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氯喹、周效磺胺/乙胺嘧啶、甲氟喹及甲氟喹-青蒿琥酯治疗缅甸北部克钦邦恶性疟的比较

Comparison of chloroquine, sulfadoxine/pyrimethamine, mefloquine and mefloquine-artesunate for the treatment of falciparum malaria in Kachin State, North Myanmar.

作者信息

Smithuis Frank, Shahmanesh Maryam, Kyaw Moe Kyaw, Savran Olivia, Lwin Saw, White Nicholas J

机构信息

Medecins sans Frontieres-Holland, Yangon, Myanmar.

出版信息

Trop Med Int Health. 2004 Nov;9(11):1184-90. doi: 10.1111/j.1365-3156.2004.01323.x.

Abstract

Multi-drug resistant falciparum malaria is widespread in Asia. In Thailand, Cambodia and Vietnam the national protocols have changed largely to artesunate combined treatment regimens but elsewhere in East and South Asia chloroquine (CQ) and sulfadoxine-pyrimethamine (SP) are still widely recommended by national malaria control programmes. In Kachin State, northern Myanmar, an area of low seasonal malaria transmission, the efficacy of CQ (25 mg base/kg) and SP (1.25/25 mg/kg), the nationally recommended treatments at the time, were compared with mefloquine alone (M; 15 mg base/kg) and mefloquine combined with artesunate (MA; 15:4 mg/kg). An open randomized controlled trial enrolled 316 patients with uncomplicated Plasmodium falciparum malaria, stratified prospectively into three age-groups. Early treatment failures (ETF) occurred in 41% (32/78) of CQ treated patients and in 24% of patients treated with SP (18/75). In young children the ETF rates were 87% after CQ and 35% after SP. Four children (two CQ, two SP) developed symptoms of cerebral malaria within 3 days after treatment. By day 42, failure rates (uncorrected for reinfections) had increased to 79% for CQ and 81% for SP. ETF rates were 2.5% after treatment with M and 3.9% after treatment with MA (P > 0.2). Overall uncorrected treatment failure rates at day 42 following M and MA were 23% and 21%, respectively. Chloroquine and SP are completely ineffective for the treatment of falciparum malaria in northern Myanmar. Mefloquine treatment is much more effective, but three day combination regimens with artesunate will be needed for optimum efficacy and protection against resistance.

摘要

耐多药恶性疟在亚洲广泛流行。在泰国、柬埔寨和越南,国家治疗方案已大幅转向青蒿琥酯联合治疗方案,但在东亚和南亚的其他地区,国家疟疾控制项目仍广泛推荐使用氯喹(CQ)和磺胺多辛-乙胺嘧啶(SP)。在缅甸北部的克钦邦,这是一个疟疾季节性传播较低的地区,当时国家推荐的治疗药物CQ(25毫克碱基/千克)和SP(1.25/25毫克/千克)的疗效与单独使用甲氟喹(M;15毫克碱基/千克)以及甲氟喹与青蒿琥酯联合使用(MA;15:4毫克/千克)进行了比较。一项开放性随机对照试验纳入了316例非复杂性恶性疟患者,前瞻性地分为三个年龄组。早期治疗失败(ETF)在接受CQ治疗的患者中占41%(32/78),在接受SP治疗的患者中占24%(18/75)。在幼儿中,CQ治疗后的ETF率为87%,SP治疗后的ETF率为35%。4名儿童(2名CQ治疗,2名SP治疗)在治疗后3天内出现了脑型疟症状。到第42天,失败率(未校正再感染)CQ组升至79%,SP组升至81%。M治疗后的ETF率为2.5%,MA治疗后的ETF率为3.9%(P>0.2)。M和MA治疗后第42天的总体未校正治疗失败率分别为23%和21%。氯喹和SP对缅甸北部恶性疟的治疗完全无效。甲氟喹治疗效果要好得多,但为了达到最佳疗效和预防耐药性,需要三天的青蒿琥酯联合治疗方案。

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