Abstract |
Thai adult males (N = 85) with acute Plasmodium vivax malaria and normal glucose-6-phosphate dehydrogenase screening were randomized to receive 30 mg or 60 mg primaquine daily for 7 days (N = 43 and 42, respectively). The regimens were well tolerated and all patients recovered fully. Median fever clearance (47 hours; range 4 to 130 hours), mean + or - SD parasite clearance times (87.7 + or - 25.3 hours), gametocyte clearance, and adverse effects were similar in the 2 groups. Two patients, 1 from each group, had a 30% reduction in hematocrit. The cumulative 28 day relapse rate (95% confidence interval) by Kaplan Meier survival analysis was 29% (16-49%) in the 30 mg group compared with 7% (2-24%) in the 60 mg group; P = 0.027. Comparison with previous data obtained at this same site suggests that the recurrences comprised approximately 17% recrudescences and 12% relapses in the 30 mg/day group compared with 3% recrudescences and 4% relapses in the 60 mg/day group. These data suggest that the dose-response relationships for primaquine's asexual stage and hypnozoitocidal activities in-vivo are different. A 1 week course of primaquine 60 mg daily is an effective treatment of vivax malaria in this region.
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Authors | Sasithon Pukrittayakamee, Mallika Imwong, Kesinee Chotivanich, Pratap Singhasivanon, Nicholas P J Day, Nicholas J White |
Journal | The American journal of tropical medicine and hygiene
(Am J Trop Med Hyg)
Vol. 82
Issue 4
Pg. 542-7
(Apr 2010)
ISSN: 1476-1645 [Electronic] United States |
PMID | 20348496
(Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
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Topics |
- Adolescent
- Adult
- Animals
- Antimalarials
(administration & dosage, therapeutic use)
- Dose-Response Relationship, Drug
- Drug Administration Schedule
- Humans
- Malaria, Vivax
(drug therapy)
- Male
- Middle Aged
- Plasmodium vivax
(drug effects)
- Primaquine
(administration & dosage, therapeutic use)
- Thailand
(epidemiology)
- Young Adult
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