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蒿甲醚-本芴醇(科泰复®)治疗非洲非复杂性恶性疟的疗效:一项系统评价

Therapeutic Efficacy of Artemether-Lumefantrine (Coartem®) for the Treatment of Uncomplicated Falciparum Malaria in Africa: A Systematic Review.

作者信息

Derbie Awoke, Mekonnen Daniel, Adugna Meseret, Yeshitela Biruk, Woldeamanuel Yimtubezinash, Abebe Tamrat

机构信息

Department of Medical Microbiology, College of Medicine and Health Sciences, Bahir Dar University, Ethiopia.

Centre for Innovative Drug Development and Therapeutic Trials for Africa (CDT-Africa), Addis Ababa University, Ethiopia.

出版信息

J Parasitol Res. 2020 Oct 20;2020:7371681. doi: 10.1155/2020/7371681. eCollection 2020.

Abstract

BACKGROUND

Africa still bears the largest burden of malaria as the majority of infections in the continent are caused by . Artemether-lumefantrine (AL, Coartem®) is the most widely used artemisinin-based combination therapy (ACT), for treating uncomplicated falciparum malaria globally. However, the development of resistance to antimalarial drugs is a major challenge for malaria control. In this review, the efficacy of AL for the treatment of uncomplicated falciparum malaria in Africa was evaluated.

METHODS

Articles published between January 2015 and July 2019 were systematically searched using comprehensive search strings from PubMed/Medline, SCOPUS, and grey literature from Google Scholar. Interventional studies that followed patients for at least 28 days were included. Two reviewers independently assessed study eligibility, extracted data, and assessed risk of bias. All the included articles were measured to be good quality. While computing the efficacy of AL, polymerase chain reaction (PCR)-corrected cure rate (adequate clinical and parasitological response, ACPR) at day 28 was considered as the main endpoint. Meta-analysis was computed using STATA v 15 to calculate the pooled ACPR.

RESULTS

In this review, 39 articles that reported the treatment outcome of 8,320 patients were included. After 28 days of follow-up, the pooled PCR uncorrected and corrected APCR was at 87% (95% CI: 85-90%) and 97.0% (95% CI: 96-98%), respectively. Moreover, the proportion of early treatment failure (ETF) was almost 0%, while most of the included articles reported <8% late treatment failures. The reinfection and recrudescence rate was less than 10% and 2.6%, respectively, within 28 days. We noted rapid fever and parasite clearance in which greater than 93% and 94% patients were parasite and fever free at day three following AL treatment.

CONCLUSIONS

This review discovered that despite more than a decade since its introduction, Coartem® remains effective and thus could continue to be the drug of choice for the treatment of uncomplicated falciparum malaria for all age groups in Africa. However, the risk of new emerging resistance for this combination warrants regular monitoring of its efficacy across the continent.

摘要

背景

非洲仍然承担着最大的疟疾负担,因为该大陆的大多数感染是由……引起的。蒿甲醚-本芴醇(AL,科泰复®)是全球治疗非复杂性恶性疟最广泛使用的青蒿素联合疗法(ACT)。然而,抗疟药物耐药性的出现是疟疾控制的一项重大挑战。在本综述中,评估了AL治疗非洲非复杂性恶性疟的疗效。

方法

使用来自PubMed/Medline、SCOPUS的全面检索词以及谷歌学术的灰色文献,系统检索2015年1月至2019年7月发表的文章。纳入对患者随访至少28天的干预性研究。两名评审员独立评估研究的合格性、提取数据并评估偏倚风险。所有纳入的文章质量均被判定为良好。在计算AL的疗效时,第28天经聚合酶链反应(PCR)校正的治愈率(充分的临床和寄生虫学反应,ACPR)被视为主要终点。使用STATA v 15进行荟萃分析以计算汇总的ACPR。

结果

本综述纳入了39篇报告8320例患者治疗结果的文章。随访28天后,汇总的未经PCR校正和经PCR校正的ACPR分别为87%(95%CI:85 - 90%)和97.0%(95%CI:96 - 98%)。此外,早期治疗失败(ETF)的比例几乎为0%,而大多数纳入文章报告的晚期治疗失败率<8%。在28天内,再感染率和复发率分别低于10%和2.6%。我们注意到发热和寄生虫清除迅速,在接受AL治疗后的第3天,超过93%和94%的患者寄生虫转阴且不再发热。

结论

本综述发现,尽管科泰复®自引入以来已有十多年,但它仍然有效,因此可以继续作为非洲所有年龄组治疗非复杂性恶性疟的首选药物。然而,这种联合用药出现新耐药性的风险使得有必要在整个非洲大陆定期监测其疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29ae/7599419/1c01971e7ac2/JPR2020-7371681.001.jpg

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