5 years and 2.5mg stat for infants) can be given to children
with clinical signs of anaemia.
7.7.3 Antibiotics
Antibiotics should be given to every patient with SAM, even if they do not
have clinical signs of systemic infection.
 If no complications, give first line antibiotics: oral Amoxicillin for 7 days
(preferred) or cotrimoxazole.
 If complications present, give second line antibiotics: Gentamicin, plus
IV Ampicillin for 2 days followed by Amoxicillin depending on the
condition of the child, for a total treatment duration of 7 days.
 If the child fails to improve within 48 hours, add chloramphenicol or
change to Amxicillin/clavulinic acid or
 Ceftriaxone

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  Use the dose and schedule in table 7.2
 Route of administration: best route is oral or through NGT
 Duration: In-patient care: every day during Phase 1 + four more days
or until transfer to OTP; Out-patient care: for 7 days total.
 If specific infections are identified which require a specific antibiotic
not already being given, give an additional antibiotic to address that
infection. For example, dysentery may require additional antibiotics.
Certain skin infections such as Candidiasis require specific antifungals.
Antimalarial treatment if the child has a positive blood film for
malaria parasites.
 Frequently a systemic anti-fungal (Fluconazole) is added for any
patient who has signs of severe sepsis or systemic candidiasis
Table 7.5 choice of antibiotics for children with SAM

IF: GIVE:
Oral Amoxicillin for 7 days or Cotrimoxazole for 5
NO COMPLICATIONS
days if Amoxicillin is not available
COMPLlCATIONS(shock,
hypoglycaemia, hypothermia, Gentamicin1 IV or IM once daily for 7 days, plus:
dermatosis with raw skin/fissures, Ampicillin IV or IM every 6 hours for 2 days
respiratory or urinary tract infections, followed by oral Amoxicillin for 5 days
or lethargic/sickly appearance)
Chloramphenicol IV or IM every 8 hours for 5
If child fails to improve within 48 days. (Give every 6 hours if suspect meningitis.) Or
hours, ADD: ceftriaxone 100 mg/kg divided into 2 doses IV or
IM + gentamicin once daily for a total of 10 days.
If a specific infection requires an Specific antibiotic as indicated.
additional antibiotic, ALSO GIVE:

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Table 7.6 Dosage of selected oral antibiotics in SAM

Table 7.7 Dosage of selected parenteral antibiotics in SAM

7.7.4 Iron
It is added to the F100 in Phase 2. Add 1 crushed tablet of ferrous sulphate
(200mg) to each 2 litres to 2.4 litres of F100. For lesser volumes: 1000 to
1200ml of F100, dilute one tab of ferrous sulphate (200mg) in 4ml water
and add 2ml of the solution. For 500ml to 600ml of F100, add 1ml of the
solution. RUTF already contains the necessary iron.

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 7.7.5. Measles vaccine
All children from 9 months without a vaccination card should be given
measles vaccine both on admission and discharge after Phase 2.
7.7.6. Deworming
Albendazole or Mebendazole is given for children ≥1 year at the start of
Phase 2 for patients that will remain as in patients. For both those
transferred from in-patients to Phase 2 as out-patients and those admitted
directly to OTP de-worming is given at the 2nd out-patient visit (after 7
days).
Table 7.8 Deworm the child as in the table below

Age < 1 year 1-2 years > 2 years

Albendazole 400 mg Not given Half tablet once one tablet once
Mebendazole 100 mg Not given One and half tablet Five tablets once
once

Table 7.9 Summary of routine medicines in SAM

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7.8 Dietary Treatment
To prevent death, feeding should begin as soon as possible with F-75, the
“starter” formula used until the child is stabilized. F-75 is specially made to
meet the child’s needs without overwhelming the body’s systems at this
early stage of treatment. F-75 contains 75 kcal and 0.9 g protein per 100
ml. F-75 is low in protein and sodium and high in carbohydrate, which is
more easily handled by the child and provides much-needed glucose.

When the child is stabilized (usually after 2 to 7 days), the “catch-up”

formula F-100 or RUTF is used to rebuild wasted tissues. F-100 contains
more calories and protein: 100 kcal and 2.9 g protein per 100 ml. This
section will describe the three phases (Phase I, Transition phase and Phase
2) of feeding for in-patient care for children 6 moths- 5 years and under 6
months separately.

7.8.1 Feeding of Children 6 months to 5 years

I. Phase I Feeding
Use the F-75 table below (Table 7.9) to determine the amount F-75 and
frequency of feeding. This amount of F-75 will give the child 100
kcal/kg/day and 1 - 1.5 g protein/kg/day and it is enough until the child is
stabilized. Eight feeds per day are given for 24h in care units where there
are sufficient staff to prepare and distribute the feeds at night. Six feeds
per day are given where there are few staff at night.

It is best to feed the child with a cup (and spoon, if needed). It may be
necessary to feed a very weak child with a dropper or syringe. Do not use a
feeding bottle. Very occasionally it may be necessary to use a nasogastric
(NG) tube if the child is very weak, has mouth ulcers that prevent drinking,
has pneumonia with rapid respiration or if the child cannot take al least
75% F-75 by mouth.
Remove the NG tube when the child takes 75 % of the day’s amount orally
for two consecutive feeds.

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Table 7.9.1 Amounts of F75 to give during Phase 1

Monitor and Record:

 Weight is measured, entered and plotted on the multichart each day.
 The degree of oedema (0 to +++) is assessed each day.
 Body temperature is measured four times per day.
 The standard clinical signs (stool frequency and consistency, vomiting,
dehydration, cough, respiration, liver size, etc.) are assessed noted in
multi-chart each day.
 Amounts of feed offered and left over

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II. Transition Phase Feeding Treatment

It may take 2-7 days for the child to stabilize on F-75. When the child has
stabilized, transfer into transition phase and offer F-100 or RUTF, the
higher calorie, higher protein “catch-up” feed intended to rebuild wasted
tissues. The following are signs of readiness to progress from Phase 1 to
transition phase:

 Return of appetite (easily finishes 4-hourly feeds of F-75) and

 Reduced oedema or minimal oedema (++ or less) and
 No IV line, No NGT
During transition phase F-100 or RUTF should be given as follows:

 Give RUTF (Plumpy Nut) if children are going to continue

treatment as out-patients (OTP) with take-home treatment rather
than F100. Use Table 7.9.1 to determine the total amount of RUTF
(Plumpy Nut) that should be taken during the day.

 Children who are not taking sufficient RUTF should be given F100
to make up any deficit in intake. Give F-100 every 4 hours in the
same amount as you last gave F-75 if children can’t take RUTF or
are not going to continue treatment in OTP. Give F-100 based on
the F-100 for transition (Table 7.9.1). Do not increase this amount
for 2 days.

 Encourage the mother to breastfeed before and on demand

between feeds of F-100 if the child is on breast feeding. As the
patient is now taking more than maintenance amounts of food,
weight gain is expected. The expected rate of weight gain, for
marasmic patients, during transition phase is about 6 g/kg/day.
Note that some of the patients may regress to phase 1
management.

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III. Phase 2 Feeding

Transfer the child from transition phase to phase 2 if:

 The child finish 90% of the RUTF or F 100
 If the child has oedema and will continue phase 2 as inpatient,
transfer if they lost the oedema. If they will continue phase 2 as an
outpatient, transfer them if the oedema starts to reduce and
become +.
 During phase 2, a child can feed freely on F-100 or RUTF. Most
children will consume at least 150 kcal/kg/day; any amount less
than this indicates that the child is not being fed freely or is
unwell. Use the table below to determine the total amount of
RUTF (Plumpy Nut) or F 100 that should be given to a child during
phase 2. There are two options for Phase 2 feeding:
 If there is OTP in the area the child is living, transfer the child to
Out Patient Treatment (OTP) to be treated at home with RUTF.
The child should be transferred with sufficient RUTF (at least one
week supply of RUTF.)
 Continue Phase 2 as in-patient: Treat with F-100 or RUTF in an in-
patient care if there is no OTP service in the area where the child
is living or for other medical reason the child should stay inpatient.
 If the child has been on RUTF during transition, continue RUTF as
Table 7.9.1 below. If the child has been on F-100 during transition,
preferably use RUTF as above or continue with F-100. On the first
day of Phase 2, increase F-100 at each feed by 10 ml as long as the
child is finishing feeds. If the child does not finish a feed, offer the

303
 same amount at the next feed; then if feed finished, increase by
10 ml. Continue increasing the amount until some food is left
after most feeds. Breast-fed children should always get the breast-
milk before they are given F100 or RUTF

Table 7.9.2 Transition Phase: amounts of RUTF to give

Move the child back to Phase 1 if:

 The patient gains weight more rapidly than 10g/kg/d (this
indicates excess fluid retention)
 There is increasing oedema
 A child who does not have oedema develops oedema
 There is a rapid increase in the size of the liver
 Any other signs of fluid overload develop.
 Tense abdominal distension develops
 The patient gets significant re-feeding diarrhoea so that there is
weight loss.
 Patient develops medical complication
 Naso-Gastric Tube is needed

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  Patient takes less than 75% of the feeds in Transition Phase
even after interchange between RUTF and F100
Criteria to transfer the child from transition phase to Phase 2:
 If the child has good appetite (taking at least 90% of the RUTF
or F100).
 Oedematous children should remain in Transition Phase until
there is a definite and steady reduction in oedema:
o For those who are going to remain as inpatients they should
normally remain in Transition Phase until they have lost their
oedema entirely.
o For those who are going to continue as OTP they can go when
their appetite is good and they have reduced their oedema to
++ or +.
Table 7.9.3 Phase 2 Amount of F100 or RUTF to give at each feed for
5 or 6 feeds per day

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Table 7.9.4 Phase 2 (out-patients): amounts of RUTF to give
Follow Up for phase 2 is summarized in the table below

Table 7.9.5 Surveillance of response for phase 2

Frequency
Parameter
Inpatient Out patient
Weight and oedema 3 times per week Every visit
Height/Length is Every 3 weeks As required Every
measured month
Body temperature is Every morning Every visit
measured
The standard clinical Every day Every visit
signs (stool, vomiting,
etc)
MUAC is taken Every week Every visit

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 Appetite test is done Intake record is kept Every visit
on chart
Transfer the child from phase 2 to Phase 1 if the child:
 Develops any signs of a complication
 Develops or has increased oedema
 Develops refeeding diarrhoea sufficient to lead to weight loss.
 Loses weight for 2 consecutive weighing
 Has static weight for 3 consecutive weighing
 Fulfills any of the criteria of “failure to respond to treatment”
7.8.2 Feeding of infants less than 6 months

The feeding of infants is different from older children and it is also different
for infants on breast feeding or with a caretaker willing to breast feed and
for infants who can not be breast-fed. RUTF is not suitable for all infant less
than 6 months, as the reflex of swallowing is not present yet.
1. Infants below six months on breast feeding or with a caretaker
willing to breast feed
Infants who are malnourished are weak and do not suckle strongly enough
to stimulate adequate production of breast milk. The feeding of these
infants is to return them to full exclusive breastfeeding using
supplementary suckling (SS) and feeding with diluted F-100. These infants
have to be fed as follows:
 Breastfeed every three hours for at least 20 minutes (more if
the child cries or demands more)
 Between one and a half hours after a normal breastfeed give
maintenance amounts of F100-diluted using the SS technique
(see the explanation below).
 Give diluted F100 in 8 feeds ( use table 7.9.5 below to

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 determine the amount of diluted F-100 )
 If the infant has no edema, there are not separate phases in the
treatment of infants with the SS technique. There is no need to
start with F75 and then switch to F100 diluted unless the infant
has oedema.
 If the infant presents with oedema, start treatment with F75
instead of F100 diluted. After resolution of oedema, change to
F100 diluted.
Supplementary suckling technique: The mother holds a cup with the F100
diluted. The end of a NG tube (size nº8) is put in the cup, and the tip of the
tube on the breast, at the nipple. The infant is offered the breast in the
normal way. The cup is placed 5 – 10 cm below the
level of the nipple for easy suckling. When the child suckles more strongly it
can be lowered to up to 30 cm.

Figure 7.5 Suplementary suckling technique

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Table 7.9.6 Amounts of F100 diluted (or infant formula) to give for
infants during Supplementary Suckling (The quantity is NOT increased
as the infant starts to gain weight)

Follow up: The child is weighed every day. When the child is gaining we
Follow-uo: The child is weighed every day. When the child is gaining weight
at 20 g/day (absolute weigh gain) the quantity of F100 diluted in the cup is
reduced so that the child gets more breast milk. If after this, weight gain is
maintained then stop the supplement suckling completely. When it is
certain that the child is gaining weight on breast milk alone he/she should
be discharged, whatever his weight or weight-for-length. If the child is not
gaining weight then continue with the SS technique, but increase the
quantity of F100 diluted in the cup to 5 mls for each feed.
Care for the mothers: Check nutritional status of the mother (MUAC and
oedema). Explain the treatment and discourage self-criticism for the lack of
milk. She should drink at least 2 litres of water per day, and eat about 2500
kcal/day. She should also receive Vitamin A (200 000 IU unless there is a
risk of pregnancy). Micronutrient supplementation must also be given to
the mother.

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II. Infants below six months who can not be breast-fed
Malnourished infants for whom there is no prospect of being breast-fed
(e.g. no mother, no wet-nurse, or other medical indications) should be fed
as follows:
Standard protocols are followed except that F100 is given diluted in the
phase 1 (stabilization phase) (instead of F75) for children without edema
(See table 7.9.6 to determine the amount).
Children with oedema are fed with F75. In transition and phase 2 use
diluted F100 (RUTF is not suitable for these children) at inpatient facility.
 During Transition Phase, the amount of the diluted F100 in
phase 1 is increased by one third.
 During phase 2, give diluted F 100 using table 7.9.7.
Table 7.9.7Amounts of F100 diluted to give for infants not breast-fed in Phase 1

Table 7.9.8 Amounts of F100 diluted to give for infants not breast-fed in Phase 2

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7.9 Failure to respond
It is only when children fulfill the criteria for “failure to respond” as stated
in 7.9.9 and 7.9.10 (below) that they need to have an extensive history and
examination or laboratory investigations conducted. Failure to respond to
standard treatment is a “diagnosis” in its own right. Usual causes and
general management of failure to respond is also summarized in table
7.9.11 below. The common causes should be systematically examined to
determine and rectify the problems.

Table 7.9.9 Criteria of failure to respond for inpatients

Criteria for failure to respond Time after admission
Primary failure to respond (phase 1)
Failure to regain appetite Day 4
Failure to start to loose Edema Day 4
Oedema still present Day 10
Failure to enter phase 2 and gain > 5g/kg/d Day 10
Secondary failure to respond
Failure to gain more than 5g/kg/d for 3 successive days During Phase 2

Table 7.9.10 Criteria of failure to respond for outpatients

Criteria for failure to respond Time after admission
Primary failure to respond
Failure to gain any weight (non-oedematous 21 days
children)
Failure to start to loose Edema 14 days
Oedema still present 21 days
Secondary failure to respond
Failure of Appetite test At any visit
Weight loss of 5% of body weight At any visit
Weight loss for two successive visits During OTP care
Failure to gain more than 2.5g/kg/d for 21days During OTP care
(after loss of oedema (kwashiorkor) or after day
14 (marasmus)

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Table 7.9.11 Possible causes of failure to respond

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7.10 Discharge Criteria
Children should be discharged from therapeutic feeding Program (TFP) or
in-patient care if they fulfill the following criteria:

Age Discharge Criteria

6 months – 5 years • Weight-for-length or height ≥ 85%
and no oedema for 10 days (In-
patient) or
• Target weight gain if the child is
admitted with MUAC

Note: Transfer from in-patient care to OTP is not considered as an early

discharge

Age Discharge Criteria

<6 monthson Infant gaining weight on breast milk alone
breastfeeding or No medical problem
with a caretaker Mother is adequately supplemented with
willing to breast vitamins and minerals
feed There are no anthropometric criteria for
discharge of the fully breast-fed infant who is
gaining weight.

Age Discharge Criteria

<6 months who When they reach 85% weight for length, they
cannot be breast-fed can be switched to infant formula.

If early discharge is necessary, many preparations must be made to ensure

that the parents can continue care at home. Follow-up visits are essential.

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7.11 Monitoring the quality of care
7.11.1 Mortality audit
A register of admissions, discharges and deaths should be kept. This should
contain information about the children (such as weight, age and sex), day
of admission, date of discharge or date and time of death.
To identify factors that can be changed to improve care, determine
whether most of the deaths occurred:
 Within 24 h: consider untreated or delayed treatment of
hypoglycaemia, hypothermia, septicaemia or severe anaemia,
incorrect rehydration fluid or volume of fluid or overuse of IV
fluids.
 Within 72 h: check whether the volume of feed given during re-
feeding was too high or the formulation was wrong. Were
potassium and antibiotics given?
 Over 72 h: consider nosocomial infection, re-feeding syndrome,
heart failure and HIV infection.

 At night: consider hypothermia due to insufficient covering of

the child or no night feeds.
 When beginning F-100 or RUTF: consider too rapid a transition
from starter to catch-up feeds.

7.11.2 Weight gain during rehabilitation

Standardize weighing on the hospital ward. Calibrate the scales every

day.
Weigh children at the same time each day (e.g. morning) after
removing clothes (but avoid hypothermia).
Weight gain is defined as:

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  Poor: < 5 g/kg per day
 Moderate: 5–10 g/kg per day
 Good: > 10 g/kg per day.

If the weight gain is < 5 g/kg per day, determine whether this occurred:
 In all children being treated (if so, a major review of case
management is required)
 Inspecific cases (reassess these children as if they were new
admissions).

General aspects to be checked if weight gain is poor are described below.

Inadequate feeding
Check:
 That night feeds are given
 That target energy and protein intakes are achieved. Is the
actual intake (i.e. what was offered minus what was left over)
correctly recorded? Is the quantity of feed recalculated as the
child gains weight? Is the child vomiting or ruminating?
 Feeding technique: Is the child given frequent feeds in unlimited
amounts?
 Quality of care: Are staff motivated, gentle, loving and patient?
 All aspects of feed preparation: scales, measurement of
ingredients, mixing, taste, hygienic storage, adequate stirring if
separating out
 Whether the complementary foods given to the child are
energy-dense enough
 Adequacy of multivitamin composition and shelf-life
 Preparation of mineral mix and whether correctly prescribed
and administered.

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If you are in a goitrous region, check whether potassium iodide is added to
the electrolyte/mineral mix (12 mg/2500 ml), or give all children Lugol
iodine (5–10 drops a day). if complementary foods are given, check that
they contain electrolyte/mineral solution.
Untreated infection
If feeding is adequate and there is no malabsorption, suspect a hidden
infection if there is recurrence of oedema, hypoglycaemia or hypothermia.
The following are easily overlooked: urinary tract infections, otitis media,
TB and giardiasis. In such cases:
 Re-examine carefully
 Repeat urine microscopy for white blood cells
 Examine the stools
 If possible, take a chest X-ray.
Consider treatment in the absence of a confirmatory diagnosis.

HIV/AIDS
Children with HIV and AIDS can recover from malnutrition, but it may take
longer, and treatment failures are commoner. Initial nutritional treatment
of severe acute malnutrition in children with HIV/AIDS should be the same
as for HIV-negative children.

For other HIV-related conditions, see Chapter 8.

Psychosocial stimulation
Check for abnormal behaviour, such as stereotyped movements (rocking),
rumination (i.e. self-stimulation through regurgitation) and attention-
seeking.
Treat by giving the child special love and attention. For children who
ruminate, firmness with affection can assist. Encourage the mother to

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spend time playing with her child.

Provide:
 Tender loving care
 Always uncover the child’s face to help able to see and hear
what is happening around the child wrapped or tied except for
the purpose of protecting from hypothermia.
 A cheerful stimulating environment
 Structured play therapy for 15–30 minutes a day
 Physical activity as soon as the child is well enough
 Maternal involvement as much as possible (e.g. comforting,
feeding, bathing, play).
 Provide suitable toys for the child (see chapter 10 sec 10.8).
Ideas for the organization of play activities are also given.

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CHAPTER 8 - CHILDREN WITH HIV/AIDS
8.1 HIV/AIDS
In general, the management of specific conditions in HIV-infected children
is similar to that in other children. Most infections in HIV positive children
are caused by the same pathogens as in HIV-negative children, although
they may be more frequent, more severe and occur repeatedly. Some,
infections, however, are due to unusual pathogens.

Many HIV-positive children die from common childhood illnesses, and

some of these deaths are preventable by early diagnosis and correct
management or by giving routine scheduled vaccinations and improving
nutrition. These children have a particularly greater risk for staphylococcal
and pneumococcal infections and TB. Saving children’s lives depends on
early identification, immediate treatment with ART and co-trimoxazole
prophylaxis for those who are HIV-infected.

All infants and children should have their HIV status established at their
first contact with the health system, ideally at birth or at the earliest
opportunity thereafter. To facilitate this, all areas of the hospital in which
maternal, neonatal and child services are delivered should offer HIV
serological testing to mothers and their infants and children.

This chapter covers mainly the management of children with HIV/AIDS:

diagnosis of HIV infection, counselling and testing, clinical staging, ART,
management of HIV-related conditions, supportive care, breastfeeding,
planning discharge and follow-up and palliative care for terminally ill
children.

8.2 Sick child with suspected or confirmed HIV infection

8.2.1 Clinical diagnosis
The clinical expression of HIV infection in children is highly variable. Many
HIV-positive children show severe HIV-related signs and symptoms in the
first year of life, while others may remain asymptomatic or mildly
symptomatic for more than a year and may survive for several years.

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Clinical experience indicates that children infected with HIV perinatally who
are not on antiretroviral therapy fit into one of three categories:
 Those with rapid progression (25–30%), most of whom die before
their first birthday; they are thought to have acquired the
infection in utero or during the early postnatal period;
 Children, who develop symptoms early in life, then follow a
downhill course and die at the age of 3–5 years (50–60%);
 Long-term survivors, who live beyond 8 years of age (5–25%); they
tend to have lymphoid interstitial pneumonitis and stunting, with
low weight and height for age.
Suspect HIV if any of the following signs, which are not common in HIV-
negative children, are present:

Signs that may indicate possible HIV infection

 Recurrent infection: three or more severe episodes of a bacterial
infection (such as pneumonia, meningitis, sepsis, cellulitis) in the
past 12 months
 Oral thrush: erythema and white-beige pseudomembranous
plaques on the palate, gums and buccal mucosa. After the
neonatal period, the presence of oral thrush is highly suggestive of
HIV infection when it lasts > 30 days despite antibiotic treatment,
recurs, extends beyond the tongue or presents as oesophageal
candidiasis.
 Chronic parotitis: unilateral or bilateral parotid swelling (just in
front of the ear) for ≥ 14 days, with or without associated pain or
fever.

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  Generalized lymphadenopathy: enlarged lymph nodes in two or
more extrainguinal regions with no apparent underlying cause.
Hepatomegaly with no apparent cause: in the absence of concurrent viral
infections such as cytomegalovirus.

Persistent and/or recurrent fever: fever (> 38 °C) lasting ≥ 7 days or

occurring more than once over 7 days.

 Neurological dysfunction: progressive neurological impairment,

microcephaly, delay in achieving developmental milestones,
hypertonia or mental confusion.
 Herpes zoster (shingles): painful rash with blisters confined to one
dermatome on one side
 HIV dermatitis: erythematous papular rash. Typical skin rashes
include; extensive fungal infections of the skin, nails and scalp and
extensive molluscum contagiosum.
 Chronic suppurative lung disease
Signs or conditions specific to HIV-infected children

Strongly suspect HIV infection if the following are present:

 Pneumocystis jiroveci (formerly carinii) pneumonia (PCP)

 Oesophageal candidiasis
 Lymphocytic interstitial pneumonia
 Kaposi sarcoma
 Acquired recto-vaginal fistula (in girls)
Signs common in HIV-infected children but which also occur in ill children
with no HIV infection
 Chronic otitis media: ear discharge lasting ≥ 14 days
 Persistent diarrhoea: diarrhoea lasting ≥ 14 days

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  Moderate or severe acute malnutrition: weight loss or a gradual
but steady deterioration in weight gain from that expected, as
indicated on the child’s growth chart. Suspect HIV particularly in
breastfed infants < 6 months old who fail to thrive.
8.2.2 HIV Counseling
HIV provider-initiated testing and counseling should be offered to all
under-five children attending clinical services. If the child’s HIV status is not
known, counsel the family and offer diagnostic testing for HIV.

As the majority of children are infected by vertical transmission from the

mother, the mother and often the father are probably infected but may not
know it. HIV still remains a stigmatizing condition, and the parents may
feel reluctant to undergo testing.

In HIV counseling, the child should be treated as part of the family by

taking into account the psychological implications of HIV for the child,
mother, father and other family members. Counselors should stress that,
although there is no definitive cure, early initiation of ART and supportive
care can greatly improve the child’s and the parents’ quality of life and
survival.
Counseling requires time and must be done by trained staff. If there are no
trained staff, assistance should be sought from local AIDS support
organizations.
HIV testing should be voluntary, with no coercion, and informed consent
should be obtained before testing is performed.
Indications for HIV counseling and testing
All infants and children with unknown HIV status should be offered
counseling and testing. In most cases, the HIV status of the child is
established by asking about maternal HIV testing during pregnancy, labour

321
or postpartum and checking the child’s or mother’s health card. If the HIV
status is not known, counselling and testing should be offered in the
following situations to:

 All under-five children visiting health facilities

 All HIV-exposed infants at 6 weeks of age or at the earliest
opportunity thereafter.
 Any infant or child presenting with signs, symptoms or medical
conditions that could indicate HIV infection.
 All pregnant women and their partners

8.2.3 Testing and diagnosis of HIV infection

Diagnosis of HIV infection in perinatally exposed infants and young children

< 18 months of age is difficult, because passively acquired maternal HIV
antibodies may still be present in the child’s blood. Additional diagnostic
challenges arise if the child is still breastfeeding or has been breastfed.
Although many children will have lost HIV antibodies between 9 and 18
months, a virological test is the only reliable method for determining the
HIV status of a child < 18 months of age.
When either the mother or the child has a positive serological HIV test and
the child has specific symptoms suggestive of HIV infection but virological
testing is not available, the child may presumptively be diagnosed as having
HIV infection. However, HIV virological testing should be done at the
earliest opportunity to confirm infection.
All diagnostic HIV testing of children must be confidential, be accompanied
by counseling and conducted only with informed consent, so that it is both
informed and voluntary.

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HIV serological antibody test (ELISA or rapid tests)
Rapid tests are widely available, sensitive and reliable for diagnosing HIV
infection in children 18 months and above. For children < 18 months, HIV
antibody tests are a sensitive, reliable way of detecting exposure and of
excluding HIV infection in non-breastfeeding children.
Rapid HIV tests can be used to exclude HIV infection in a child presenting
with severe acute malnutrition, or TB or any other serious clinical event in
areas of high HIV prevalence. For children aged < 18 months, confirm all
positive HIV serological results by virological testing as soon as possible
(see below). When this is not possible, repeat antibody testing at 18
months.

Virological tests
Virological testing for HIV-specific RNA or DNA is the most reliable method
for diagnosing HIV infection in children < 18 months of age. This may
require sending a blood sample to a specialized laboratory that can
perform this test. The tests are relatively cheap, easy to standardize and
can be done on dried blood spots. The following assays (and respective
specimen types) may be available:

 HIV DNA on whole blood specimen or dried blood spots

 HIV RNA on plasma or dried blood spots
 Ultrasensitive p24 antigen detection in plasma or dried blood
spots
 One positive virological test is sufficient to diagnose HIV infection
in a young infant. ART should be started without delay, and, at the
same time, a second specimen should be collected to confirm the
positive virological test result.

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  If the infant is still breastfeeding and the virological test is
negative, it should be repeated 6 weeks after complete cessation
of breastfeeding to confirm that the child is not infected with HIV.
 The results of virological testing in infants should be returned to
the clinic and to the child, mother or carer as soon as possible but
at the very latest within 4 weeks of specimen collection.
8.2.4 Diagnosing HIV infection in breastfeeding infants
A breastfeeding infant is at risk of acquiring HIV infection from an infected
mother throughout the period of breastfeeding. Breastfeeding should not
be stopped in order to perform diagnostic HIV viral testing. Positive test
results should be considered to reflect HIV infection. The interpretation of
negative results is, however, difficult because a 6-week period after
complete cessation of breastfeeding is required before negative viral test
results can reliably indicate HIV infection status.

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Algorithm for testing of HIV Exposed Infants <18 months

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Clinical staging

In a child with diagnosed or highly suspected HIV infection, the clinical

staging system helps to determine the degree of damage to the immune
system and to plan treatment and care.

The clinical stages represent a progressive sequence from least to most

severe, each higher clinical stage indicating a poorer prognosis. Initiating
ART, with good adherence, dramatically improves the prognosis. Clinical
staging events can be used to identify the response to ART if there is no
easy access to tests for viral load or CD4 count.

CLINICAL STAGING
WHO paediatric clinical staging system for HIV infection

For use in children aged <14 years with confirmed laboratory evidence of
HIV infection (HIV antibodies for children > 18 months, virological testing
for those aged < 18 months)

STAGE 1
o Asymptomatic
o Persistent generalized lymphadenopathy
STAGE 2
o Hepatosplenomegaly
o Papular pruritic eruptions
o Seborrhoeic dermatitis
o Fungal nail infections
o Angular cheilitis
o Linear gingival erythema
o Extensive human papillomavirus infection or molluscum infection
(> 5% body area)
o Recurrent oral ulcerations (two or more episodes in 6 months)

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 o Parotid enlargement
o Herpes zoster
o Recurrent or chronic upper respiratory tract infection (otitis
media, otorrhoea, sinusitis; two or more episodes in any 6-month
period)
STAGE 3
o Unexplained moderate malnutrition that does not respond to
standard therapy
o Unexplained persistent diarrhoea (> 14 days)
o Unexplained persistent fever (intermittent or constant, for > 1
month)
o Oral candidiasis (outside neonatal period)
o Oral hairy leukoplakia
a
o Pulmonary TB
o Severe recurrent presumed bacterial pneumonia (two or more
episodes in 6 months)
o Acute necrotizing ulcerative gingivitis or periodontitis
o Lymphoid interstitial pneumonia
o Unexplained anaemia (< 8 g/dl), neutropenia (< 500/mm3) or
thrombocytopenia (< 30 000/mm3) for > 1 month
o HIV-related cardiomyopathy
o HIV-related nephropathy
STAGE 4

o Unexplained severe wasting or severe malnutrition that does not

respond to standard therapy
o PCP
o Recurrent severe presumed bacterial infections (two or more
episodes within 1 year, e.g. empyema, pyomyositis, bone or joint
infection, meningitis, but excluding pneumonia)

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 o Chronic orolabial or cutaneous herpes simplex infection (lasting >
1 month)
o Disseminated or extrapulmonary TB
o Kaposi sarcoma
o Oesophageal candidiasis
o Symptomatic HIV seropositive infant < 18 months with two or
more of the following: oral thrush, severe pneumonia, failure to
b
thrive, severe sepsis
o Cytomegalovirus retinitis
o Central nervous system toxoplasmosis
o Any disseminated endemic mycosis, including cryptococcal
meningitis (e.g. extrapulmonary cryptococcosis, histoplasmosis,
coccidiomycosis, penicilliosis)
o Cryptosporidiosis or isosporiasis (with diarrhoea lasting > 1 month)
o Cytomegalovirus infection (onset at age > 1 month in an organ
other than liver, spleen or lymph nodes)
o Disseminated mycobacterial disease other than TB
o Candida of trachea, bronchi or lungs
o Acquired HIV-related rectovesical fistula
o Cerebral or B cell non-Hodgkin lymphoma
o Progressive multifocal leukoencephalopathy
o HIV encephalopathy
A. TB may occur at any CD4 count; the percentage CD4 should be considered
when available.

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B. Presumptive diagnosis of stage 4 disease in seropositive children < 18
months requires confi rmation with HIV virological tests or an HIV
antibody test after 18 months of age.

8.3 Antiretroviral therapy

The current standard first-line treatment for HIV infection is use of three
antiretroviral medications (triple drug therapy) to suppress viral replication
as much as possible and thus arrest the progression of HIV disease. Fixed-
dose combinations are now available and are preferable to syrups or single
drugs because they encourage adherence to treatment, and reduce the
cost. Clinicians should be familiar with the national paediatric HIV
treatment guidelines.

The underlying principles of ART and the choice of first-line drugs for
children are largely the same as for adults. Suitable formulations for
children may not be available for some antiretroviral drugs (particularly the
protease inhibitor class). It is nevertheless important to consider:
 The availability of a suitable formulation that can be taken in
appropriate doses
 The simplicity of the dosage schedule
 The taste and palatability, and hence compliance, for young
children.
 It is also important to ensure that HIV-infected parents access
treatment; and ART should ideally be ensured for other family
members.
8.3.1 Antiretroviral drugs
Antiretroviral drugs fall into three main classes:
 Nucleoside reverse transcriptase inhibitors (NRTIs),
 Non-nucleoside reverse transcriptase inhibitors (NNRTIs), and
 Protease inhibitors

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Triple therapy is the standard of care, and first-line regimens should be
based on two NRTIs plus one NNRTI or protease inhibitor.
All infants and children < 3 years of age should be started on
Lopinavir/Ritonavir (LPV/r) plus two NRTIs, regardless of exposure to
nevirapine (NVP) to prevent mother-to-child transmission. When viral load
monitoring is available, consideration can be given to substituting LPV/r
with an NNRTI after virological suppression is sustained.
For children ≥ 3 years, efavirenz (EFV) is the preferred NNRTI for first-line
treatment particularly once daily therapy, although NVP may be used as an
alternative especially for children who are on twice daily therapy. Efavirenz
is also the NNRTI of choice in children who are on rifampicin, if treatment
has to start before anti-TB therapy is completed.

Age Preferred first line Alternative first line regimen

regimen
< 3 yrs ABC or ABC+3TC+NVP
AZT+3TC+LPV/r AZT+3TC+NVP
3-10 yrs AZT/ABC+3TC+EFV ABC+3TC+NVP
AZT+3TC+NVP
TDF+3TC+EFV
TDF+3TC+NVP
10-19 yrs TDF+3TC+EFV (FDC) ABC+3TC+EFV
AZT+3TC+NVP
TDF+3TC+NVP
Table 8.1 First-line treatment regimens for children

Dosing in children is usually based on either body surface area or weight,

or, more conveniently, on weight bands. As these change with growth,
drug doses must be adjusted in order to avoid the risk for under-dosage.

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ANTIRETROVIRAL DRUGS
Table 8.2 Classes of antiretroviral drugs recommended for use in children

Nucleoside analogue reverse transcriptase inhibitors

Zidovudine ZDV (AZT)

Lamivudine 3TC

Abacavir ABC
Emtricitabine FTC
Tenofovir TDF
Non-nucleoside analogue reverse transcriptase inhibitors
Nevirapine NVP
Efavirenz EFV
Protease inhibitors
Lopinavir/ritonavir LPV/RTV
Atazanavir ATZ
8.3.2 When to start antiretroviral therapy

Infants and young children have an exceptionally high risk of poor

outcomes from HIV infection. Up to 52% and 75% of children die before the
age of two and five years respectively in the absence of any intervention.
By five years of age, the risk of mortality and disease progression in the
absence of treatment falls to rates similar to those of young adults.

Diagnosing and retaining children exposed to HIV and children infected

with HIV in care also presents unique challenges because of their
dependence on a caregiver.

Loss to follow-up has been particularly high along the continuum of care,
with retention especially challenging for children who are in HIV care but
not yet eligible for ART.Where access to immunological testing is limited,
the burden of pediatric HIV disease is high and pediatric ART coverage is

331
low, simplifying the eligibility criteria for initiating ART may significantly
improve the overall health outcomes for children with HIV.

ART is recommended for all HIV infected children less than 15 years
regardless of CD4 count and WHO clinical stage. Treating all children
younger than fifteen years of age is expected to simplify pediatric
treatment and facilitate a significant expansion of ART coverage for young
children. Note that late diagnosis is still occurring, and a large proportion of
the children identified as infected with HIV would already be eligible for
ART based on previous recommendations.

Children < 15 years All children with HIV infection regardless of

CD4 count and WHO clinical stage

8.3.3 What ART regimen to start with (first-line ART)

Using simplified, less toxic and more convenient regimens as fixed-dose
combinations is recommended for first-line ART. Once-daily regimens
comprising NRTI backbone (TDF + 3TC) and one NNRTI (EFV) are
maintained as the preferred choices in adults, adolescents and children
older than ten years. For children younger than three years a PI-based
regimen is the preferred approach.
Occasionally immediate initiation of ART treatment may be deferred until
the child is stabilized during treatment of acute infections.
In the case of confirmed or presumptive TB, initiating TB treatment is the
priority.
Any child with active TB should begin TB treatment immediately and start
ART as soon as it can be tolerated but within the first 8 weeks of TB
therapy.
For children on TB treatment:
 Children> 3 years and at least 10 kg, a regimen containing EFV is
preferred.

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  Children< 3 years of age, if the child is on a LPV/r-containing
regimen, consider adding RTV in a 1:1 ration of LPV: RTV to
achieve a full therapeutic dose of LPV.
 A triple NNRTI-containing regimen may be used as an alternative.
8.3.4 Side-effects and monitoring

a
Drug Abbreviation Side-effects Comments
Nucleoside reverse transcriptase inhibitors (NRTIs)

Lamivudine 3TC Headache, abdominal pain, Well tolerated

pancreatitis

Zidovudine ZDV (AZT) Headache, anaemia,

neutropenia
Abacavir ABC Hypersensitivity reaction, Tablets can be
fever mucositis rash If these crushed
occur, stop the drug.
Emtricitabine FTC Headache, diarrhoea, nausea,
and rash. May cause
hepatotoxicity or lactic
acidosis.
Tenofovir TDF Renal insufficiency,
decrease in bone
mineral density
Non-nucleoside reverse transcriptase inhibitors (NNRTIs)
Efavirenz EFV Strange dreams, Take at night; avoid
sleepiness, rash taking with fatty
food

Nevirapine NVP Rash, liver toxicity When given with

rifampicin, increase
nevirapine dose by
~30% or avoid use.
Drug interactions

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Protease inhibitors

Lopinavir/ LPV/RTV Diarrhoea, nausea Take

with food; bitter taste
b
ritonavir

Atazanavir ATZ Jaundice, prolonged

PR interval,

nephrolithiasis

Common side-effects of antiretroviral drugs (Table 8.3)

a. General long-term side-effects of ART include lipodystrophy.

b. Requires cold storage and cold chain for transport
The response to and side-effects of ART should be monitored in all children
on ART. A child’s responses to therapy (i.e. reassessment of clinical status
and stage, laboratory parameters and, symptoms of potential drug side
effects or toxicity) should be done regularly. Common side effects are
summarized in the table above.

Immune reconstitution inflammatory syndrome

Immune reconstitution inflammatory syndrome (IRIS) is a spectrum of
clinical signs and symptoms associated with immune recovery brought
about by a response to antiretroviral treatment. Although most HIV-
infected children experience rapid benefi t from ART, some undergo clinical
deterioration. This is the result of either the unmasking of latent or
subclinical infection or the reactivation of previously diagnosed, and often
treated, conditions (infectious or non-infectious).

The onset of IRIS in children usually occurs within the fi rst weeks to
months after initiation of ART and is seen most often in children who

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initiate ART with very low percentge CD4+ levels (< 15%). The commonest
opportunistic infections associated with IRIS in children include:

 TB the commonest;
 Pneumocystis pneumonia (PCP) or cryptosporidiosis;
 Herpes simplex virus (HSV) infection;
 Fungal, parasitic or other infections.

Where BCG immunization of infants and children is routine, BCG-associated

IRIS (localized and systemic) is frequently observed.
Most cases of paradoxical IRIS resolve spontaneously, or can be managed
with non-steroidal anti-infl ammatory drugs, although some episodes can
be severe and even lead to death.
Give specifi c treatment for the opportunistic infection
Start on anti-infl ammatory therapy.
Occasionally, IRIS becomes progressively worse and may require a short
course of treatment with corticosteroids and, rarely, temporary
discontinuation of ART. The same ART regimen should be restarted once
IRIS has improved.
8.3.5 Monitoring the response to ART and the diagnosis of Treatment
Failure

In addition to checking for ART side effects, a clinical assessment should be

made of the child’s or caregiver’s adherence to therapy and the need for
additional support. The frequency of clinical monitoring depends on the
response to ART. At a minimum, after the start of ART, follow-up visits
should be made:
For infants < 12 months, at weeks 2, 4 and 8 and then every 4 weeks for
the first year
 For children > 12 months, at weeks 2, 4, 8 and 12 and then every
2–3 months once the child has stabilized on ART
 Any time there is a problem of concern to the caregiver or
intercurrent illness.

335
Important signs of infants’ and children’s responses to ART include:
 Improvement in the growth in children who have been failing to
grow
 Improvement in neurological symptoms and development of
children with encephalopathy or who had delayed achievement of
developmental milestones
 decreased frequency of infections (bacterial infections, oral thrush
and other opportunistic infections)
Long-term follow-up

 A clinician should see the child at least every 3 months.

 A non-clinician (ideally, the provider of ART, such as a pharmacist)
should assess adherence and provide adherence counselling.
Children who are clinically unstable should be seen more frequently,
preferably by a clinician.
The organization of follow-up care depends on local expertise, and should
be decentralized as much as possible.
Monitoring response at each visit
 Weight and height
 Neurodevelopment
 Adherence to treatment
 CD4 (%) count, if available (every 6 months)
 Baseline Hb or Hct (if on ZDV/AZT) and alanine aminotransferase
activity, if available
Symptom-directed laboratory testing: Hb, Hct or full blood count, alanine
aminotransferase activity

336
When to change treatment
When to substitute
If toxic effects can be associated with an identifi able drug in a regimen, it
can be replaced by another drug in the same class that does not have the
same adverse effect. As few antiretroviral drugs are available, drug
substitutions should be limited to:
 Severe or life-threatening toxicity, such as:
 Stevens Johnson syndrome
 Severe liver toxicity
 Severe haematological effects
 Drug interaction (e.g. TB treatment with rifampicin interfering
with nevirapine or protease inhibitor).
 Potential lack of adherence by the patient if he or she cannot
tolerate the regimen.
When to switch
Monitoring individuals receiving ART is important to ensure successful
treatment, identify adherence problems and determine whether and which
ART regimens should be switched in case of treatment failure.

ART failure may be due to:

 Poor adherence
 Inadequate drug level
 Prior or treatment experienced drug resistance
 Inadequate potency of the drug
 A reasonable trial of the therapy is required before ART is
determined to be failing on clinical criteria alone:
 The child should have received the regimen for at least 24 weeks.

337
  Adherence to therapy should be considered optimal.
 Any opportunistic infections have been treated and resolved.
 IRIS has been excluded.
 The child is receiving adequate nutrition.
 Definitions of clinical, Immunological and Virological Failure
 Clinical failure (clinical criteria): appearance or reappearance of
WHO clinical stage 3 or 4 events (with the exception of TB) after at
least 24 weeks on ART, with adherence to treatment
 Immunological failure (CD4 criteria): count of < 200 cells/mm3 or
CD4 < 10% for a child aged < 5 years and in a child aged > 5 years
persistent CD4 levels < 100 cells/mm3
Virological failure (viral load criteria): persistent viral load > 1000 RNA
copies/ml after at least 24 weeks on ART, and based on two consecutive
measurements within 3 months, with adherence to treatment.
When treatment failure is confirmed, switching to a second-line regimen
becomes necessary.
Second-line treatment regimens
In the event of treatment failure, the entire regimen should be changed
from a fi rst-line to a second-line combination. The second-line regimen
should include at least three new drugs, one or more of them in a new
class. Recommending potent, effective second-line regimens for infants
and children is particularly difficult because of the lack of experience in use
of second-line regimens in children and the limited number of formulations
appropriate for children.

After failure of a first-line NNRTI-based regimen, a regimen with boosted

protease inhibitor plus two NRTIs is recommended for second-line ART.
LPV/RTV is the preferred boosted protease inhibitor for a second-line ART

338
regimen after failure of a fi rst-line NNRTI-based regimen. Recommended
second-line treatment is indicated in Table 8.4 below.

Table 8.4: Recommended second-line regimen for children

8.4 Supportive care for HIV-positive children

8.4.1 Vaccination
HIV-exposed infants and children should receive all vaccines in the
Expanded Programme for Immunization, including H. infl uenzae type B
and pneumococcal vaccine, according to the national schedule. The only
exception is that infants with symptomatic HIV should not receive BCG.
8.4.2 Co-trimoxazole prophylaxis
Co-trimoxazole prevents PCP in infants and reduces morbidity and
mortality among infants and children living with, or exposed, to HIV. Co-
trimoxazole also protects against common bacterial infections,
toxoplasmosis and malaria.
Who should receive co-trimoxazole?

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 All infants born to HIV-infected mothers should receive co-trimoxazole 4–6
weeks after birth or at their fi rst encounter with the health care system.
They should continue until HIV infection has been excluded and they are no
longer at risk of acquiring HIV from breast milk.
All infected children should be continued on co-trimoxazole even when on
ART.
How long co-trimoxazole should be given?
Adherence should be discussed at initiation and monitored at each visit.
Cotrimoxazole must be taken as follows:
 HIV-exposed children: for the fi rst year or until HIV infection has
been defi nitively ruled out and the mother is no longer
breastfeeding
 When on ART: Co-trimoxazole may be stopped once clinical or
immunological indicators confi rm restoration of the immune
system for ≥ 6 months. It is not known whether co-trimoxazole
continues to provide protection after the immune system is
restored.
 Children with a history of PCP: Continue indefinitely.
 Under what circumstances co-trimoxazole should be
discontinued?
 If the child develops severe cutaneous reactions such as Stevens
Johnson syndrome, renal or hepatic insuffi ciency or severe
haematological toxicity.
After HIV infection has confi dently been excluded in an HIV-exposed child:
 In a non-breastfed child aged < 18 months by a negative
virological test

340
  In a breastfed child aged < 18 months by a negative virological test
conducted 6 weeks after cessation of breastfeeding.
 In a breastfed child aged > 18 months by a negative HIV serological
test 6 weeks after cessation of breastfeeding
In HIV-infected children, co-trimoxazole should be continued until they are
5 years of age and on ART with a sustained CD4 percentage > 25%.

Co-trimoxazole should not be discontinued if not on ART.

What doses of co-trimoxazole should be used?

Recommended dosages of 6–8 mg/kg trimethoprim once daily should be

used.

Table 8.5: Co-trimoxazole (CPT) dosing for children

Age (weight) Co-trimoxazole Co-trimoxazole Co-trimoxazole

(240 mg/5ml) single strength double strength
suspension tab (480 mg) tab (960 mg)

Up to 6 months 2.5 ml/day ½ tab/day -

(5 kg)

6 months to 5 yr 5 ml/day ½ tab/day -

(5-15 kg)

6-14 yr (15-30 kg) 10 ml/day 1 tab/day ½ tab/day

If the child is allergic to co-trimoxazole, dapsone is the best alternative can

be given from 4 weeks of age at 2 mg/kg per day orally once daily.

What follow-up is required?

341
Assessment of tolerance and adherence: Co-trimoxazole prophylaxis
should be a routine part of the care of HIV-infected children and be
assessed at all regular clinic or follow-up visits by health workers or other
members of multidisciplinary care teams. Clinical follow-up could initially
be monthly, then every 3 months, if co-trimoxazole is well tolerated.

8.4.3 Nutrition
The mothers of infants and young children known to be infected with HIV
are strongly encouraged to breastfeed them exclusively for 6 months and
to continue breastfeeding up to the age of 1 year. Older children should eat
varied, energy-rich food to increase their energy intake and to ensure
adequate micronutrient intake.

Children should be assessed routinely for nutritional status, including

weight and height, at scheduled visits. Their energy intake might have to be
increased by 25–30% if they lose weight or grow poorly.

HIV-infected children who have severe acute malnutrition should be

managed according to the guidelines for uninfected children and given 50–
100% additional energy-rich foods

8.5 Management of HIV-related conditions

The treatment of most infections (such as pneumonia, diarrhoea and
meningitis) in HIV-infected children is the same as in other children. In
cases of treatment failure, consider giving a second-line antibiotic.
Treatment of recurrent infections is the same, regardless of the number of
recurrences.

Some HIV-related conditions that require specific management are

described below.

8.5.1 Tuberculosis
In a child with suspected or proven HIV infection, a diagnosis of TB should
always be considered, although it is often diffi cult to confi rm. Early in HIV
infection, when immunity is not impaired, the signs of TB are similar to

342
those in a child without HIV infection. Pulmonary TB is still the commonest
form of TB, even in HIV-infected children. As HIV infection progresses and
immunity declines, dissemination of TB becomes more common, and
tuberculous meningitis, miliary TB and widespread tuberculous
lymphadenopathy occur.

HIV-infected infants and children with active TB should begin TB treatment

immediately. If they are not yet started on ART, this should be started as
soon as it is tolerated, within the fi rst 8 weeks of TB therapy, irrespective
of CD4 count and clinical stage.
In the case of confirmed or presumptive TB, initiating TB treatment is the
priority.
Any child with active TB should begin TB treatment immediately and start
ART as soon as it can be tolerated but within the first 8 weeks of TB
therapy.
For children on TB treatment:

 Children> 3 years and at least 10 kg, a regimen containing EFV is

preferred.
 Children< 3 years of age, if the child is on a LPV/r-containing
regimen, consider adding RTV in a 1:1 ratio of LPV:RTV to achieve
a full therapeutic dose of LPV.
 A triple NNRTI-containing regimen may be used as an alternative.
 Treat TB in HIV-infected children with the same anti-TB drug
regimen as for uninfected children with TB.
Isoniazid preventive therapy
All HIV-infected infants and children should be screened for TB infection, as
they are at special risk. If a child has cough, fever or weight loss, assess for
TB. If the child does not have TB, give isoniazid preventive therapy (IPT)
daily for 6 months.

Give isoniazid preventive therapy to:

343
  All HIV-infected infants and children exposed to TB from
household contacts, but with no evidence of active disease, are
well and thriving.
 children > 12 months living with HIV infection, including those
previously treated for TB, who are not likely to have active TB and
are not known to be exposed to TB
 Give 10 mg/kg isoniazid daily for at least 6 months. See the child
monthly and give a 1-month supply of isoniazid at each visit.
Note: Infants living with HIV infection who are unlikely to have active TB
and are not known to have been exposed to TB should not receive isoniazid
preventive therapy as part of HIV care.

8.4.2 Pneumocystis jiroveci pneumonia

PCP should be suspected in any HIV-positive infant with severe pneumonia.

If PCP is untreated, mortality from this condition is very high. It is therefore

imperative to provide treatment as early as possible.

Diagnosis

 Is most likely in a child < 12 months (peak age, 4–6 months),

 Subacute or acute onset of non-productive cough and diffi culty in
breathing,
 No or low-grade fever,
 Cyanosis or persistent hypoxia,
 Poor response to 48 h of fi rst-line antibiotics for pneumonia, and
 Elevated levels of lactate dehydrogenase.
Although clinical and radiological signs are not diagnostic, the presence of
severe respiratory distress (tachypnoea, chest indrawing and cyanosis),

344
with disproportionate clear chest or diffuse signs on auscultation and low
oxygen saturation are typical of PCP infection.
A chest X-ray is falsely negative in 10–20% of proven cases of PCP but
typically shows a bilateral diffuse interstitial reticulogranular (‘ground
glass’) pattern, with no hilar lymph nodes or effusion. PCP may also present
with pneumothorax.

Induced sputum and nasopharyngeal aspiration are useful for obtaining

sputum for examination.

Treatment
Promptly give oral or preferably IV high-dose co-trimoxazole (8 mg/kg
trimethoprim–40 mg/kg sulfamethoxazole) three times a day for 3 weeks.

If the child has a severe drug reaction, change to pentamidine (4 mg/kg

once a day) by IV infusion for 3 weeks. Prednisolone at 1–2 mg/kg per day
for 1 week may be helpful early in the disease if severe hypoxia or severe
respiratory distress is present.

Continue co-trimoxazole prophylaxis on recovery, and ensure that ART is

given

8.4.3 Lymphoid interstitial pneumonitis (LIP)

Diagnosis

LIP is one of the most common chronic lower respiratory conditions

occurring in up to 25% of children with HIV/AIDS.

The child is often asymptomatic in the early stages but may later have:
 Persistent cough, with or without diffi culty in breathing,

345
  Bilateral parotid swelling,
 Persistent generalized lymphadenopathy,
 Hepatomegaly and other signs of heart failure, and
 Finger-clubbing.
 Chest X-ray: Suspect lymphoid interstitial pneumonitis if the chest
X-ray shows a bilateral reticulonodular interstitial pattern, which
should be distinguished from pulmonary TB and bilateral hilar
adenopathy
Treatment

Give a trial of antibiotic treatment for bacterial pneumonia before starting

treatment with prednisolone.

Start treatment with steroids only if the chest X-ray shows lymphoid
interstitial pneumonitis, plus any of the following signs:

 Fast or difficult breathing

 Cyanosis
 Pulse oximetry reading of oxygen saturation ≤ 90%.
 Give oral prednisolone at 1–2 mg/kg per day for 2 weeks. Then
decrease the dose over 2–4 weeks, depending on the response to
treatment. Beware of reactivating TB.
 Start ART if not already on treatment.
8.4.4 Fungal infections
Oral and oesophageal candidiasis

 Treat oral thrush with nystatin (100 000 U/ml) suspension. Give 1–
2 ml into the mouth four times a day for 7 days. If this is not

346
 available, apply 1% gentian violet solution. If these are ineffective,
give 2% miconazole gel at 5 ml twice a day, if available.
 Suspect oesophageal candidiasis if the child has difficulty or pain
while vomiting or swallowing is reluctant to take food, is salivating
excessively or cries during feeding. The condition may occur with
or without evidence of oral thrush.
 If oral thrush is not found, give a trial of treatment with fl
uconazole. Exclude other causes of painful swallowing (such as
cytomegalovirus, herpes simplex, lymphoma and, rarely, Kaposi
sarcoma), if necessary by referral to a larger hospital where
appropriate testing is possible.
 Give oral fl uconazole (3–6 mg/kg once a day) for 7 days, except if
the child has active liver disease.
 Give amphotericin B (0.5 mg/kg once a day) by IV infusion for 10–
14 days to children who don’t respond to oral therapy or are
unable to tolerate oral medications or risk disseminated
candidiasis (e.g. a child with leukopenia).
Cryptococcal meningitis
 Suspect cryptococcus as a cause in any HIV-infected child with
signs of meningitis.
 The presentation is often subacute, with chronic headache or only
mental status changes. An India ink stain of CSF confi rms the
diagnosis.
 Treat with amphotericin at 0.5–1.5 mg/kg per day for 14 days,
then with fluconazole 6–12 mg/kg (maximum 800 mg) for 8
weeks.

347
  Start fluconazole 6 mg/kg daily (maximum 200 mg) prophylaxis
after treatment.

8.4.5 Kaposi sarcoma

Consider Kaposi sarcoma in children presenting with nodular skin lesions,

diffuse lymphadenopathy and lesions on the palate and conjunctiva with
periorbital bruising. Diagnosis is usually clinical but can be confi rmed by a
needle biopsy of skin lesions or lymph node. Suspect Kaposi sarcoma also
in children with fungal infections, persistent diarrhoea, weight loss,
intestinal obstruction, abdominal pain or large pleural effusion. Consider
referral to a larger hospital for management.

Figure 8.1 Lymphocytic interstitial Figure 8.2 Pneumocystis jiroveci

pneumonia: typical hilar pneumonia (PCP): typical ‘ground
lymphadenopathy and lace-like infiltrates glass’ Appearance

8.6 Prevention of mother-to-child HIV transmission, and infant feeding

8.6.1 Prevention of mother-to-child HIV transmission

 HIV may be transmitted during pregnancy, labour and delivery or

through breastfeeding. The best way to prevent transmission is to
prevent HIV infection in general, especially in pregnant women, and
to prevent unintended pregnancies in HIV-positive women. If an HIV-

348
 infected woman becomes pregnant, she should be provided with
ART, safe obstetric care and counselling and support for infant
feeding.

 HIV-infected pregnant women should be given ART both to benefit

their own health and to prevent HIV transmission to their infants
during pregnancy and breastfeeding.

 Starting lifelong ART for all pregnant women with HIV infection
regardless of symptoms is referred to as Option B+

 Option B+: A Triple ARV treatment regimen for the mother

beginning in pregnancy and continued for life, as well as infant
prophylaxis for 6 weeks after birth, whether or not the infant is
breastfeeding. Since 2013 Ethiopia has rolled out option B+ for
PMTCT using combination of TDF, 3TC and EFF, which is given daily
as a single pill. This strategy has greatly simplified PMTCT regimen
and will also improve adherence.

8.6.2 Infant feeding in the context of HIV infection

 In the absence of any interventions, 15–25% of HIV-positive mothers
will infect their infants during pregnancy or delivery; if they breastfeed,
there is an additional absolute risk of 5–20%. Although avoidance of
breastfeeding eliminates the risk for HIV transmission through breast
milk, replacement feeds have been associated with increased infant
morbidity and mortality.

 Exclusive breastfeeding during the first 6 months of life carries less risk
for HIV transmission than mixed feeding, and it provides considerable
protection against infectious diseases and other benefits.

ART greatly reduces the risk for HIV transmission, while simultaneously
ensuring that the mother receives appropriate care to improve her own
health. If an HIV-positive mother breastfeeds her infant while taking ART
and gives ART to her infant each day, the risk for transmission is reduced to

349
2% or 4% if she breastfeeds for 6 or 12 months, respectively. It is important
to:
 Support mothers known to be HIV-positive in achieving the
greatest likelihood that their child will be HIV-free and survive,
while taking into consideration their own health.
 Balance the prevention of HIV transmission against meeting the
nutritional requirements and protection of infants against non-HIV
morbidity and mortality.
 HIV-positive mothers should receive lifelong ART treatment to
improve their own health, and the infant should be put on ART
prophylaxis while breastfeeding.
Infant feeding advice
 Our national guideline recommends that HIV-positive mothers
should breastfeed their infants exclusively for the first 6 months of
life, introducing appropriate complementary foods thereafter, and
should continue breastfeeding for the first 12 months of life.
 When a decision has been taken to continue breastfeeding
because the child is already infected, ART treatment and infant
feeding options should be discussed for future pregnancies.
 Mothers will require continued counselling and support to feed
their infants optimally. Counselling should be done by a trained,
experienced counsellor.
 Local people experienced in counselling should be consulted, so
that the advice given is consistent. If the mother is using breast-
milk substitutes, counsel her about their correct use and
demonstrate safe preparation.

350
8.7 Follow-up
8.7.1 Discharge from hospital
HIV-infected children may respond slowly or incompletely to the usual
treatment. They may have persistent fever, persistent diarrhoea and
chronic cough. If the general condition of these children is good, they need
not remain in hospital but can be seen regularly as outpatients.

8.7.2 Referral
If the necessary facilities are not available, consider referring a child
suspected of having HIV infection:

 For HIV testing with pre- and post-test counseling

 To another centre or hospital for further investigations or second-
line treatment if there has been little or no response to treatment
 To a trained counsellor for HIV and infant feeding, if the local
health worker cannot do this
 To a community or home-based care programme, a community or
institutionbased voluntary counselling and testing centre or a
community-based social support programme for further
counselling and continuing psychosocial support.
 Orphans must be referred to essential services, including health
care education and birth registration.
8.7.3 Clinical follow-up
Children who are known to be HIV-infected should, when not ill, attend
well-infant clinics like other children. In addition, they need regular clinical
follow-up at fi rst-level facilities to monitor their:

 Clinical condition
 Growth
 Nutritional intake

351
  Vaccination status
They should also be given psychosocial support, if possible in community
programmes

8.8 Palliative and end-of-life care

An HIV-infected, immunologically compromised child often has
considerable discomfort, so good palliative care is essential. All decisions
should be taken with the parents or caretaker, and the decisions should be
clearly communicated to other staff (including night staff). Consider
palliative care at home as an alternative to hospital care. Some treatments
for pain control and relief of distressing conditions (such as oesophageal
candidiasis or convulsions) can significantly improve the quality of the
child’s remaining life.

Give end-of-life (terminal) care if:

 The child has progressively worsening illness
 Everything possible has been done to treat the presenting illness.
Ensuring that the family has appropriate support to cope with the
impending death of the child is an important part of care in the terminal
stages of HIV/AIDS. Parents should be supported in their efforts to give
palliative care at home so that the child is not kept in hospital
unnecessarily
8.8.1 Pain control
The management of pain in HIV-infected children follows the same
principles as for other chronic diseases, such as cancer and sickle-cell
disease. Particular attention should be paid to ensuring that the care is
culturally appropriate and sensitive. (see chapter 10)
8.8.2 Management of anorexia, nausea and vomiting
Loss of appetite during a terminal illness is diffi cult to treat. Encourage
carers to continue providing meals and to try:

352
Giving small feeds more frequently, particularly in the morning when the
child’s appetite may be better

Giving cool foods rather than hot foods

Avoiding salty or spicy foods

Giving oral metoclopramide (1–2 mg/kg) every 2–4 h, if the child has
distressing nausea and vomiting.

8.8.3 Prevention and treatment of pressure sores

Teach carers to turn the child at least once every 2 h. If pressure sores
develop, keep them clean and dry. Use local anaesthetics such as
tetracaine, adrenaline and cocaine to relieve pain.
8.8.4 Care of the mouth

Teach carers to wash out the mouth after every meal. If mouth ulcers
develop, clean the mouth at least four times a day with clean water or salt
solution and a clean cloth rolled into a wick. Apply 0.25% or 0.5% gentian
violet to any sores. If the child has a high fever or is irritable or in pain, give
paracetamol.

Crushed ice wrapped in gauze and given to the child to suck may give some
relief. If the child is bottle-fed, advise the carer to use a spoon and cup
instead.

If a bottle continues to be used, advise the carer to clean the teat with
water before each feed.

If oral thrush develops, apply miconazole gel to the affected areas at least
three times a day for 5 days, or give 1 ml nystatin suspension four times a
day for 7 days, pouring it slowly into the corner of the mouth so that it
reaches the affected parts.

353
If there is pus due to a secondary bacterial infection, apply tetracycline or
chloramphenicol ointment. If there is a foul smell in the mouth, give IM
benzylpenicillin (50 000 U/kg every 6 h), plus oral metronidazole
suspension (7.5 mg/kg every 8 h) for 7 days.

8.8.5 Airway management

Give priority to keeping the child comfortable rather than prolonging life.

8.8.6 Psychosocial support

Helping parents and siblings through their emotional reaction towards the
dying child is one of the most important aspects of care in the terminal
stage of HIV disease. How this is done depends on whether care is being
given at home, in hospital or in a hospice. At home, much of the support
can be given by close family members, relatives and friends.

Keep up to date on how to contact local community home care

programmes and HIV/AIDS counselling groups. Find out if the carers are
receiving support from these groups. If not, discuss the family’s attitude
towards these groups and the possibility of linking the family with them.

354
CHAPTER 9 - COMMON SURGICAL PROBLEMS

Infants and children develop distinct surgical diseases and have special
perioperative needs. This chapter provides guidelines for the supportive
care of children with surgical problems and briefly describes the
management of the most common surgical conditions.

9.1 Care before, during and after surgery

Good surgical care neither begins nor ends with the procedure. In most
instances it is the preparation for surgery, the anaesthetic and the
postoperative care that ensures a good outcome.

9.1.1 Preoperative Care

Both the child and the parents need to be prepared for the procedure and
need to consent.
 Explain why the procedure is needed, the anticipated outcome
and the potential risks and benefits.
 Ensure that the child is medically fit for an operation.
 Correct fluid deficits prior to emergency procedures. Restoration
of urine output implies adequate volume resuscitation. Collect and
measure the urine.
 Correct electrolyte deficits as appropriate.
 Correct anemia: Ideally, the child’s hematocrit should be checked
to see if it is normal for the age and population. Prepare blood for
major surgical procedures. Correct iron deficiency anemia in
elective surgical children with oral medications.
 Check that the child is in the best nutritional state possible. Good
nutrition is needed to heal wounds.

355
  Check that the child has an empty stomach prior to a general
anaesthesia. Infants under 12 months: the child should be given
no solids orally for 8 hrs, no formula for 6 hrs, no clear liquids for
4 hrs, or no breast milk for 4 hrs before the operation. If
prolonged periods of fasting are anticipated (>6 hrs) give
intravenous fluids that contain glucose. Young infants may need IV
fluids.
Additional preoperative lab screening is generally not essential. However,
carry out the following if possible.
Infants less than 6 months: check hematocrit and do blood group and Rh
status
Children 6 months–12 years: no need of investigation for minor surgery;
check hematocrit for major surgery.
Preoperative antibiotics should be given for:

 Infected and contaminated cases (e.g. those requiring bowel or

bladder surgery)
 Bowel: give ampicillin (25–50 mg/kg IV four times a day),
gentamicin (7.5 mg/kg IV once a day) and metronidazole
(7.5 mg/kg three times a day) at least 24 hrs before and for 3–5
days after the operation.
 Urinary tract: give ampicillin (25–50 mg/kg IV four times a day),
and gentamicin (7.5 mg/kg IV once a day) before and for 3–5 days
after the operation.
Children at risk for endocarditis (children with congenital heart disease or
valvular heart disease) undergoing dental, oral, respiratory and

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oesophageal procedures: give amoxicillin 50 mg/kg orally 1 hr before the
operation or, if unable to take oral medications, ampicillin 50 mg/kg IV
within 30 minutes before the surgery. If the child has penicillin allergy,
consider oral clinadamycin/cefalexin /clarithromycin / azithromycin PO or
IV. For GI and GU procedures, IM/IV ampicillin 50 mg/kg IV plus gentamicin
7.5 mg/kg IM or IV within 30 minutes before the surgery and IM/IV
ampicillin or oral amoxicillin 6hrs later.
9.1.2 Intraoperative care
Anaesthesia
Infants and children experience pain just like adults, but may express it
differently.
Make the procedure as painless as possible.
For minor procedures in co-operative children: give a local anaesthetic such
as lidocaine 4–5 mg/kg or bupivacaine 0.25% (dose not to exceed 1 mg/kg).
For major procedures: give general anaesthesia
Ketamine is an excellent anaesthetic when muscle relaxation is not
required.
Insert an intravenous cannula (it may be more convenient to delay this
until after ketamine has been given IM).
 Give ketamine 5–8 mg/kg IM or 1–2 mg/kg IV; following IV ketamine,
the child should be ready for surgery in 2–3 minutes, if given IM in 3–5
minutes.
 Give a further dose of ketamine (1–2 mg/kg IM or 0.5–1 mg/kg IV) if
the child responds to a painful stimulus.
 At the end of the procedure turn the child into the lateral position
and closely supervise the recovery possibly in an ICU.

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  Special considerations
 Airway: The smaller diameter airway in children makes them
especially susceptible to airway obstruction so they often need
intubation to protect their airway during surgical procedures. Small
children also have difficulty in moving heavy columns of air making
adult vaporiser units unacceptable. Endotracheal tube sizes for
children are given in Table 9.1.
Table 9.1 Endotracheal tube size by age

Age (years) Tube size (mm)

Premature infant 2.5–3.0
Newborn 3.5
1 4.0
2 4.5
2–4 5.0
5 5.5
6 6
6–8 6.5
8 Cuffed 5.5
10 Cuffed 6.0

Alternatively, as a rough guide for normally nourished children more than

2 years old, use the following formula:

Internal diameter of the tube (mm) = [(Age in years) ÷ 4] + 4

 Another rough indicator of the correct tube size is the diameter of the
child’s little finger. Always have tubes one size bigger and smaller
available. With a non-cuffed tube there should be a small air leak.
Listen to the lungs with a stethoscope following intubation to ensure
the breath sounds are equal on both sides.

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 Hypothermia: Prevent hypothermia in the operating room by turning
off the air conditioner, warming the room (aim for a temperature of
>28 ° C when operating on an infant or small child) and covering
exposed parts of child.

Use warmed fluids (but not too hot),

Monitor the child’s temperature as frequently as possible and at the

completion of the operation.

Hypoglycaemia: Infants and children are at risk for developing

hypoglycaemia because of a limited ability to utilize fat and protein to
synthesize glucose. Use glucose infusions during anaesthesia to help
maintain blood sugar level. For most paediatric operations, other than
minor ones, give Ringer's lactate plus glucose 5% (or glucose 5% with saline
0.9%) at a rate of 5 ml/kg of body weight per hour in addition to replacing
the measured fluid losses.

 Blood loss: Children have smaller blood volumes than adults. Even
small amounts of blood loss can be life threatening.
 Measure blood loss during operations as accurately as possible.
 Consider blood transfusion if blood loss exceeds 10% of blood
volume (Table 9.2).
 Have blood readily available in the operating room if blood loss is
anticipated.
 Monitor pulse rate and BP.
Table 9.2 Blood volume of children by age

Age ml/kg body weight

Neonate 85–90
Children 80

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Communicate to the family the outcome of the operation, problems
encountered during the procedure, and the expected postoperative
course.

9.1.3 Postoperative care

Immediately following surgery:

 Ensure that the child recovers safely from the anaesthesia.

 Monitor the vital signs—respiratory rate, pulse) and, if necessary,
blood pressure every 15–30 minutes until stable (see Table 9.3)
 Avoid settings where high-risk children cannot be adequately
monitored.
 Investigate and treat abnormal vital signs.
Table 9.3 Normal pulse rate and blood pressure in children

Systolic blood
pressure (normal)
Age Pulse rate (normal range)

0–1 year 100–160 Above 60

1–3 years 90–150 Above 70

3–6 years 80–140 Above 75

Note: normal pulse rates are 10% slower in sleeping children.

In infants and children a presence or absence of a strong central pulse is

often a more useful guide to the presence or absence of shock than a blood
pressure reading. Also, equally important may be assessing capillary refill if
there is no cold exposure of the extremities.

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Fluid management
Postoperatively, children commonly require more than maintenance fluid.
Children with abdominal operations typically require 150% of baseline
requirements and even larger amounts if peritonitis is present. Preferred IV
fluids are Ringer's lactate with 5% glucose or normal saline with 5% glucose
or half-normal saline with 5% glucose. Note that normal saline and Ringer's
lactate do not contain glucose and there is risk of hypoglycaemia, and large
amounts of 5% glucose contain no sodium and may lead to hyponatraemia.

Monitor fluid status closely.

 Record inputs and outputs (intravenous fluids, nasogastric drainage,

urine drain outputs) every 4–6 hours.
 Urine output is the most sensitive indicator of fluid status in a child.
 Normal urine output: Infants 1–2 ml/kg/hour, children 1 ml/kg/hour.
 If urinary retention is suspected, pass a urinary catheter. This also
allows for hourly measurements of urine output to be made, which
can be invaluable in severely ill children. Suspect urinary retention if
bladder is palpable or the child is unable to void urine.
Pain control

Have a plan for postoperative pain management.

 Mild pain: Give paracetamol (10–15 mg/kg every 4–6 hours)

administered by mouth or rectally. Oral paracetamol can be given
several hours prior to operation or rectally at the completion of
surgery.

 Moderate to severe pain: Give intravenous narcotic analgesics (IM

injections are painful). Morphine sulfate 0.05–0.1 mg/kg IV every 2–4
hours can be given if pain warrants. IV morphine is not usally

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 available. In this situation give morphine sulphate 0.15-0.2 mg/kg
orally every 2-4 hours.

Nutrition
Many surgical conditions increase caloric needs or prevent adequate
nutritional intake. Many children with surgical problems present in a
debilitated state. Poor nutrition adversely affects their response to injury
and delays wound healing.

 Feed children as soon as possible after surgery depending on the

type of surgery.
 Provide a high calorie diet containing adequate protein and vitamin
supplements.
 Consider feeding by nasogastric tube for children whose oral intake
is poor.
 Monitor the child’s weight.
Common postoperative problems
Tachycardia (raised pulse rate see Table 9. 3): May be caused by pain,
hypovolaemia, anaemia, fever, hypoglycaemia, and infection.
Review the child’s preoperative and intraoperative care.
Monitor the response to pain medication, boluses of IV fluids, dextrose,
oxygen, and IV transfusions, where appropriate.
Bradycardia in a child should be considered as a sign of hypoxia until
proven otherwise.
Fever: May be due to tissue injury, wound infections, atelectasis, urinary
tract infections (from indwelling catheters), phlebitis (from an intravenous
catheter site), or other concomitant infections (e.g. malaria).

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Low urine output: May be due to hypovolaemia, urinary retention or renal
failure. Low urine output is almost always due to inadequate fluid
resuscitation.
Review the child’s fluid record.

If hypovolaemia is suspected; give normal saline (10–20 ml/kg) and repeat

as needed

If urinary retention is suspected (the child is uncomfortable and has a full

bladder on physical examination): pass a urinary catheter

9.2 Congenital anomalies

9.2.1 Cleft lip and palate
These may occur together or separately (see figure). Reassure the parents
that the problem can be dealt with, as there may be concern about the
unattractive appearance.

Figure 9.1: Cleft lip and palate

Treatment
Babies with isolated cleft lip can feed normally. Cleft palate is associated
with feeding difficulties. The baby is able to swallow normally but unable to

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suck adequately and milk regurgitates through the nose and may be
aspirated into the lungs.

 Feed using expressed breast milk via a cup and spoon, or if

available AND adequate sterility of bottles can be ensured, a
special teat may be used. The technique of feeding is to deliver a
bolus of milk over the back of the tongue into the pharynx by
means of a spoon, pipette, or some other pouring device. The
baby will then swallow normally.
 Close follow-up in infancy is required to monitor feeding and
growth.
 Surgical closure of the lip is performed at 3 months of age (may be
revised at 4-5 years of age) and of the palate is performed around
1 year of age.
 Follow-up after surgery to monitor hearing (middle-ear infections
are common) and speech development.
9.2.2 GI obstruction
Hypertrophic pyloric stenosis, bowel atresia, malrotation with volvulus,
meconium plug syndrome, Hirschsprung’s disease (colonic aganglionosis),
or imperforate anus are the common causes of bowel obstruction.

Diagnosis
The level of obstruction determines the clinical presentation. Proximal
obstruction: vomiting with minimal distension. Distal obstruction:
distension with vomiting occurring late.
Bile-stained (green) vomiting in an infant is due to a bowel obstruction until
proven otherwise and is a surgical emergency.

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Pyloric stenosis presents as progressive, projectile (forceful) non-bilious
vomiting. Dehydration, weight loss, and failure to thrive can develop
later. Typically occurs between 3 and 6 weeks of age.

Dehydration and electrolyte abnormalities are common

An olive like mass (the enlarged pylorus) may be palpated in the right
upper abdomen
Consider other causes of abdominal distension (such as ileus related to
sepsis, necrotizing enterocolitis and ascites)
Investigation: plain film of the abdomen, abdominal ultrasound if available.

Treatment
Prompt resuscitation and URGENT REVIEW by a surgeon experienced in
paediatric surgery.

Give nothing orally. Pass a nasogastric tube if there is vomiting or

abdominal distension.

 Intravenous fluid: use 0.45-0.9% saline + 5-10% glucose

(dextrose)+ KCL 30-50Meq/L after ensuring good urine output (in
case of IHPS)
 Give 10–20 ml/kg to correct dehydration
 Then give maintenance fluid plus the same volume that comes
out of the nasogastric tube
 Antibiotics prophylaxis depending on the procedure
9.2.3 Abdominal wall defects
The abdominal wall does not fully develop and remains open.

Diagnosis
There may be exposed bowel (gastroschisis) or a thin layer covering the
bowel (omphalocele) (see figure).

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 Figure 9.2: Newborn with an
omphalocele

Treatment
 Apply a sterile dressing and cover with a plastic bag (to prevent
fluid loss). Exposed bowel can lead to rapid fluid loss and
hypothermia.
 Give nothing orally. Pass a nasogastric tube for free drainage.
 Give intravenous fluids: use normal saline + glucose (dextrose):
 Give 10–20 ml/kg to correct dehydration.
 Then give maintenance fluid requirements (chapter 10) plus the
same volume that comes out of the nasogastric tube.
 Antibiotics (section 9.1.1)
 URGENT REVIEW by a surgeon experienced in paediatric surgery.
9.2.3 Myelomeningocele
Diagnosis

 A sac containing meninges and a malformed spinal cord that

protrudes through defective vertebrae. The most common site is
the lumbar region.
 Maybe associated with neurological problems (bowel, bladder and
motor deficits in the lower extremities) and hydrocephalus.

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  Maternal oral folic acid supplementation prior to conception and
throughout the first trimester reduces the risk of
myelomenigocele by 50% to 70%.
 There is high risk of recurrence in the family than in the general
population.
Treatment
 Apply a sterile dressing.
 If ruptured, and any signs of infection give ampicillin (25–50
mg/kg IV four times a day) plus gentamicin (7.5 mg/kg once per
day) for 10-14 days.
 Catheterize regularly to prevent pyelonephritis and
hydronephrosis.
 REVIEW by a sergeon experienced in paediatric surgery.

Figure 9.3: Myelomeningocele

Developmental Dyspalsia of the Hip

(DDH)
Diagnosis
 Severe cases should be detected by routine physical examination
at birth.

 When unilateral, the limb is short, there is limited abduction when

the hip is flexed, and the skin crease at the back of the hip appears
asymmetrical. When the flexed hip is abducted, a clunk (not an

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 audible click) can often be felt as the dislocated femoral head
enters the acetabulum (Ortolani’s sign).

 In the older infant, confirm the diagnosis with X-ray. X-rays in

neonates are difficult to interpret as the epiphysis of the femur
and the femoral head do not appear until 3–4 months of age (see
figure), so ultrasound of the hip can be done earlier usually at
3 weeks of life if this is available. Positioning the lower limb in
45° abduction demonstrates a break in the continuity of a line
drawn along the upper margin of the obturator foramen and
lower aspect of the femoral neck.The figure below shows: A)
Normal Shenton’s line, B) The line is broken in dislocation of the
hip.

A
B

Figure 9.4: Radiological diagnosis of congenital dislocation of the hip

Treatment
In milder cases, keep the hip in flexion and abduction through double
nappies or an abduction brace in an abducted position for 2–3 months. In
more severe cases, keep the hip abducted and flexed in a splint.

REVIEW by a surgeon experienced in paediatric orthopedics.

9.2.4 Talipes equinovarus (club foot)

Diagnosis
The foot cannot be placed into the normal position.

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The commonest form is congenital form and accounts for 75% of case. In
50 % of cases it occurs bilaterally. It includes three deformities: hind foot
equinus, hind and mid foot varus, fore foot adduction.

Hind foot equinus

Hind and
mid foot
Fore foot adduction varus

Figure 9.5: Club foot

Treatment
Non operative
 Mild positional deformity (the foot can be passively corrected):
simple Stretching of foot beginning shortly after birth
 Moderate deformity: serial manipulations beginning shortly after
birth
 Maintain position with tape strapping or well-padded plaster of
 Paris casts. Apply this in the sequence 1, then 2, then 3 as in Figure
below.
 These manipulations should be repeated every 2 weeks or until the
deformity is corrected.
 Special splints may need to be worn until the child begins to walk.
Operative:
 If cast fails, surgery is indicated at 6-12 months of age.
 If child presents beyond 3 months of age

Figure 9.5: Treating talipes

with tape strapping

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9.3 Injuries
Injuries are the most common surgical problems affecting children. Proper
treatment can prevent death and lifelong disability. Whenever possible, try
to prevent childhood injuries from occurring.
See Chapter 1 for guidelines for assessing children with severe injuries.
More detailed surgical guidance is given in the WHO manual of surgical
care in the district hospital.

9.3.1 Burns
Burns are associated with a high risk of mortality in children. Those who
survive may suffer from disfigurement and psychological trauma as a result
of a painful and prolonged stay in the hospital.

Assessment
Burns may be partial or full thickness. A full thickness burn means the
entire thickness of the skin is destroyed, and the skin will not regenerate.

Ask two questions:

How deep is the burn?

 Full thickness burns are black or white, usually dry, have no feeling
and do not blanch on pressure.

 Partial thickness burns are pink or red, blistering or weeping, and

painful.

How much of the body is burnt?

 Use a body surface area chart according to age

 Alternatively, use the child’s palm to estimate the burn area. A

child’s palm is approximately 1% of the total body surface area.

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 Figure 9.10.Estimation of the total area burned in percentage

Table 9.4 Tools for estimating the percentage of body surface burned

IN Areas A-F the percentage changes according to the age of

the child
Area % By age in years
0 1 5 10
Head (A/D) 10% 9% 7% 6%
Thigh (B/E) 3% 3% 4% 5%
Leg (C/F) 2% 3% 3% 3%

Treatment
 Admit all children with burns >10% of their body surface; those
involving the face, neck, hands, feet, perineum, across joints, high
tension electrical burns; burns that are circumferential and those
that cannot be managed as outpatients.

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  Consider whether the child has a respiratory injury due to smoke
inhalation.
 If there is evidence of respiratory distress, then provide
supplemental oxygen
 Severe facial burns and inhalational injuries may require early
intubation or tracheostomy to prevent or treat airway obstruction.
 Fluid resuscitation (required for >10% total body surface burn).
Use Ringer's lactate with 5% glucose, normal saline with 5%
glucose or half-normal saline with 5% glucose.
1st 24 hours: Calculate fluid requirements by adding maintenance fluid
requirements and additional resuscitation fluid requirements (volume
equal to 4 ml/kg for every 1% of surface burned) (Section 10.2)

Administer 1/2 of total fluid in first 8 hours, and remaining in next 16

hours.
Example: 20 kg child with a 25% burn:
Total fluid in 1st 24 hrs = (1500ml) + 4 ml x 20kg x 25% burn
= 1500 ml + 2000 ml
= 3500 ml (1750 ml over 1st 8 hours)

Second 24 hours: give 1/2 to 3/4 of fluid required during the first day.

Monitor the child closely during resuscitation (pulse, respiratory rate, blood
pressure and urine output).

Blood may be given to correct severe anemia or for deep burns to replace
blood loss.

Prevent infection
 If skin is intact, clean with antiseptic solution gently without
breaking the skin

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  If skin is not intact, carefully debride the burn. Blisters should be
pricked and dead skin removed.
 Give topical antibiotics/antiseptics (there are several options
depending on resources available and these include: silver nitrate,
silver sulfadiazine, gentian violet, betadine and even mashed
papaya). Clean and dress the wound daily.
 Small burns or those in areas that are difficult to cover can be
managed by leaving them open to the air and keeping them clean
and dry.
 Oral or IV penicillin for 5 days (standard dose QID)
 Treat secondary infection if present.
 If septicaemia is suspected, use gentamicin (7.5 mg/kg IM or IV
once a day) plus cloxacillin (25–50 mg/kg IM or IV four times a
day). If infection is suspected beneath an eschar, remove the
eschar.
Pain control (see chapter 10)
 Make sure that pain control is adequate including before
procedures such as changing dressings.
 Give paracetamol (10–15 mg/kg every 6 hours) by mouth or
 If pain is severe can give Morphin syrup or intravenous narcotic
analgesics (IM injections are painful), such as morphine sulfate
(0.05–0.1 mg/kg IV every 2–4 hours)
 Check tetanus vaccination status and treat as per Table 9.5.

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Table 9.5 Indications for Tetanus prophylaxis

Prior Tetanus Toxoid doses TT/DPT TAT/TIG

Unknown/<3 Yes Yes
≥3, last <5yrs ago No No
≥3, last >5yrs ago Yes No

Nutrition
 Begin feeding as soon as practical in the first 24 hours.
 Children should receive a high calorie diet containing adequate
protein, and vitamin and iron supplements.
 Children with extensive burns require about 1.5 times the normal
calorie and 2–3 times the normal protein requirements.
Burn contractures: Burn scars across flexor surfaces contract. This happens
even with the best treatment.

Prevent contractures by passive mobilization of the involved areas and by

splinting flexor surfaces. Splints can be made of plaster of Paris. Splints
should be worn at night.

Physiotherapy and rehabilitation

 Should begin early and continue throughout the course of the

burn care.
 If the child is admitted for a prolonged period, ensure the child has
access to toys and is encouraged to play.
9.3.2 Principles of wound care
The goal of caring for any wound is to stop bleeding, prevent infection,
assess damage to underlying structures and promote wound healing.

Stop bleeding
 Direct pressure will control any bleeding.

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  Bleeding from extremities can be controlled for short periods of
time (<10 minutes) using a sphygmomanometer cuff inflated
above the arterial pressure.
 Prolonged use of tourniquets can damage the extremity. Never
use a tourniquet in a child with sickle-cell anemia.
Prevent infection
 Cleaning the wound is the most important factor in preventing a
wound infection. Most wounds are contaminated when first seen.
May contain blood clots, dirt, dead or dying tissue and perhaps
foreign bodies.
 Clean the skin around the wound thoroughly with soap and water
or antiseptic. Water and antiseptic should be poured into the
wound.
 After giving a local anaesthetic such as bupivacaine 0.25% (not to
exceed 1ml/kg), search carefully for foreign bodies and carefully
excise any dead tissue. Determine what damage may have been
done. Major wounds require a general anaesthetic.
Antibiotics are usually not necessary when wounds are carefully cleaned.
However, there are some wounds that should be treated with antibiotics
(see below).
 Wounds older than 12 hours
 Wounds penetrating deep into tissue (e.g. a dirty stick or knife
wound).
Tetanus prophylaxis
See table 9.5 above

Wound closure
 If the wound is less than 6 hrs old and has been cleaned
satisfactorily, the wound can be closed (called primary closure).

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  The wound should not be closed if it is more than 6 hours old, there
has been a lot of dirt and foreign material in the wound, or if the
wound has been caused by an animal bite including human bite
 Wounds not treated with primary closure should be packed lightly
with damp gauze. If the wound is clean 48 hours later, the wound
can then be closed (delayed primary closure).
 If the wound is infected, pack the wound lightly and let it heal on its
own.
Wound infections
Clinical signs: pain, swelling, redness, warmth and pus drainage from the
wound.
Treatment
 Open wound if pus suspected
 Clean the wound with disinfectant.
 Pack the wound lightly with damp gauze. Change the dressing every
day, more frequently if needed.
Antibiotics until surrounding cellulitis has resolved (usually 5 days):
 Give cloxacillin (25–50 mg/kg orally four times a day) for most
wounds to deal with Staphylococcus.
 Give ampicillin (25–50 mg/kg orally four times a day), gentamicin
(7.5 mg/kg IM or IV once a day) and metronidazole (7.5 mg/kg three
times a day) if bowel flora is suspected.
Controlling external bleeding
Elevate the limb, apply direct pressure then put a pressure bandage

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9.3.3 Fractures
Children have a remarkable ability to heal fractures if the bones are aligned
properly.

Diagnosis
Pain, swelling, deformity, crepitus, unnatural movement, and loss of
function.

Fractures can be closed (where the skin is intact) or open (where there is a
wound of the skin). Open fractures may lead to serious bone infection.
Suspect an open fracture if there is an associated wound. A child’s bones
are different from adults; instead of breaking they often bend like a stick

X-ray-to locate and know the extent of fracture

Treatment
Ask two questions: - Is there a fracture? - Which bone is broken (either by
clinical exam or X-ray)?

Consider referral for REVIEW by a surgeon experienced in paediatric

orthopedics for complicated fractures such as those that are displaced or
involve growth plates or are open.

Open fractures require antibiotics: cloxacillin (25–50 mg/kg orally four

times a day), and gentamicin (7.5 mg/kg IM or IV once a day) and
meticulous cleaning to prevent osteomyelitis).

Figures shown below describe simple methods for treating some of the
most common childhood fractures. For further details of how to manage
these fractures, consult the WHO manual of surgical care at the district
hospital or a standard textbook of (surgical) paediatrics.

A posterior splint can be used for upper and lower extremity injuries. The
extremity is first wrapped with soft padding (e.g. cotton), then a plaster of
Paris splint is placed to maintain the extremity in a neutral position. The
posterior splint is held in place with an elastic bandage. Monitor the fingers

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(capillary refill and temperature) to ensure the splint has not been placed
too tightly.

The treatment of a mid-shaft femoral fracture in a child under 3 years of

age is by gallows splint and is shown in the figure. It is important that every
few hours the attendant should check that the circulation of the feet is
good and the toes are warm.

The treatment of a mid-shaft femoral fracture in an older child is by skin

traction. This is a simple and effective method for treating femur fractures
in children aged 3–15 years. If the child can raise his leg off the bed the
fracture has united and the child is ready for ambulation on crutches
(usually about 3 weeks).

Figure 9.12 Posterior splint

Figure 9.13: Sling and

Tractions

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Figure 9.14: Treatment of a supracondylar fracture

A. X-ray of displaced supracondylar fracture

B. Pull as shown to reduce the fracture displacement.

C. Carefully bend the elbow maintaining traction. Hold the elbow flexed
and keep the fracture in position as shown
D. Apply a back slab
E. Check the position of the fracture on X-ray.

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An important complication of this fracture is constriction of the artery at
the elbow—where it can become entrapped. Assess the blood flow to the
hand. If the artery is obstructed the hand will be cool, capillary refill will be
slow and the radial pulse will be absent. If the artery is obstructed,
reduction needs to be done urgently.

9.3.4 Head injuries

Brain injuries fall into four categories (3 C’s +L).

 Concussion: the mildest injury where loss of brain function is

temporary.
 Contusion: the brain is bruised and function may be affected for
hours to days, or even weeks.
 Compression: may result from swelling or a growing blood clot
(epidural or subdural haematoma). If compression is due to a
blood clot, urgent operation may be required.
 Laceration: visible cut to the brain tissue
Diagnosis
 History of head trauma.
 Diminished level of consciousness, confusion, seizure and signs of
increased intracranial pressure (increased BP, drop in pulse,
unequal pupils, rigid posture, focal paralysis and irregular
breathing).
 Skull X-ray
Treatment
 Give nothing orally
 Protect the child’s airway (see Chapter 1).
 Limit fluid intake (to 2/3 of maintenance fluid requirements
 Elevate the head of the bed to 30 degrees.
 Diagnose and treat other injuries.

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  URGENT REVIEW by a surgeon experienced in paediatric surgery.
9.3.5 Chest and abdominal injuries
These can be life threatening and may result from blunt or penetrating
injuries. Types of injuries include:

 Chest injuries include rib fractures, pulmonary contusions,

pneumothorax and haemothorax. Because the ribcage of children
is more pliable than that of adults, there may be extensive chest
injuries without rib fractures.
 Blunt and penetrating trauma to the abdomen may injure a
variety of organs. Splenic injuries from blunt trauma are especially
common.
 Assume that a penetrating wound to the abdominal wall has
entered the abdominal cavity and that there may be injuries to the
intra-abdominal organs.
 Be especially cautious with injuries around the anus—as
penetrating rectal injuries can be easily missed.
Treatment
Suspected chest or abdominal injuries require URGENT REVIEW by a
surgeon experienced in paediatric surgery.
See guidelines given in Chapter 1.
9.4 Abdominal problems
9.4.1 Abdominal pain

Abdominal pain lasting longer than four hours should be regarded as a

potential abdominal emergency.

Assessment
Ask three questions:

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  Are there associated symptoms? The presence of nausea, vomiting,
diarrhoea, constipation, fever, cough, headache, sore throat or
dysuria (pain on passing urine) helps determine the severity of the
problem and can help narrow the diagnosis.
 Where does it hurt? Ask the child to point to where it hurts most.
This can also help narrow the diagnosis. Periumbilical pain is a
nonspecific finding.
 Does the child have peritonitis: inflammation of the lining of the
peritoneal cavity? This is a critical question, as most causes of
peritonitis in children require operation.
 Signs of peritonitis include tenderness during palpation, pain in the
abdomen when the child jumps or has his pelvis shaken and
involuntary guarding (spasm of the abdominal musculature following
palpation). A rigid abdomen that does not move with respiration is
another sign of peritonitis.
Treatment
 Give the child nothing orally.
 If vomiting or abdominal distension, place a nasogastric tube.
 Give intravenous fluids (most children presenting with abdominal
pain are dehydrated) to correct fluid deficits (Ringers lactate 10–20
ml/kg repeated as needed) followed by 150% maintenance fluid
requirements. Add glucose 5-10% for the maintenance fluid.
 Give analgesics if the pain is severe (this will not mask a serious
intra-abdominal problem, and may even facilitate a better
examination).
 Repeat the examinations if the diagnosis is in question.
 Give antibiotics if there are signs of peritonitis. To deal with enteric
flora (Gram-negative rods, Enterococcus, and anaerobes): give

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 ampicillin (25–50 mg/kg IV four times a day), gentamicin (7.5 mg/kg
IV once a day) and metronidazole (7.5 mg/kg three times a day).
 URGENT REVIEW by a surgeon experienced in paediatric surgery.

9.4.2 Appendicitis
This is caused by obstruction of the lumen of the appendix. Fecoliths,
lymphoid hyperplasia and gastrointestinal parasites can cause obstruction.
If not recognized the appendix ruptures leading to peritonitis and abscess
formation.
Diagnosis
Clinical:
 Fever, anorexia, vomiting (variable)
 May begin as periumbilical pain, but the most important clinical
finding is persistent pain and tenderness in the right lower
quadrant.
 May be confused with urinary tract infections, kidney stones,
ovarian problems, mesenteric adenitis, and ileitis.
Lab:
 Nonspecific
 WBC count may be normal or mildly elevated
 U/A frequently demonstrates a few white or red blood cells
Treatment
 Give the child nothing orally.
 Give intravenous fluids. See above
 Give antibiotics in patients (with suspected perforation) once
diagnosis established: see above

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  URGENT REVIEW by a surgeon experienced in paediatric surgery.
Appendectomy should be done as soon as possible to prevent
perforation, peritonitis and abscess formation.

9.5 Bowel obstruction beyond the newborn period

This may be caused by incarcerated hernias, adhesions (scarring from
previous surgery), Ascaris infection, and intussusception (see next section).
Diagnosis

Clinical:
 Clinical presentation is determined by the level of obstruction.
Proximal obstruction—presents with vomiting with minimal
distension. Distal obstruction—presents with distension,
obstipation with vomiting occurring later.
 Typically there is cramping abdominal pain, distension and no
flatus.
 Sometimes peristalsis waves can be seen through abdominal wall.
Investigation:
 Plain film of the abdomen shows distended loops of bowel with air
fluid levels.
 Ultra sound – transverse image doughnut or target appearance

Treatment
 Give the child nothing orally
 Give fluid resuscitation. See above
 Pass a nasogastric tube—this relieves nausea and vomiting, and
prevents bowel perforation by keeping the bowel decompressed.
 URGENT REVIEW by a surgeon experienced in paediatric surgery.
9.5.1 Intussusceptions

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This is form of bowel obstruction in which one segment of the intestine (a
proximal segment of bowel) telescopes into the next (distal portion of
intestine). This most commonly occurs at the ileal-caecal junction.

Diagnosis
Usually occurs in children between 3 months to 6 years, and 80% occurs in
<2 years.

Clinical presentation

 Early: colicky abdominal pain with vomiting. The child cries with
pain, doubles over, and pulls the legs up.
 Late: pallor, abdominal distension, tenderness, bloody diarrhoea
(“red currant jelly stool”) and dehydration.
 Palpable abdominal mass most often in the right upper quadrant
(begins in right lower quadrant and may extend along the line of
colon).
 Barium Enema: see below

Treatment
Give an air or barium enema if gangrene is excluded (this can both
diagnose and reduce the intussusception). An unlubricated 35 ml
Foley catheter is passed into the rectum; the bag is inflated and the
buttocks strapped together. A warm solution of barium in normal saline is
allowed to flow in under gravity from a height of 1 meter and its entrance
into the colon is observed using an abdominal X-ray. The diagnosis is
confirmed when the barium outlines a concave ‘meniscus’. The pressure of
the column of barium slowly reduces the intussusception; the reduction is
only complete when several loops of small bowel are seen to fill with
barium.

 Pass a nasogastric tube.

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  Give fluid resuscitation.
 Give antibiotics if there are signs of infection (fever, peritonitis)—
give ampicillin (25–50 mg/kg IV four times a day), gentamicin (7.5
mg/kg IV once a day) and metronidazole (7.5 mg/kg three times a
day). The duration of the post-operative antibiotics depends on
the severity of the disease: in an uncomplicated intussusception
reduced with an air enema, give for 24–48 hours postoperatively;
in a child with a perforated bowel with resection, continue
antibiotics for one week.
 Arrange URGENT REVIEW by a surgeon experienced in paediatric
surgery. Proceed to an operation if air or barium enema is unable
to reduce the intussusception. If the bowel is ischaemic or dead,
then a bowel resection will be required.

9.5.2 Umbilical hernia

Diagnosis
Soft reducible swelling at umbilicus.
Treatment
 Most close spontaneously.
 Repair if not closed by age 6 years, or if there is a history of the
hernia being difficult to reduce.
9.5.3 Inguinal hernia
Diagnosis
 Intermittent reducible swelling in the groin that is observed when
the child is crying or straining.
 Occurs where the spermatic cord exits the abdomen (inguinal
canal).

386
  Distinguish from a hydrocele (fluid that collects around testicle
due to a patent processus vaginalis). Hydroceles trans-illuminate
and usually do not extend up into the inguinal canal.
 Can also occur rarely in girls.

Fig 9.15: Inguinal hernia

Treatment
Uncomplicated inguinal hernia: elective surgical repair to prevent
incarceration.
Hydrocele: repair if not resolved by age 1 year. Unrepaired hydroceles will
lead to inguinal hernias.
Incarcerated hernias
These occur when the bowel or other intra-abdominal structure (e.g.
omentum) is trapped in the hernia.
Diagnosis
 Non-reducible tender swelling at the site of an inguinal or
umbilical hernia.
 There may be signs of intestinal obstruction (vomiting and
abdominal distension) if the bowel is trapped in the hernia.
Treatment
 Attempt to reduce by steady constant pressure. If the hernia does
not reduce easily, an operation will be required.

387
  Give the child nothing orally.
 Give intravenous fluids.
 Pass a nasogastric tube if there is vomiting or abdominal
distension.
 Give antibiotics if compromised bowel is suspected: give ampicillin
(25–50 mg/kg IV four times a day), gentamicin (7.5 mg/kg IV once
a day) and metronidazole (7.5 mg/kg three times a day).
 URGENT REVIEW by a surgeon experienced in paediatric surgery.
9.5.4 Rectal prolapse
This is caused by straining during a bowel motion and is associated with
chronic diarrhoea and malnutrition. Causative factors include
gastrointestinal parasites (such as Trichuris)

Diagnosis
 The prolapse occurs on defecation. Initially the prolapsed section
reduces spontaneously, but later may require manual reduction.
 May be complicated by bleeding or even strangulation with
gangrene
Treatment
 Provided that the prolapsed rectum is not dead (it is pink or red
and bleeds), reduce with gentle constant pressure.
 Firm strapping across buttocks to maintain the reduction.
 Correct underlying cause of diarrhoea and malnutrition.
 Treat for a helminth infection (such as mebendazole 100 mg orally
twice a day for 3 days or 500 mg once only).
 REVIEW by a surgeon experienced in paediatric surgery. Recurrent
prolapse may require a Thirsch stitch.

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9.6 Infections requiring surgery
9.6.1 Abscess
Infection can cause a collection of pus in almost any area of the body.

Diagnosis
Fever, swelling, tenderness, and fluctuant mass.

Question what might be the cause of the abscess (e.g., injection, foreign
body or underlying bone infection). Injection abscesses usually develop 2–3
weeks after injection.

Treatment
 Incision and drainage

 Large abscesses may require general anaesthesia.

 Antibiotics: cloxacillin (25–50 mg/kg four times a day) for 5 days or

until surrounding cellulitis resolved. If bowel flora is suspected
(e.g., perirectal abscess): give ampicillin (25–50 mg/kg IV four
times a day), gentamicin (7.5 mg/kg IV once a day) and
metronidazole (7.5 mg/kg three times a day).

B C
A

E
D
Figure 9.16: Incision and drainage of an abscess

389
A. Aspirating to identify site of pus; B. Elliptical incision; C–D. Breaking up
loculations; E. Loose packing in place.

9.6.2 Osteomyelitis
Infection of a bone usually results from blood spread. It may be caused by
open fractures. The most common organisms include Staphylococcus, H.
influenza type b, Salmonella (sickle-cell children) and Mycobacterium
tuberculosis.

Diagnosis
Acute osteomyelitis
Clinical:

 Pain and tenderness of the involved bone (± fever).

 Refusal to move the affected limb.
 Refusal to bear weight on leg.
Investigation:
CBC, ESR, CRP

 X ray: In early osteomyelitis the X-ray may be normal (it usually

takes 12–14 days for X-ray changes to appear).
 Chronic osteomyelitis
 Chronic draining sinuses over the involved bone.
 X-ray: elevated periosteum and sequestrum (collection of dead
bone).
Treatment
 REVIEW by a surgeon experienced in paediatric orthopedics

 Less than 5 years of age ceftriaxone 100 mg/kg/day in two divided

doses

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  Cloxacillin (100 mg/kg in four divided doses) is given for children
above 5 years of age. Total duration of treatment extends from 3-
6 weeks depending on the etiologies. Chronic osteomyelitis:
sequestrectomy (removal of dead bone) is usually necessary as
well as antibiotic treatment, as above.

9.6.3 Septic arthritis

The most common organism is Staphylococcus aureus, H. influenza type b,
and streptococcus.

Diagnosis
Clinical:

 Pain and swelling of the joint (± fever).

 Examination of the joint shows two important physical signs:
 Swelling and tenderness over the joint.
 Decreased range of movement.
 Investigation: CBC, ESR, CRP, X ray, Synovial fluid analysis, culture
and sensitivity
 DDx: always exclude hemophilia in a male child
Treatment

 URGENT REVIEW by a surgeon experienced in paediatric surgery

for washout of the joint. Pus under pressure in a joint destroys the
joint.
 Less than 5 years of age: ceftriaxone 100 mg/kg/day in two
devided doses three weeks.
 Cloxacillin (100 mg/kg in four divided doses) is given for children
above 5 years of age. Total duration of treatment 3 weeks
depending on the etiologies.

391
A B

D
C

Figure 9.17: Technique for

aspirating hip (A,B), knee (C,D) and
elbow (E) joints.

9.6.4 Pyomyositis
This is a condition where there is pus within the substance of a muscle.

Diagnosis
Fever, tenderness and swelling of the involved muscle. A fluctuant mass
may not be a sign as the inflammation is deep in the muscle.

Commonly occurs in the thigh.

Treatment
 Incision and drainage (usually requires a general anaesthetic).
 Leave a drain in the abscess cavity for 2–3 days.
 X-ray to exclude underlying osteomyelitis.
 Give cloxacillin (50 mg/kg IM or IV four times a day) for 5–10 days
as the most common organism is Staphylococcus aureus.

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CHAPTER 10 - SUPPORTIVE CARE

In order to provide good patient care, hospital policies and working

practices should promote the basic principles of child care, such as:

 Communicating with the parents/child

 Arranging the paediatric ward so that the most seriously ill
children get the closest attention and are close to oxygen and
other emergency treatments
 Keeping the child comfortable
 Preventing the spread of nosocomial infection by encouraging
staff to handwash regularly, and other infection prevention
measures
 Keeping warm the area in which young infants or children with
severe malnutrition are being looked after, in order to prevent
complications like hypothermia.
10.1 Nutritional management
The health worker should follow the counseling process outlined in chapter
12. A mother’s card containing a pictorial representation of the advice
should be given to the mother to take home as a reminder

10.2 Supporting breastfeeding

Breastfeeding is most important for the protection of infants from illness
and for their recovery from illness. It provides the nutrients needed for a
return to good health. The national infant and young child feeding
recommendation follows the global strategy on infant and young child
feeding recommendations irrespective of HIV status of the mother and
child.

 Exclusive Brest Feeding (EBF) for the first 6 months

393
  Initiation of complementary feeding at 6 months with
continuation of breastfeeding until two years and beyond.
Health workers treating sick young children have a responsibility to
encourage mothers to breastfeed and to help them overcome any
difficulties. Additional national recommendation is that every facility that
provides antenatal, maternity and care for newborns should:

1. Have a written breastfeeding policy that is routinely

communicated to all healthcare staff.
2. Train all healthcare staff in the skills necessary to implement this
policy.
3. Inform all pregnant women about the benefits and management
of breastfeeding
4. Help mothers initiate breastfeeding within half an hour of birth.
5. Show mothers how to breastfeed and how to maintain lactation
even if they are separated from their infants.
6. Give newborns no food or drink other than breast milk unless
medically indicated.
7. Encourage rooming in—this is a hospital arrangement where the
mother and baby stay in the same room day and night.
8. Encourage breastfeeding on-demand
9. Give no artificial feeds or pacifiers to breastfeeding babies.
10. The key to best breastfeeding practices is continued day-to-day
support for the breastfeeding mother within her home and
community.

394
 Steps for promoting breast feeding
Assessing a breastfeed
Take a breastfeeding history by asking about the baby’s feeding and
behavior. Observe the mother while breastfeeding to decide whether she
needs help. Observe:

 How the mother holds her baby.

 Baby should be held close to the mother.
 Baby should face the breast.
 Baby’s body should be in a straight line with the head.
 Baby’s whole body should be supported.
How the baby is attached to the breast. Signs of good attachment are:
 More areola visible above baby’s mouth
 Mouth wide open
 Lower lip turned out
 Baby’s chin touching the breast.
 How the mother holds her breast.

Figure 10.1 Good (left) and poor (right) attachment of infant to the
mother’s breast

395
Figure 10.2: Good (left) and poor (right) attachment; cross-sectional view
of the breast and baby

Figure 10.3 Good (left) and poor (right) positioning of infant

for breastfeeding

Overcoming difficulties
‘Not enough milk’:

396
  Almost all mothers can produce enough breast milk for one or
even two babies. However, sometimes the baby is not getting
enough breast milk. The signs are:

 Poor weight gain (<500 g a month, or <125 g a week, or less than

the birth weight after 2 weeks)
 Passing a small amount of concentrated urine (less frequent,
yellow and strong-smelling).
Common reasons why a baby may not be getting enough breast milk are:

 Poor breastfeeding practices: poor attachment (very common

cause), delayed start of breastfeeding, feeding at fixed times, no
night feeds, short feeds, use of bottles, pacifiers, other foods

and other fluids.

 Psychological factors in the mother: lack of confidence, worry,
stress, depression, dislike of breastfeeding, rejection of baby,
tiredness.
 Mother’s physical condition: chronic illness (e.g. tuberculosis,
severe anaemia or rheumatic heart disease), contraceptive pill,
diuretics, pregnancy, severe malnutrition, alcohol, smoking,
retained piece of placenta (rare).
 Baby’s condition: illness, or congenital anomaly (such as cleft
palate or congenital heart disease) which interferes with feeding.
 A mother whose breast milk supply is reduced will need to
increase it, while a mother who has stopped breastfeeding may
need to relactate if HIV negative.
Help a mother to breastfeed again by:

397
  Keeping the baby close to her and not giving him/her to other
carers
 Having plenty of skin-to-skin contact at all times
 Offering the baby her breast whenever the baby is willing to
suckle
 Helping the baby to take the breast by expressing breast milk into
the baby’s mouth, and positioning the baby so that the baby can
easily attach to the breast
 Avoiding use of bottles, teats and pacifiers. If necessary, express
the breast milk and give it by cup. If this cannot be done, artificial
feeds may be needed until an adequate milk supply is established
How to increase the milk supply:
 The main way to increase or restart the supply of breast milk is for
the baby to suckle often in order to stimulate the breast.
 Give other feeds from a cup while waiting for breast milk to come.
 Do not use bottles or pacifiers.
 Reduce the other milk by 30–60 ml per day as her breast milk
starts to increase.
 Monitor the baby’s weight gain.
Refusal or reluctance to breastfeed:
 The main reasons why a baby might refuse to breastfeed are:
 The baby is ill, in pain or sedated.
 If the baby is able to suckle, encourage the mother to breastfeed
more often. If the baby is very ill, the mother may need to express
breast milk and feed by cup or tube until the baby is able to
breastfeed again.

398
  If the baby is in hospital, arrange for the mother to stay with the
baby in order to breastfeed
 Help the mother to find a way to hold her baby without pressing
on a painful place
 Explain to the mother how to clear a blocked nose. Suggest short
feeds, more often than usual, for a few days.
 A sore mouth may be due to Candida infection (thrush) or
teething. Treat the infection with nystatin (100 000 units/ml)
suspension. Give 1–2 ml dropped into the mouth, 4 times a day for
7 days. If this is not available, apply 1% gentian violet solution.
Encourage the mother of a teething baby to be patient and keep
offering the baby the breast.
 If the mother is on regular sedation, reduce the dose or try a less
sedating alternative
If there is difficulty with the breastfeeding technique:

 Help the mother with her technique: ensure that the baby is
positioned and attached well without pressing on the baby’s head,
or shaking the breast.
 Advise her not to use a feeding bottle or pacifier; if necessary, use
a cup
 Treat engorgement by removing milk from the breast; otherwise
mastitis or an abscess may develop.
 If the baby is not able to suckle, help the mother to express her
milk

399
  Help reduce oversupply. If a baby is poorly attached and suckles
ineffectively, the baby may breastfeed more frequently or for a
longer time, stimulating the breast so that more milk is produced
than required. Oversupply may also occur if a mother tries to
make her baby feed from both breasts at each feed, when this is
not necessary. A change has upset the baby:

Figure Figure 10.4: Getting a baby to suckle using a breastfeeding

supplementer (knot in tubing to control flow rate

Changes such as separation from the mother, a new carer, illness of the
mother, or in the family routine or the mother’s smell (due to a different
soap, food or menstruation) can upset the baby and cause refusal to
breastfeed.

 Low-birth-weight and sick infants

 Infants with a birth weight < 2.5 kg need breast milk even more
than larger infants; often, however, they cannot breastfeed
immediately after birth, especially if they are very small.
 For the first few days, an infant may not be able to take oral feeds
and may have to be fed IV. Initiate early feeding with small oral

400
 feeds even on day 1 or as soon as the infant can tolerate enteral
feeds.
 Very low-birth-weight infants (< 1.5 kg) may have to be fed by
naso- or oro-gastric tube during the first days of life. Preferably
give the mother’s expressed breast milk. The mother can let the
infant suck on her cleaned finger while being tube fed. This may
stimulate the infant’s digestive tract and help weight gain.
 Low-birth-weight infants at ≥ 32 weeks’ gestational age can start
suckling on the breast. Let the mother put her infant to the breast
as soon as the infant is well enough. Continue giving expressed
breast milk by cup or tube to make sure that the infant gets all the
nutrition needed.
 Infants at ≥ 34–36 weeks’ gestational age can usually take all that
they need directly from the breast.
 Babies who cannot breastfeed

Non-breastfed babies should receive either:

 Expressed breast milk (preferably from their own mothers)

 Formula milk prepared with clean water according to instructions
or, if possible, ready-made liquid formula
 Replacement feeding using home modified animal milk is not
recommended for infants less than 6 months of age.
 If the child is too weak to suck, feeding can be done with a cup.
 Feed by nasogastric tube if the child is lethargic or severely
anorexic.

401
 Figure 10.5: Feeding
infant with expressed
breast milk using a cup

Nutritional management of sick children

 The principles for feeding sick infants and young children are:
 Continue breastfeeding
 Do not withhold food
 Give frequent small feeds, every 2–3 hours
 Coax, encourage, and be patient
 Feed by nasogastric tube if the child is severely anorexic
 Promote catch-up growth after the appetite returns.
The food provided should be:
 Palatable (to the child)
 Easily eaten (soft or liquid consistency)
 Easily digested
 Nutritious (rich in energy and nutrients).
The basic principle of nutritional management is to provide a diet with
sufficient energy-producing foods and high-quality proteins. Foods with a
high oil or fat content are recommended. Up to 30–40% of the total
calories can be given as fat. In addition, feeding at frequent intervals is
necessary to achieve high energy intakes. If there is concern about the
nutritional content of the food, provide multivitamin and mineral
supplements.

402
The child should be encouraged to eat relatively small amounts frequently.
If young children are left to feed by themselves, or have to compete with
siblings for food, they may not get enough to eat.

A blocked nose, with dry or thick mucus, may interfere with feeding. Put
drops of salted water or saline into the nose with a moistened wick to help
soften the mucus.

In a minority of children who are unable to eat for a number of days (e.g.
due to impaired consciousness in meningitis or respiratory distress in
severe pneumonia), it may be necessary to feed by nasogastric tube. The
risk of aspiration can be reduced if small volumes are given frequently.

To supplement the child’s nutritional management in the hospital, feeding

should be increased during convalescence to make up for any lost weight.
It is important that the mother or carer should offer food to the child more
frequently than normal (at least one additional meal a day) after the child’s
appetite increases.

403
404
405
 Feeding recommendations during sickness and health

Table 10.1: Feeding recommendation during sickness and health in

Ethiopia - For infants up to 6 months of age

Birth up to 6 months

Breastfeed as often as the child wants, day and

night, at least 8 times in 24 hours.
Feed your child only breast milk for the first 6
months, not even giving water.
Empty one breast before switching to the other for your baby to get the
most nutritious hind milk.
During illness and for at least up to 2 weeks after the illness, increase the
frequency of breastfeeding to recover faster.
Expose child to sunshine for 20 to 30 minutes daily.

Table 10.2.Feeding recommendation during sickness and health in Ethiopia - For

infants 6-24 months of age
6-24 months
 Breastfeed as often as the child wants.
 Start complementary foods at 6 months.
 Give adequate servings of freshly prepared and enriched foods; porridge
made of cereal and legume mixes, shirofitfiit, merekfitfit, mashed
potatoes and carrot, mashed gommen, eggs and fruits.
 Enrich the food by adding some oil or butter every time;
give also animal foods (meat, liver, fish, eggs), legumes,
vegetables (green leafy, carrots) and yellow fruits (orange,
papaya, mangos).
 Give these foods 3 times per day if breastfed, 5 times per day if not

406
 breastfed (3 main meals and 2 snacks).
 Babies who stopped breastfeeding at 6 months should also get
adequate milk replacement besides complementary feeding.
 Increase intake of food and fluids during illness, and give one additional
meal of solid food for about 2 weeks after illness for fast recovery.
 Give Vitamin A supplements from the age of 6 months, 2 times per year.
 Expose child to sunshine.

------------------------------------------------------------------------------

 By 6 months of age, all children should be receiving a soft, nutritious

complementary food.
 It is important to actively feed the child. Active feeding means
encouraging the child to eat. The child should not have to compete with
older brothers and sisters for food from a common plate. He should have
his own serving. Until the child can feed himself, the mother or another
caretaker (such as an older sibling, father, or grandmother) should sit
with the child during meals and help get the spoon into his mouth.
 An "adequate serving" means that the child does not want any more
food after active feeding.
 A good daily diet should be adequate in quantity and include an energy-
rich food (for example, soft cereal based porridge with added oil); meat,
fish, eggs, or pulses; and fruits and vegetables.

407
Table 10.3 Feeding recommendation during sickness and health in Ethiopia-
2 years and above

Two years and above

 Breastfeed as often as the child wants.

 Give adequate servings of enriched

family foods: and porridge made of cereal and legume mixes,
shiro, kik, merekfitfit, mashed potatoes and carrot, gommen,
undiluted milk and egg and fruits.

 Add some extra butter or oil to child’s food. Give also animal foods
(meat, liver, fish, eggs), legumes, vegetables (green leafy, carrots)
and yellow fruits (orange, papaya, mangos)

 Give these foods at least 5 times per day (3 meals and 2

snacks/mekses).

 Babies who stopped breast feeding at early age should also get
adequate milk replacement besides complementary feeding.

 Give your baby his/her own servings and actively feed the child

 Give freshly prepared food and use clean utensils

 Increase intake of food and fluids during illness, and give one
additional meal of solid food for about 2 weeks after illness for
fast recovery

 Give Vitamin A supplements and Mebendazole every 6 months

---------------------------------------------------------------------------------

408
 During this period the mother should continue to breastfeed as
often as the child wants and also give nutritious complementary
foods. The variety and quantity of food should be increased.
Family foods should become an important part of the child's diet.
Family foods should be appropriately prepared, so that they are
easy for the child to eat.

 Give nutritious complementary foods or family foods 5 times a

day.

 Adequate servings and active feeding (encouraging the child to

eat) continue to be important.

 Give adequate servings of freshly prepared enriched family foods,

3-4 meals a day.

 Also, twice daily, give nutritious food between meals, such as: Egg,
milk, fruits, kitta, dabo, ripe yellow fruits.

 Give your baby his/her own servings and actively feed the child.

 Give freshly prepared food and use clean utensils.

 Increase intake of food and fluids during illness, and give one
additional meal of solid food for about 2 weeks after illness for
fast recovery.

 Give Vitamin A supplements and Mebendazole every 6 months.

---------------------------------------------------------------------------

409
At this age the child should be taking a variety of family foods in 3 meals
per day. The child should also be given 2 extra feedings between meals
(snacks) per day. These may be family foods or other
nutritious foods which are convenient to give between
meals. Examples are listed on the COUNSEL chart and
below.

10.3 Fluid management

The total daily fluid requirement of a child is calculated with the following
formula: 100 ml/kg for the first 10 kg, then 50 ml/kg for the next 10 kg,
thereafter 25 ml/kg for each subsequent kg. For example, an 8 kg baby
receives 8 x 100 ml = 800 ml per day, a 15 kg child (10 x 100) + (5 x 50) =
1250 ml per day.

Table 10.5 Maintenance fluid requirements

Body weight of child Fluid (ml/day)

2 kg 200 ml/day
4 kg 400 ml/day
6 kg 600 ml/day
8 kg 800 ml/day
10 kg 1000 ml/day
12 kg 1100 ml/day
14 kg 1200 ml/day
16 kg 1300 ml/day
18 kg 1400 ml/day
20 kg 1500 ml/day
22 kg 1550 ml/day
24 kg 1600 ml/day
26 kg 1650 ml/day
Give the sick child more than the above amounts if there is fever (increase
by 10% for every 1°C of fever).

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Monitoring fluid intake
Pay careful attention to maintaining adequate hydration in very sick
children, who may have had no oral fluid intake for some time. Fluids
should preferably be given orally (by mouth or nasogastric tube).

If fluids need to be given intravenously, it is important to monitor closely

any infusion of I.V fluid given to a sick child because of the risk of fluid
overload leading to heart failure or cerebral oedema. If it is impossible to
monitor the I.V fluid infusion closely, then the I.V route should be used only
for the management of severe dehydration, septic shock, the delivery of I.V
antibiotics, and in children in whom oral fluids are contraindicated (such as
in perforation of the intestine or other surgical abdominal problems).

IV maintenance fluids should preferably be isotonic fluids with 5%

dextrose. Possible fluids include isotonic saline and Ringer’s lactate. Do not
give 5% glucose alone for extended periods as this can lead to
hyponatraemia.

Example: to prepare 700 ml of normal saline in 10% dextrose, we need to

add 70 grams of glucose. If the source of glucose is 40 % dextrose, we need
175 ml of 40% dextrose in water. Because of the 175 ml of 40% glucose,
the total fluid becomes 875 ml 10% dextrose in normal saline.

10.4 Management of fever

Temperatures referred to in these guidelines are rectal temperatures,
unless otherwise stated. Oral and axillary temperatures are lower by
approximately 0.5°C and 0.8°C respectively.

Fever is not an indication for antibiotic treatment, and may help the
immune defenses against infection. However, high fever (>39°C or
>102.2°F) can have harmful effects such as:

 Reducing the appetite

 Making the child irritable

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  Precipitating convulsions in some children aged between 6
months and 5 years
 Increasing oxygen consumption (e.g. in a child with very severe
pneumonia, heart failure or meningitis)
 All children with fever should be examined for signs and
symptoms which indicate the underlying cause of the fever, and
should be treated accordingly.

Antipyretic treatment
Paracetamol
Treatment with oral paracetamol should be restricted to children aged ≥ 2
months who have a fever of ≥ 39°C (≥ 102.2°F), and are uncomfortable or
distressed because of the high fever. Children who are alert and active are
unlikely to benefit from paracetamol treatment. The dose of paracetamol is
15 mg/kg 6-hourly.

Ibuprofen
The effectiveness in lowering temperature and the safety of ibuprofen and
acetaminophen are comparable, except that ibuprofen, like any NSAID, can
cause gastritis and is slightly more expensive.

Ibuprofen dose is 10 mg/kg every 6–8 h.

Other agents
Aspirin is not recommended as a first-line antipyretic because it has been
linked with Reye’s syndrome, a rare but serious condition affecting the liver
and brain. Avoid giving aspirin to children with acute viral infections such as
chicken pox.

Other agents are not recommended because of their toxicity and inefficacy
(dipyrone, phenylbutazone).

Supportive care

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Children with fever should be lightly clothed, kept in a warm but well-
ventilated room, and encouraged to increase their oral fluid intake.
Sponging with tepid water lowers the temperature during the period of
sponging only.

10.5 Pain control

Why do we treat pain?
The unchecked release of stress hormones by untreated pain may
exacerbate injury, prevent wound healing, lead to infection, prolong
hospitalization, and even lead to death.

Pain may also persist not only secondary to ongoing injury but rather from
persistent or abnormal excitability in the peripheral or central nervous
system in the absence of ongoing tissue injury; this form of pain is known
as neuropathic.

Assessment of pain in children

Good assessment of pain contributes to the prevention and/or early
recognistion of pain as well as its effective management. Proper pain
assessment requires proper communication skills between the patient/and
or the care taker (the family). There are many pain assessment tools but
their application depends on the age of the child, level of consciousness
and cognitive development.

The three fundamental methods for pain assessment tools are:

Physiological: primarily measuring physiological arousal consequent to

pain. This includes increase in heart rate, blood pressure, respiratory rate,
autonomic symptoms like vomiting, sweating, etc. These are non-specific
and can be signs of other common childhood illnesses and therefore not
usually used for pain management.

Behavioral-observation: measuring behavioral distress associated with

pain. It mostly emphasizes on facial expression, crying and body
movements. Facial expression measurements are most useful and specific.

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We can use FLACC pain scale for children up to 3 years. FLACC scoring
system may be used in children 0-3 years of age and in mechanically
ventilated or cognitively impaired children. It is an acronym that includes
five indicators, each scored as a 0, 1, or 2 that forms a ten point composite
scale with a range from “0” (no pain) to “10” (worst pain).

Table 10.6 behavioral Observation Pain Rating Scale (FLACC scale)

Score: 0 1 2

Face No particular Occasional Frequent to

expression or smile; grimace or constant frown
disinterested frown, clenched jaw;
withdrawn quivering chin

Legs Normal, relaxed Restless or tense Kicking, legs

withdrawn

Activity Quiet, moves easily, Shifting or tense, Rigid, arched,

normal position moving back and jerking
forth

Cry None (awake or Moan, whimper Steady crying,

asleep) screaming,
sobbing, or
frequent
complaints

Consolability Content, relaxed Consolable Inconsolable

(reassured by
occational
touching or
hagging

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Self reporting of pain (measuring expressed experience of pain): mostly
children who are less than 3 years old cannot express their pain. Whenever
feasible, it is preferred to try to get the level of pain from the patient and
trust patients pain, as pain is a subjective experience. It is the best and
golden standard approach.

For children between 3-8 years

They can quantify their pain and are able to translate it to visual
representation. Therefore we use the visual analog scale which quantifies
pain based up on a series of faces in different phases of happiness and
crying. Wong Baker FACES Pain Rating Scale allows ranking the level of pain
by observing the child’s face

Figure 10.5 Pediatric faces scale for rating the intensity of pain

For children 8 years and above

Usually have a word for pain and can articulate more detail about the
presence and location of pain. Therefore verbal rating scale can be used:

415
this is categorical scale for rating pain based on the patient’s description.
The response ranges from no pain to mild and moderate to severe pain.

Management of pain
Non-pharmacological treatment of pain:

 Distraction: is used to direct the child’s attention away from the

pain- various distractive techniques might be used like songs, play
therapies, movies, bubbles, games etc
 Hot or cold therapy: hot or cold application at the source of pain
might be helpful
 Massage therapy: massaging or rubbing is helpful. It enhances a
sense of wellbeing and comfort
 Physical therapy: like exercise, rest, breathing exercise
 Diet: feeding the child with fruits, vegetables etc which are liked
by the child
 Prayer
 Social support: encouragement, keeping the child near peer
groups, story telling, reading books
 Bright or dim light

Use of anti-pains
Analgesics can be divided into three classes:

 Non-opioid (antipyretics)
 Opioid
 Adjuvants
Non-opioid and opioid analgesics both act peripherally and centrally. The
principles governing analgesic use include:

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  By the mouth: the oral route is the standard route for analgesics,
including morphine and other strong opioids.
 By the clock: persistent pain requires preventive therapy.
Analgesics should be given regularly and prophylactically; as
needed (p.r.n.) medication alone is irrational and inhumane.
 By the ladder: use the analgesic ladder. If after optimizing the
dose a drug fails to relieve, move up the ladder, do not move
sideways in the same efficacy group.
Individualized treatment: the right dose is the one which relieves pain;
doses should be titrated upwards until the pain is relieved or undesirable
effects prevent further escalation.
Use of adjuvant drugs: in the context of analgesic ladder these include:
other drugs which relieve pain in specific situations, drugs to control the
undesirable effects of analgesics, concurrently prescribed psychotropic
medications e.g. anxiolytics.
Non- opioid (antipyretic) analgesics

The non-opioid (antipyretic) analgesics include:

 Paracetamol
 Non-steroidal anti-inflammatory drugs (NSAIDS)
Paracetamol
Inhibits cyclo-oxygenase in the CNS. Though it has a peripheral analgesic
effect, it doesn’t have an anti-inflammatory effect in inflamed joints.
Paracetamol is different from NSAIDS in that:

 Side effects are uncommon

 Doesn’t injure the gastric mucosa
 Well tolerated by patients with peptic ulcer
 Doesn’t affect plasma uric acid concentration

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  Has no effect on platelet function
NSAIDS can be used with paracetamol for additive effect. It has a potential
hepatotoxicity.

NSAIDS
Have particular benefit for pains associated with inflammation. Drugs in
this group include: Ibuprofen, diclofenac and naproxen. These drugs inhibit
cyclo oxygenase, an important enzyme in the Arachidonic acid cascade
which results in the production of tissue and inflammatory prostaglandins.
Aspirin, because of its side effects like irreversible platelet dysfunction, is
not recommended.

Adjuvants
Drugs in this group include:

 Corticosteroids
 Antidepressants, anti-epileptics
 NMDA-receptor-channel blockers
 Antispasmodics, muscle relaxants
 Biphosphonates
OPIOID analgesics
Weak opioids

Tramadol: Tramadol is another analgesic with opioid effects that has been
considered for the control of moderate pain. However, there is currently
no available evidence for its comparative effectiveness and safety in
children. Furthermore, tramadol is not licensed for paediatric use in several
countries. More research on tramadol and other intermediate potency
opioids is needed.

Strong opioids: pain is a physiological antagonist to the central depressant

effects of opioids. Strong opioids do not cause clinically important
respiratory depression in patients in pain.

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Morphine is metabolized mainly to morphine-3-glucoronide (M3G) and
morphine-6-glucoronide (M6G). M3G is inactive but M6G is more potent
than morphine. Both glucoronides accumulate in renal failure so the dose
needs to be adjusted.

The recommended analgesic ladder for pain management

Strong opiod + non-opiod + adjuvant

Step 2

Non-opiod (antipyretic) + adjuvant

Step 1

Non-pharmacologic and pharmacologic treatments have to be combined

for an effective pain management.

Pharmacologic treatment of pain using a two-step strategy

Recommendation

It is recommended to use the analgesic treatment in two steps according to

the child’s level of pain severity.

The first step: mild pain

Paracetamol and ibuprofen are the medicines of choice in the first step
(mild pain).

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Table 10.7 Non-opioid analgesics for the relief of mild pain in neonates,
infants and children

The second step: moderate to severe pain

Morphine is the medicine of choice for the second step, although other
strong opioids should be considered and made available to ensure an
alternative to morphine in case of intolerable side-effects.

Opioid analgesics
To obtain a dose that provides adequate relief of pain with an acceptable
degree of side-effects the doses of morphine or other strong opioids need
to be gradually increased until effective. Unlike paracetamol and NSAIDs,
there is no upper dosage limit for opioid analgesics because there is no
“ceiling” analgesic effect. The appropriate dose is the dose that produces
pain relief for the individual child. The goal of titration to pain relief is to
select a dose that prevents the child from experiencing pain between two
doses using the lowest effective dose. This is best achieved by frequent
assessment of the child’s pain relief response and adjusting the analgesic
doses as necessary.

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The opioid dose that effectively relieves pain varies widely between
children, and in the same child at different times, and should, therefore, be
based on the child’s pain severity assessment. Large opioid doses given at
frequent intervals may be necessary to control pain in some children; these
doses may be regarded as appropriate, provided that the side-effects are
minimal or can be managed with other medicines. An alternative opioid
should be tried if patients experience unacceptable side-effects such as
nausea, vomiting, sedation and confusion.

The use of strong opioid analgesics is recommended for the relief of

moderate to severe persisting pain in children with medical illnesses.

Choice of strong opioids

Morphine is recommended as the first-line strong opioid for the treatment

of persisting moderate to severe pain in children with medical illnesses.

There is insufficient evidence to recommend any alternative opioid in

preference to morphine as the opioid of first choice.

Selection of alternative opioid analgesics to morphine should be guided by

considerations of safety, availability, cost and suitability including patient-
related factors.

The strong opioid that we have in Ethiopia is Ethio-morph. It is immediate

release morphine syrup manufactured by EPHARM with different
concentrations (5mg/5ml, 20 mg/5ml, and 50 mg/5ml in 120 ml.

The actual dose for each individual child is the dose that controls pain.

The oral initial dose would be:

 Infants less than 6 months of age 0.02 mg/kg q4h PO.

 Infants/children more than 6 months old 0.15-0.3 mg/kg/dose

every 4 hours

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  The child might require higher doses. The dose could be escalated
by 33-50% depending on the response. If there is breakthrough
pain in between the regular doses, the dose should be 5-15% of
the total 24 hours dose or 50% of the 4 hours dose.
 If there are only 1-3 rescue doses no need of adjustment.
 If there are 4-5 rescue doses, assess and increase the scheduled
dose
Side effects of morphine and their intervention
 Gastric stasis: metoclopramide 10-20 mg q4h
 Sedation: reduce the dose or give methylphenidate 10 mg o.d-b.d
 Agitation, delirium: haloperidol 3-5 mg stat
 Multifocal twitching: diazepam or lorazepam
 Movement induced vomiting: promethazine
 Constipation: start with bisacodyl suppository or cascara tabs.
Use the following local anesthetics for effective pain control:
 Local anaesthetics: for painful lesions in the skin or mucosa or
during painful procedures.
 Lidocaine: apply on gauze to painful mouth ulcers before feeds
(apply with gloves, unless the family member or health worker is
HIV-positive and does not need protection from infection); it acts
in 2–5 minutes.
 Tetracaine: apply to a gauze pad and place over open wounds; it is
particularly useful when suturing

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10.6 Management of anaemia
Anaemia (non-severe)

Young children (aged <6 years) are anaemic if their haemoglobin is 9.3 g/dl
(approximately equivalent to a haematocrit of <27%). If anaemia is present,
begin treatment except if the child is severely malnourished.

Investigation

 CBC, peripheral morphology

 RBC indices if possible
 Stool exam for ova of parasite
If the cause of anemia is iron defficiency
 Give (home) treatment with iron (daily dose of iron/folate tablet
or iron syrup) for 14 days.

 Ask the parent to return with the child after 14 days. Treatment
should be given for 3 months, where possible. It takes 2–4 weeks
to correct the anaemia and 1–3 months after the haemoglobin
reverts to normal to build up iron stores.

If the child is ≥ 2 years and has not had mebendazole in the previous
6 months, give one dose of mebendazole (500 mg) for possible hookworm
or whipworm). Advise the mother about good feeding practices.

Blood transfusion
10.6.1 Storage of blood

Use blood that has been screened and found negative for transfusion-
transmissible infections. Do not use blood that has passed its expiry date or
has been out of the refrigerator for more than 2 hours.

Large volume rapid transfusion at a rate >15 ml/kg/hour of blood stored at

4 ° C may cause hypothermia, especially in small babies.

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10.6.2 Problems in blood transfusion

Blood can be the vehicle for transmitting infections (e.g. malaria,

syphilis, hepatitis B and C, HIV). Therefore, screen donors for as
many of these infections as possible. To minimize the risk, only give
blood transfusions when essential.

10.6.3 Indications for blood transfusion

There are five general indications for blood transfusion:

 Severe anaemia:
 All children with a haematocrit of ≤ 12% or Hb of ≤ 4 g/dl
 Acute blood loss, when 20–30% of the total blood volume has
been lost and bleeding is continuing
 Less severely anaemic children (haematocrit 13–18%; Hb 4–6 g/dl)
with any of the following clinical features
 Septic shock (if IV fluids are insufficient to maintain adequate
circulation and in addition to antibiotic therapy)
 To provide plasma and platelets for clotting factors, if specific
blood components are not available
 Exchange transfusion in neonates with severe jaundice.
10.6.4 Giving a blood transfusion
Before transfusion, check the following:
 The blood is the correct group and the patient’s name and number
are on both the label and the form (in an emergency, reduce the
risk of incompatibility or transfusion reactions by cross-matching
group-specific blood or giving O-negative blood if available)
 The blood transfusion bag has no leaks

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  The blood pack has not been out of the refrigerator for more than
2 hours, the plasma is not pink or has large clots, and the red cells
do not look purple or black
 No sign of heart failure. If present, give 1mg/kg of furosemide IV
at the start of the transfusion in children whose circulating blood
volume is normal. Do not inject into the blood pack.
 In severely malnourished children, fluid overload is a common and
serious complication. Give packed cells where available or whole
blood, 10 ml/kg body weight (rather than 20 ml/kg), once only and
do not repeat the transfusion
 Do a baseline recording of the child’s temperature, respiratory
rate and pulse rate. The volume transfused should initially be 20
ml/kg body weight of whole blood, given over 3–4 hours.
During transfusion:

 If available, use an infusion device to control the rate of the

transfusion
 Check that the blood is flowing at the correct speed
 Look for signs of a transfusion reaction (see below), particularly
carefully in the first 15 minutes of the transfusion
 Record the child’s general appearance, temperature, pulse and
respiratory rate every 30 minutes
 Record the time the transfusion was started and ended, the
volume of blood transfused, and the presence of any reactions.

425
After transfusion:

Reassess the child. If more blood is needed, a similar quantity should be

transfused and the dose of furosemide (if given) repeated.

Giving a blood transfusion: Note: A burette can be used to measure the blood
volume, and the arm is splinted to prevent flexion of the elbow.

10.6.5 Transfusion reactions

If a transfusion reaction occurs, first check the blood pack labels and
patient’s identity. If there is any discrepancy, stop the transfusion
immediately and notify the blood bank.

Mild reactions (due to mild hypersensitivity)

Signs and symptoms:

Itchy rash
Management:
 Slow the transfusion
 Give chlorphenamine 0.1 mg/kg IM, if available

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  Continue the transfusion at the normal rate if there is no
progression of symptoms after 30 minutes
 If symptoms persist, treat as moderate reaction (see below).
 Moderately severe reactions (due to moderate hypersensitivity,
non-haemolytic reactions, pyrogens or bacterial contamination)
Signs and symptoms:

 Severe itchy rash (urticaria)

 Flushing
 Fever >38 ° C (Note: fever may have been present before the
transfusion)
 Rigors
 Restlessness
 Raised heart rate.
Management:

Stop the transfusion, but keep the IV line open with normal saline

 Give IV 200 mg hydrocortisone, or chlorphenamine 0.25 mg/kg IM,

if available
 Give a bronchodilator, if wheezing (see chapter 1).
 Send the following to the Blood Bank: the blood-giving set that
was used, blood sample from another site, and urine samples
collected over 24 hours.
 If there is improvement, restart the transfusion slowly with new
blood and observe carefully
 If no improvement in 15 minutes, treat as life-threatening reaction
(see below), and report to doctor in charge and to the Blood Bank.

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  Life-threatening reactions (due to haemolysis, bacterial
contamination and septic shock, fluid overload or anaphylaxis)
Signs and symptoms:
 Fever >38°C (note: fever may have been present before the
transfusion)
 Rigors
 Restlessness
 Raised heart rate
 Fast breathing
 Black or dark red urine (haemoglobinuria)
 Unexplained bleeding
 Confusion
 Collapse
 Note that in an unconscious child, uncontrolled bleeding or shock
may be the only signs of a life-threatening reaction.
Management:

 Stop the transfusion, but keep the IV line open with normal saline
 Maintain airway and give oxygen (see chapter 1). Give epinephrine
(adrenaline) 0.01 mg/kg body weight (equal to 0.1 ml of 1 in 10
000 solution
 Treat shock (see chapter 1)
 Give IV 200 mg hydrocortisone, or chlorpheniramine 0.1 mg/kg
IM, if available
 Give a bronchodilator, if wheezing

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  Report to doctor in charge and to blood laboratory as soon as
possible
 Maintain renal blood flow with IV furosemide 1 mg/kg
 Give antibiotic as for septicaemia
10.7 Oxygen therapy
Indications: Where available, oxygen therapy should be guided by pulse
oximetry. Give oxygen to children with SaO 2 <90%, and increase oxygen to
achieve a SaO 2 >90%. Where pulse oximeters are not available, the need
for oxygen therapy needs to be guided by clinical signs, which are less
reliable. Where the oxygen supply is limited, priority should be given to
children with very severe pneumonia, bronchiolitis, or asthma who:

 Have central cyanosis, or

 Are unable to drink (where this is due to respiratory distress).
 Where the oxygen supply is more plentiful, it should be given to
children with any of the following:
 Severe lower chest wall indrawing
 Respiratory rate of 70/min or above
 Grunting with every breath (in young infants)
 Head nodding
Sources:
Oxygen supplies should be available at all times. The two main sources of
oxygen are cylinders and oxygen concentrators. It is important that all
equipment is checked for compatibility.

Oxygen cylinders and concentrators

See list of recommended equipment for use with oxygen cylinders and
concentrators and instructions for their use in the WHO technical review
paper, Oxygen therapy in the management of a child with an acute
respiratory infection and the WHO manual Clinical use of oxygen.

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 Oxygen delivery
Three methods are recommended for the delivery of oxygen: nasal prongs,
nasal catheter and nasopharyngeal catheter. Nasal prongs or a nasal
catheter are preferred in most circumstances. Nasal prongs are the best
method for delivering oxygen to young infants and children with severe
croup or pertussis.

Use of a nasopharyngeal catheter calls for close monitoring and prompt

action, in case the catheter enters the oesophagus or other serious
complications develop. The use of face masks or head boxes is not
recommended.

Nasal prongs: These are short tubes inserted into the nostrils. Place them
just inside the nostrils and secure with a piece of tape on the cheeks near
the nose (see figure). Care should be taken to keep the nostrils clear of
mucus, which could block the flow of oxygen.

 Set a flow rate of 1–2 litres/min (0.5 litre/min in young infants) to

deliver an inspired oxygen concentration of 30–35%.
Humidification is not required with nasal prongs.

Figure 10.6: Oxygen therapy: Nasal prongs correctly

positioned and secured.

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Nasal catheter: This is a 6 or 8 FG catheter which is passed to the back of
the nasal cavity. Place the catheter at a distance from the side of the nostril
to the inner margin of the eyebrow.

 Set a flow rate of 1–2 litres/min. Humidification is not required

with a nasal catheter.

40-45% o2 Figure 10.7: Oxygen therapy:

correct position of nasal
catheter (cross-sectional view)

Figure 10.8: A: Measuring the

distance from nose to the
tragus of the ear for the
insertion of a nasopharyngeal
catheter

Figure 10.9: B. Cross sectional

view of the position of the
nasopharyngeal catheter

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Nasopharyngeal catheter: This is a 6 or 8 FG catheter which is passed to
the pharynx just below the level of the uvula. Place the catheter at a
distance equal to that from the side of the nostril to the front of the ear
(see figure B, above). If it is placed too far down, gagging and vomiting and,
rarely, gastric distension can occur.

 Set a flow rate of 1–2 litres/min, which delivers an inspired oxygen

concentration of 45–60%. It is important that this flow rate is not
exceeded because of the risk of gastric distension. Humidification
is required.

Monitoring
Train the nurses to place and secure the nasal prongs or catheter correctly.
Check regularly that the equipment is working properly, and remove and
clean the prongs or catheter at least twice a day.

Monitor the child at least every 3 hours to identify and correct any
problems, including:

 SaO 2 by pulse oximeter

 Nasal catheter or prongs out of position

 Leaks in the oxygen delivery system

 Oxygen flow rate not correct

 Airway obstructed by mucus (clear the nose with a moist wick or

by gentle suction)

 Gastric distension (check the catheter’s position and correct it, if

necessary).

Pulse oximetry
A pulse oximeter is a machine which measures non-invasively the oxygen
saturation in the blood. For this, it transmits a light beam through tissue

432
such as a finger, a toe, or in small children the whole hand or foot. The
saturation is measured in the small arteries, and is therefore referred to as
the arterial oxygen saturation (SaO2). There are reusable probes which last
several months, and disposable ones.

Normal oxygen saturation at sea level in a child is 95–100%; with severe

pneumonia, as oxygen uptake in the lung is impeded, it can drop. Oxygen is
usually given with a saturation <90% (measured at room air). Different cut-
offs might be used at altitude or if oxygen is scarce. The response to oxygen
therapy can be measured with the pulse oximeter as well, as the SaO 2
should increase if the child has lung disease (with cyanotic heart disease,
SaO 2 does not change when oxygen is given). The oxygen flow can be
titrated with the pulse oximeter to obtain a stable SaO 2 >90% without
wasting too much oxygen.

Duration of oxygen therapy

Continue giving oxygen continuously until the child is able to maintain a

SaO 2 >90% in room air. When the child is stable and improving, take the
child off oxygen for a few minutes. If the SaO 2 remains above 90%,
discontinue oxygen, but check again 1/2 hour later, and 3 hourly thereafter
on the first day off oxygen to ensure the child is stable. Where pulse
oximetry is not available, the duration of oxygen therapy is guided by
clinical signs, which are less reliable.

10.8 Toys and Play Therapy

Each play session should include language and motor activities, and
activities with toys.

Language activities
Teach the child local songs. Encourage the child to laugh, vocalize and
describe what he or she is doing.

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Motor activities
Always encourage the child to perform the next appropriate motor activity.

Activities with toys

Ring on a string (from 6 months)

Thread cotton reels and other small objects (e.g. cut from the neck of
plastic bottles) on to a string. Tie the string in a ring, leaving a long piece of
string hanging.

Figure 10.10: Ring on a string

(from 6 months)

Figure 10.11: Blocks (from 9 months) Small

blocks of wood: Smooth the surfaces with
sandpaper and paint in bright colors, if possible.

Figure 10.12: Nesting toys (from 9

months).Cut off the bottom of two bottles of
identical shape, but different size. The smaller
bottle should be placed inside the larger

Figure 10.13 In-and-out toys (from 9 months).

Any plastic or cardboard container and small
objects (not small enough to be swallowed)

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Figure 10.14: Rattle (from 12 months)Cut long strips of plastic
from colored plastic bottles. Place them in a small transparent
plastic bottle and glue the top on firmly.

Figure 10.15 Doll (from 12 months)

Cut out two doll shapes from a piece of cloth
and sew the edges together, leaving a small
opening. Turn the doll inside-out and stuff with
scraps of materials. Stitch up the opening and
sew or draw a face on the doll.

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436
CHAPTER 11 - MONITORING THE CHILD’S PROGRESS

Monitoring is a regular follow up of treatment out comes for patients

under medical care. It starts from the time when patients present to the
health facility seeking care.

11.1 Monitoring procedures

In order for monitoring to be effective, the health worker needs to know:

 the correct diagnosis of the illness

 the importance of shared confidentiality
 the correct management protocol and administration of the
treatment
 the expected progress of the child
 the possible adverse effects of the treatment
 the complications that may arise and how these can be identified
 the possible alternative diagnoses in a child not responding to
treatment
 the importance of parental involvement in the management of the
child
 the importance of complete documentation of findings
Children treated in hospital should be checked regularly so that any
deterioration in their condition, as well as complications, adverse effects of
treatment, or errors in the administration of treatment can be identified
promptly. The frequency of monitoring depends on the severity and nature
of the illness.

Details of the child’s condition and progress should be recorded so that the
documents can be reviewed by other members of staff. A senior health

437
worker who is responsible for the care of the child, and has the authority to
change treatment, should supervise these records and examine the child
on a regular basis.
Children who are seriously ill should be visited if possible by a senior health
professional soon after the child’s admission to hospital. These visits should
also be seen as an opportunity to encourage communication between the
families of sick children and hospital staff.

11.2 Monitoring chart

A monitoring chart should include the following items.

1. Patient’s details
2. Vital signs (Temperature, Respiratory Rate, Pulse Rate, Blood
Pressure)
3. Anthropometry (Weight, Height, Head Circumference)
4. Relevant systemic findings
5. Level of consciousness, coma score (AVPU)
6. Fluid balance (input/output measurement)
7. Clinical diagnosis: presence of clinical signs and complications. At
each review of the child, record whether these signs are still
present. Record any new signs or complications and progressive
assessment.
8. Treatments given
9. Investigation findings
10. Adverse events of treatment (if any).
11. Feeding/nutrition (type, amount, frequency, any feeding problems
( see Chapter 7&10)
12. Outcome on discharge, advice and follow-up

438
11.3 Quality and audit of paediatric care

Quality of health service is defined as “the degree to which health services

for individuals and populations increase the likelyhood of achieving desired
health outcomes and are consistent with current professional knowledge”.
It is becoming a public health concern in many countries including Ethiopia.

All stakeholders (government administrators, funding agencies,

beneficiaries and providers) are raising quality as a policy and basic right
issues.

Quality is determined by structural (administrative competencies, provision

of necessary inputs, etc) and technical (staff competency, motivation, etc)
factors. Ethiopia has started quality improvement as an essential element
of health services while the country is undergoing a rapid and voluminous
expansion of health services to improve the coverage and access. Quality of
service must be the concern in every unit/department in health institutions
including pediatrics units (OPD, in patient unit, etc).

The quality of care given to sick children in hospital can be improved if

there is a system for reviewing the outcomes of each child admitted to the
hospital. At a minimum, the system should keep records of all children who
died in the hospital. Trends in case fatality rates over time can then be
compared, and the treatment given can be discussed by all staff with the
aim of identifying any problems and devising solutions. Clinical audit
meetings to discuss near-death events or deaths in children, especially
those in which some aspect of treatment might have gone wrong, can also
be helpful. The aim is to improve care and solve problems, not to attribute
blame for errors.

An audit of hospital paediatric care can be carried out by comparing the

quality of care actually given with a recognized national standard, such as
the recommendations contained in this pocket book. A successful audit
calls for the full and constructive participation of all medical and nursing
staff.

439
 The audit should be simple and not take up too much time, which
is required for caring for the sick children.

 One suggestion is to ask medical and nursing staff for their views
on improving the quality of care, and to give priority to these
conditions or problems.

 Communication among hospital administration, pediatrics care

team and client is of paramount importance to improve the
quality of pediatrics care.

 There must be an understanding of the fact that proper

documentation of child’s medical information (clinical evaluation,
treatment and progress) is part and parcel of a good quality
pediatrics care.

440
CHAPTER 12 - COUNSELING AND DISCHARGE FROM HOSPITAL

The discharge process for all children should include:

 Correct timing of discharge from hospital

 Counseling the mother on treatment and feeding of the child at

home

 Ensuring that the child’s immunization status and record card are
up-to-date

 Communicating with the health worker who referred the child or

who will be responsible for follow-up care

 Giving instructions on when to return to the hospital for follow-up

and on symptoms and signs indicating the need to return urgently.
Written instruction for medication type , dose and duration of
treatment

 Assisting the family with special support (e.g. providing equipment

for a child with a disability, or linking with community support
organizations for children with HIV/AIDS)

12.1 Timing of discharge from hospital

In general, in the management of acute infections, the child can be
considered ready for discharge after the clinical condition has improved
markedly (afebrile, alert, eating and sleeping normally) and oral treatment
has been tolerated.

Decisions on when to discharge should be made on an individual basis,

taking into consideration a number of factors, such as:

 The family’s home circumstances and how much support is

available to care for the child

441
  The staff’s judgment of the likelihood that the treatment course
will be completed at home

 The staff’s judgment of the likelihood that the family will return
immediately to the hospital if the child’s condition should worsen

Timing of discharge of the child with severe malnutrition is particularly

important and is discussed separately (See Chapter 7). In every case, the
family should be given adequate and convincing information as to the
discharge date so that appropriate arrangements can be made to support
the child at home.

If the family wants to take the child prematurely against the advice of the
hospital staff, every effort must be made to counsel the mother on how to
continue treatment at home and encourage her to bring the child for
follow-up after 1–2 days, and to make contact with the local health worker
for help in the follow-up care of the child.

12.2 Counseling
Counseling of the caregivers is integral part of the comprehensive care
delivered to any sick child. Counseling needs time, concern to parental
feelings, empathy and recognizing the understanding level of parents.
Counseling must be participatory and may be done repeatedly. Messages
must be brief and easy to remember. Communication skill of health
workers is of paramount importance in delivering a proper counseling.
Older children can be involved in the counseling process. Tools for
counseling will help facilitate communication and can build confidence for
the caregivers. During counseling provide an effective interpreter if
language is a barrier

Mother’s Card
A simple, pictorial card reminding the mother of home care instructions,
when to return for follow-up care, and the signs indicating the need to
return immediately to the hospital can be given to each mother. Mother’s

442
Card will help her to remember the appropriate foods and fluids, and when
to return to the health worker.

Appropriate Mother’s Cards are already developed as part of training for

Integrated Management of Neonatal and Childhood Illness (IMNCI) in the
country.

When reviewing the Mother’s Card with the mother:

 Hold the card so that she can easily see the pictures, or allow her
to hold it herself.

 Point to the pictures as you talk, and explain each one; this will
help her to remember what the pictures represent.

 Mark the information that is relevant to the mother. For example,

put a circle round the feeding advice for the child’s age, and round
the signs to return immediately. If the child has diarrhoea, tick the
appropriate fluid(s) to be given. Record the date for the next
immunization.

 Watch to see if the mother looks worried or puzzled. If so,

encourage questions.

 Ask the mother to tell you in her own words what she should do at
home. Encourage her to use the card to help her remember.

 Give her the card to take home. Suggest she show it to other
family members. (If you do not have a large enough supply of
cards to give to every mother, keep several in the clinic to show to
mothers.)

12.3 Nutrition counseling

For HIV counseling, see chapter 8
Identifying feeding problems

443
First, identify any feeding problems which have not been fully resolved.

Ask the following questions:

 Do you breastfeed your child?

 How many times during the day?
 Do you also breastfeed during the night?
 Does the child take any other food or fluids?
 What food or fluids?
 How many times a day?
 What do you use to feed the child?
 How large are the servings?
 Does the child receive his/her own serving?
 Who feeds the child and how?
Compare the child’s actual feeding with the recommended guidelines for
feeding a child of that age (see chapter 10). Identify any differences and list
these as feeding problems.

In addition, consider:

 Difficulty in breastfeeding
 Use of a feeding bottle
 Lack of active feeding
 Not feeding well during the illness
Advise the mother how to overcome problems and how to feed the child.
Counsel the mother to give locally appropriate energy-rich and nutrient-
rich complementary foods. Even when specific feeding problems are not
found, praise the mother for what she does well. Give her advice that
promotes:

444
Breastfeeding

Improved complementary feeding practices using locally available energy-

and nutrient-rich foods
 Giving nutritious snacks to children aged >2 years.
 Examples of nutritionally adequate diets (see chapter 10)
12.4 Home treatment
 Use words the mother understands.

 Use teaching aids that are familiar (e.g. common containers for
mixing ORS).

 Allow the mother to practice what she must do, e.g. preparing
ORS solution or giving an oral medication, and encourage her to
ask questions.

 Give advice in a helpful and constructive manner, praising the

mother for correct answers or good practice.

 Teaching mothers is not just about giving instructions. It should

include the following steps:

o Give information: Explain to the mother how to give the

treatment, e.g. preparing ORS, giving an oral antibiotic, or
applying eye ointment.

o Show an example: Show the mother how to give the

treatment by demonstrating what to do.

o Let her practice: Ask the mother to prepare the medicine or

give the treatment while you watch her. Help her as needed,
so that she does it correctly.

445
 o Check her understanding: Ask the mother to repeat the
instructions in her own words, or ask her questions to see
that she has understood correctly.

12.5 Checking the mother’s health

If the mother is sick, provide treatment for her and help to arrange follow-
up at a first-level clinic close to her home. Check the mother’s nutritional
status and give any appropriate counseling. Check the mother’s
immunization status and, if needed, arrange so that she can get tetanus
toxoid. Make sure the mother has access to family planning, birth spacing
and counseling about preventing sexually-transmitted diseases and HIV. If
the child has tuberculosis, the mother should also be investigated for TB
including having chest X-ray.

12.6 Checking immunization status

Ask to see the child’s immunization card, and determine whether all the
immunizations recommended for the child’s age have been given. Note any
immunizations the child still needs and explain this to the mother; then
carry them out before the child leaves hospital and record them on the
card.
Recommended immunization schedule:

Table 12.1 National EPI vaccines and schedule

Age Vaccine

Birth BCG and OPV0

6 weeks DPT1-HepB1-Hib1,rota , pneumococcal and OPV1

10 weeks DPT2-HepB2-Hib2,rota, pneumococcal and OPV2

14 weeks DPT3-HepB3-Hib3 pneumococcal and OPV3

9 months Measles* and Vitamin A

446
*In exceptional situations give an extra dose of measles vaccine at 6
months of age for groups at high risk of measles death, such as infants in
refugee camps, child with severe acute malnutrition and infants affected by
disasters and during outbreaks of measles.

Contraindications
It is important to immunize all children, including those who are sick and
malnourished, unless there are contraindications. There are only 3
Contraindications to immunization:

Do not give BCG vaccines to a child with symptomatic HIV infection/AIDS,

but do give the other vaccines.

 Give all immunizations, including BCG to a child with

asymptomatic HIV infection.

 Do not give DPT-2 or -3 to a child who has had convulsions or

shock within 3 days of the most recent dose.

 Do not give DPT to a child with recurrent convulsions or an active

neurological disease of the central nervous system.

A child with diarrhoea who is due to receive OPV should be given a dose of
OPV. However, this dose should not be counted in the schedule. Make a
note on the child’s immunization record that it coincided with diarrhoea, so
that the health worker will know this and give the child an extra dose
during the next visit.

12.7 Communicating with the first-level health worker

Information needed
The first-level health worker who referred the child to hospital should
receive information about the child’s care in hospital, which should include:

 Diagnosis/diagnoses
 Treatment(s) given (and duration of stay in hospital)

447
  Response of the child to this treatment
 Instructions given to the mother for follow-up treatment or other
care at home
 Other matters for follow-up (e.g. immunizations).

These details should be recorded in a short note for the mother and
health worker on the referral slip as a feedback. If there is further
information that is important to be told to the health worker,
telephone communication can be used if applicable.
12.8 Providing follow-up care
Children who do not require hospital admission but can be treated at home

Advise all mothers who are taking their children home, after assessment in
the hospital, when to go to a health worker for follow-up care. Mothers
may need to return to hospital:

 For a follow-up visit in a specific number of days (e.g. when it is

necessary to check progress or the response to an antibiotic)

 If signs appear that suggest the illness is worsening

 For the child’s next immunization.

It is especially important to teach the mother the signs indicating the need
to return to hospital immediately. Guidance on the follow-up of specific
clinical conditions is given in appropriate sections of this pocket book.

Follow-up for feeding and nutritional problems

 If a child has a feeding problem and you have recommended

changes in feeding, follow up in 5 days to see if the mother has
made the changes, and give further counseling if needed.

 If a child has anaemia, follow up in 14 days to give more oral iron

448
  Use also follow up schedule after management of severe acute
malnutrition.

When to return immediately

Advise the mother to return immediately if the child develops any of the
following signs:

 Not able to drink or breastfeed

 Becomes sicker
 Develops a fever
 Signs of illness return again after successful treatment in hospital
 In a child with a cough or cold: fast or difficult breathing
 In a child with diarrhoea: blood in stool or drinking poorly

Next well-child visit

Remind the mother about the child’s next visit for immunization and record
the date on the Mother’s Card or the child’s immunization record.

449
ANNEX 1: Practical Procedures

450
451
452
453
454
455
456
457
458
459
460
461
462
463
464
465
466
467
468
ANNEX 2: Drug dosages and regimens

469
470
471
472
473
474
475
476
477
478
479
480
481
482
483
484
485
486
487
488
489
ANNEX 3: Eguipment Sizes

490
ANNEX 4: Intravenous fluids

491
492
ANNEX 5: Assessing nutritional status

493
494
495
496
497
498
499
500
501
502
503
504
505
506
507
508
509
510
511
512
513
514
515
516
ANNEX 6: BP Levels for Boys and Girls

517
518
519
520
Inderx
A
B
abdominal distension, 190, 210, 365,
382, 385, 387, 388 BCG, 123, 130, 178, 446, 447
abdominal pain, 209, 211, 252, 253, benzathine penicillin, 167
382, 384, 385 benzyl penicillin, 367
Abdominal tenderness, 216 benzylpenicillin, 248
abscess, 140, 161, 162, 172, 177, Birth trauma, 118
218, 221, 253, 254, 255, 383, 384, Bitot’s spot, 279
389, 392, 399 Bleeding, 282, 375
acidosis, 120, 231 blood transfusion, 172, 230, 359,
adrenaline, 149, 154, 156, 157, 428 424, 426
AIDS, X, 177, 178, 441, 447 bowel obstruction, 176, 364, 385
Airway management, 174 breast feeding, 119, 148, 302, 307,
airway obstruction, 150, 164, 165, 395, 408
166, 167, 171, 358, 372 Bronchiectasis, 172
aminophylline, 156 bronchiolitis, 148, 150, 151, 429
amoebiasis, 203, 211 bronchodilators, 148, 150, 154, 155,
amoxicillin, 137, 258, 357 156, 158, 160, 171
ampicillin, 137, 185, 251, 258, 356, Brucellosis, 222
357, 367, 376, 383, 386, 388, 389 Bull neck, 162
anemia, 187, 231, 253, 292, 355, Burns, 370
372, 375, 423
antibiotics, 190, 203, 204, 207, 210, C
238, 289, 296, 297, 298, 356, 373,
375, 377, 382, 383, 386, 388, 411 Candidiasis, 295, 297
Appendicitis, 383 Cardiac failure, 132, 222
Artemether, 227 catch-up growth, 402
arthritis, 217, 221, 391 Ceftriaxone, 239, 253, 296
asphyxia, 183 chest drainage, 144, 145
aspirin, 412 chest indrawing, 149
asthma, 130, 147, 148, 150, 154, chest X-ray, 63, 133, 134, 136, 138,
159, 170, 171, 429 139, 144, 153, 160, 172, 178, 184,
atropine, 147, 294 186, 222, 279, 446
chloramphenicol, 173, 260, 294, 296
chloroquine, 233

521
chlorpheniramine, 428 dexamethasone, 164
cholera, 188, 189, 190, 194 diarrhea, 61, 188, 190, 191, 247, 284
ciprofloxacin, 257 diazepam, 175, 224, 244
Cleft lip, 117, 363 difficult breathing, 129, 132, 136,
cloxacillin, 138, 251, 373, 376, 377, 148, 449
389, 392 digoxin, 187
club foot, 117, 368 discharge from hospital, 244, 441
codeine, 147
coma, 229, 230, 248, 251, 253 E
congenital heart disease, 185, 356,
397 empyema, 133, 136, 138, 144
Congenital syphilis, 121 encephalopathy, 175
Conjunctivitis, 110, 247 endocarditis, 185, 222, 356
Convulsions, 175, 212, 230, 244, 248 epinephrine, 137, 149, 154, 155,
Corneal clouding, 219, 245 156, 157, 428
corneal ulceration, 278 Erythromycin, 261
cotrimoxazole, 173, 210, 258, 296 ethambutol, 181
cough, 61, 129, 132, 133, 135, 147,
150, 154, 160, 161, 162, 163, 170, F
171, 172, 173, 174, 176, 177, 183,
217, 245, 249, 278, 301, 382, 449 F-100, 300, 302, 303, 307, 308
counseling, 63, 441, 442, 443, 446, F-75, 283, 290, 300, 302
448 febrile illness, 252
croup, 161, 162, 163, 164, 165, 246, Fever, 132, 150, 161, 162, 216, 217,
430 221, 247, 249, 259, 282, 362, 383,
cyanosis, 116, 119, 129, 130, 132, 389, 392, 411
133, 136, 149, 161, 171, 173, 174, Fluid management, 361, 410
187, 232, 429 fluid overload, 185, 243, 411, 425,
428
follow-up care, 276, 441, 442, 448
D foreign body aspiration, 171
dehydration, 61, 173, 188, 189, 190, fractures, 118, 377, 378, 381, 390
191, 192, 193, 194, 195, 196, 199,
200, 202, 203, 204, 206, 207, 209, G
210, 211, 231, 246, 248, 251, 253,
259, 278, 282, 284, 285, 301, 365, Gentamicin, 296
366, 385, 411 gentian violet, 247, 295, 373, 399

522
giardiasis, 204
J
glomerulonephritis, 185, 186
glucose, X, 63, 116, 117, 118, 119, jaundice, 214, 424
120, 121, 144, 203, 206, 231, 232,
238, 243, 293, 300, 356, 359, 361, K
365, 366, 372, 382, 411
keratomalacia, 278

H Ketamine, 357
kwashiorkor, 277, 278, 311
Haemophilus, 239
heart failure, 120, 167, 186, 224, L
288, 289, 290, 292, 411, 412, 425
hernia, 120, 386, 387 lumbar puncture, X, 238
herpes zoster, 172 lumefantrine, 227, 233
hip, 117, 222, 367, 368, 392
hypoglycemia, 116, 290, 294 M
Hypothermia, 120, 282, 290, 359
malaria, 63, 132, 223, 225, 231, 233,
292, 297, 362, 424
I malnutrition, XI, 173, 176, 178, 185,
immunization, X, 130, 133, 165, 171, 188, 190, 207, 210, 246, 276, 277,
176, 219, 441, 443, 446, 447, 448, 282, 283, 285, 292, 293, 388, 393,
449 397, 442, 449
IMNCI, 61, 443 marasmus, 277, 311
injections, 181, 361, 373 Mastoiditis, 217, 254
intracranial pressure, 236, 380 Measles, 219, 244, 247, 299, 446
intravenous fluids, 286, 288, 356, Mebendazole, 299, 408
361, 366, 382, 383, 388 meningitis, 82, 177, 178, 219, 229,
intubation, 164, 166, 167, 358, 372 238, 244, 252, 254, 255, 403, 412
intussusception, 384, 385, 386 Meningococcal infection, 219
iron, 298, 355, 374, 423, 448 metronidazole, 203, 204, 248, 356,
isoniazid, 123 376, 383, 386, 388, 389
IV fluids, 185, 187, 243, 289, 290, miliary tuberculosis, 133, 141
356, 361, 362, 424 mineral supplements, 402
Monitoring chart, 438
Morphine, 361
MUAC, 276, 306, 309, 313
Myelomeningocele, 366

523
myocarditis, 165, 167, 185, 187 penicillin, 121, 122, 166, 238, 239,
260, 261, 357, 373
N pericarditis, 185
pertussis, X, 147, 170, 172, 173, 175,
nasal catheter, 174, 430, 431, 432 176, 430
nasal flaring, 136 pharyngeal membrane, 161, 162
nasal prongs, 120, 164, 166, 174, Phenobarbital, 230
430, 432 Plan A, 191, 207, 211
nasogastric tube, 93, 138, 174, 175, Plan B, 191, 199, 201
243, 248, 253, 362, 365, 366, 382, Plan C, 191, 193, 201
384, 385, 388, 401, 402, 403, 411 Plasmodium falciparum, 223
necrotizing enterocolitis, 365 play therapy, 317
neonatal resuscitation, 65 Pleural effusion, 144
Nutritional management, 212, 393, Pneumococcus, 239
402 PPD skin test, 178
nystatin, 295, 399 Pyrazinamide, 181

O Q
oedema, 162, 186, 212, 232, 285, quinine, 226, 227
294, 296, 301, 302, 303, 306, 308,
309, 310, 311, 313, 411
R
oral polio vaccine, X
Oral thrush, 172 Ready to Use Therapeutic Food, XI
Osteomyelitis, 217, 221, 390 rectal prolapse, 209, 212
Otitis media, 217, 247 relactation, 204
Oxygen therapy, 136, 429, 430, 431 ReSoMal, XI, 285, 287
respiratory distress, 62, 120, 121,
P 122, 129, 130, 133, 136, 149, 151,
152, 153, 154, 155, 156, 160, 161,
pain control, 373, 422 175, 185, 187, 372, 403, 429
palmar pallor, 131, 132, 186, 278 rheumatic fever, 185
Paracetamol, 137, 412 Ringer's lactate, 359, 361, 372
paraldehyde, 175 RUTF, XI, 298, 300, 302, 303, 304,
parotitis, 172 305, 306, 307, 310
PCP, X, 133

524
 S tuberculosis, XI, 123, 129, 139, 145,
147, 172, 176, 177, 178, 182, 184,
Salbutamol, 157 222, 278, 390, 397, 446
Salmonella, 221, 250, 390 typhoid, 252
sepsis, 65, 122, 203, 207, 210, 297, typhus, 219, 252
365
septic shock, 289, 411, 424, 428 U
shock, 251, 252, 253, 278, 285, 288,
289, 360, 428, 447 unconscious child, 231, 242, 428
Skin infection, 172 urinary tract infection, XI, 203, 207
skin pinch, 189, 191, 192, 194, 196
some dehydration, 192, 196 V
spacer device, 137, 149, 156, 157
steroids, 160, 256 Vitamin A, 246, 249, 296, 309, 406,
stiff neck, 214, 236, 252 408
stridor, 133, 146, 161, 162, 163, 165,
171, 183, 246 W
sulfamethoxazole, XI, 258
supportive care, 146, 155, 163, 173, wheeze, 133, 137, 148, 149, 150,
176, 355 151, 154, 170, 171, 183, 184
surface area, 370 wound care, 374
surgical problems, 355, 362, 370
X
T xerophthalmia, 279
tracheostomy, 163, 166, 167, 184,
372 Z
transfusion reactions, 424
trimethoprim, XI, 258 zinc, 188, 194, 201, 208, 210, 295

525