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泡罩包装对青蒿琥酯+甲氟喹在缅甸社区治疗非重症恶性疟中疗效优于单用青蒿琥酯的影响。

Influence of blister packaging on the efficacy of artesunate + mefloquine over artesunate alone in community-based treatment of non-severe falciparum malaria in Myanmar.

作者信息

Shwe T, Lwin M, Aung S

机构信息

Department of Medical Research (DMR), Ministry of Health, Yangon, Myanmar.

出版信息

Bull World Health Organ. 1998;76 Suppl 1(Suppl 1):35-41.

Abstract

Three studies were carried out to determine the need, acceptability, and efficacy of adding mefloquine to artemisinin derivatives (AD) for the first-line treatment of uncomplicated falciparum malaria. The first was a retrospective study of 255 basic health workers which showed that their recommendation of AD to patients depended on their level of training. None of the paramedics/midwives and only 9% of 129 doctors had prescribed AD, and no one had recommended AD in combination with mefloquine; 72% of patients used courses that were too short for parasitological cure. To promote the addition of mefloquine to AD regimens we conducted intervention workshops with health care providers and subsidized the cost of mefloquine to patients. In the second study, we interviewed 200 patients before and after the intervention to evaluate drug compliance with full doses of AD and use of subsidized mefloquine. After the intervention, we found that only 3.6% had used mefloquine and 62% had taken non-curative doses of AD. In the third study, we provided blister packs of medication in daily doses and compared the intake of AD + placebo (158 patients) with that of AD + mefloquine (222 patients) for 5 days. The compliance with both regimens was 99%. Blood smears for parasites on day 28 showed one positive in the AD + mefloquine group and 7 positive in the AD group. We conclude that provision of blister packs of daily doses is a very effective way to improve compliance with short courses and drug combinations, but the efficacy of the combination in Myanmar in this particular study was only marginally higher than that of AD alone.

摘要

开展了三项研究,以确定在一线治疗单纯性恶性疟中,将甲氟喹添加到青蒿素衍生物(AD)中的必要性、可接受性和疗效。第一项是对255名基层卫生工作者的回顾性研究,结果表明他们向患者推荐AD取决于其培训水平。没有一名护理人员/助产士开具过AD,在129名医生中只有9%开具过AD,而且没有人推荐过AD与甲氟喹联合使用;72%的患者使用的疗程过短,无法实现寄生虫学治愈。为了促进在AD治疗方案中添加甲氟喹,我们与医疗服务提供者举办了干预研讨会,并为患者补贴了甲氟喹的费用。在第二项研究中,我们在干预前后对200名患者进行了访谈,以评估患者对全剂量AD和补贴甲氟喹的药物依从性。干预后,我们发现只有3.6%的患者使用了甲氟喹,62%的患者服用了非治愈剂量的AD。在第三项研究中,我们提供了每日剂量的泡罩包装药物,并比较了158名服用AD + 安慰剂的患者与222名服用AD + 甲氟喹的患者5天的药物摄入量。两种治疗方案的依从性均为99%。第28天的寄生虫血涂片显示,AD + 甲氟喹组有1例阳性,AD组有7例阳性。我们得出结论,提供每日剂量的泡罩包装是提高对短疗程和药物组合依从性的非常有效的方法,但在缅甸的这项特定研究中,联合用药的疗效仅略高于单独使用AD。

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