World Health Organization · 1st edition, 2025 · 125 pages
Evidence-based GRADE recommendations for clinicians managing suspected or confirmed arboviral infections in all settings
- Issuer
- World Health Organization
- Edition
- 1st edition, 2025
- Audience
- Clinicians managing arboviral infections (community care, primary care, emergency departments, hospital wards); policymakers and health facility administrators developing national/regional protocols
- Evidence
- GRADE-rated recommendations based on systematic review of RCTs (predominantly dengue, applied to other arboviruses as indirect evidence); some recommendations based on sepsis literature applied to arboviral context; GDG consensus where evidence limited
- Reviewed
- 14 Oct 2026 · GMJ
What this guideline says
GMJ summary
These guidelines provide the first comprehensive GRADE-methodology recommendations for managing dengue, chikungunya, Zika and yellow fever. They address both non-severe (outpatient) and severe (hospitalized) disease, recognizing that clinical differentiation between arboviruses is often impossible at presentation, particularly in resource-limited settings without rapid diagnostics.
Key recommendations include using crystalloids over colloids for intravenous resuscitation, measuring capillary refill time and lactate to guide fluid therapy, and avoiding NSAIDs due to bleeding risk. For symptom control, paracetamol or metamizole are suggested; corticosteroids are not recommended for non-severe disease. For yellow fever with liver failure, N-acetylcysteine is suggested while specific antivirals remain investigational.
The guidance emphasizes that most evidence derives from dengue studies but is applied across arboviruses given diagnostic uncertainty at presentation. Recommendations balance benefits and harms in the context of limited certainty evidence, with strong emphasis on individualized clinical decision-making and careful monitoring to prevent both under- and over-resuscitation.
Key points
For clinicians — doses and thresholds as stated in the guideline
- Protocolized oral fluids (measured intake, ~3000 ml/24h in adults) suggested for non-severe disease to potentially reduce hospitalization
- Paracetamol 500 mg–1 g every 4–6 hours (max 4 g/day adults; 10–15 mg/kg every 4–6h in children, max 60 mg/kg/day) suggested for fever/pain
- NSAIDs strongly recommended against in all suspected arboviral disease (any severity) due to bleeding risk, unless dengue definitively ruled out
- Crystalloids recommended over colloids for IV resuscitation in severe disease; colloids associated with 27 more adverse events per 1000 patients
- Capillary refill time >3 seconds (measured on index finger at heart level, 10-second pressure) recommended to guide IV fluid therapy
- Lactate monitoring (target ≥10–30% decrease every 2 hours) recommended to guide resuscitation where available; unreliable in liver failure
- Passive leg raise test (cardiac output increase >10%) suggested when uncertain if more IV fluids warranted in shock
- Prophylactic platelet transfusion not recommended for thrombocytopenia <50,000/µL without active bleeding; corticosteroids and IVIG not recommended for severe disease
Recommendations summary by disease severity
Table extracted from the guideline
| Intervention | Non-severe disease | Severe disease (hospitalized) | Strength |
|---|---|---|---|
| Protocolized oral fluids | Suggested FOR | N/A | Conditional |
| Paracetamol | Suggested FOR | N/A | Conditional |
| Metamizole | Suggested FOR (where licensed) | N/A | Conditional |
| NSAIDs | Recommended AGAINST | Recommended AGAINST | Strong |
| Corticosteroids | Suggested AGAINST | Suggested AGAINST | Conditional |
| Crystalloids vs colloids | N/A | Crystalloids suggested | Conditional |
| Capillary refill time monitoring | N/A | Recommended FOR | Strong |
| Lactate monitoring | N/A | Recommended FOR | Strong |
| Passive leg raise test | N/A | Suggested FOR (when uncertain) | Conditional |
| Platelet transfusion (prophylactic) | N/A | Suggested AGAINST | Conditional |
| IVIG | N/A | Suggested AGAINST | Conditional |
| N-acetylcysteine (yellow fever liver failure) | N/A | Suggested FOR | Conditional |
Source: World Health Organization, Guidelines for clinical management of arboviral diseases: dengue, chikungunya, Zika and yellow fever. Reproduced in summary form.
What changed in this edition
Versus the previous edition
- First WHO global guideline using GRADE methodology for arboviral disease management; previous guidance was expert opinion-based
- Supersedes all specific recommendations in Dengue guidelines for diagnosis, treatment, prevention and control (2009)
- Integrates evidence across four arboviral diseases (dengue, chikungunya, Zika, yellow fever) recognizing diagnostic uncertainty
- Strong recommendation against NSAIDs replaces previous conditional guidance, based on bleeding risk despite low certainty evidence
- New recommendations on fluid resuscitation monitoring (CRT, lactate, PLR) based on sepsis literature applied to arboviral context
- Explicit recommendations against corticosteroids and IVIG where previously practice varied by region
From the guideline
Verbatim
“WHO recommends against the use of non-steroidal anti-inflammatory medications (NSAIDs) in patients with acute suspected or confirmed arboviral disease, irrespective of severity.”
Editor’s perspective
Why this matters for Georgia and the region
Prof. Giorgi Pkhakadze, MD, MPH, PhD
Editor-in-Chief, Georgian Medical Journal · Chair, Public Health Institute of Georgia · WHO consultant, health and migration
As Georgia strengthens its surveillance for emerging vector-borne diseases and the South Caucasus experiences warmer temperatures conducive to Aedes mosquito expansion, these guidelines provide essential preparation for arboviral threats that are no longer confined to tropical regions. The strong recommendation against NSAIDs is critical for our clinicians to internalize now, before we face our first dengue outbreak, because ibuprofen and diclofenac are currently first-line antipyretics in many Georgian primary care settings and changing prescribing culture takes time. I would stress the capillary refill time measurement protocol to our hospital teams: it requires only training and a chronometer, no expensive equipment, yet provides evidence-based guidance for fluid resuscitation that could prevent both fatal under-resuscitation and harmful pulmonary oedema from over-treatment. The realistic implementation challenge for Georgia will be establishing reliable arbovirus diagnostics and ensuring that emergency departments stock adequate crystalloid volumes during potential summer epidemics, when our health system already faces seasonal respiratory illness and tourism-related demands. Our National Centre for Disease Control should adapt these WHO protocols now, while transmission pressure is low, rather than attempting guideline development during an outbreak when clinical and public health capacity is overwhelmed.
ORCID 0000-0001-7609-4515 · Perspective written for the GMJ Guidelines Library, 14 Oct 2026
Applicability
Georgia and the South Caucasus
Georgia and the South Caucasus currently have minimal autochthonous arboviral transmission, but climate change, urbanization and expansion of Aedes albopictus vectors into temperate zones increase introduction risk. European Region has documented sporadic dengue and chikungunya transmission in Mediterranean countries since 2007, with autochthonous cases in France, Italy, Spain and Croatia. National programmes should consider: establishing arbovirus surveillance and diagnostic capacity before local transmission occurs; training clinicians in early recognition using the clinical differentiation tables (fever, rash, arthralgia patterns); ensuring essential medicines availability (paracetamol, crystalloids) and basic monitoring tools (chronometers for CRT, lactate measurement where feasible); and developing protocols for travel-associated cases given increasing global connectivity. The guideline’s emphasis on low-cost interventions (CRT, protocolized oral fluids) suits all resource settings, while acknowledging that some monitoring (lactate, cardiac output during PLR) requires equipment investment.
Questions this guideline answers
Quick answers
Can I use ibuprofen or aspirin for fever in suspected dengue?
No. WHO strongly recommends against NSAIDs in all suspected arboviral disease, any severity, due to platelet inhibition and bleeding risk. Use paracetamol 500 mg–1 g every 4–6 hours (adults) or metamizole where licensed instead. Only consider NSAIDs if dengue definitively ruled out or for confirmed chikungunya/Zika with inflammatory arthritis.
How do I measure capillary refill time correctly?
Place patient's hand at heart level, apply firm pressure to ventral surface of index finger distal phalanx for 10 seconds, release and time return to baseline colour using a chronometer. CRT >3 seconds is abnormal. Ensure warm room, standardized technique. Use to guide IV fluid therapy in hospitalized patients alongside other monitoring.
What IV fluid should I use for dengue shock and how much?
Use crystalloids (Ringer's lactate or 0.9% saline) rather than colloids. Volume and rate depend on age, weight, severity and response. Monitor using CRT (target ≤3 sec), lactate (target ≥10% decrease every 2h where available), BP, urine output, haematocrit. Use passive leg raise test if uncertain whether more fluid needed. Refer to regional protocols for specific volumes.
Should I give platelets prophylactically if platelet count is 20,000/µL but no bleeding?
No. WHO suggests against prophylactic platelet transfusion for platelet counts <50,000/µL without active bleeding. Transfuse only for active major bleeding or invasive procedures. Thrombocytopenia alone is not an indication; focus on careful monitoring and minimizing invasive interventions to reduce bleeding risk.
Related on GMJ
Interconnected resources
Dictionary of Public Health
Drugs A–Z
GMJ News coverage
- Sri Lanka deploys military to combat surging dengue epidemic as hospitals reach capacityAug 2026
- Tropical Cyclones Dramatically Amplify Dengue Transmission, Study FindsJul 2026
- Climate Change May Turn North America and Europe into Chikungunya Hotspots by 2070Jul 2026
- Genetic Factors May Explain Why Some Chikungunya Infections Turn ChronicMay 2026
Quality & accreditation
Other guidelines on this topic
- Guidelines for the management of severe dengue in intensive care units
- Consolidated guidelines for the prevention, diagnosis and treatment of postpartum haemorrhage
- Acute diarrhoea — MSF Clinical guidelines
- Guidelines on the Management of Advanced HIV Disease
- Consolidated guidelines for the management of common childhood illness: management of asthma in children and adolescents and bronchiolitis in infants and young children
- Issuer
- World Health Organization
- Type
- Guideline
- Edition
- 1st edition, 2025
- Status
- Current
- Published
- 2025-07-04
- Languages
- English
- Scope
- Clinical management of suspected/confirmed dengue, chikungunya, Zika, yellow fever in non-severe (outpatient) and severe (hospitalized) patients; symptomatic treatment, fluid resuscitation, monitoring, adjunctive therapies
- Audience
- Clinicians managing arboviral infections (community care, primary care, emergency departments, hospital wards); policymakers and health facility administrators developing national/regional protocols
- Pages
- 125
- Licence
- CC BY-NC-SA 3.0 IGO
- ISBN
- 978-92-4-011111-0
- Evidence
- GRADE-rated recommendations based on systematic review of RCTs (predominantly dengue, applied to other arboviruses as indirect evidence); some recommendations based on sepsis literature applied to arboviral context; GDG consensus where evidence limited
- Next review
- Not specified; stated as living guideline to be updated according to emerging evidence
- Record history
- Created 14 Oct 2026 · updated 14 Oct 2026 · next check Apr 2027
World Health Organization. WHO guidelines for clinical management of arboviral diseases: dengue, chikungunya, Zika and yellow fever. Geneva: World Health Organization; 2025. Licence: CC BY-NC-SA 3.0 IGO.GMJ Guidelines Library records are original summaries written by the GMJ editorial team from the issuer’s published document and reviewed by a physician. They do not replace the full guideline. The document is the copyright of its issuer and is linked, not hosted. Spotted an error or a newer edition? Tell the Guidelines Desk.
Was this article helpful?

