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Crimean-Congo Haemorrhagic Fever

GMJ News knowledge hub · last reviewed August 2026 · Georgian Medical Journal

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Crimean-Congo haemorrhagic fever (CCHF) — caused by CCHF virus (a Nairovirus) transmitted by Hyalomma ticks — is one of the most feared tick-borne viral diseases globally, with case fatality rates of 10-40% and no approved vaccine or specific antiviral treatment (WHO). A WHO R&D Blueprint priority pathogen, CCHF is endemic across Africa, the Balkans, the Middle East and Central Asia — covering over 30 countries — with the geographic range of Hyalomma ticks actively expanding into previously unaffected European countries including Spain, France and Germany, driven by climate change.

Key messages

10-40% case fatality — expanding globally
Crimean-Congo haemorrhagic fever (CCHF) — caused by CCHF virus transmitted by Hyalomma ticks — has a case fatality rate of 10-40% and is expanding its geographic range into previously unaffected European countries as tick habitats expand with climate change (WHO).
WHO R&D Blueprint priority pathogen
CCHF is on the WHO R&D Blueprint list of priority pathogens — alongside Ebola, Nipah and Lassa — because of its potential for nosocomial spread, high case fatality, and absence of approved vaccines or effective antivirals.
Endemic across 30+ countries
CCHF is endemic across Africa, the Balkans (Turkey, Bulgaria, Kosovo, Serbia), the Middle East, and Central Asia — with Turkey reporting the highest case burden (hundreds of cases annually). Spain, Germany and France have documented autochthonous cases as Hyalomma ticks expand northward.
Healthcare worker risk
Nosocomial CCHF transmission — to healthcare workers without PPE, through blood or body fluids of infected patients — has caused multiple hospital outbreaks. Strict contact and droplet precautions and PPE are essential when CCHF is suspected.
Ribavirin — limited evidence
Ribavirin is recommended by WHO based on in vitro activity and observational studies, though randomised trial evidence is limited. Early initiation (within 4 days of symptoms) is most important.
Tick prevention is primary
Personal protection measures: avoiding tick habitats; use of repellents; regular tick checks; proper tick removal; and livestock tick control are the primary prevention strategies in endemic areas.

Key statistics

10-40%
case fatality rate
WHO
30+
endemic countries
WHO
~1,000
reported CCHF cases/year (massively underreported)
WHO/ECDC
Turkey
highest CCHF case burden globally (hundreds/year)
WHO
0
approved vaccines or specific antivirals
WHO 2024
Europe
autochthonous cases now documented in Spain, France
ECDC

CCHF cases by region — WHO reported data trend

Source: WHO. Turkey reports the most cases; Africa substantially underreported.

Glossary of key terms

CCHF virus
WHO
A negative-sense RNA Nairovirus (Bunyavirales) — the causative agent of CCHF. Maintained in a tick-animal-tick cycle; humans are incidental dead-end hosts. The virus is highly resistant to drying and can survive for days in blood at room temperature.
Hyalomma ticks
WHO/ECDC
The primary CCHF vector — large, distinctive ticks with striped legs (ornate hyalomma) found on cattle, sheep, goats, camels, hares and other animals. Hyalomma tick range is expanding northward into Europe with rising temperatures — explaining the emergence of autochthonous CCHF cases in Spain and France.
Haemorrhagic phase
WHO/Clinical
The most severe CCHF phase — occurring approximately 3-6 days after illness onset — characterised by haemorrhagic manifestations: petechiae, ecchymoses, nosebleeds, gum bleeding, haematemesis, melaena, haematuria. Thrombocytopenia, elevated liver enzymes and coagulopathy (DIC) are laboratory hallmarks.
Nosocomial CCHF transmission
WHO
Transmission of CCHF from infected patients to healthcare workers — through contact with blood, body fluids or tissues without adequate PPE. Multiple healthcare worker deaths have occurred globally. Patients with suspected CCHF require strict contact and droplet precautions; healthcare workers need PPE training.
Ribavirin for CCHF
WHO EML
An antiviral recommended by WHO for CCHF treatment and post-exposure prophylaxis based on in vitro activity and observational studies. IV ribavirin preferred; oral acceptable if IV unavailable. No completed randomised controlled trial. Early initiation important. WHO Essential Medicine for viral haemorrhagic fevers.
DNA vaccine (INO-4500)
CEPI/Research
A CCHF DNA vaccine — in Phase 2 trials (CEPI-funded) as of 2024. Encodes the CCHF virus glycoprotein. Other candidates: MVA-based and virus-like particle vaccines. CCHF vaccine development is a WHO R&D Blueprint priority.

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