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六剂蒿甲醚-本芴醇(苯芴醇)治疗耐多药恶性疟原虫疟疾的疗效

Efficacy of six doses of artemether-lumefantrine (benflumetol) in multidrug-resistant Plasmodium falciparum malaria.

作者信息

Vugt M V, Wilairatana P, Gemperli B, Gathmann I, Phaipun L, Brockman A, Luxemburger C, White N J, Nosten F, Looareesuwan S

机构信息

Shoklo Malaria Research Unit, Mae Sot, Tak Province, Thailand.

出版信息

Am J Trop Med Hyg. 1999 Jun;60(6):936-42. doi: 10.4269/ajtmh.1999.60.936.

Abstract

The new oral fixed combination artemether-lumefantrine (CGP 56697) has proved to be an effective and well-tolerated treatment of multi-drug resistant Plasmodium falciparum malaria, although cure rates using the four-dose regimen have been lower than with the currently recommended alternative of artesunate-mefloquine. Two six-dose schedules (total adult dose = 480 mg of artemether and 2,880 mg of lumefantrine) were therefore compared with the previously used four-dose regimen (320 mg of artemether and 1,920 mg of lumefantrine) in a double-blind trial involving 359 patients with uncomplicated multidrug-resistant falciparum malaria. There were no differences between the three treatment groups in parasite and fever clearance times, and reported adverse effects. The two six-dose regimens gave adjusted 28-day cure rates of 96.9% and 99.12%, respectively, compared with 83.3% for the four-dose regimen (P < 0.001). These six-dose regimens of artemether-lumefantrine provide a highly effective and very well-tolerated treatment for multidrug-resistant falciparum malaria.

摘要

新型口服固定复方蒿甲醚-本芴醇(CGP 56697)已被证明是治疗多重耐药恶性疟原虫疟疾的一种有效且耐受性良好的疗法,尽管使用四剂疗法的治愈率低于目前推荐的青蒿琥酯-甲氟喹替代疗法。因此,在一项涉及359例非复杂性多重耐药恶性疟患者的双盲试验中,将两种六剂方案(成人总剂量=480毫克蒿甲醚和2880毫克本芴醇)与先前使用的四剂方案(320毫克蒿甲醚和1920毫克本芴醇)进行了比较。三个治疗组在寄生虫清除时间、发热清除时间和报告的不良反应方面没有差异。两种六剂方案的28天校正治愈率分别为96.9%和99.12%,而四剂方案为83.3%(P<0.001)。这些蒿甲醚-本芴醇六剂方案为多重耐药恶性疟提供了一种高效且耐受性非常好的治疗方法。

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