Teklemariam Michael, Assefa Ashenafi, Kassa Moges, Mohammed Hussien, Mamo Hassen
Department of Microbial, Cellular and Molecular Biology; College of Natural Sciences, Addis Ababa University, Addis Ababa, Ethiopia.
Bacterial, Parasitic and Zoonotic Diseases Research Directorate, Ethiopian Public Health Institute, Addis Ababa, Ethiopia.
PLoS One. 2017 Apr 26;12(4):e0176004. doi: 10.1371/journal.pone.0176004. eCollection 2017.
Malaria, particularly due to Plasmodium falciparum, remains a major public health threat in Ethiopia. Artemether-lumefantine (AL) has been the first-line antimalarial drug against uncomplicated P. falciparum malaria in the country since 2004. Regular monitoring of antimalarial drugs is recommended by the World Health Organization (WHO) to help early detection of drug resistant strains of the parasite and contain their rapid spread. The objective of this study was to assess the therapeutic efficacy of AL in a high-transmission setting in Ethiopia. The study site was Setit Humera, northwest Ethiopia. Single-arm prospective study of a 28-day follow-up was conducted from October 2014 to January 2015 according to the revised WHO 2009 drug efficacy study protocol. Study end-points were classified into primary end-point and secondary end-point. While the primary end-point was the day-28 adequate clinical and parasitological response the secondary end-points were clinical and parasitological evaluations (parasite, fever and gametocyte clearance rate, incidence of drug adverse events) and the relative increment in hemoglobin (Hb) level from baseline to day (D) 14 and D28. A total of 92 patients were enrolled and 79 had completed the 28-day follow-up period. The overall cure rate was 98.8% with 95% confidence interval of 0.915-0.998 without polymerase chain reaction correction. The parasite clearance rate was high with fast resolution of clinical symptoms; 100% of the study participants cleared parasitaemia and fever on D3. Gametocyte carriage was reduced from 7% on D0 to 1% on D3 and complete clearance was achieved on D14. Mean Hb concentration significantly increased on D28 compared to that on D14. There was no serious adverse event. AL was efficacious and safe in a high-transmission setting for treatment of uncomplicated falciparum malaria.
疟疾,尤其是由恶性疟原虫引起的疟疾,在埃塞俄比亚仍然是一个重大的公共卫生威胁。自2004年以来,蒿甲醚-本芴醇(AL)一直是该国治疗非复杂性恶性疟原虫疟疾的一线抗疟药物。世界卫生组织(WHO)建议定期监测抗疟药物,以帮助早期发现寄生虫的耐药菌株并遏制其快速传播。本研究的目的是评估AL在埃塞俄比亚高传播环境中的治疗效果。研究地点是埃塞俄比亚西北部的塞蒂特胡梅拉。根据修订后的WHO 2009年药物疗效研究方案,于2014年10月至2015年1月进行了一项为期28天随访的单臂前瞻性研究。研究终点分为主要终点和次要终点。主要终点是第28天的充分临床和寄生虫学反应,次要终点是临床和寄生虫学评估(寄生虫、发热和配子体清除率、药物不良事件发生率)以及从基线到第14天和第28天血红蛋白(Hb)水平的相对增量。总共招募了92名患者,其中79名完成了28天的随访期。总体治愈率为98.8%,95%置信区间为0.915 - 0.998,未进行聚合酶链反应校正。寄生虫清除率高,临床症状迅速缓解;100%的研究参与者在第3天清除了寄生虫血症和发热。配子体携带率从第0天的7%降至第3天的1%,并在第14天实现了完全清除。与第14天相比,第28天的平均Hb浓度显著增加。没有严重不良事件。AL在高传播环境中治疗非复杂性恶性疟原虫疟疾是有效且安全的。