Current Efficacy of the First Line Uncomplicated Malaria Treatment in Two Sentinels Sites of Côte d’Ivoire

O. Touré, N’Guessan Tiacoh Landry, Ira Bonouman Ama Valerie, Assi Serge Brice, K. Emmanuel, Kokora Adonis, Yao Serge Stéphane, A. Eric, Kinifo-Lawson Viviane, Adji Eric Gbessi, Beourou Sylvain, Tuo Karil, A. Bérenger, G. Albert, D. Joseph
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引用次数: 3

Abstract

Background: Artemisinin combination therapies have been wildly used in the treatment of uncomplicated falciparum malaria in most endemic countries. This strategy has been implemented in Cote d’Ivoire since 2005 with Artesunate + Amodiaquine (AS + AQ) and Artemether + lumefantrine (AL). The goal of this study was to assess efficacy and safety of these two drugs in two sentinel’s sites, Man and Abidjan in Cote d’Ivoire. Methods: An open label, randomized, clinical trial was conducted in Man in the west and Abidjan in the south of Cote d’Ivoire. Patients older than 6 months with uncomplicated falciparum malaria after consent were randomized in AS+AQ and AL group and were followed up for 42 days. The first endpoint was Adequate Clinical and Parasitological Response adjusted by PCR at day 42. The second endpoints were fever and parasite clearance time, crude cure rate at day 42 and safety of the two ACTs. Results: A total of 241 patients were randomized in AS+AQ (120) and AL (121) group. The crude cure rate at day 42 in PP analysis was 95.8% and 87.9% in AS+AQ and AL respectively. After correction by PCR ACPR at day 42 was 99.2% in AS+AQ group and 97.4% in AL group. The two ACTs were well tolerated. Conclusion: AS+AQ and AL remains efficacious in the uncomplicated malaria treatment in the two areas but continue monitoring is needed particularly for AL.
目前在Côte科特迪瓦两个哨点一线简单疟疾治疗的疗效
背景:在大多数流行国家,青蒿素联合疗法已被广泛用于治疗无并发症的恶性疟疾。自2005年以来,这一战略已在科特迪瓦通过青蒿琥酯+阿莫地喹(AS + AQ)和蒿甲醚+甲苯胺(AL)实施。这项研究的目的是评估这两种药物在科特迪瓦的曼和阿比让两个哨点的疗效和安全性。方法:在科特迪瓦西部的曼和南部的阿比让进行了一项开放标签、随机的临床试验。年龄大于6个月且同意后无并发症的恶性疟疾患者随机分为AS+AQ组和AL组,随访42 d。第一个终点是在第42天通过PCR调整的充分的临床和寄生虫学反应。第二个终点是发热和寄生虫清除时间,第42天的粗治愈率和两种ACTs的安全性。结果:共241例患者随机分为AS+AQ组(120例)和AL组(121例)。PP分析第42天的粗固成率AS+AQ和AL分别为95.8%和87.9%。经PCR校正,第42天AS+AQ组ACPR为99.2%,AL组为97.4%。这两种ACTs耐受性良好。结论:AS+AQ和AL在两个地区的简单疟疾治疗中仍然有效,但需要继续监测特别是AL。
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