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Clinical Trial
. 1983 Jan 29;1(8318):210-3.
doi: 10.1016/s0140-6736(83)92588-6.

Comparison of two dosage schedules of sodium stibogluconate in the treatment of visceral leishmaniasis in Kenya

Clinical Trial

Comparison of two dosage schedules of sodium stibogluconate in the treatment of visceral leishmaniasis in Kenya

G M Anabwani et al. Lancet. .

Abstract

The efficacy and safety of a single daily dose of sodium stibogluconate, 20 mg/kg body weight, given by deep intramuscular injection was compared with the conventional dose of 10 mg Sb/kg body weight in a randomised trial in Kenyan children and adults with visceral leishmaniasis. Splenic aspiration proved a safe and simple method for assessing parasitological response to treatment. In children the higher dose was associated with a faster clinical and parasitological response, and 100% were cured within 4 weeks, compared with 60% receiving the lower dosage. This difference is statistically significant by life-table analysis (x2 = 4.41, p less than 0.05). The superiority of the higher dose was not, however, seen in adults. In both children and adults the higher dose given daily for 2--4 weeks and in one patient for up to 7 weeks was found to be safe and well tolerated. It is likely, but not proven, that the use of sodium stibogluconate in a dose of 20 mg/kg bw daily for 4 weeks will reduce the relapse-rate in Kenyan children with visceral leishmaniasis.

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