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Therapeutic efficacy and safety of artesunate + amodiaquine and artemether + lumefantrine in treating uncomplicated Plasmodium falciparum malaria in children on the rainy south-east coast of Madagascar

机译:青蒿琥酯 + 阿莫地喹和蒿甲醚 + 苯芴醇治疗马达加斯加多雨东南海岸儿童单纯性恶性疟原虫疟疾的治疗疗效和安全性

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摘要

Malaria is a major public health problem in Madagascar, particularly in coastal areas. We conducted a randomized, controlled, parallel-group study of artemisinin-based combination therapy (ACT) in Mananjary and Farafangana, two localities on the rainy south-east coast of Madagascar, from March to September 2018. The efficacy and safety of artesunate + amodiaquine (ASAQ) and artemether + lumefantrine (AL) were assessed according to the WHO protocol with a 28-day follow-up. Children aged 6 months to 14 years with uncomplicated Plasmodium falciparum malaria were randomized to receive ASAQ or AL for three days (1:1). 347/352 (98.5%) randomized patients reached the study endpoint on day 28. Crude adequate clinical and parasitological response (ACPR) rates were 100% (95% CI: 98.8–100%) in the ASAQ group and 96% (95% CI: 93.1–98.9%) in the AL group (per protocol population). However, the PCR-corrected ACPR rate was 97.7% (95% CI: 95.4–100%) in the AL group. Two cases of recrudescence and three of re-infection were observed. Mild and moderate adverse events, including gastrointestinal and/or nervous disorders, were reported in 11.9% (42/352) of patients. We found that ASAQ and AL were safe and efficacious for treating uncomplicated P. falciparum malaria. They may be used for treatment at health facilities and at the community level, and for mass drug administration campaigns.
机译:疟疾是马达加斯加的一个主要公共卫生问题,尤其是在沿海地区。我们于 2018 年 3 月至 9 月在马达加斯加多雨的东南海岸的两个地区 Mananjary 和 Farafangana 进行了一项基于青蒿素的联合疗法 (ACT) 的随机、对照、平行组研究。根据 WHO 方案评估青蒿琥酯 + 阿莫地喹 (ASAQ) 和蒿甲醚 + 苯芴醇 (AL) 的有效性和安全性,并进行 28 天的随访。患有无并发症的恶性疟原虫疟疾的 6 个月至 14 岁儿童被随机分配接受 ASAQ 或 AL 治疗 3 天 (1:1)。347/352 名 (98.5%) 随机分配的患者在第 28 天到达研究终点。ASAQ 组粗略足够的临床和寄生虫学反应 (ACPR) 率为 100% (95% CI: 98.8-100%),AL 组为 96% (95% CI: 93.1-98.9%) (每个方案人群)。然而,AL 组的 PCR 校正 ACPR 率为 97.7% (95% CI: 95.4–100%)。观察到 2 例复发和 3 例再感染。11.9% (42/352) 的患者报告了轻度和中度不良事件,包括胃肠道和/或神经疾病。我们发现 ASAQ 和 AL 对治疗单纯性恶性疟原虫疟疾是安全有效的。它们可用于卫生机构和社区一级的治疗,以及用于大规模药物管理运动。

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