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[蒿甲醚-本芴醇治疗尼日尔疟疾三个流行区5至15岁儿童单纯性恶性疟的疗效和安全性]

[Therapeutic effectiveness and safety of artemether lumefantrine for the treatment of uncomplicated Plasmodium falciparum malaria in children aged 5 to 15 years in three epidemiological strata of malaria in Niger].

作者信息

Yacouba Idrissa, Issa Ibrahima, Sanoussi Maman Kabirou, Jika Mamane, Hamani Boureima Seidou, Diallo Oumarou, Issoufou Seyni, Mahamadou Aboubacar, Abou Yahaya, Koko Daniel, Moustapha Lamine Mahaman, Ibrahim Maman Laminou

机构信息

Programme National de Lutte contre le Paludisme (PNLP) Niger, BP 026 Niamey, Niger.

Centre de Recherche Médicale et Sanitaire (CERMES), BP 10887 Niamey, Niger.

出版信息

Ann Biol Clin (Paris). 2025 Jun 1;83(3):280-292. doi: 10.1684/abc.2025.1973.

Abstract

Malaria is a major public health issue in Niger. This study aims to provide information on the therapeutic efficacy of antimalarials, specifically focusing on artemether-lumefantrin (AL) in children aged 5 to 15 years in Aderbissinat, Aguié, and Baban Tabki. To evaluate the therapeutic efficacy of AL in children in the specified regions. The study was conducted from August 26 to October 25, 2022, using the standard WHO/2015 28-day follow-up method. Biological confirmation was done using rapid diagnostic tests (RDT) and microscopy, while PCR was used to distinguish between reinfections and recrudescences. Out of 352 suspected malaria patients, 263 were included in the study. There were 5 lost to follow-up, 1 voluntary withdrawal, and 3 protocol violations. The malaria prevalence was 92%, with an average parasite density of 42,606 P/μL and a sex-ratio of 1.02. The overall adequate clinical and parasitological response (ACPR) after PCR correction was 97.25%, with 100% in Aderbissinat and Aguié, and 90% in Baban Tabki. No major adverse events were recorded. The results support the use of AL for the treatment of uncomplicated malaria as per the National Malaria Control Program (NMCP).

摘要

疟疾是尼日尔的一个主要公共卫生问题。本研究旨在提供有关抗疟药治疗效果的信息,特别关注阿代尔比西纳、阿吉埃和巴巴恩塔布基5至15岁儿童使用蒿甲醚-本芴醇(AL)的情况。以评估AL对指定地区儿童的治疗效果。该研究于2022年8月26日至10月25日进行,采用世界卫生组织/2015年标准的28天随访方法。使用快速诊断测试(RDT)和显微镜检查进行生物学确认,同时使用聚合酶链反应(PCR)区分再感染和复发。在352名疑似疟疾患者中,263名被纳入研究。有5名失访,1名自愿退出,3名违反方案。疟疾患病率为92%,平均寄生虫密度为42,606个/微升,性别比为1.02。经PCR校正后的总体充分临床和寄生虫学反应(ACPR)为97.25%,阿代尔比西纳和阿吉埃为100%,巴巴恩塔布基为90%。未记录到重大不良事件。结果支持按照国家疟疾控制计划(NMCP)使用AL治疗非复杂性疟疾。

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