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Dengue, chikungunya and Zika

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Severe dengue at defervescence

Severe abdominal pain, persistent vomiting, mucosal bleeding, lethargy, restlessness, fluid accumulation, hepatomegaly, a rising haematocrit with falling platelets, shock or organ dysfunction around fever resolution indicates plasma leakage.

Action: Admit urgently, assess ABCDE and perfusion, involve infection and critical care, start carefully titrated isotonic crystalloid when shock or clinically important leakage is present, and reassess haematocrit, urine output and respiratory status after every intervention.

Synopsis

Distinguish the major Aedes-borne viral syndromes, detect dengue capillary leak before shock, investigate infection by illness timing, and protect pregnancies and future pregnancies from Zika exposure.

  • Dengue, chikungunya and Zika are transmitted by day-biting Aedes mosquitoes and overlap geographically and clinically.
  • Dengue commonly causes abrupt high fever, severe headache, retro-orbital pain, myalgia, nausea and rash; warning signs cluster near defervescence when capillary permeability rises.
  • Chikungunya is distinguished by abrupt fever with prominent, often symmetric and disabling polyarthralgia; joint symptoms can persist for months or years.

Key red flags

Deterioration as fever settles, usually during illness days three to seven, is characteristic of the dengue critical phase and must not be mistaken for recovery.

Dengue warning phase

Severe abdominal pain, repeated vomiting, mucosal bleeding, lethargy, restlessness, liver enlargement or fluid accumulation emerging near defervescence predicts deterioration.

Investigation priorities

01
First-line returning-fever assessmentFirst stepFirst line

Identify malaria, physiological instability and common organ complications before arbovirus confirmation.

Management branches

TRIAGEAssess acute arboviral illness

A traveller returns from an Aedes-risk area with fever, rash, arthralgia or conjunctivitis.

  1. Record destinations, dates, outbreak exposure, mosquito bites, day of illness, pregnancy possibility, sexual partner travel and previous flavivirus infection or vaccination.
  2. Use ABCDE, obtain urgent malaria testing and baseline haematocrit, platelets, renal and liver profiles; screen separately for high-consequence infection when epidemiology requires it.

Key medicines

ParacetamolGive 500 mg to 1 g orally every four to six hours when needed, with at least four hours between doses and no more than 4 g in 24 hours for a suitable adult.
Isotonic crystalloid for dengue shockGive a protocolised intravenous crystalloid bolus or infusion matched to shock severity, then reassess perfusion, urine output, haematocrit and respiratory findings before any further fluid.
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Sources and review status8 sources · checked 27 Aug 2026 · clinical review pending
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom