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This document provides guidelines for diagnosing and managing dengue fever cases. It outlines the criteria for presumptive diagnosis of dengue which includes living in a dengue endemic area and having fever with two of the following: anorexia, rash, aches and pains, warning signs, leukopenia, or a positive tourniquet test. It further classifies dengue cases into those without or with warning signs and provides treatment protocols for oral or intravenous fluid replacement depending on the classification and the patient's condition. Close monitoring of vital signs and lab tests is emphasized.

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0% found this document useful (0 votes)
18 views

ch2 fs1

This document provides guidelines for diagnosing and managing dengue fever cases. It outlines the criteria for presumptive diagnosis of dengue which includes living in a dengue endemic area and having fever with two of the following: anorexia, rash, aches and pains, warning signs, leukopenia, or a positive tourniquet test. It further classifies dengue cases into those without or with warning signs and provides treatment protocols for oral or intravenous fluid replacement depending on the classification and the patient's condition. Close monitoring of vital signs and lab tests is emphasized.

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ry be
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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PRESUMPTIVE DIAGNOSIS DENGUE CASE MANA

Live in/travel to dengue endemic area.


Fever and two of the following criteria:
• Anorexia and nausea
ASSESSMENT

• Rash
• Aches and pains
• Warning signs
• Leukopenia WARNING SIGNS*
• Tourniquet test positive • Abdominal pain or tenderness
• Persistent vomiting
Laboratory confirmed dengue • Clinical fluid accumulation
(important when no sign of plasma leakage) • Mucosal bleed
• Lethargy, restlessness
• Liver enlargment >2 cm
• Laboratory: increase in HCT concurrent
with rapid decrease in platelet count
*(requiring strict observation and medical intervention)
CLASSIFICATION

NEGATIVE

Co-existing conditions
POSITIVE
Social circumstances

NEGATIVE

DENGUE WITHOUT WARNING SIGNS DENGUE WITH WARNING SIGNS

Group A Group B
(May be sent home) (Referred for in-hospital care)

Group criteria Group criteria OR: Existing warning signs Group criter
Patients who do not have warning signs Patients with any of the following features: Patients with
AND • co-existing conditions such as Laboratory tests • severe pla
who are able: pregnancy, infancy, old age, diabetes • full blood count (FBC) • severe ble
• to tolerate adequate volumes of oral mellitus, renal failure • haematocrit (HCT) • severe org
fluids • social circumstances such as living
• to pass urine at least once every alone, living far from hospital Treatment Laboratory t
6 hours Obtain reference HCT before fluid therapy. • full blood
Laboratory tests Give isotonic solutions such as 0.9 % saline, • haematoc
Laboratory tests • full blood count (FBC) Ringer’s Lactate. Start with 5–7 ml/kg/hr for • other orga
• full blood count (FBC) • haematocrit (HCT) 1–2 hours, then reduce to 3–5 ml/kg/hr for
• haematocrit (HCT) 2–4 hr, and then reduce to 2–3 ml/kg/hr Treatment of
Treatment or less according to clinical response. Start IV fluid
Treatment • Encouragement for oral fluids. If not
If patient imp
Advice for: tolerated, start intravenous fluid Reassess clinical status and repeat HCT: • IV fluids sh
• adequate bed rest therapy 0,9% saline or Ringer’s Lactate • if HCT remains the same or rises only
MANAGEMENT

then to 2-
• adequate fluid intake at maintenance rate. minimally -> continue with 2–3 ml/kg/ • IV fluids c
• Paracetamol, 4 gram maximum per hr for another 2–4 hours;
day in adults and accordingly in Monitoring • if worsening of vital signs and rapidly If patient is s
children. Monitor: rising HCT -> increase rate to 5–10 • check HC
Patients with stable HCT can be sent home. • temperature pattern ml/kg/hr for 1–2 hours. • if HCT inc
• volume of fluid intake and losses Reassess clinical status, repeat HCT and • if there is
Monitoring • urine output (volume and frequency) review fluid infusion rates accordingly: • if HCT de
Daily review for disease progression: • warning signs • reduce intravenous fluids gradually when
• decreasing white blood cell count • HCT, white blood cell and platelet the rate of plasma leakage decreases Treatment of
• defervescence counts. towards the end of the critical phase. Initiate IV flui
• warning signs (until out of critical period). This is indicated by: If patient imp
Advice for immediate return to hospital if • adequate urine output and/or fluid • give a cry
development of any warning signs, and intake If patient is s
• written advice for management (e.g. • HCT deceases below the baseline value • review the
home care card for dengue). in a stable patient. • if HCT wa
the need t
Monitoring • if HCT wa
Monitor: reassess a
• vital signs and peripheral perfusion (1–4 • If patient
hourly until patient is out of critical phase • if patient’
• urine output (4–6 hourly) • If HCT de
• HCT (before and after fluid replacement, • if HCT inc
then 6–12 hourly) then reduc
• blood glucose
• other organ functions (renal profile, liver Treatment of
profile, coagulation profile, as indicated). Give 5–10 m
CASE MANAGEMENT Days of illness 1 2 3 4 5 6 7 8 9 10

40°

Temperature

Dehydration Shock Reabsorption


Potential clinical issues
bleeding Fluid overload

Organ impairment

Platelet
Laboratory changes

Hematocrit

IgM/IgG
Serology and virology Viraemia

on)
Course of dengue illness: Febrile Critical Recovery phases

POSITIVE

SEVERE DENGUE

Group C
(Require emergency treatment)

Group criteria
Patients with any of the following features:
• severe plasma leakage with shock and/or fl uid accumulation with respiratory distress
• severe bleeding
• severe organ impairment

Laboratory tests
e fluid therapy. • full blood count (FBC)
as 0.9 % saline, • haematocrit (HCT)
–7 ml/kg/hr for • other organ function tests as indicated
–5 ml/kg/hr for
2–3 ml/kg/hr Treatment of compensated shock
response. Start IV fluid resuscitation with isotonic crystalloid solutions at 5–10 ml/kg/hr over 1 hour. Reassess patients’ condition.

If patient improves:
repeat HCT: • IV fl uids should be reduced gradually to 5–7 ml/kg/hr for 1–2 hours, then to 3–5 ml/kg/hr for 2–4 hours,
or rises only then to 2-3 ml/kg/hr for 2–4 hours and then reduced further depending on haemodynamic status;
h 2–3 ml/kg/ • IV fl uids can be maintained for up to 24–48 hours.

s and rapidly If patient is still unstable:


ate to 5–10 • check HCT after fi rst bolus;
• if HCT increases/still high (>50%), repeat a second bolus of crystalloid solution at 10–20 ml/kg/hr for 1 hour;
eat HCT and • if there is improvement after second bolus, reduce rate to 7–10 ml/kg/hr for 1–2 hours and continue to reduce as above;
ccordingly: • if HCT decreases, this indicates bleeding and need to cross-match and transfuse blood as soon as possible.
gradually when
ge decreases Treatment of hypotensive shock
itical phase. Initiate IV fluid resuscitation with crystalloid or colloid solution at 20 ml/kg as a bolus for 15 minutes.
If patient improves:
d/or fl uid • give a crystalloid/colloid solution of 10 ml/kg/hr for 1 hour, then reduce gradually as above.
If patient is still unstable:
e baseline value • review the HCT taken before the fi rst bolus;
• if HCT was low (<40% in children and adult females, <45% in adult males) this indicates bleeding,
the need to cross-match and transfuse (see above);
• if HCT was high compared to baseline value, change to IV colloids at 10–20 ml/kg as a second bolus over 30 minutes to 1 hour;
reassess after second bolus.
perfusion (1–4 • If patient is improving reduce the rate to 7–10ml/kg/hr for 1–2 hours, then back to IV cystalloids and reduce rates as above;
of critical phase • if patient’s condition is still unstable, repeat HCT after second bolus.
• If HCT decreases, this indicates bleeding (see above);
id replacement, • if HCT increases/remains high (>50%), continue colloid infusion at 10–20 ml/kg as a third bolus over 1 hour,
then reduce to 7–10 ml/kg/h 1–2 hours, then change back to crystalloid solution and reduce rate as above.

nal profi le, liver Treatment of haemorrhagic complications


e, as indicated). Give 5–10 ml/kg of fresh packed red cells or 10–20 ml/kg of fresh whole blood.

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