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Randomized, comparative study of the efficacy and safety of artesunate plus amodiaquine, administered as a single daily intake versus two daily intakes in the treatment of uncomplicated falciparum malaria

机译:青蒿琥酯与阿莫地喹的疗效和安全性的随机对照研究,以每日一次服用与每天两次服用来治疗单纯性恶性疟疾

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Background Artesunate plus amodiaquine is a coblistered ACT, given as a single daily intake. It has been suggested that, in view of the number of tablets to be taken (particularly in adults), it may be possible to improve compliance by allowing patients to divide the daily dose. The objectives of this randomized, comparative, open-label, multicentre study, conducted in Senegal and in Cameroon in 2005, was to demonstrate the non-inferiority and to compare the safety of artesunate plus amodiaquine, as a single daily intake versus two daily intakes. Methods A three-day treatment period and 14-day follow-up period was performed in any subject weighting more than 10 kg, presenting with a malaria paroxysm confirmed by parasitaemia ≥ 1,000/μl, after informed consent. Patients were randomly allocated into one of the two regimens, with dosage according to bodyweight range. All products were administered by an authorized person, blinded to both the investigating physician and the biologist. The primary endpoint was an adequate response to treatment on D14 (WHO definition). The two-sided 90% confidence interval of the difference was calculated on intent to treat (ITT) population; the acceptance limit for non-inferiority was 3%. The safety was evaluated by incidence of adverse events. Results Three-hundred and sixteen patients were included in the study. The two patient groups were strictly comparable on D0. The adequate responses to treatment were similar for the two treatment regimens on D14, PCR-corrected (99,4% in the one-daily intake group versus 99,3% in the comparative group). The statistical analyses demonstrated the non-inferiority of administering artesunate/amodiaquine as two intakes. The drug was well tolerated. The main adverse events were gastrointestinal disorders (2.5%) and pruritus (2.5%); safety profiles were similar in the two groups. Conclusion This pilot study confirms the efficacy and good tolerability of artesunate plus amodiaquine, administrated either in one or in two daily intakes.
机译:背景青蒿琥酯加阿莫地喹是一种联合治疗的ACT,每天服用一次。已经提出,考虑到要服用的片剂数量(特别是在成年人中),可以通过允许患者划分每日剂量来改善依从性。这项于2005年在塞内加尔和喀麦隆进行的随机,比较,开放标签,多中心研究的目的是证明非劣势并比较青蒿琥酯和阿莫地喹的单日摄入量与每日两次摄入量的安全性。方法对任何体重超过10 kg的受试者进行三天的治疗期和14天的随访期,经知情同意后,其表现为疟原虫病,经寄生虫血症≥1000 /μl证实。根据患者体重范围,将患者随机分配为两种方案之一。所有产品均由授权人员管理,对研究医师和生物学家均不知情。主要终点是对D14治疗的适当反应(WHO定义)。差异的双向90%置信区间是根据治疗意愿(ITT)人群计算的;非自卑感的接受极限为3%。通过不良事件的发生率评估安全性。结果本研究共纳入316例患者。这两个患者组在D0上严格可比。对于D14的两种治疗方案,经PCR校正后,对治疗的充分反应相似(一日摄入量组为99.4%,对比组为99.3%)。统计分析表明,将青蒿琥酯/阿马地喹作为两个摄入量服用是非劣效的。该药耐受性良好。主要不良事件为胃肠道疾病(2.5%)和瘙痒(2.5%);两组的安全性相似。结论这项初步研究证实了青蒿琥酯和阿莫地喹的疗效和良好的耐受性,每天一次或两次摄入均可。

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