Laury Jessica E, Mugittu Kefas, Kajeguka Debora C, Kamugisha Erasmus, Ishengoma Deus S, Mandara Celine I, Ngasala Billy, Chiduo Mercy G, Mahende Muhidin K, Kitau Jovin, Ahmed Maimuna M, Mkumbaye Sixbert I, Francis Filbert, Chacky Frank, Warsame Marian, Serbantez Naomi, Kitojo Chonge, Reaves Erik J, Bishanga Dunstan R, Bajic Marko, Kabula Bilali I, Muro Florida, Kavishe Reginald A
Global Health Fellowship Program, Public Health Institute, Oakland, California.
Division of Parasitic Diseases and Malaria, National Center for Emerging and Zoonotic Infectious Diseases.
J Infect Dis. 2025 Feb 4;231(1):251-259. doi: 10.1093/infdis/jiae425.
Artemether-lumefantrine (AL) is the first-line antimalarial drug for the treatment of uncomplicated malaria in Tanzania. The World Health Organization (WHO) recommends regular efficacy monitoring of antimalarial drugs to inform case management policy decisions. This study assessed the safety and efficacy of AL for treating uncomplicated Plasmodium falciparum malaria in Tanzania in 2022.
Children aged 6 months to 10 years with uncomplicated P falciparum malaria were recruited from 4 sentinel sites and treated with the standard 6-dose, 3-day regimen for AL. Clinical and parasitological responses were monitored for 28 days using the WHO standard protocol. Genotyping based on msp1, msp2, and glurp was used to distinguish recrudescence from reinfection. Sanger sequencing was used to detect K13 mutations.
Three hundred fifty-two participants, 88 per site, were enrolled. Four withdrew and 55 experienced parasite recurrence. The polymerase chain reaction (PCR)-corrected Kaplan-Meier efficacies were 89.9% in Pwani, 95.0% in Kigoma, 94.4% in Tanga, and 98.9% in Morogoro. No K13 mutations were found.
Artemether-lumefantrine remains highly efficacious in 3 regions of Tanzania, but the PCR-corrected efficacy in Pwani fell below the WHO-defined 90% threshold at which policy change is recommended. Implementing strategies to diversify artemisinin-based combination therapies to ensure effective case management in Tanzania is critical.
蒿甲醚-本芴醇(AL)是坦桑尼亚治疗非复杂性疟疾的一线抗疟药物。世界卫生组织(WHO)建议定期对抗疟药物的疗效进行监测,以为病例管理政策决策提供依据。本研究评估了2022年AL在坦桑尼亚治疗非复杂性恶性疟原虫疟疾的安全性和疗效。
从4个哨点招募6个月至10岁患有非复杂性恶性疟原虫疟疾的儿童,并采用标准的6剂、3天疗程的AL进行治疗。使用WHO标准方案对临床和寄生虫学反应进行28天的监测。基于msp1、msp2和glurp的基因分型用于区分复发和再感染。采用桑格测序法检测K13突变。
共纳入352名参与者,每个哨点88名。4人退出研究,55人出现寄生虫复发。经聚合酶链反应(PCR)校正的Kaplan-Meier疗效在滨海省为89.9%,在基戈马为95.0%,在坦噶为94.4%,在莫罗戈罗为98.9%。未发现K13突变。
蒿甲醚-本芴醇在坦桑尼亚的3个地区仍然高度有效,但滨海省经PCR校正的疗效低于WHO定义的90%阈值,即建议改变政策的阈值。实施基于青蒿素的联合疗法多样化策略以确保坦桑尼亚有效的病例管理至关重要。