Treatment of Dengue Fever
Dengue treatment is entirely supportive and symptomatic, as no specific antiviral therapy is currently approved—the cornerstone is careful fluid management, acetaminophen for pain/fever, and vigilant monitoring for progression to severe disease. 1, 2, 3
General Management Principles
- Symptomatic management is the only available treatment since no antiviral therapy exists for dengue infection 1, 2, 3
- Acetaminophen (paracetamol) at standard doses is the only acceptable analgesic for pain and fever relief 1, 4, 5
- Aspirin and NSAIDs must be strictly avoided due to significantly increased bleeding risk from platelet dysfunction and potential hemorrhagic complications 1, 4, 5, 6
- Daily complete blood count monitoring is essential to track platelet counts and hematocrit levels, particularly during the critical phase (days 3-7 of illness) 1, 4, 5
Fluid Management Strategy
For Patients Without Shock
- Ensure adequate oral hydration with oral rehydration solutions, aiming for more than 2500 mL daily intake 1, 4, 5
- Oral rehydration is appropriate for patients without signs of shock or warning signs 1
- Avoid routine bolus intravenous fluids in patients with febrile illness who are not in shock, as this can lead to fluid overload 1
For Dengue Shock Syndrome
- Administer an initial fluid bolus of 20 mL/kg crystalloid solution with careful patient reassessment afterward 1, 4, 5
- Crystalloid solutions (normal saline or Ringer's lactate) are first-line for moderate shock 1
- Colloid solutions may be beneficial for severe dengue shock syndrome when available 1, 4
- For persistent tissue hypoperfusion despite adequate fluid resuscitation, vasopressors such as dopamine or epinephrine may be required 1, 4
Critical Monitoring Parameters
Warning Signs Requiring Immediate Attention
- Monitor for clinical indicators of progression to severe disease: persistent vomiting, severe abdominal pain, lethargy or restlessness, mucosal bleeding, and high hematocrit with rapidly falling platelet count 1, 4, 5
- Watch for signs of adequate tissue perfusion: normal capillary refill time, absence of skin mottling, warm and dry extremities, well-felt peripheral pulses, return to baseline mental status, and adequate urine output (>0.5 mL/kg/hour in adults) 1, 4
Laboratory Monitoring
- Daily complete blood count to track platelet counts and hematocrit levels 1, 4
- Rising hematocrit with falling platelet count indicates plasma leakage and impending shock 1, 4
Management of Complications
- Blood transfusion may be necessary in cases of significant bleeding with close monitoring of hemoglobin and hematocrit 1, 4, 5
- Consider abdominal ultrasound to evaluate for ascites, hepatomegaly, and plasma leakage if severe abdominal pain develops 5
- For severe pain not responding to acetaminophen, opioid analgesics may be considered with careful monitoring 5
Critical Pitfalls to Avoid
- Administering excessive fluid boluses in patients without shock leads to fluid overload and pulmonary edema, particularly during the recovery phase 1, 5
- Failing to recognize the critical phase (days 3-7 of illness) when plasma leakage can rapidly progress to shock is a common error 1, 4
- Never use aspirin or NSAIDs under any circumstances due to high bleeding risk 1, 4, 5, 6
- Delaying fluid resuscitation in patients with dengue shock syndrome significantly worsens outcomes 1, 5
- Inadequate monitoring during the critical phase of illness can miss early signs of deterioration 1, 4
Discharge Criteria
Patients can be discharged when ALL of the following are met:
- Afebrile for at least 48 hours without antipyretics 4
- Resolution or significant improvement of symptoms including abdominal pain 4, 5
- Stable hemodynamic parameters for at least 24 hours without support (normal heart rate, blood pressure, capillary refill) 4
- Adequate oral intake and urine output (>0.5 mL/kg/hour) 4
- Laboratory parameters returning to normal ranges 4
Post-Discharge Instructions
- Monitor and record temperature twice daily 4
- Return immediately if temperature rises to ≥38°C on two consecutive readings or if any warning signs develop (persistent vomiting, severe abdominal pain, bleeding, lethargy) 4
Diagnostic Confirmation
- For patients presenting ≤7 days after symptom onset, nucleic acid amplification tests (NAATs/PCR) on serum are the preferred diagnostic method 7, 4
- For patients presenting >7 days after symptom onset or with negative NAAT results, IgM antibody testing should be performed 7
- Cross-reactivity with other flaviviruses (yellow fever, Japanese encephalitis, Zika) complicates antibody interpretation, so vaccination history is essential 7