Primaquine therapy for malaria.

Primaquine is the only available drug for preventing relapse of malaria, and confusion surrounds its use. This review examines the wide range of clinical applications of primaquine described in the medical literature between 1946 and 2004. The risk of relapse of Plasmodium vivax malaria without prim...

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Main Authors: Baird, J, Hoffman, S
Format: Journal article
Language:English
Published: 2004
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author Baird, J
Hoffman, S
author_facet Baird, J
Hoffman, S
author_sort Baird, J
collection OXFORD
description Primaquine is the only available drug for preventing relapse of malaria, and confusion surrounds its use. This review examines the wide range of clinical applications of primaquine described in the medical literature between 1946 and 2004. The risk of relapse of Plasmodium vivax malaria without primaquine therapy ranged from 5% to 80% or more, depending largely upon geographic location. Supervision of therapy profoundly impacts the risk of relapse, and almost all reports of malaria resistant to primaquine are associated with lack of such supervision. We nonetheless suspect that there is widespread resistance to the standard course of primaquine therapy, which is 15 mg primaquine base daily for 14 days. Clinical evidence confirms that a course of 15 mg daily for just 5 days, a regimen widely used in areas where malaria is endemic, has no discernible efficacy. This review supports a recommendation for a regimen of 0.5 mg/kg primaquine daily for 14 days, on the basis of superior efficacy and good tolerability and safety in nonpregnant persons without glucose-6-phosphate dehydrogenase deficiency.
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spelling oxford-uuid:5cbd6f05-30f2-4f88-b0de-43f674be67b42022-03-26T17:30:02ZPrimaquine therapy for malaria.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:5cbd6f05-30f2-4f88-b0de-43f674be67b4EnglishSymplectic Elements at Oxford2004Baird, JHoffman, SPrimaquine is the only available drug for preventing relapse of malaria, and confusion surrounds its use. This review examines the wide range of clinical applications of primaquine described in the medical literature between 1946 and 2004. The risk of relapse of Plasmodium vivax malaria without primaquine therapy ranged from 5% to 80% or more, depending largely upon geographic location. Supervision of therapy profoundly impacts the risk of relapse, and almost all reports of malaria resistant to primaquine are associated with lack of such supervision. We nonetheless suspect that there is widespread resistance to the standard course of primaquine therapy, which is 15 mg primaquine base daily for 14 days. Clinical evidence confirms that a course of 15 mg daily for just 5 days, a regimen widely used in areas where malaria is endemic, has no discernible efficacy. This review supports a recommendation for a regimen of 0.5 mg/kg primaquine daily for 14 days, on the basis of superior efficacy and good tolerability and safety in nonpregnant persons without glucose-6-phosphate dehydrogenase deficiency.
spellingShingle Baird, J
Hoffman, S
Primaquine therapy for malaria.
title Primaquine therapy for malaria.
title_full Primaquine therapy for malaria.
title_fullStr Primaquine therapy for malaria.
title_full_unstemmed Primaquine therapy for malaria.
title_short Primaquine therapy for malaria.
title_sort primaquine therapy for malaria
work_keys_str_mv AT bairdj primaquinetherapyformalaria
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