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dc.contributor.authorNaamara, W
dc.contributor.authorKunimoto, DY
dc.contributor.authorD'Costa, LJ
dc.contributor.authorNdinya-Achola, JO
dc.contributor.authorNsanze, H
dc.contributor.authorRonald ., AR
dc.contributor.authorPlummer, FA
dc.date.accessioned2013-04-26T11:08:39Z
dc.date.available2013-04-26T11:08:39Z
dc.date.issued1988
dc.identifier.citationGenitourin Med. 1988 Jun;64(3):189-92en
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/3044978
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/17068
dc.description.abstractIncreasing resistance of Haemophilus ducreyi to antimicrobials necessitates further trials of new antimicrobial agents for treating chancroid. Enoxacin has excellent in vitro activity against H ducreyi, and a randomised clinical trial of three doses of enoxacin 400 mg at intervals of 12 hours compared with a single dose of trimethoprim/sulphametrole (TMP/SMT) 640/3200 mg was therefore conducted. Of 169 men enrolled in the study, 86 received enoxacin and 83 received TMP/SMT. Ulcers were improved or cured in 65/73 men treated with enoxacin and 57/70 men treated with TMP/SMT. This difference was not significant. At 72 hours after treatment, H ducreyi was eradicated from ulcers of 72/77 men treated with enoxacin and of 67/74 of those treated with TMP/SMT. Patients with buboes responded equally well to both treatments. Of 100 H ducreyi strains tested, all were susceptible to both 0.25 mg/l enoxacin and the combination of 0.25 mg/l TMP and 5 mg/l SMT. Although most men treated with either regimen were cured, neither regimen appeared to be the optimum treatment for chancroid. This study shows the efficacy of enoxacin for a soft tissue infection caused by Gram negative organisms.en
dc.language.isoenen
dc.titleTreating chancroid with enoxacinen
dc.typeArticleen
local.publisherCentre for Microbiology Research, Kenya Medical Research Instituteen


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