NBSU Participants Module PDF
NBSU Participants Module PDF
NBSU Participants Module PDF
Newborn
StabiliZation Unit Training
PARTICIPANTS’ MODULE
2020
Dr HarshDr
Vardhan
Harsh Vardhan
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t; foKku Dr Harsh Vardhan
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Union Minister for Health & Familyfor
Union Minister Welfare,
Health & Family Welfare,
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Union Minister for Health &
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Vikas, Sabka Vishwas Government of India
Message
It gives me immense pleasure to commemorate the National Newborn Week from 15th to 21st
November, 2020 and launch the training module on "Newborn Stabilization Units (NBSUs)" for
optimal management of newborn care at First Referral Units (FRU).
The health of children including newborns continues to be of highest priority to our Government.
We are committed to reducing Neonatal Mortality Rate to single digit by the year 2030 - a target which
has been much appreciated globally and is more ambitious than the targets set under Sustainable
Development Goals.
I am also happy to note that to provide quality services to newborns at FRUs, my Ministry has
developed a training module for NBSUs. I am sure this will help doctors and nurses to acquire essential
knowledge and skills for optimal care of neonates thereby improving health status of newborns.
I wish all the best and hope this module will work as a good resource for capacity building of our
healthcare personnel.
348, - 110011 • Office: 348, A-Wing, Nirman Bhawan, New Delhi - 110011
Tele.: (0): +91-11-23061661, 23063513 • Telefax: 23062358 • E-mail: hfwminister@gov.in, hfm@gov.in
- 110011 • Residence: 8, Tees January Marg, New Delhi -110011
Tele.: (R): +91-11-23794649 • Telefax. 23794640
MINISTER OF STATE FOR
HEALTH & FAMILYMINISTER
WELFAREOF STATE FOR
HEALTH
GOVERNMENT OF INDIA& FAMILY WELFARE
GOVERNMENT OF INDIA
Ashwini Kumar Choubey
shwini Kumar Choubey
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MINISTER OF STATE FOR
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HEALTH & FAMILY WELFARE
GOVERNMENT OF INDIA
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Message
The Ministry of Health and Family Welfare, Govt. of India has implemented a number of policies and programmes aimed at
ensuring universal access to health coverage and reducing child and neonatal mortality.
Under the umbrella of RMNCAH+N strategy in National Health Mission, Child Health have always been of high priority.
In 2014, the Government of India launched the India Newborn Action Plan (INAP) in order to intensify the efforts towards
improving newborn health. INAP has successfully brought a sharper focus on implementation of the existing and new
initiatives for the newborns both for their survival and subsequent growth and development.
To fulfill the role of providing quality service for newborn care in the health facilities, Ministry of Health and Family Welfare,
Government of India has developed training packages for Newborn Stabilization Units. Capacity building of the service
providers are of utmost importance as newborn care and survival necessitate knowledge and skills of high order in the
providers.
I would like to express my heartfelt appreciation to all those who contributed to the preparation of these documents. I am
sure that these packages will help in delivering newborn health services with quality care, all across the country.
Message
Childhood and infant mortality in India has reduced substantially during the last decade, but the rate of neonatal
mortality continues to remains high. Nearly two-thirds of infant deaths each year occur within the first four weeks of life
and about two-thirds of these occur within the first week itself. Thus, the first few days and weeks of life are extremely
critical for survival of a child. Therefore, newborns must be provided special attention during their birth for a healthy and
safe start to life.
India Newborn Action Plan envisages that the country will make all possible endeavors and attain the target of
single digit newborn mortality by 2030, a target which is more ambitious than even the corresponding global SDG target.
Effective and quality Newborn care is a critical challenge faced by every health care setting dealing in child birth and child
care. Building capacities of Doctors, Nurses and ANMs to improve quality of services in low resource settings remains a
challenge but is urgently required for our country.
Newborn Stabilization Units (NBSUs) are an important part of the facility based newborn care at the first referral units
to provide basic stabilization and feeding support to babies delivered at the facility and to sick and small babies referred to
the facilities from outside. The NBSU training package has been developed with an aim to empower the health care providers
with essential knowledge and skills for optimal management of any newborn presenting at NBSU. This aims to bring about
the desired changes in quality of services at these units established at the sub district level.
I am sure that the NBSU training package will act as an enabling tool for health care providers. Functionalization
of the NBSUs will result in effective utilization of resources and contribute in a significant way to reduce preventable
mortality in the country.
(Rajesh Bhushan)
As a part of the Reproductive, Maternal, Newborn, Child, Adolescent Health and Nutrition (RMNCAH+N) strategy
of the National Health Mission, newborn health has always been at priority. A well-defined multi level care system for
newborn care at public health facilities has been scaled up massively and is supported by community level interventions.
Health systems strengthening over the last 15 years has brought about considerable improvement in the infrastructure,
availability of human resources, availability of drugs & equipment along with ancillary services.
Under facility based newborn care, “Newborn Stabilization Units” at the first referral units have been part of the care
system since 2011. However, these units continue to remain underutilized, one of the main reasons being the lack of
confidence and poor skills of healthcare providers working in these units. As a part of the strategy to revitalize these units,
a new “NBSU Training Package” for both doctors and nurses has been developed by the Child Health Division, GoI with
technical support from the Norway India Partnership Initiative (NIPI), technical experts and other development partners.
I do hope that this new package will be rolled out across the States and UTs to reinvigorate the facility based newborn care
system and pave way towards strengthening of timely and quality care for the newborns, closer to their homes.
(Vandana Gurnani)
Foreword
With the National Health Policy-2017 and the India Newborn Action Plan, India is committed to accelerate reduction in
the newborn deaths by more than half, by the year 2030. Newborn health occupies the centre-stage in the Reproductive,
Maternal, Newborn, Child Health, Adolescent Health and Nutrition (RMNCAH+N) strategy and inter linkages between
various components have a significant impact on the mortality and morbidity rates of a newborn.
Under the National Health Mission, newer interventions and improved service delivery platforms have been included in
the newborn health programme over a period of time. This mandates a review of existing training packages and strategies
in order to incorporate these new topics and skills sets emerging out of new evidences and technological advances which
will work towards improving the quality of care at the health facilities.
With this background, the Child Health Division along with the support of technical experts and development partners
including NIPI, has developed a “NBSU Training Package” for training of doctors and nurses working in the Newborn
Stabilization Units (NBSU). Until now, the Facility Based IMNCI package was being used for this purpose. This new
package equips both doctors and nurses to deliver interventions for management and stabilization of small and sick
newborns. It is further envisioned that these units will play a key role in scaling up Kangaroo Mother Care Services, one
of the most effective interventions , to save lives of preterm and low birth weight babies.
I do hope that by adopting this training package, a large number of babies will receive quality care at the sub district level
thus preventing referral and overburdening of district level facilities, resulting in improvement of neonatal survival to a
great extent.
Acknowledgement
India witnessed a consistent and sharp decline in maternal and child mortality in comparison to global averages since
the inception of National Health Mission (NHM). India’s newborn mortality has reduced by more than one-third in the
last decade. With the National Health Policy 2017 in place and with sight on the Sustainable Development Goal agenda,
the opportunity now is to build upon the gains made in the last decade, accelerate and sustain the pace of improvement.
In order to scale up the implementation of the facility based newborn care programme, at New Born Stabilization Units
(NBSUs) at sub district level, it was a felt need that a training package should be designed exclusively for training of the
health care providers to deliver full set of services at the NBSUs. Accordingly, the Child Health Division along with the
technical support from the Norway India Partnership team has developed the “NBSU Training Package” for doctors and
nurses to equip them with the necessary technical knowledge and skills for provision of quality care to small and sick
newborns in these units.
I sincerely thank my colleagues Dr. Ajay Khera, Ex-Commissioner MCH & Dr. P. K. Prabhakar, Ex- JC, Child Health, for
starting the process. I specially acknowledge the efforts of Dr. Harish Kumar, Dr. Harish Chellani, Dr. Renu Srivastava,
Dr. Deepti Agrawal and NIPI team for their assistance in the development of this package.This was an intensive process that
required a lot of brainstorming and deliberations. I would therefore take this opportunity to thank all the academicians,
technical experts from NCC, State Programme officers, Child Health Division officers and consultants who participated
in the discussions and shared their valuable experiences and suggestions.
As a next step, I will urge the State / UTs, to roll out this package at the earliest. Concerted, consistent efforts of all
concerned stakeholders are solicited for achieving significant decrease in neonatal mortality.
CHAPTER 2
Referral and Transport of Sick Babies & Communication with the Family / 41
CHAPTER 3
Assessment of Newborns for Admission in NBSU / 49
CHAPTER 4
Supportive Care / 59
CHAPTER 5
Management of Jaundice and Sepsis in Newborn / 73
5.1: Management of Jaundice / 75
5.2: Management of Sepsis in Newborn / 81
CHAPTER 6
Postnatal Care of the Newborn in the Health Facility / 87
SKILL STATIONS / 95
ANNEXURE
Annexure 1: Examination of Newborn from head to toes for Common Birth Defects / 125
Annexure 2: NBSU Stationery and Formats / 127
Annexure 3: Mentoring Checklist / 142
CHAPTER 1
Assessment & Management of
Newborns with Emergency Signs
INTRODUCTION
Newborn Stabilization Units (NBSU) are an important part of the facility based newborn care. They
have been established at the sub district level (First Referral Unit/Community Health Centre) in order to
provide facility based newborn care to babies delivered at the same health facility and to sick and small
babies delivered at other health facilities closer to FRU/CHC. The advantage of a functional NBSU is that
it adds to the total bed capacity available in the district for newborn care, while making provision for
newborn care closer to home for many sick and small babies. Current data shows that the mortality is
higher in babies referred from home/other health facilities (out born), as compared to the facility born
babies (inborn). This could be due to the fact that currently newborns are referred to Special Newborn
Care Unit (SNCU), without adequate pre referral management. This gap can be addressed at an optimally
functioning NBSU. NBSUs have an important role of stabilizing these sick & small newborns before they
reach SNCU and managing not so seriously sick newborns so that the limited SNCU beds are utilized for
those who need advanced care.
To fulfil your role as quality service provider for newborn care in the FRU/CHC, this course will help you
in acquiring essential knowledge and skills for optimal management of newborns presenting at NBSU.
• The first step is rapid screening to identify life threatening conditions. This is known as triage or ‘sorting’.
A few of them may have emergency signs indicating that the problem is so serious that the newborn
may die within minutes, if not immediately treated.
E Emergency
P Priority
N Non-urgent
Signs of triage
Emergency signs
• Low body temperature (Temp.<35.5°C)
• Not breathing at all "OR" gasping respiration
• Severe respiratory distress
• Central cyanosis
• Shock
• Convulsions/Unconsciousness
✓ Place the newborn on a warm surface under a Radiant warmer and under good light and record
temperature.
✓ Check for the Emergency signs and institute appropriate treatment while planning for referral to
SNCU/higher facility.
✓ If there is an emergency sign perform bedside diagnostics (check blood glucose & oxygen saturation).
Give priority to stabilizing the sick or small baby before assessing and treating the underlying cause of
the problem.
✓ Place the newborn on a warm surface under a radiant warmer and under good light
Placing the baby on a warm surface under a radiant warmer and under good light is the first essential
step that you should perform in every baby irrespective of the underlying condition. This is important
as many sick babies are hypothermic and their survival chances increase, if hypothermia is taken care,
of even before instituting any resuscitation measure.
In hypothermia, the temperature is below 36.5°C. The common signs and symptoms in a hypothermic
newborn are lethargy, irritability, poor feeding and breathing difficulty (tachypnoea/apnoea).
Tactile assessment of temperature: Temperature of a baby can be assessed with reasonable precision by
human touch, the reliability of which can be enhanced by practice. Abdominal temperature is representative
of the core temperature and it is reliable in the diagnosis of hypothermia. The warm and pink feet of the
newborn indicate that the newborn is in thermal comfort, but when feet are cold and abdomen is warm,
it indicates that the newborn is in cold stress. In hypothermia, both feet and abdomen are cold to touch.
In a newborn being nursed under a radiant warmer, temperature is usually recorded by a thermistor probe.
The thermistor probe is attached to the skin over upper right side of the abdomen. The thermistor senses
the skin temperature and displays it on the panel.
Ensure:
Assessment for other emergency signs is started while recording temperature.
Treatment is initiated immediately when an emergency sign is detected, while simultaneously completing
the assessment for other emergency signs.
• Look at breathing & count respiratory rate: • Not breathing at all or gasping respiration
Not breathing at all, even when stimulated; or
gasping; or
Slow breathing - Respiratory Rate <20/min
Apnoea – Breathing with prolonged, intermittent
pauses lasting >20 seconds or less if associated
with bradycardia/cyanosis
1.
2.
3.
ACTIVITY 1.2:
DRILL TO IDENTIFY: WHICH CONDITIONS REQUIRE EMERGENCY MANAGEMENT?
Observe breathing effort and count the respiratory rate, for at least one minute, if the baby is not breathing;
or is gasping; or respiratory rate is less than 20 breaths per minute, initiate immediate management.
LOOK: Count the breaths in one minute. Repeat the count if elevated.
Count the breaths in one minute to decide if the newborn has fast breathing. Tell the mother you are going
to count her newborn's breathing. The newborn must be calm and quiet when you count the respiratory
rate. If the newborn is crying or agitated, you will not be able to obtain an accurate count of the newborn 's
breaths. If the newborn is sleeping, do not wake him. To count the number of breaths in one minute, use a
watch with a second’s hand or a digital watch. Look for breathing movement, anywhere on the newborn's
chest or abdomen. Usually you can see breathing movements even in a newborn who is clothed. If you
cannot see the movement easily, ask the mother to lift the newborn 's shirt. If the newborn starts to cry, ask
the mother to calm the newborn before you start counting. If you are not sure about the number of breaths
you counted (for example, if the newborn was actively moving and it was difficult to watch the chest, or if
the newborn was upset or crying), repeat the count.
Mild chest indrawing is normal in a young infant (till two months' age) because the chest wall is soft.
Severe chest indrawing is very deep and easy to see. Severe chest indrawing is a sign of pneumonia and is
serious in a young infant.
Identification of central cyanosis can be difficult. Examine the tongue or gums (not the lips) in natural light
or the light from an incandescent light bulb (even healthy people may look slightly blue under fluorescent
light). If unsure, compare the colour of the baby’s tongue with that of the mother’s. Bluish discoloration of the
nail-beds indicates peripheral cyanosis, which can occur with vasoconstriction as a result of hypothermia.
This is not central cyanosis and does not denote low oxygen level.
Assess circulation
Assess if a newborn has a poor circulation:
• Does the newborn have cold hands?
• Is the capillary refill time (CRT) longer than 3 seconds?
• Is the pulse weak and fast?
Feel the temperature of extremities. If the newborn’s hands feel cold, you need to assess the capillary refill.
Jitteriness
Jitteriness must be differentiated from seizures in neonates.
1. Jitteriness is not associated with ocular deviation.
2. It is stimulus sensitive (e.g., triggered by stimulation or easily stopped with change in position or
restraining of the limb).
3. The movement resembles a tremor and no autonomic changes, such as tachycardia, are associated with it.
Seizures, often, are associated with ocular deviation and are not stimulus sensitive. Autonomic changes
frequently accompany them.
The assessment of a seizure is based on observation; convulsion must be witnessed by a health care worker
in the health facility. A convulsion can be recognised as sudden loss of consciousness, associated with
uncontrolled jerky movements of the limbs and/or the face. The same may be associated with stiffening of
the arms and legs or uncontrolled movements of the limbs.
Sometimes, in newborns, jerky movements may be absent, but there may be twitching (abnormal facial
movements)/abnormal movements of the eyes, hands or feet and the neonate may appear awake but
unresponsive. These are classified as subtle seizures.
Subtle convulsion
• Repetitive blinking, eye deviation, or staring
• Repetitive movements of mouth or tongue
• Purposeless movement of the limbs, as if bicycling or swimming
• Apnoea (spontaneous cessation of breathing for more than 20 seconds or less, if associated with
cyanosis and bradycardia)
A newborn who does not respond to any of the above stimuli, may be lethargic or unconscious.
Lethargy is decreased level of consciousness from which the newborn can be aroused, but with difficulty.
Unconscious babies have profound sleep; are unresponsive to stimuli and may not respond to a painful
stimulus.
Add 1.3 ml sterile Oral syrup (contains Undiluted 2 ml vial Add 6 ml sterile water to 2
water to a vial of 250 125 mg in 5 ml) containing 20 mg=2 or ml vial containing 80 mg
mg=250 mg/1.5ml ml at 10 mg/ml in 2 ml=8 ml at 10 mg/ml
WEIGHT
< 1.5 kg 0.4 ml 2.0 ml* 0.5 ml
1.5 - 2.0 kg 0.5 ml 2.0 ml* 1.0 ml
2.0 - 3.0 kg 0.5 ml 2.5 ml* 1.0 ml
3.0 - 4.0 kg 1.0 ml 3.0 ml* 1.5 ml
4.0 - 5.0 kg 1.25 ml 4.0 ml* 2.0 ml
*Determine if the child is able to take orally
Oxygen therapy
For all sick neonates, assess oxygen saturation using a pulse oximeter. Heated and humidified oxygen
should be given if the oxygen saturation is ≤ 90%, and the oxygen flow should be regulated to maintain
saturation between 91-95%. Use a pulse oximeter to guide oxygen therapy. Oxygen can be discontinued
once the infant can maintain saturation > 90% in room air.
Oxygen delivery devices available for babies include nasal cannula, nasal prongs and head box. Nasal
cannula, nasal prongs should be snugly fitting inside the nostrils, without blanching the nares. Ends of
prongs should be cleaned twice daily, with saline and checked to avoid plugging by mucous or secretions.
• A flow rate of 0.5-1 litres/min should be maintained for nasal prongs
• Nasal prongs carry the advantage of permitting breast feeding while newborn is on oxygen therapy.
• Head box should allow for newborn’s head movement within the box.
• Oxygen flow rate of 5-7 Litres/min is required for the headbox.
• Meticulous monitoring of SpO2 and general condition should be ensured while the baby is on oxygen
therapy.
Figure 1.1: Oxygen delivery devices- Nasal prongs and head box
Figure 1.1: Oxygen delivery devices- Nasal prongs and head box
Video 1 1
Video
Oxygen delivery in neonates
Administer IV fluids
To administer IV fluids, superficial distal veins over dorsum of hands or feet are preferred.
• Fluid may be administered using a micro drip set or an infusion pump. Each mL of micro drip set equals
60 micro drops; thus, the amount of fluid required in mL/hour equals number of drops per minute.
• Always check the fluid bottle for type of fluid, bottle’s seal, date of expiry and whether it contains clear
fluid or not.
• Check the Intravenous site for leakage or displacement of cannula.
Monitoring: The clinical signs that should be monitored during treatment of shock to evaluate for response
to therapy include:
• Heart rate [decrease in heart rate by at least 10 beats per minute]
• Respiratory Rate (normalization of RR)
• Capillary refill time (Improvement of CRT)
• Oxygen saturation (Imrpovement in SpO2)
Look for signs of over-hydration
• Puffiness of eyes
• Weight gain
• Increasing liver size on per abdomen examination
In case of excess fluid administration, further fluid bolus should be stopped and only maintenance
fluid therapy should be continued.
Video 2
IV access in newborns
Convulsions/Unconsciousness
a. Maintain temperature under radiant warmer
b. Position the newborn to maintain airway
c. Clear the airway, if required
d. Maintain SpO2 between 91-95%
e. Check glucose levels; if blood glucose <45mg/dl, then treat with 10% dextrose as described below.
f. Give IV 10% Calcium gluconate at 2ml/kg (in equal dilution with distilled water), slowly over 5-10
minutes under cardiac monitoring.
Note that generalized and subtle convulsions are both managed in the same way.
Treatment of hypoglycaemia:
• If blood Sugar >45mg: Give breastfeed/20-30ml EBM/top feed, continue feeding and ensure 6 hourly
blood sugar estimation.
• If blood glucose <45mg/dl by glucometer (if possible get confirmation done by plasma blood sugar
levels), give treatment.
Asymptomatic newborn: Provide one oral feed (direct breastfeed or EBM 20ml by spoon).
Assess blood sugar after an hour, if blood sugar remains below 45mg/dl, treat with IV dextrose as for
symptomatic newborn (given below).
Symptomatic newborn (lethargy, limpness, sweating, respiratory distress, apnoea etc.): Give a bolus
of 10% Dextrose @2ml/kg slowly over a minute (If IV access is difficult, give the same amount through
OG tube) and follow by Dextrose infusion @6mg/kg/min. Start infusion of dextrose containing fluid
at the daily maintenance volume according to the baby's age so as to provide a glucose infusion rate
(GIR) of 6 mg/kg/min.(Refer to the table below)
Repeat blood glucose after half an hour. Refer to SNCU for further management.
How to prepare glucose infusion rates@6mg/kg/min for neonates with Birth weight ≥ 1500 gms
using a mixture of D10 and D25 Volume (ml/kg/d)
Appropriate mixture of these two fluids will achieve the GIR @ 6mg/Kg/min.
It is mandated that an early referral for such a baby is planned by the team at NBSU
Treatment of hypocalcaemia
Collect the sample for estimation of Calcium levels if facility is available. Give 10% Calcium gluconate
2ml/Kg IV over 5-10 minutes. 10% Calcium gluconate is diluted with equal volume of distilled water
and administered slowly under cardiac monitoring, preferably by an infusion pump (withhold infusion if
HR< 100/min).
Do not add calcium to maintenance IV Fluid.
Inj. Phenobarbitone Intravenous (200 mg/ml) 0.1 ml diluted with 0.9 ml saline (20 mg/ml)
Weight of Infant Initial Repeat dose
2 kg or less 2 mL 0.5 mL
2 to 3 kg 3 mL 0.75 mL
3 to 4 kg 4 mL 1 mL
Caution- Do not use Inj. Diazepam for control of convulsions in Neonates < 2 weeks
Phenytoin is used as a second line drug, when full dose of phenobarbitone fails to resolve seizures. If
used, it should only be mixed with saline and not with dextrose as it precipitates in dextrose.
Continue supportive management while preparing for referral to higher centre for further management.
SIGN CRITERIA
Shock
Hypothermia
Cyanosis
Hypoglycemia
Severe Respiratory Distress
Jitteriness
Subtle convulsions
Apnoea
Activity 1.4:
CASE STUDIES
1. A 7 days old baby weighing 2.5 kg is admitted with refusal to feeds, fast breathing, cold extremities
and CRT of 5 seconds. What are the steps for stabilization of this newborn?
2. A 7 days old baby girl with birth weight 2.8 kg is brought with the inability to breastfeed.
On examination you find that the newborn has subtle seizures, temperature is 36°C and respiratory
rate is 56/min.
Write down initial steps of management.
Babies who are seriously ill at the time of presentation and cannot be cared for at NBSU need to be
transferred to a special neonatal care unit (SNCU). In such instances, communication with the family
is important for ensuring that the referral to the SNCU materializes successfully. It is also necessary to
arrange for timely transport and provide care during transfer.
The mother should be encouraged to stay in the health facility with the baby. She should be counseled
to provide care to her baby including feeding, which should be transitioned to spoon and finally direct
breastfeeding as baby improves. In addition, the healthcare provider should ensure communication
regarding all other associated problems of her infant.
All babies need to be assessed for four vital parameters- TOPS (Temperature, Oxygenation, Perfusion
and Sugar). Babies need to be stabilized for all these parameters before & during transport:
6. Referral note
The referral note should mention the following:
• Case particulars- Name, age, gender, address
• Chief complaints
Ask the participants to go through the referral note given in the annexure. (page-136)
The baby should be referred and transported safely from the health facility to a higher centre. The transport
facilities can be availed free of cost through the National Ambulance Service. The Government of India has
provided for free transport to the mother and infant (upto one year of age) under the Janani Shishu Suraksha
Karyakram (JSSK). Wherever available, prefer transportation in an ALS (Advanced Life Support) ambulance.
The GPS fitted vehicles target to reach the beneficiary within a fixed response time of 30 to 45 minutes. The
facilities under this initiative, include:
• Free transfer from home to facility,
• Inter facility transfer in case of referral, and
• Drop back for mother and newborn, after 48 hours of delivery.
The transport vehicle should be equipped to shift the baby in a secure manner and stabilize the baby
en-route. The minimum requirements that should be available in a transport vehicle are shown below:
If a SNCU/Referral unit is very far or not available, the baby should be managed in the NBSU.
The prognosis and outcome of the baby should be explained in detail to the family.
A 2 days old baby, with birth weight 1.6 kg is brought to your facility with refusal to feed and subtle
convulsions. You have taken steps to stabilize the baby and now you are preparing for referral and transfer.
II. What steps will you take to complete the referral process?
Babies who are sick, but do not present with an emergency sign(s) require detailed assessment as described
below:
• Detailed history of the baby and the mother.
• Complete examination of the baby
• Performing appropriate laboratory investigations, and
• Recording all information, including:
Relevant history
Examination findings and laboratory investigations
3.1. History
Review the referral notes or records of the birth, if available. A good history along with the findings of the
examination and laboratory investigations, will point towards a probable diagnosis.
Ask the mother or attendant and validate from records:
Pregnancy
Did she develop any complications, such as fever, any time from the onset of labour to three
days after birth?
When did the membranes rupture (assess if the duration was more than 18 hours before birth)?
Was the labour or birth difficult or complicated, including any of the following:
§ Prolonged labour
§ Caesarean section
§ Instrumental vaginal delivery (e.g. forceps or vacuum extraction)
§ Malposition of the baby (e.g. breech)
§ Any other complications.
Did she develop any complications after the birth?
Record weight
All babies presenting to the facility must be weighed.
• Newborns weighing 1500-1800 grams can be managed at either NBSU or SNCU depending on the
place of delivery and sickness. In case baby requires referral, ensure prereferral stabilization.
• Those weighing more than 1800 grams, do not require urgent referral and can be managed at NBSU.
However, all babies above 1800 grams, having emergency signs should also be referred after stabilization
• Babies above 1800 grams, with no emergency signs, but having feeding problem or any other sickness
should be managed in NBSU.
Assess breathing
1. Count the breaths in one minute to decide if the newborn has fast breathing. The newborn must be
calm and quiet when you count the respiratory rate. If the newborn is crying or agitated, you will not be
able to obtain an accurate count of the newborn 's breaths. The cut-off rate to identify fast breathing is
60 breaths per minute or more. If the count is 60 breaths or more, the count should be repeated, because
the breathing rate of a newborn is often irregular. The newborn may occasionally stop breathing for a
few seconds, followed by a period of faster breathing. If the second count is also 60 breaths or more,
the newborn has fast breathing.
Fast breathing is considered serious in a newborn and needs management in a health facility. Babies
with only fast breathing can be managed in NBSU. If the baby has severe respiratory distress (as
explained in earlier section), baby should be referred to SNCU.
Assess feeding
Ask the mother how is the baby feeding at the breast. Any difficulty mentioned by the mother is important.
A newborn who was feeding well earlier but is not feeding well now, may have a serious illness. These
newborns, who are either not able to feed or are not feeding well, should be evaluated urgently in a
health facility. Babies requiring continuous IV support or oxygen should be managed in SNCU.
Table 3.1: Differential diagnosis in a newborn presenting with lethargy, unconsciousness or convulsions
Condition Symptoms and signs
• Perinatal asphyxia • Onset in first 3 days of life
• Hypoxic ischaemic encephalopathy • History of difficult delivery
• Birth trauma • Gestation: Term or preterm
• Intracranial haemorrhage
• Haemolytic disease of the newborn • Onset in first 3 days of life
• Kernicterus • Jaundice
• Pallor
• Serious bacterial infection
• No H/o Inj. vitamin K at birth
Neonatal tetanus • Onset at age 3–14 days
• Home delivery, asepsis not maintained
• Irritability
• Difficulty in breastfeeding
• Trismus
• Muscle spasms
Meningitis • Lethargy
• Fever
• Apnoeic episodes
• Convulsions
• High-pitched cry
• Tense or bulging fontanelle
Sepsis • Fever or hypothermia
• Inability to feed
• Respiratory distress
• Shock (lethargy, fast breathing, cold skin, prolonged
capillary refill, fast weak pulse, and sometimes low blood
pressure)
Assess diarrhoea
Infective diarrhoea is seldom seen in exclusively breast fed babies, however if the baby presents with
diarrhoea suspect sepsis. Assess for dehydration and also ask for blood in stool.
• If the baby has signs of dehydration or blood in stool, establish an IV line and start IV fluid, while
arranging for referral.
• Blood in stool in a young infant may be because of serious infection or surgical problem. Such babies
should be given 1 mg intramuscular dose of Vitamin K and referred to higher centre with pre-referral
dose of antibiotics.
54 | Newborn Stabilization Unit Training Participants’ Module
Look for abdominal distension
Abdominal distension may be a sign of serious illness (sepsis, necrotizing enterocolitis or gastrointestinal
malformation or obstruction) and needs management in a higher centre.
These congenital malformations are not life threatening and may not require immediate referral. The
provider must connect with Rashtriya Bal Swasthya Karyakram (RBSK) manager after reporting the
congenital defect, for facilitating any further support required by the family, in terms of surgery etc. which
is available free of cost under RBSK. Congenital defects which are life threatening should be stabilized and
referred to SNCU for example- a baby with meningomyelocele should be transported after covering the
same with saline soaked sterile gauze during transport.
# Newborns weighing 1500-1800 grams can be managed at either a functional NBSU or SNCU
depending on the place of delivery and sickness
While babies with emergency signs and also those without emergency signs, but who fulfill the criteria
for admission to SNCU would be referred, there may be situations, where referral is not possible. Further
management of these cases, along with those who should be managed in a NBSU (Table 3.2) is given below.
KMC can be initiated immediately in all babies, except those clinically unstable. The ongoing
medical support, like intravenous fluids and tube feeding are not contraindications to KMC. In
India KMC is prioritized in babies weighing less than 2000 grams.
Video 3
KMC
If baby has hyperthermia, maintain optimal room temperature, correct environmental factors (such as
removal of any heat source), ensure that the baby is not overly clothed or covered by blankets. Antipyretics
are not recommended. Adequate amount of fluids should be given.
Perform sepsis screening in babies, where fever continues after excluding environmental cause.
4.3. Feeding
Most newborns weighing 1800 grams or more will be able to suckle at the breast. Those who cannot
breastfeed should be given expressed breast milk with a cup. Infants unable to feed from a cup should be
given intermittent bolus feeds through an oro-gastric tube. When the newborn starts to suckle well and is
gaining weight, reduce the cup/orogastric feeds gradually.
Breastfeeding is ideal for all newborns and should be supported. Breast milk is the ideal feed for all
infants, including LBW infants. Anything other than breast milk is less than optimal.
In exceptional situations, when mother’s own milk (MOM) is not available, donor human milk can be
given, only when safe milk-banking facilities are available. Formula feeds should only be given, if neither of
the above is possible. Babies should be fed every two hours and the amount to be fed should be calculated
according to the weight and day of life (Table 4.2).
Video 4
Expression of breast milk & feeding by paladai/cup and spoon
Type of fluid:
• During the first 2 days of life, give 10% dextrose as IV infusion. After the first 2 days of life, use IV
dextrose with low sodium, such as commercially available Isolyte P.
Administration of IV fluids:
• Use syringe infusion pump or paediatric microdrip infusion set to administer IV fluids in newborns.
• Calculate the drip rate: first calculate the total fluid requirement per day and divide by 24. This will give
the estimate of fluids in ml per hour which can be set on the syringe infusion pump. In microdrip set, 1
ml=60 micro drops. The number of drops per minute is equal to ml of fluid per hour. So if a baby needs
5 ml/hour, then set the drop rate at 5 drops per minute).
• Record the drip rate and volume infused every hour in the case sheet.
• Weigh the infant daily. Watch for weight loss/gain and urine output and increase/reduce IV fluids accordingly.
• Check IV catheter site for signs of leakage, swelling or redness, in which case IV access at a new site
should be established.
• Introduce breastfeeding or milk feeding by orogastric tube, as soon as it is safe to do so.
Excessive weight loss (greater than 3-5% in 24 hours): Check for inadequate feeding, and manage
underlying conditions, if any (cold stress, excessive insensible water loss or systemic illness).
Video 5
OG tube insertion & feeding
If active, or crying, the newborn is obviously breathing. Look for slow breathing with prolonged intermittent
pauses (lasting >20 seconds) with or without central cyanosis or bradycardia. If present, it means newborn
has apnoea.
• Monitor all small babies for occurence of apnoea.
• If the newborn stops breathing, stimulate the newborn to breathe by rubbing the newborn’s back.
• If the newborn does not begin to breathe by tactile stimulation, resuscitate the newborn using a bag and
mask.
• In addition, maintain temperature, oxygen saturation and glucose levels.
• If the apnoeic episodes become more frequent, refer to SNCU for further management.
Family participatory care (FPC) in newborn care units entails supervised delivery of care to haemo-
dynamically stable, sick & preterm newborns by the parents/attendants, in addition to the standard care
provided by the healthcare providers in the nursery.
Detailed operational guidelines on FPC have been issued by the Government of India and should be
referred to for making newborn care family participatory.
Temperature maintenance:
• The best way to maintain temperature is by placing the baby in skin-to-skin contact (KMC) with the
mother (or any adult). KMC can also be used to keep a baby warm during transport and at home.
Breastfeeding:
• Optimum nutrition for the baby is its own mother’s milk. Mother should be advised and supported to
exclusively breastfeed her baby. The healthcare worker needs to assess the adequacy of breastfeeding.
In case of any concern regarding adequacy of breastfeeding, the newborn can be weighed on the same
weighing scale that was used to weigh the infant at birth. Excessive weight loss (normal 8-10% of birth
• Baby is maintaining normal body temperature (in room temperature/when cared for by the mother)
• Baby not requiring IV fluids/medications
• Baby is accepting breastfeeds/assisted feeds well and gaining weight for 3 consecutive days
• IV antibiotic therapy has been completed
• Baby admitted for neonatal jaundice and has completed treatment with phototherapy
• Mother has been counselled for danger signs*, assisted feeding (as required) , KMC (as required) and
follow up plan.
*Danger signs: Refusal to feed; Fast or difficult breathing, Cold or Hot to touch, jaundice involving palms and soles
Pallor/Cyanosis, Abdominal distension, Abnormal movements, Bleeding from any site or Diarrhoea with blood in stool.
• Advise mother to give home care: Breastfeed infant exclusively, keep infant warm, keep cord
clean and dry, importance and correct method of handwashing & danger signs.
• Low weight babies (1.8-2.5 Kg) should be followed up within 14 days of discharge. Date and time of
follow up should be informed to the parents . The same must be recorded in the discharge summary.
Rub palms together Rub the back of both hands Interface fingers and rub
hands together
Interlock fingers and rub the back of Rub thumb in a rotating manner Rub fingertips on palm for
fingers of both hands followed by the area between index both hands
finger and thumb for both hands
Hands should be allowed to dry on their own without use of any mop/ cloth/ paper.
Hands should
Rub both
5. Additional wrists inbe allowed
a rotating
practices- In to dry on
manner.
addition, their which
policies own without
promote useexclusive
of any mop/ cloth/ paper.
breastfeeding, rooming
Rinse and dry thoroughly
in with mother and maintenance of maternal hygiene should be promoted. The health
Hands should
5. Additional be allowed
practices- to dry on
In addition, their which
policies own without
promote useexclusive
of any mop/ cloth/ paper.
breastfeeding, rooming
care facility should also avoid cross-infection at all times by practising barrier nursing.
in with mother and maintenance of maternal hygiene should be promoted. The health
Hands should be allowed to dry on their own without use of any mop/cloth/paper.
5. Additional
care facilitypractices-
should also In addition, policies which
avoid cross-infection atpromote
all times exclusive breastfeeding,
by practising rooming
barrier nursing.
in with mother
3. Additional and maintenance
practices- In addition, adoptofpolicies
maternal
which hygiene
promote: should be promoted. The health
care
a. facility should
Early enteral also avoid cross-infection at all times by practising barrier nursing.
feeding
b. Exclusive breastmilk feeding
c. Rooming in with mother
d. Maintenance of maternal hygiene
The health care facility should also avoid cross-infection at all times by practicing strict hand hygiene.
50
50
70 | Newborn Stabilization Unit Training Participants’ Module
50
Exercise 4.1:
CASE STUDIES
1. Ranno delivered a 2.0 Kg baby 48 hours ago. There are no emergency signs. The baby is feeding well
at the breast and maintaining temperature. How will you manage this baby?
2. Baby of Shanti, weighing 2 kg, was admitted with fast breathing on day 1 of life. He was started on IV
fluids. On day 3, his distress has stabilized. How will you plan the feeding transition? When will you
plan for discharge?
3. Baby of Malti, weight 1900 grams is being discharged from NBSU at day 6 of life after receiving
phototherapy. What feeding advice will you give to the mother? What supplements will you advise,
in what quantity and for how much duration?
A baby who has physiological jaundice can be sent home on exclusive breastfeeding. The baby should be
re-assessed for any fresh symptoms or progression of jaundice, after 48 hours of discharge.
Assessment of jaundice
When a neonate is clinically jaundiced, the total serum bilirubin (TSB) is usually >5-7mg/dl.
Jaundice in newborn progresses in cephalocaudal (head to toe) direction and thus the extent of yellowness
of the skin is useful to assess the level of bilirubin. Kramer’s criteria is used to clinically assess jaundice.
However, serum bilirubin levels must be done to guide management.
12
15
18-20
Figure 5.1
Figure 5.1: Clinical
: Clinical visualvisual perception of
perception of jaundice:
jaundice:Kramer 1969 1969
Kramer
Investigations to be done:
What
1. Send bloodto investigate in case of of
samples for estimation jaundice:
Send
1.Total blood
serum samples for estimation of
bilirubin
MotheroandTotalbaby’sserum bilirubin
blood group (Collect cord blood when mother's blood group is known to be O or
Rh negative)
2. Look
2. Look for associated
for associated risk factors
risk factors for jaundice
for jaundice like:asphyxia
like: Sepsis, Sepsis,orasphyxia or haemolysis
haemolysis due to blooddue to
group blood group incompatibility
incompatibility (mother O+ and(mother O+ and
baby A+/B+ baby A+/B+/
or mother AB+ and
Rh negative or mother
baby Rh Rh negative an
positive).
If thesebaby Rh positive).
are suspected, then relevant investigations (like sepsis screen, baby's peripheral blood smear for
evidence of haemolysis
If these and haemoglobin
are suspected, levels, etc.)
then relevant should be performed.
investigations (like blood group of baby and mother,
peripheral
3. Determine baby’s blood
weightsmear for evidence
and gestational of haemolysis,
age {from haemoglobin
mother’s last levels,
menstrual period etc.) -should
(LMP)} To be
performed.
interpret bilirubin values for phototherapy and exchange transfusion according to baby’s gestational age.
Management ofbaby’s
3. Determine newborns
weightwith jaundice:
and mother’s last menstrual period (LMP) - To interpret bilirubin
values
Management for phototherapy
of jaundice and exchange
is directed towards transfusion
reducing the according
level of bilirubin to baby’s central
and preventing gestational age.
nervous
system toxicity and has two main components:
1. Prevention of hyperbilirubinemia: by early and frequent feeding
2. Reduction of bilirubin: This is achieved by phototherapy, and/or exchange transfusion.
The decision to treat depends on the severity and the cause of jaundice.
Phototherapy should be initiated (after sending blood sample for TSB), if:
• Jaundice appears on day 1
• Jaundice is severe i.e. involving palms and soles
• S. Bilirubin level is in phototherapy range as per American Academy of Paediatrics (AAP) charts (Refer
Figure 5.2).
Continue phototherapy until the serum bilirubin level is 2-3 mg lower than the phototherapy range.
Important information:
1. Prophylactic phototherapy is not recommended
2. Sunlight exposure or exposure to artificial light at home like a bulb has no effect on bilirubin levels
Figure 5.3: Chart for exchange transfusion as per AAP Guidelines 2004 56
Table 5.1: Guidelines to start phototherapy for <35 weeks and birth weight <2000 g
Source: Martin & Fanaroff, Neonatal -Perinatal medicine, 8th edition, p1450
Side Effects
1. Transient maculopapular rash on the trunk
2. Hyperthermia/Hypothermia
3. Increased insensible water loss and dehydration
4. Loose stools
5. Bronzing of the skin
Ineffective Phototherapy
1. Baby covered or frequently removed from phototherapy
2. Low irradiance (tubes old, flickering, black ends, bulbs covered with dust or reflectors dirty)
3. Distance between phototherapy lights and baby is more than recommended
4. Hemolytic conditions can cause bilirubin to rise, in spite of phototherapy
When to refer
1. Serum bilirubin increasing despite phototherapy
2. Neurological signs develop
3. Jaundice requiring exchange transfusion
4. Jaundice persisting after three weeks and/or associated with clay coloured stools
1. Ram, a 5 days old baby, born full term with birth weight of 2.8 kg, is brought to health facility with
jaundice on the face and chest which developed over last 24 hours. Baby is feeding well. There are no
risk factors.
a. How will you manage this baby?
b. What advise should be given to the mother?
2. Baby Prerna was born at 34 weeks and has been brought to FRU with yellow palms and soles. The
baby is four days old.
a. How will you manage this baby?
b. What additional information and investigations are required?
General Symptoms Refusal to suckle, not arousable, comatose, poor cry, poor weight gain, abdominal distension,
vomiting, poor perfusion, shock, bleeding
Suggestive of Cyanosis, tachypnea, chest retractions, grunt, apnoea/gasping
pneumonia
Suggestive of Fever, seizures, blank look, high pitched cry, excessive crying/irritability, neck retraction
meningitis bulging fontanelle
Diarrhoea Diarrhoea is suspected if there is passage of watery stool or an increase in usual stool
frequency
Sclerema Sclerema neonatorum manifests as diffuse hardening of the subcutaneous tissue resulting in a
tight smooth skin that feels bound to the underlying structures
Renal failure Renal failure can be suspected clinically by presence of oedema/excessive weight gain and
oliguria/anuria
Diagnosis of sepsis
Isolation of microorganisms from blood, CSF, urine or pus is diagnostic of sepsis. In clinically
suspected cases of sepsis, blood culture should be sent prior to starting antibiotics. As culture facility
may not be available at most NBSUs, indirect method such as sepsis screen may be used to diagnose
sepsis.
Sepsis screen: This is a combination of laboratory parameters which help in predicting sepsis in
newborns, with clinical features suggestive of sepsis. It should be done in all babies with probable
sepsis and in babies born to mothers with risk factors for sepsis. A positive “sepsis screen” takes into
account two or more positive tests as given below:
Sepsis screen
Maintain TABC
1. Maintain normothermia
2. Position and clear airway if required
3. Ensure optimum oxygenation (maintain SpO2 91-95%)
4. Shock to be treated with NS bolus of 10ml/kg over 30 mins
5. Maintain normoglycemia
6. If hemodynamically compromised, avoid enteral feed and give maintenance IV fluids. Start orogastric
feeds, as soon as hemodynamically stable.
7. Consider referral for exchange transfusion, if there is sclerema.
Antibiotic Policy:
Each facility is required to have its own policy based on profile of pathogens and, local sensitivity patterns.
Antibiotic therapy should cover the common causative bacteria, namely, Escherichia coli, Staphylococcus
aureus and Klebsiella pneumoniae.
Administration of Antibiotics:
• Give Injection ampicillin and gentamicin, as first line of treatment.
• Give cloxacillin (if available) instead of ampicillin, if there are extensive skin pustules or abscesses, as
these might be signs of Staphylococcus infection.
• Antibiotics should be given slowly, after dissolving in 5-10 ml fluid using a microdrip set or infusion
pump.
• Never mix two antibiotics in same syringe.
• If baby has been referred/shifted from SNCU, total duration of antibiotics should be as per treatment
plan from SNCU. In babies admitted and managed at NBSU/FRU alone, antibiotics should be given for
7-10 days.
Any baby who is being treated with antibiotics but fails to improve by 48-72 hours of admission
should be referred to SNCU/referral unit.
*This frequency of antibiotics is valid in babies weighing < 2kg. In baby weighing ≥ 2kg, the frequency remains as (a) from
0-7 days of life and (b) from > 7 days of life.
Meningitis
Suspect meningitis if signs of serious bacterial infection are present, particularly if the infant is:
• Drowsy, lethargic or unconscious
• Convulsing
• Has a bulging fontanelle
• Irritable
• Has a high-pitched cry.
Treat with antimicrobials as given below in the table.
Baby Tara, 10 day old baby has come with refusal of feeds, fever and excessive crying. On examination,
temperature is 39oC, heart rate is 170/minute, respiratory rate 66/minute, capillary refill time is 3
seconds. There is pus discharge from umbilicus. Her weight is 2.5 kg and blood sugar is 50mg/dl.
a. Are there any emergency signs ?
b. How will you proceed?
All babies delivered at the health facility should be monitored and provided routine care, support for
feeding difficulties, appropriate treatment for danger signs* and prompt referral if required. [* danger signs
are same as described in Chapter 1 & and Mother & Child Protection Card (MCP)]
The baby should be thoroughly examined at birth from head to toe to clinically screen for any life threatening
congenital anomalies, malformations and birth injuries# and findings should be recorded in the case sheet.
Remember that routine passage of catheter in the stomach, nostrils and the rectum is not recommended
but do give special attention to identify and document the anal opening. Some of the birth defects to be
reported as per RBSK Operational Guidelines are: (Refer to pictures in annexure 1)
1. Neural Tube Defect
2. Down’s Syndrome
3. Cleft Lip & Palate
4. Talipes (club foot)
5. Developmental Dysplasia of Hip
6. Congenital Cataract
7. Congenital Deafness
8. Congenital Heart Disease
(# cephalohematoma, brachial plexus injury, facial paralysis, fracture & dislocation of hip)
Physiological Conditions
Mothers observe their babies very carefully and are often worried by minor physical peculiarities or
developmental variations, which may be of no consequence and do not warrant any therapy.
Peeling skin Dry skin with peeling and exaggerated transverse sole creases are seen in all post term and
some term babies
Milia Yellow – white spots on the nose or face due to retention of sebum, are present in
practically all babies and disappear spontaneously
Toxic erythema/ An erythematous rash of unknown cause with a central pallor appearing on the second
Erythema or third day in term neonates, which begins on the face and spreads down to the trunk
Neonatorum and extremities in about 24 hours. This should be differentiated from pustules which
need treatment. It disappears spontaneously after two to three days without any specific
treatment.
Storkbites (Salmon These are discrete, pinkish- gray, sparse, capillary hemangiomata commonly seen at the
patches or naevus nape of neck, upper eyelids,forehead and root of the nose which invariably disappears
simplex): after a few months.
Mongolian blue In babies of Asiatic origin irregular blue areas of skin pigmentation are often present over
spots the sacral area and buttocks, though extremities and rest of the trunk may also be affected.
These spots disappear by the age of six months.
Subconjunctival Semilunar arcs of sub-conjuctival hemorrhage are a common finding in normal babies.
hemorrhage The blood gets reabsorbed after a few days without leaving any pigmentation.
Epstein Pearls These are white spots, usually one on either side of the median raphe of the hard palate.
Similar lesions may be seen on the prepuce. They are of no significance.
Sucking callosities The presence of these button like, cornified plaques over the centre of upper lip has no
significance.
Advice at discharge
1. Maintenance of body temperature – as explained earlier
2. Breast feed every two to three hours on a semi-demand schedule both during day and night. During
each feed, one breast should be completely emptied before the baby is put to the other breast. Exclusive
breastfeeding should be advised and the mother should be counselled that there is no need for additional
water or other fluids except under medical supervision.
3. Skin care/bathing Always take special precautions during bathing to prevent draught and chilling.
Daily baths may be avoided during the winter months and the baby can be sponged in a warm room to
avoid exposure and to keep the baby clean.
4. Care of the umbilical stump: Do not apply any medication on the cord, leave it open without any
dressing. The cord usually falls after 4 to 10 days.
5. Care of the eyes: Some neonates may develop persistent epiphora (watering) due to blockage of
nasolacrimal duct by epithelial debris. The mother should be advised to massage the nasolacrimal duct
area (by massaging the either side of the nose adjacent to the medial canthus) 5 to 8 times daily, each
time before she feeds the baby. Routine application of antiseptic ointment/drops for prevention of
ophthalmia neonatorum is not recommended
Immunization: It is recommended to give BCG vaccine, zero dose of oral polio vaccine and Hepatitis B
vaccine as per schedule and document it in the MCP Card. The mother should be informed about the date
of the next visit and the same should be shown in the MCP card.
Follow up
Preferably, each baby should be followed up in the clinic for assessment of growth and development, early
diagnosis and management of illnesses and health education of parents. Routine use of MCP card should
be done to promote monitoring and awareness of parents. Immunization visits can be used for assessment
of newborn by service provider.
Preparation
Check equipment and supplies (This drill must be performed on a daily basis by the participants at
their facility )
• Check the Radiant warmer and ensure that it is in working condition.
• Place two baby sheets under the warmer
• Check the resuscitation equipment, including the mannequin and ensure functionality.
• Check suction apparatus, ensure that the pressure is <100 mm of mercury.
• Block the mask by making a tight seal with the palm of your hand, and squeeze the bag:
If you feel pressure against your hand, the bag is generating adequate pressure;
If the bag re-inflates when you release your grip, the bag is functioning properly.
Move the baby to a firm, warm surface under a radiant warmer. Keep the baby
Provide
wrapped Warmthexcept for the face and upper chest.
or covered,
• Place the baby on a firm, warm surface under a radiant warmer which was switched on in manual mode
Position 20
the babyearlier.
minutes
Do not suction deep in the throat as this may decrease the baby’s heart rate.
Evaluate: You should evaluate the newborn’s respiration and heart rate:
• If the baby is breathing and has a heart rate of >100/min, manage other emergency signs.
If the baby is not breathing (is gasping or has apnoea) or has a heart rate below 100 beats per minute (bpm),
you should immediately proceed for bag and mask ventilation.
Station 2
Bag and mask ventilation
Indications: Apnoea/gasping "OR" Heart rate < 100/min after initial steps "OR" persisting central cyanosis
despite oxygen, administration.
Ventilating
- Form a with a Bag andthe
seal between Mask
mask and the baby’s face;
• Recheck the baby’s position and ensure that the neck is slightly extended.
- Squeeze the bag with two fingers only (adult-size bag) or with the whole
• Position the mask and check the seal:
hand (newborn-size bag);
Place the mask on the baby’s face so that it covers the baby’s chin, mouth, and nose;
- Check
Checkthe
forseal
chestbetween the maskfive
rise after ventilating and the baby’s face by ventilating two times
times.
and observing the rise of the chest.
32
Station 3
Chest compressions
Indications: Heart rate <60/min after 30 seconds of effective ventilation.
• In order to support circulation start chest compressions, while continuing PPV. At this stage provide 100%
oxygen. It is strongly recommended to attach a pulse oximeter and perform endotracheal intubation (if
skilled), if not done earlier. This is for more effective coordination of chest compressions and PPV.
Compressions and ventilation should be coordinated. For every 3 compressions, 1 breath is delivered.
Thus, the ratio is 90 chest compressions coordinated with 30 breaths per min.
Technique of chest compressions: The technique for providing chest compressions is the "Thumb
Technique" :
• Place thumbs just below the line connecting the nipples on the sternum (see below).
• Compress one third the anterior–posterior diameter of the chest.
The sternum should be depressed to a depth of approximately one third of the antero-posterior diameter
of the chest.
ssions
after 30 seconds of
Station
If heart rate less than4 60
ompressions along with
Umbilical vein catheterisation
nd ventilation should be
Equipment and Supplies
ry 3 compressions, 1
• Sterile
hus the ratio is 90gloves
chest
nated with• 30Sterile umbilical catheter or ordinary feeding tube:
breaths
• Syringes- 1ml, 10ml and 20ml
• Swabs or cotton-wool balls soaked in antiseptic solution
• Sterile blade
• Sterile forceps
• Suture
ow the line
• connecting the nipples
Adhesive strapping, ontape
or thin paper the(to
sternum (see below).
secure catheter)
he anterior–posterior diameter
• Fresh umbilical of the chest.
cord for demonstrating umbilical vein catheterization
e: Procedure
d index or• ring finger are used to compress the sternum. The spine is
Gather necessary equipment and supplies.
er hand or• by placing the baby on a hard surface.
Wash hands and wear sterile gloves.
• P
repare the umbilicus and surrounding skin by cleaning in an outward circular motion starting at the
umbilicus with a swab or cotton-wool ball soaked in alcohol, allow to dry. Repeat the procedure with
be depressed to a depth
Povidone iodine swabof approximately oneswab
and finally with alcohol third
onceof theusing
more, antero-
a new swab or cotton-wool ball
f the chest. each time and allowing to dry each time.
• Fill the umbilical catheter with normal saline using a closed syringe (i.e. with the plunger completely
ease, the fingers should
inside the barrel ofremain in attached
the syringe) contactto with
the endthe
of thechest to avoid
catheter.
ession area and delay in providing the next compression.
Ensure that there is no air in the catheter and that a closed syringe is attached to the end of the
catheter; a sudden deep breath by the baby just after the catheter has been inserted may result in an
air embolus if air is inside the catheter.
NeverStabilization
102 | Newborn force the umbilical
Unit Training catheter
Participants’ Module if resistance is encountered.
• Tie the cord tie or suture around the stump of the umbilicus to hold th
Medication:
Drugs used in newborn resuscitation
When the drug is given intravenously through a catheter, you should follow the drug with a 0.5 to 1
ml flush of normal saline to be sure that the drug has reached the blood.
If the baby appears to be in shock and is not responding to resuscitation, administration of a volume
expander may be indicated.
What can you give to expand blood volume? How much and how to give it?
The recommended solution for treating hypovolemia is an isotonic crystalloid solution. Acceptable
solutions include
• 0.9% NaCl (“Normal saline”)
• O Rh-negative packed red blood cells should be considered as part of the volume replacement when
severe fetal anemia is documented or expected. If timely diagnosis permits, the donor unit can be cross-
matched with the mother who would be the source of any problematic antibody. Otherwise, emergency-
release of O-Rh negative packed cells may be necessary. (Only if facilities and expertise is available)
Procedure
Kangaroo mother care (KMC) is care of a small baby, who is continuously carried in skin-to- skin contact
by the mother and exclusively breastfed. It is the best way to keep a small baby warm and it also helps
establish breastfeeding. KMC, however, requires that the mother stays with the baby or spends most of the
day at the hospital.
Beginning KMC
• Counsel the mother and the family. Ensure that the mother has support from her family to stay at the
hospital or return when the baby is ready for KMC. Discuss with the family, if possible, how they can
support the mother so she can provide KMC.
• Explain to the mother that KMC may be the best way for her to care for her baby once the baby’s
condition permits. Enumerate the advantages of KMC:
• Clothes for the mother: light, loose clothing that is comfortable in the ambient temperature, provided
the clothing can accommodate the baby.
• Clothes for the baby: pre-warmed shirt open at the front, a napkin, a cap, and socks.
Place the baby in an upright position directly against the mother’s skin in between her breasts
Ensure that the baby’s hips and elbows are flexed into a frog-like position and the baby’s head and
chest are on the mother’s chest, with the head in a slightly extended position.
Use a soft piece of fabric (about 1 square metre), folded diagonally in two and secured with a knot.
Make sure it is tied firmly enough to prevent the baby from sliding out if the mother stands, but not
so tightly that it obstructs the baby’s breathing or movement.
Do’s
1. Demonstrate correct technique, if expression of milk is painful.
2. Milk should be expressed frequently -at least 8 times in 24 hours to stimulate and maintain milk
production
Don’ts
1. Rub or slide fingers along the skin but should be more like rolling.
2. Squeeze the nipple; pressing or pulling the nipple does not help expression of milk
3. Try to express for a shorter time.
Storage
The expressed breast milk (EBM) should be stored in a container washed thoroughly with soap and water.
The container of expressed breast milk (EBM) should be covered with a clean cloth or a lid. EBM can be
kept at room temperature for 8 hours, and in the refrigerator for 24 hours.
Procedure
1. Take 6 Fr catheter
2. Measure length from angle of mouth to tragus to midpoint between umbilicus and xiphisternum
3. Insert the tube from mouth till the desired length has been introduced
4. Check position using a syringe & a stethoscope to auscultate the gush of air
5. Tape the tube to the side of mouth, and close outer end after removing the syringe
6. To instill feed-Take a 10 ml syringe barrel without the plunger and insert nozzle into the open end of the
feeding tube. Pour milk in to the syringe and wait for it to go down slowly by gravity. After a feed, close
the open end.
7. The baby should be placed in the right lateral position for 15 to 20 minutes to avoid regurgitation. There
is no need to burp a gavage-fed baby.
8. Check abdominal girth at next feeding session & proceed to feed, if no increase in girth. If the girth
increases by 2 cm, do a pre-feed gastric aspirate and analyse the amount and content to decide about
continuing/discontinuing feeds.
9. While pulling out a feeding tube, it must be kept pinched and pulled out gently.
10. Always confirm the position of the tube prior to giving a feed.
Infection prevention:
1. Show video of infection prevention
2. Hand washing drill for all participants
Station 3 : Equipment
1. Radiant Warmer
Equipment & Supplies
Radiant warmer and adhesive tape.
Parts
1. Bassinet (for placing the neonate)
2. Radiant heat source (Quartz/ceramic or similar heating rod)
3. Skin probe (for measuring baby’s skin temperature)
4. Air probe
5. Control panel (Displays and control knobs)
6. Mode selector (selects manual or servo mode)
7. Heater output control key/knob (to increase or decrease the heater output manually)
8. Heater output display (indicates heater output)
9. Temperature selection key/knob (select the desired skin temperature)
10. Temperature display (displays temperature of baby ’s skin, the set temperature and air temperature)
11. Alarm display for power failure, system failure, skin probe failure, skin temp. high/low & heater failure.
Bassinet
1. Soap/detergent - daily
2. Clean using disinfectant like 2% Bacillocid or glutaraldehyde when the bassinet is unoccupied or weekly
(move the baby while using disinfectant)
Probe
1. Clean using Isopropyl alcohol swab before and after each use.
Problem Action
1. No power on turning instrument on - Check power supply, plug, fuse
- If above okay, call engineer
2. Power on, heater not on - Call engineer
3 No skin temperature display - Faulty skin sensor (replace/call engineer)
4. Display temperature and baby temperature variation > 1°C - Needs calibration, call engineer
2. Phototherapy Machine
Phototherapy involves exposure of the newborn with jaundice to blue light/CFL/LED of wave length 450-
460 nm. The light waves convert the bilirubin to water soluble nontoxic forms which are then easily excreted.
The advantages of phototherapy are that it is noninvasive, effective, inexpensive and easy to use. Frequent
feeding every 2 hours and change of posture should be promoted in a newborn receiving phototherapy.
Parts
Source of light
1. Fluorescent lights (Conventional phototherapy)
• 6-8 white fluorescent light OR
• A combination of 2 special blue and 4-6 white fluorescent lights with a plexiglass shield.
• White tubes
• Blue tubes
• Tube life is 1000 hours/6 months, whichever is earlier.
• Irradiance provided 6-8 uw/cm2/nm (White light), 8-12 uw/cm2/nm (Blue + White light)
Working
1. Connect to mains.
2. Switch on the unit & check that all tubes/lamps are working.
Cleaning
1. Soap/Detergent once daily
2. Clean with disinfectant once a week
3. Keep the lamps, the covering shield and the grill clean
Problem Action
1. No power on turning instrument on - Check power supply, plug, fuse
- If above okay, call enginee
2. Fan not working - Call engineer
3 Timer not working - Call engineer
4. Standard Blue units - Tubes faulty/choke needs change
- Tubes not coming on - Tubes need change
- Blackening/flickering of tubes
Side Effects
1. Transient maculopapular rash on the trunk
2. Hyperthermia/Hypothermia
3. Increased insensible water loss and dehydration
4. Loose stools
5. Bronzing of the skin
Maintenance
1. Change lights if:
1. Irradiance as measured with flux meter < 15
2. Lamp life > 1000 hours of use for fluorescent tubes, for LED > 20000-30000 and for CFL 2000 –
3000 hours/as per manufacturer’s instruction manual
3. If Flux meter and hour meter are not available, then change fluorescent tubes every 3 months
4. Tube ends are black or flickering or not working
3. Oxygen Therapy/Delivery
Equipment & Supplies
• Nasal prongs/Cannula
• Headbox/Oxygen hood
• Oxygen supply/source (oxygen cylinder with humidifier, concentrator)
Oxygen Concentrators
An oxygen concentrator is a device providing oxygen therapy to a patient at minimally to substantially
higher concentrations than available in ambient air. Oxygen concentrators are less expensive than liquid
oxygen and are the most cost-effective source of oxygen therapy and more convenient alternative to tanks
of compressed oxygen.
Room air contains 21% oxygen combined with nitrogen and a mixture of other gases. A miniaturized
compressor inside the machine pressurizes this air through a system of chemical filters. This chemical filter
is made up of silicate granules called, Zeolite. The Zeolite will sieve the nitrogen out of the air, concentrating
the oxygen. Through this process, the system is capable of producing medical grade oxygen up to 96%,
consistently. Most of the portable oxygen concentrator systems available today provide high concentration
of oxygen and also maximize the purity of the oxygen.
Safety
The concentrator’s instruction manual indicates as to what maintenance is necessary; here are some general
guidelines to follow:
• The concentrator needs good, clean air to operate properly. Hence, operate the concentrator in a
well-ventilated area.
• Wash the filters periodically (at least once in a week).
• Replace the filters periodically (at least once in a year).
• Ensure examination of the concentrator, at least once in a year by the company engineer.
There are also some very important safety issues to be kept in mind. Oxygen is most dangerous in the
presence of fire. Keep flammable materials away, and do not allow any heat sources to be near a working
oxygen concentrator. In both clinical and emergency-care situations, oxygen concentrators have the
advantage of not being as dangerous as oxygen cylinders, which can, if ruptured or leaking, greatly increases
the combustion rate of a fire.
Oxygen concentrators are considered sufficiently foolproof to be used in neonatal units. They can be used
for more than one patient by using flow splitters. However, they need a power source.
Working
1. Plug onto the power supply.
2. Switch on the concentrator using the ON/OFF button.
3. Once the concentrator is on, a yellow light will come up.
4. Next, adjust the flow to 3-4 liters. This light will be on till the desired concentration of oxygen is achieved,
which in most concentrators is nearly 90-93%, after which it goes off.
5. Every manufacturer has its own way of showing the achieved desired concentration, In some
concentrators this yellow light will become green after achieving the desired concentration.
Maintenance
1. Coarse filter –Ensure it is dust free, wash daily
2. Zeolite granules –Change every 20,000 hrs
3. Bacterial filter –Change every one year
Trouble shooting
Station 4:
Oxygen Cylinder
• Ensure the oxygen cylinder is secured on a flat surface on a trolley
• Attach regulator, flow meter and humidifier to the cylinder
• Attach the humidification bottle to the flow meter and fill with clean water up to the mark level on the
bottle (between 1/3 and 2/3)
• Use a spanner/key to open the cylinder
Bedside skills
1. Glucometer
Using a2. glucometer
IV Injection to test Blood Sugar
EQUIPMENT
3. IM AND SUPPLIES
Injection
Glucometer
4. Blood sample collection
Glucometer test strips
Sterile needle (26G) or lancet
1. Using a glucometer to test Blood Sugar
Alcohol for skin preparation
Cotton Equipment & Supplies
• Glucometer
• Glucometer test strips
PROCEDURE
• Sterile needle (26G) or lancet
Hypoglycaemia is to be suspected and managed in all sick or low birth weight newborn.
• Alcohol for skin preparation
For this blood glucose levels can be estimated at the bedside using a glucometer.
• Cotton swabs
2. IV injection
IV Access
The training for gaining an intravenous access shall be done on a model which is provided. Each participant
shall carry out this skill on this given model.
1. Select the vein (dorsum of hand/foot)
2. Wash hands and dry
3. Wear gloves
4. Prepare skin by cleaning with spirit, povidone iodine and spirit, let dry between applications
5. Hold the limb proximally to make the vein prominent
6. Pierce skin distal to the intended site of puncture
7. Insert needle into the vein (feeling of give way)
8. Ensure free flow, thread the needle further up into the vein
9. Secure the intracath by adhesive tape
10. Secure splint if needed (generally not needed)
11. Flush the cannula with normal saline 0.5ml
12. Inject fluid/medications
13. Check distal limb for adequacy of circulation
General Principles
• The sites for IM injections include the:
Quadriceps muscle group of the upper, outer thigh. This site is preferred because of the small risk of
giving the injection intravenously, hitting the femur with the needle, or injuring the sciatic nerve.
Gluteus muscle group in the buttock. This muscle group is difficult to use for IM injection because
of variable amounts of fat and subcutaneous tissue and the danger of injury to the sciatic nerve and
major blood vessels in the region. If using this site, use only the upper, outer quadrant of the muscle,
and always aspirate before injecting.
Deltoid muscle group. This site can be used for giving immunization but should not be used for
giving other injections.
Supplies
• Sterile 1-inch needle of the smallest size that will allow fluid to flow freely (e.g. 22- to 24-gauge)
• Sterile syringe of the smallest size available that has adequate markings for proper dose (e.g. 1- to 3-ml)
• Dry cotton-wool ball
Procedure
• Gather necessary supplies.
• Wash hands.
• Select the site for injection.
• Draw the drug for injection into the syringe.
• Ensure that the drug and dose are correct.
• Clean site with alcohol swab.
• Grasp the centre of the target muscle between the thumb and forefinger, if possible.
• Insert the needle at a 90-degree angle through the skin with a single quick motion.
• Withdraw the plunger of the syringe slightly to ensure that the tip of the needle is not in a vein
(i.e. no blood should enter the needle):
If the needle is in a vein:
Withdraw the needle without injecting the drug
Apply gentle pressure to the site with a dry cotton-wool ball to prevent bruising
Precautions:
• Avoid oedematous, bruised sites and excessive pressure.
• Avoid excess ambient light to shine on the probe, if so cover with an opaque material
• Do not tie the BP cuff proximal to the limb where the probe is fixed
• Do not run the oximeter on battery alone if back up power is available
Head and
Face
Fontanelle,
Facial
appearance for
dysmorphic
features
Source (RBSK)
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Admission Register
Sister Incharge...........................................................
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Date and Time of Birth ...../...../20......... ..... : ..... Birth Weight (grams) :
Date and Time of Admission ...../...../20......... ..... : ..... Age on Admission : Wt. on Admission (grams) :
Date and Time of Discharge ...../...../20......... Age on Discharge : Wt. on Discharge (grams) :
Type of Admission Inborn / Out born (Health Facility Referred) / Out born (Community Referred)
Indication for Admission ( Encircle the most relevant single indication, If multiple indication also mention all relevant numbers in the end as per priority, mention even if admitting for stabilization)
Provisional Diagnosis:
*Presumptive Diagnosis ( Encircle the most relevant single diagnosis, If multiple causes also mention all relevant numbers in the end as per sequence)
Other LBW (1000 gm – 2499 gm) : P 07.1 Neonatal Jaundice : P 59 Any Other Diagnosis (…...............…..
Prematurity (28-<37 Weeks) : P 07.3 Neonatal Diarrhoea : A 09 ...........................................................)
Small for Gestational Age (IUGR) : P 05.1 Hypothermia of Newborn : P 80 Multiple Diagnosis-
RDS of Newborn (HMD) : P 22.0 Environmental Hyperthermia of Newborn : P 81.0 Mention All Relevant Codes :
Transient Tachypnoea of Newborn : P 22.1 Congenital Malformation : a .......... b ........... c ............ d ............
Acquired Pneumonia : J 15 (a) Cong. Hydrocephalus : Q 03
Birth Asphyxia : P 21.0 (b) Meningomyelocele : Q 05
HIE of Newborn : P 91.6 (c) Imperforate anus : Q 42.3
Neonatal Sepsis : P 36.9 (d) Cleft Palate : Q 35
Meningitis : G 00 (e) Cleft Lip : Q 36
Convulsions of Newborn : P 90 (f) Cleft Palate with Cleft Lip : Q 37
(Hypoxic, Hypoglycaemic, Hypocalcaemic, (g) Congenital Deformities of Hip : Q 65
CNS Infections, Birth Trauma, Metabolic, (h) Congenital Deformities of Feet : Q 66
Other, Unknown Cause) (i) Other Malformation (.........................)
No. of doses : [1] [2] [3] [4] Foul Smelling Discharge : Yes [ ] No [ ]
Leaking P.V. > 24 Hours. : Yes [ ] No [ ] PIH : Hypertension / Pre Eclampsia / Eclampsia
Course of Labour : Uneventful / Prolonged 1st stage / Prolonged 2nd stage / Obstructed
Indication for Caesarean, : [Cephalo Pelvic Disproportion] [Malpresentation] [Placenta Previa] [Obstructed Labor] [Foetal Distress]
if Applicable
[Prolonged Labour] [Cord Prolapse] [Failed Induction (Dystocia)] [Previous LSCS] [Other ....................]
Resuscitation Required : NO [ ] Yes [ ] Tactile Stimulation /Only Oxygen / Bag & Mask [Duration....................min.]/
Intubation / Chest Compression / Adrenaline
PRESENTING COMPLAINTS:
GENERAL EXAMINATION
Tone : Limp / Active / Increase Tone Convulsions : Present on Admission / Past History / No
Jaundice : Yes [ ] No [ ] If Yes, extent [Face] [Chest] [Abdomen] [Legs] [Palms / Soles]
Sucking : [Good] [Poor] [No Sucking] Attachment : [Well attached] [Poorly attached] [Not attached]
Umbilicus : [Red] [Discharge] [Normal] Skin Pustules : [No] [Yes <10] [Yes >=10] [Abscess]
Congenital Malformation : No [ ] Yes [ ] Hydrocephalus / M.M.C. / Imperforate Anus / Cleft Palate / Cleft Lip /
Cleft Palate with Cleft Lip /Cong. Deformity of Hip / Cong. Deformity of Feet /
Other..................................
CVS : ...........................................................................................................................................................
RESPIRATORY : ...........................................................................................................................................................
CNS : ...........................................................................................................................................................
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In Case of Death : Mention Cause of Death ( The Most Relevant Cause of Death)
I / V Drugs
I / V Fluids
Oral Drugs
Feeding
Investigations
Conducted
(Results with Date)
Planning for
Next Day
MONITORING SHEET
NBSU Reg. No............................................................................... Date of Admission.........................
Weight............................................................................................ Date...............................................
Time
Activity
( Dull / Active )
Temperature
Colour
HR
RR
CRT
B.P.
O2 Flow
Rate
FIO2
Oxygen
Saturation
Blood
Glucose
Urine
Stool
Abdominal
Girth
R.T.
Aspirate
IV Patency
( Yes / No )
Blood
Collection
Other
Oral Feeds
Feeding Tube ( ml )
Oral Drugs
1. .......................................
2. .......................................
IV Drugs
(Also Record Fluid Volume)
1. .......................................
2. .......................................
3. .......................................
IV Fluids
1. ....................................... .......ml / hr .......ml / hr .......ml / hr .......ml / hr .......ml / hr .......ml / hr .......ml / hr .......ml / hr .......ml / hr .......ml / hr .......ml / hr .......ml / hr
( Enter Rate & fluid given
between each time slot ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml )
2. ....................................... ......ml / hr ......ml / hr ......ml / hr ......ml / hr ......ml / hr ......ml / hr ......ml / hr ......ml / hr ......ml / hr ......ml / hr ......ml / hr ......ml / hr
( Enter Rate & fluid given
between each time slot ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml )
IV Infusions
1. ....................................... .......ml / hr .......ml / hr .......ml / hr .......ml / hr .......ml / hr .......ml / hr .......ml / hr .......ml / hr .......ml / hr .......ml / hr .......ml / hr .......ml / hr
( Enter Rate & fluid given
between each time slot ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml )
2. ....................................... ......ml / hr ......ml / hr ......ml / hr ......ml / hr ......ml / hr ......ml / hr ......ml / hr ......ml / hr ......ml / hr ......ml / hr ......ml / hr ......ml / hr
( Enter Rate & fluid given
between each time slot ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml ) ( ........ml )
IV Bolus
................................. ml
Rate................. ml / hr
........................................................
........................................................
REFERRAL SUMMARY
Name of NBSU.....................................................
NBSU Reg. No. Sex : M / F / A Age : Weight (grams) :
Indication for Referral Ventilation / Surgical Intervention / Diagnostic Work up / Metabolic Work up / Dialysis / Other
*Final Diagnosis ( Encircle the most relevant single diagnosis, If multiple causes also mention all relevant numbers in the end as per priority)
Other LBW (1000 gm – 2499 gm) : P 07.1 Neonatal Jaundice : P 59 Any Other Diagnosis (…...............…..
Prematurity (28-<37 Weeks) : P 07.3 Neonatal Diarrhoea : A 09 ...........................................................)
Small for Gestational Age (IUGR) : P 05.1 Hypothermia of Newborn : P 80 Multiple Diagnosis-
RDS of Newborn (HMD) : P 22.0 Environmental Hyperthermia of Newborn : P 81.0 Mention All Relevant Codes :
Transient Tachypnoea of Newborn : P 22.1 Congenital Malformation : a .......... b ........... c ............ d ............
Acquired Pneumonia : J 15 (a) Cong. Hydrocephalus : Q 03
Birth Asphyxia : P 21.0 (b) Meningomyelocele : Q 05
HIE of Newborn : P 91.6 (c) Imperforate anus : Q 42.3
Neonatal Sepsis : P 36.9 (d) Cleft Palate : Q 35
Meningitis : G 00 (e) Cleft Lip : Q 36
Convulsions of Newborn : P 90 (f) Cleft Palate with Cleft Lip : Q 37
(Hypoxic, Hypoglycaemic, Hypocalcaemic, (g) Congenital Deformities of Hip : Q 65
CNS Infections, Birth Trauma, Metabolic, (h) Congenital Deformities of Feet : Q 66
Other, Unknown Cause) (i) Other Malformation (.........................)
*( Based on WHO, ICD - 10 Version: 2010 )
TREATMENT GIVEN
......................................................................................................
1. Oxygen : Yes / No ( If yes duration..............................................)
2. Phototherapy : Yes / No ( If yes duration..............................................)
......................................................................................................
3. Antibiotics : Yes / No ( If yes fill the details below)
Treatment Given No. of Days ......................................................................................................
a) .................................................................................. .......................
b) .................................................................................. ....................... ......................................................................................................
c) .................................................................................. .......................
d) .................................................................................. ....................... ......................................................................................................
RELEVANT INVESTIGATIONS
Date & Time of Discharge ....../....../20.... .... : .... Age on Discharge : Wt. on Discharge (grams) :
Other LBW (1000 gm – 2499 gm) : P 07.1 Neonatal Jaundice : P 59 Any Other Diagnosis (…...............…..
Prematurity (28-<37 Weeks) : P 07.3 Neonatal Diarrhoea : A 09 ...........................................................)
Small for Gestational Age (IUGR) : P 05.1 Hypothermia of Newborn : P 80 Multiple Diagnosis-
RDS of Newborn (HMD) : P 22.0 Environmental Hyperthermia of Newborn : P 81.0 Mention All Relevant Codes :
Transient Tachypnoea of Newborn : P 22.1 Congenital Malformation : a .......... b ........... c ............ d ............
Acquired Pneumonia : J 15 (a) Cong. Hydrocephalus : Q 03
Birth Asphyxia : P 21.0 (b) Meningomyelocele : Q 05
HIE of Newborn : P 91.6 (c) Imperforate anus : Q 42.3
Neonatal Sepsis : P 36.9 (d) Cleft Palate : Q 35
Meningitis : G 00 (e) Cleft Lip : Q 36
Convulsions of Newborn : P 90 (f) Cleft Palate with Cleft Lip : Q 37
(Hypoxic, Hypoglycaemic, Hypocalcaemic, (g) Congenital Deformities of Hip : Q 65
CNS Infections, Birth Trauma, Metabolic, (h) Congenital Deformities of Feet : Q 66
Other, Unknown Cause) (i) Other Malformation (.........................)
* ( Based on WHO, ICD - 10 Version: 2010 )
TREATMENT GIVEN
1. Oxygen : Yes / No ( If yes duration..............................................)
2. Phototherapy : Yes / No ( If yes duration..............................................)
3. KMC : Yes / No ( If yes duration..............................................)
4. Antibiotics : Yes / No ( If yes fill the details below)
CONDITION ON DISCHARGE (Mention Vitals, Provisional Diagnosis, General Condition, Persisting Health Problems)
BCG
.........................................................................................................................................................
OPV (0 Dose)
Hepatitis B (Birth Dose) .........................................................................................................................................................
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Final Diagnosis
Final Outcome
PRESENTING COMPLAINTS :
T.T. Doses :__________ Gestation Weeks :__________ Gravida :__________ Para :__________
Antenatal Steroids :________________ Number of Doses :_________________ Foul Smelling Discharge :______________
Leaking P.V. > 24 Hours :____________ PIH :___________________________ Course of Labour :____________________
E/O Feotal Distress :_______________ Type of Delivery :___________________ Indication of Caesarean, If Applicable
Cried Immed. after Birth :__________ Wt. at Birth :__________Kgs. Gestational Age_______(in completed weeks)
Maturity :__________
Resuscitation Required :__________ Vitamin K Given :__________ Breast Fed within 1 Hour :________
GENERAL EXAMINATION
General Condition :___________ Temperature :_______ºC Heart Rate :________/min Apnea:_________ RR :________/min
Jaundice :________________ Bleeding :__________ Bulging Anterior Fontanel :_____ Taking Breast Feed :__________
SYSTEMIC EXAMINATION
CVS : ...........................................................................................................................................................
RESPIRATORY : ...........................................................................................................................................................
CNS : ...........................................................................................................................................................
RELEVANT INVESTIGATIONS
CONDITION ON DISCHARGE (Mention Vitals, Provisional Diagnosis, General Condition, Persisting Health Problems)
.....................................................................................................................................
.....................................................................................................................................
Mentoring Checklists are available online on NHM portal under Child Health guidelines:
https://nhm.gov.in/index1.php?lang=1&level=3&sublinkid=1184&lid=368