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A Comparison of Two Short-Course Primaquine Regimens for the Treatment and Radical Cure of Plasmodium vivax Malaria in Thailand

机译:两种治疗泰国间日疟原虫的短疗程伯氨喹治疗方案的比较

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摘要

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 ± SD parasite clearance times (87.7 ± 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.
机译:将患有间日疟原虫疟疾和正常葡萄糖-6-磷酸脱氢酶筛查的泰国成年男性(N = 85)随机接受7天每天30 mg或60 mg primaquine(分别为N = 43和42)。该方案耐受良好,所有患者均完全康复。两组的中位发烧清除率(47小时;范围为4至130小时),平均±SD寄生虫清除时间(87.7±25.3小时),配子细胞清除及不良反应相似。 2名患者(每组1名)的血细胞比容降低了30%。 Kaplan Meier生存分析的28天内累积复发率(95%置信区间)在30 mg组为29%(16–49%),而60 mg组为7%(2–24%)。 P = 0.027。与在同一地点获得的先前数据的比较表明,在30 mg /天的组中复发包括约17%的复发和12%的复发,而在60 mg /天的组中复发包括3%的复发和4%的复发。这些数据表明,伯氨喹的无性阶段和体内杀豚子杀虫活性的剂量反应关系是不同的。每天60 mg的primaquine疗程为1周,是该地区间日间疟疾的有效治疗方法。

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