Objectives-To determine the effectiveness of intramuscular (IM) ceftri
axone sodium in the treatment of chronic donovanosis, and the acceptab
ility to patients and staff of supervised outpatient treatment in rura
l clinics. Methods-We collected demographic and sexual health data fro
m participants using a standard questionnaire, recorded lesions baseli
ne diagrams. Treatment consisted of a single daily IM injection of 1 g
ceftriaxone diluted in 2 ml of 1% lignocaine. Clinic staff followed p
atients for between three and 12 months, enabling the detection of lat
e recurrences. Setting-Rural Aboriginal communities in central Austral
ia. Participants-The study describes eight women and four men with chr
onic donovanosis in detail, and summarises the outcome in 12 additiona
l cases. All cases presented with advanced lesions which had failed to
heal on the standard oral antibiotic regimens used in the region. Res
ults-The mean duration of infection was 3.0 years (SD 1.9 years), and
between four and ten courses of antibiotics had been prescribed for si
x of the 12 patients. Patients received between 7-26g of ceftriaxone s
odium. Clinical improvement was in most lesions, and four healed compl
etely without recurrence after a total 7-10g of ceftriaxone. Mild recu
rrences responded to further ceftriaxone or short courses of oral anti
biotics. Treatment was tolerated, and both patient and compliance high
. Conclusion-Donovanosis is an important cause of chronic genital ulce
ration in central Australia, and is potentially an important risk fact
or for HIV transmission in Aboriginal communities. The pharmacokinetic
s and safety profile of ceftriaxone make it a useful and cost-effectiv
e agent in the ambulatory management of donovanosis, especially in rem
ote communities. Supervised multidrug regimens of two or more long-act
ing agents may provide the best answer in donovanosis, administered th
rough the existing health care infrastructure.