Crimean-Congo Haemorrhagic Fever (CCHF) is an often-lethal haemorrhagi
c fever caused by a tick-borne virus. There are no published data on r
ibavirin treatment of CCHF-infected patients, despite established in-v
itro and in-vivo sensitivity. We report three health workers-two surge
ons and a hospital worker-infected with CCHF Virus ill Pakistan who we
re treated with oral ribavirin 4 g/day for four days, then 2.4 g/day f
or six days. Intravenous ribavirin was unavailable. All three patients
were severely ill with low platelet and white-cell counts, raised asp
artate transaminase acid evidence of impaired haemostasis. Based on pu
blished reports, all had an estimated probability of death of 90% or m
ore. The patients became afebrile, and their haematological and bioche
mical abnormalities returned to normal within 48 h of ribavirin treatm
ent; all made a complete recovery, and developed IgG and IgM antibody
to CCHF virus. Our experience with ribavirin treatment is encouraging,
but does not constitute evidence of efficacy. Given the difficulties
in gathering adequate treatment data, we propose a consensus protocol
for both intravenous and oral treatment of CCHF. This protocol could b
e distributed to key medical personnel in areas endemic for CCHF and u
sed to provide a firm basis for effective treatment recommendations.