School of Medical Laboratory Science, Institute of Health, Jimma University, Jimma, Ethiopia.
Department of Biomedical, College of Public Health and Medical Science, Mettu University, Mettu, Ethiopia.
Malar J. 2020 Jul 10;19(1):240. doi: 10.1186/s12936-020-03307-4.
The efficacy of artemether-lumefantrine (AL) for treatment of uncomplicated Plasmodium falciparum malaria in south-western Ethiopia is poorly documented. Regular monitoring of drug efficacy is an important tool for supporting national treatment policies and practice. This study investigated the therapeutic efficacy of AL for the treatment of P. falciparum malaria in Ethiopia.
The study was a one-arm, prospective, evaluation of the clinical and parasitological, responses to directly observed treatment with AL among participants 6 months and older with uncomplicated P. falciparum malaria. Real-time polymerase chain reaction (PCR) and nested PCR reaction methods were used to quantify and genotype P. falciparum. A modified protocol based on the World Health Organization 2009 recommendations for the surveillance of anti-malarial drug efficacy was used for the study with primary outcomes, clinical and parasitological cure rates at day-28. Secondary outcomes assessed included patterns of fever and parasite clearance. Cure rate on day-28 was assessed by intention to treat (ITT) and per protocol (PP) analysis. Parasite genotyping was also performed at baseline and at the time of recurrence of parasitaemia to differentiate between recrudescence and new infection.
Of the 80 study participants enrolled, 75 completed the follow-up at day-28 with ACPR. For per protocol (PP) analysis, PCR-uncorrected and-corrected cure rate of AL among the study participants was 94.7% (95% CI 87.1-98.5) and 96% (95% CI 88.8-99.2), respectively. For intention to treat (ITT) analysis, the cure rate was 90% (95% CI 88.8-99.2). Based on Kaplan-Meier survival estimate, the cumulative incidence of failure rate of AL was 3.8% (95% CI 1.3-11.4). Only three participants 3.8% (95% CI 0.8-10.6) of the 80 enrolled participants were found to be positive on day-3. The day three-positive participants were followed up to day 28 and did not correspond to treatment failures observed during follow-up. Only 7.5% (6/80) of the participants were gametocyte-positive on enrollment and gametocytaemia was absent on day-2 following treatment with AL.
The therapeutic efficacy of AL is considerably high (above 90%). AL remained highly efficacious in the treatment of uncomplicated malaria in the study area resulted in rapid fever and parasite clearance as well as low gametocyte carriage rates despite the use of this combination for more than 15 years.
在埃塞俄比亚西南部,青蒿琥酯-咯萘啶(AL)治疗无并发症恶性疟原虫疟疾的疗效记录不佳。定期监测药物疗效是支持国家治疗政策和实践的重要工具。本研究调查了 AL 治疗恶性疟原虫疟疾的疗效。
该研究是一项前瞻性、观察性研究,对 6 个月及以上患有无并发症恶性疟原虫疟疾的参与者进行直接观察治疗,评估临床和寄生虫学反应。实时聚合酶链反应(PCR)和巢式 PCR 反应方法用于定量和基因分型恶性疟原虫。采用世界卫生组织 2009 年抗疟药物疗效监测建议的改良方案进行研究,主要结局为第 28 天的临床和寄生虫学治愈率。次要结局评估包括发热和寄生虫清除模式。第 28 天的治愈率采用意向治疗(ITT)和方案(PP)分析进行评估。寄生虫基因分型也在基线和寄生虫血症复发时进行,以区分复发和新感染。
在 80 名入组的研究参与者中,有 75 名在第 28 天完成了随访。对于方案(PP)分析,AL 在研究参与者中的未校正和校正 PCR 治愈率分别为 94.7%(95%CI 87.1-98.5)和 96%(95%CI 88.8-99.2)。对于意向治疗(ITT)分析,治愈率为 90%(95%CI 88.8-99.2)。基于 Kaplan-Meier 生存估计,AL 的累积失败率为 3.8%(95%CI 1.3-11.4)。仅 3 名参与者(3.8%(95%CI 0.8-10.6))在 80 名入组参与者中在第 3 天呈阳性。第 3 天阳性的参与者随访至第 28 天,与随访期间观察到的治疗失败无关。仅 7.5%(6/80)的参与者在入组时为配子体阳性,并且在用 AL 治疗后第 2 天没有配子体血症。
AL 的治疗效果非常高(超过 90%)。尽管该组合已使用了 15 年以上,但 AL 在研究地区治疗无并发症疟疾的疗效仍然很高,导致快速退热和寄生虫清除,配子体携带率也很低。