Fluconazole for the Treatment of Cutaneous Leishmaniasis Caused by Leishmania major
Abdulrahman A. Alrajhi, M.D., M.P.H., Elfaki A. Ibrahim, Ph.D., Edward B. De Vol, Ph.D., Mohammad Khairat, M.D., Rajab M. Faris, M.D., and James H. Maguire, M.D., M.P.H.
Background Whereas certain oral antifungal azoles are well documentedto have activity against leishmania, data on the efficacy offluconazole for leishmaniasis are limited. We conducted a controlledtrial in Saudi Arabia of fluconazole for the treatment of cutaneousleishmaniasis caused by Leishmania major.
Methods This randomized, double-blind, placebo-controlled trialassessed the efficacy of oral fluconazole, in a dose of 200mg daily for six weeks, in the treatment of parasitologicallyconfirmed cutaneous leishmaniasis. The primary outcome measurewas the time to the complete healing of all lesions.
Results A total of 106 patients were assigned to receive fluconazole,and 103 patients were assigned to receive placebo. Follow-updata were available for 80 and 65 patients, respectively. Atthe three-month follow-up, healing of lesions was complete for63 of the 80 patients in the fluconazole group (79 percent)and 22 of the 65 patients in the placebo group (34 percent;relative risk of complete healing, 2.33 [95 percent confidenceinterval, 1.63 to 3.33]). According to an intention-to-treatanalysis, the rates of healing were 59 percent and 22 percent,respectively (relative risk, 2.76 [95 percent confidence interval,1.84 to 4.12]). Sodium stibogluconate was offered to 11 patientsin the fluconazole group who returned for follow-up (14 percent)and 33 of those in the placebo group (51 percent) in whom oraltreatment was judged to have failed. According to a KaplanMeieranalysis, the time to healing was shorter for the fluconazolegroup (median, 8.5 weeks, as compared with 11.2 weeks in theplacebo group; P<0.001 by the log-rank test). Side effectswere mild and similar in both groups.
Conclusions A six-week course of oral fluconazole is a safeand useful treatment for cutaneous leishmaniasis caused by L.major.
Source Information
From the Department of Immunology and Infectious Diseases, Harvard School of Public Health, and the Division of Infectious Diseases, Department of Medicine, Brigham and Women's Hospital both in Boston (A.A.A., J.H.M.); and the Ministry of Health of Saudi Arabia (E.A.I., M.K., R.M.F.); the Section of Infectious Diseases, Department of Medicine (A.A.A.), and the Department of Biostatistics, Epidemiology, and Scientific Computing (E.B.D.V.), King Faisal Specialist Hospital and Research Centre both in Riyadh, Saudi Arabia.
Address reprint requests to Dr. Alrajhi at the Department of Medicine, MBC No. 46, King Faisal Specialist Hospital and Research Centre, P.O. Box 3354, Riyadh 11211, Saudi Arabia.
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