# Dengue Fever

> The content on this page is for informational and educational purposes only. It does not constitute medical advice, diagnosis, or treatment recommendations. If you have health concerns, consult a qualified healthcare professional. Medova is not a medical service provider.

Source: https://medova.health/en/knowledge/diseases/dengue-fever · Language: en

## Overview

Mosquito-borne viral infection causing high fever, severe pain, and potentially fatal hemorrhagic complications. The fastest-spreading arboviral disease globally with ~390 million infections per year.

## Medical Information

- ICD-10: A90
- ICD-11: 1D40
- Causative Agent: virus
- Severity: Severe
- Incubation Period: 3–14 days
- Infectious Period: 4–5 days
- Mortality Rate: 1%
- Vaccine available: Yes

## Symptoms

- Arthralgia (55%)
- Bone pain (45%)
- Fatigue (70%)
- High fever (97%)
- Itching (60%)
- Loss of appetite (55%)
- Maculopapular rash (50%)
- Myalgia (85%)
- Nausea (60%)
- Retro-orbital pain (70%)
- Severe headache (90%)
- Swollen lymph nodes (30%)
- Vomiting (45%)
- Abdominal pain (40%)
- Bleeding gums (15%)
- Bruising (10%)
- Hemorrhage (10%)
- Hepatomegaly (15%)
- Hypotension (8%)
- Petechiae (20%)
- Sore throat (35%)
- Tachycardia (12%)
- Altered consciousness (5%)
- Edema (8%)

## Transmission

- Mosquito Bite (Primary route)
- Blood transfusion
- Congenital (mother-to-child)
- Needle sharing
- Vector Borne

## Overview

Dengue fever is a viral disease transmitted by mosquitoes, occurring in tropical and subtropical regions. It can cause severe flu-like symptoms and, in some cases, life-threatening complications.

## Overview

Dengue is caused by four serotypes (DENV-1 to DENV-4) of the Dengue virus, a single-stranded RNA flavivirus transmitted primarily by Aedes aegypti (and secondarily by Ae. albopictus) mosquitoes. These day-biting urban mosquitoes breed in standing water near human habitation. Infection with one serotype confers lifelong immunity to that serotype but only temporary cross-protection (2–3 months) against others — subsequent infection with a different serotype carries increased risk of severe dengue due to antibody-dependent enhancement (ADE).

## Emergency Signs

Seek emergency medical care immediately if:

- Severe abdominal pain or persistent vomiting

- Bleeding from gums, nose, or in vomit/stool

- Rapid breathing or difficulty breathing

- Extreme fatigue, restlessness, or confusion

- Skin feels cold and clammy (sign of shock)

- No urination for 4–6 hours

- Symptoms worsening AFTER fever breaks (days 3–7) — this is the danger period

- Rash that turns into bruise-like purple patches

## Detailed Symptoms

Incubation: 4–10 days (typically 5–7 days). WHO classifies dengue into three categories:

**Dengue without warning signs:**

- Sudden high fever (40°C/104°F)

- Severe headache (retro-orbital pain is characteristic)

- Intense myalgia and arthralgia — "breakbone fever" (joint pain so severe it gave the disease its name)

- Nausea, vomiting, anorexia

- Maculopapular rash (appears days 3–7; may be pruritic)

- Mild hemorrhagic manifestations: petechiae, positive tourniquet test

- Leukopenia

**Dengue with warning signs (critical to recognize — requires close monitoring):**

- Abdominal pain or tenderness

- Persistent vomiting

- Clinical fluid accumulation (ascites, pleural effusion)

- Mucosal bleeding (gums, epistaxis)

- Lethargy or restlessness

- Liver enlargement >2 cm

- Increasing hematocrit with decreasing platelets

**Severe dengue (medical emergency):**

- Severe plasma leakage → shock (dengue shock syndrome — DSS)

- Severe hemorrhage (GI bleeding, hematemesis)

- Severe organ impairment (liver: AST/ALT >1000; brain: encephalitis; heart: myocarditis)

## Course of Disease

Dengue can progress from mild to severe forms, including dengue hemorrhagic fever and dengue shock syndrome.

## Diagnosis

Diagnosis depends on timing relative to fever onset:

- **Days 1–5 (acute/viremic phase):**
  – NS1 antigen rapid test: sensitivity 60–95% (highest days 1–3); highly specific
  – RT-PCR: gold standard during viremia; identifies serotype

- **Days 5+:**
  – Anti-dengue IgM (ELISA/rapid test): positive from day 5; persists 2–3 months. Cross-reacts with Zika and other flaviviruses.
  – Anti-dengue IgG: rises in secondary infection; IgG/IgM ratio >1.2 suggests secondary infection (higher ADE risk)

- **Full blood count (essential):**
  – Rising hematocrit (>20% above baseline) = plasma leakage
  – Thrombocytopenia (<100,000/mm³) — correlates with severity
  – Leukopenia — common in first few days

- **Liver function:** AST often elevated more than ALT (hepatitis pattern)

- **Tourniquet test:** ≥20 petechiae per 1 inch² is positive (low sensitivity, moderate specificity)

NOTE: In dengue-endemic areas, NS1 + IgM combination testing provides optimal accuracy.

## Treatment

No specific antiviral therapy. Management stratified by WHO severity classification:

**Group A (outpatient — dengue without warning signs):**

- Oral rehydration (ORS): 2–3 L/day minimum

- Paracetamol for fever and pain (max 4 g/day in adults)

- **AVOID:** NSAIDs (ibuprofen, aspirin, diclofenac) — increase bleeding risk

- Daily platelet and hematocrit monitoring; return if warning signs develop

**Group B (hospital observation — warning signs present):**

- IV fluid: isotonic crystalloid (0.9% NaCl or Ringer lactate) at 5–7 mL/kg/hr

- Strict fluid balance monitoring (avoid overhydration — pulmonary edema risk)

- 6-hourly hematocrit and platelet monitoring

- Monitor urine output (≥0.5 mL/kg/hr target)

**Group C (emergency — severe dengue/DSS):**

- Rapid IV fluid resuscitation: 10–20 mL/kg bolus over 15–30 min

- Colloids if no response to crystalloid

- Blood product transfusion for severe hemorrhage

- ICU care; vasopressors for refractory shock

- Platelet transfusion only for active bleeding with <10,000/mm³ (routine transfusion not recommended)

**Critical phase:** Days 3–7 of illness (defervescence period) — this is when severe dengue develops. Paradoxically, patients often feel better as fever drops while plasma leakage peaks.

## Prevention Details

**Vector control (primary prevention):**

- Eliminate Aedes breeding sites: empty standing water containers, flower pots, old tires, water storage

- Use mosquito repellent containing DEET (20–30%), picaridin, or IR3535 — reapply every 4–6 hours

- Wear long sleeves and light-colored clothing (Aedes bites during daytime, especially early morning and late afternoon)

- Sleep under permethrin-treated bed nets or in air-conditioned/screened rooms

- Mosquito coils and electric vaporizers as supplementary measures

**Vaccination:**

- **Dengvaxia (CYD-TDV — Sanofi):** Live recombinant tetravalent vaccine; licensed in ~20 countries for ages 6–45 with confirmed prior dengue infection (seropositive). Contraindicated in seronegative individuals (increases severe dengue risk via ADE). 3-dose schedule (0, 6, 12 months). NOT recommended for travelers.

- **TAK-003 (Qdenga — Takeda):** Live attenuated tetravalent; 2-dose schedule (0, 3 months); approved in EU, UK, Brazil, Indonesia, Thailand. Can be given regardless of prior dengue status. Efficacy ~80% against hospitalization. WHO recommended (2024) for high-burden settings.

- No dengue vaccine is currently recommended for short-term travelers.

## Travel Advice

Risk to travelers:

- **High risk:** Southeast Asia (Thailand, Indonesia, Philippines, Vietnam), South Asia (India, Sri Lanka, Bangladesh), Latin America (Brazil, Mexico, Caribbean), Sub-Saharan Africa

- **Moderate risk:** Pacific Islands, Southern China, Middle East

- **Emerging risk:** Southern Europe (France, Italy, Spain) — autochthonous transmission

- No vaccine is currently recommended for short-term travelers; prevention relies entirely on mosquito bite avoidance

- Peak Aedes biting: early morning (6–9 AM) and late afternoon (4–7 PM) — do NOT rely on nighttime bed nets alone

- Travelers returning with fever within 2 weeks of travel to endemic areas should be tested for dengue (and Zika, chikungunya — same vector)

- Avoid aspirin and ibuprofen if dengue suspected — use only paracetamol for fever

- Previous dengue infection increases risk of severe disease on re-exposure to a different serotype — disclose prior infection at travel clinic

## How common is it?

Dengue is the most rapidly expanding arboviral disease globally. WHO estimates 390 million infections/year (96 million symptomatic), 500,000 severe dengue cases, and ~40,000 deaths annually. 2024 saw record-breaking outbreaks:

- **Americas:** >16 million cases reported in 2024 (largest year ever); Brazil alone had >13 million suspected cases

- **Southeast Asia:** Thailand, Vietnam, Philippines, Indonesia — endemic with periodic epidemics every 3–5 years

- **South Asia:** India, Bangladesh, Sri Lanka — expanding range and intensity

- **Pacific Islands:** Major outbreaks in endemic cycles

- **Africa:** Emerging — likely vastly underreported; Burkina Faso, Kenya, Sudan outbreaks in 2024

- **Europe:** Autochthonous (local) transmission confirmed in France, Italy, Spain (Ae. albopictus range expansion due to climate change)

Risk factors for expansion: urbanization, climate change (warmer temperatures expand Aedes range), globalization, and water storage practices. The disease has expanded from 9 endemic countries in 1970 to 130+ countries today.

## Risk Factors

Traveling to endemic areas during peak transmission seasons, outdoor activities during mosquito activity hours.

## Complications Details

Severe dengue (formerly "dengue hemorrhagic fever/dengue shock syndrome") occurs in 1–5% of cases:

- **Dengue shock syndrome (DSS):** Plasma leakage causes hypovolemic shock

- mortality 1–5% with treatment, 20–50% without. Critical window: hours around defervescence (days 3–7)

- **Severe hemorrhage:** GI bleeding, hematemesis, menorrhagia

- more common in secondary infections and patients on anticoagulants

- **Organ involvement:**
  – Liver: Fulminant hepatitis (AST/ALT >1,000)

- may progress to acute liver failure
  – Brain: Encephalitis, encephalopathy (rare, 0.5–6% of hospitalized dengue)
  – Heart: Myocarditis, cardiac arrhythmias
  – Kidneys: Acute kidney injury (AKI) from shock and rhabdomyolysis

- **Fluid overload:** Iatrogenic complication from excessive IV fluids during recovery phase (plasma reabsorption causes fluid shifts → pulmonary edema, respiratory distress)

- **Secondary infection risk factors:** Prior infection with different serotype (ADE), age extremes, pregnancy, chronic diseases (diabetes, asthma)

- **Case fatality:** <1% with early recognition and proper fluid management

- 2–5% in severe dengue

- >20% if shock untreated

## Recovery & Outlook

Prognosis is generally good with supportive care. Severe dengue can be life-threatening.

## Available Vaccines

- [Dengue Vaccine](https://medova.health/en/knowledge/vaccines/dengue-vaccine)

## Sources & content verification

- Data sources: WHO/ICD-11, CDC Yellow Book 2024, ECDC (SafeTripVax QMR-004, 2026-03-23), WHO Disease Factsheets 2024 + CDC Travelers' Health 2024 + Heymann CDD 21st ed.
- Generated by: AI + Human review
- Review status: Awaiting medical review
- Last updated: 2026-03-29
- [www.who.int](https://www.who.int/emergencies/disease-outbreak-news)

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The content on this page is for informational and educational purposes only. It does not constitute medical advice, diagnosis, or treatment recommendations. If you have health concerns, consult a qualified healthcare professional. Medova is not a medical service provider.

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