Show simple item record

dc.contributor.authorAnabwania, GM
dc.contributor.authorDimitia, G
dc.contributor.authorNgira, JA
dc.contributor.authorBryceso, ADM
dc.date.accessioned2013-06-30T08:46:13Z
dc.date.available2013-06-30T08:46:13Z
dc.date.issued1983-01
dc.identifier.citationThe Lancet Volume 321, Issue 8318, 29 January 1983, Pages 210–212en
dc.identifier.urihttp://www.sciencedirect.com/science/article/pii/S0140673683925886
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/42776
dc.description.abstractThe 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 (χ2=4·41, p<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.en
dc.language.isoenen
dc.publisherUniversity of Nairobien
dc.titleComparison Of Two Dosage Schedules Of Sodium Stibogluconate In The Treatment Of Visceral Leishmaniasis In Kenyaen
dc.typeArticleen
local.publisherDepartment of Paediatricsen


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record