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Compliance with a three-day course of artesunate-mefloquine combination and baseline anti-malarial treatment in an area of Thailand with highly multidrug resistant falciparum malaria

机译:在泰国具有高度多药耐药性的恶性疟疾地区遵从为期三天的青蒿琥酯-甲氟喹联合用药和基线抗疟疾治疗的规定

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摘要

BackgroundArtemisinin-based combination therapy (ACT) is presently recommended by the World Health Organization as first-line treatment for uncomplicated Plasmodium falciparum malaria in several countries, as a mean of prolonging the effectiveness of first-line malaria treatment regimens. A three-day course of artesunate-mefloquine (4 mg/kg body weight once daily for three consecutive days, plus 15 and 10 mg/kg body weight mefloquine on the first and second days) has been adopted by Malaria Control Programme of Thailand as first-line treatment for uncomplicated falciparum malaria all over the country since 2008. The gametocytocydal anti-malarial drug primaquine is administered at the dose of 30 mg (0.6 mg/kg) on the last day. The aim of the present study was to assess patient compliance of this combination regimen when applied to field condition.
机译:背景技术目前,世界卫生组织推荐基于青蒿素的联合治疗(ACT)作为一些国家中单纯性恶性疟原虫疟疾的一线治疗,以延长一线疟疾治疗方案的有效性。泰国的疟疾控制计划采用了为期三天的青蒿琥酯甲氟喹治疗(连续三天每天一次4 mg / kg体重,第一天和第二天分别加15和10 mg / kg体重甲氟喹),作为自2008年以来,在全国范围内对一例简单的恶性疟疾进行了一线治疗。在最后一天,以30 mg(0.6 mg / kg)的剂量施用了杀细胞杀伤剂的抗疟药伯氨喹。本研究的目的是评估应用于现场条件时该组合方案的患者依从性。

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