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蒿甲醚-本芴醇和青蒿琥酯-阿莫地喹治疗儿童非复杂性恶性疟的体内疗效:莫桑比克的一项多中心、开放标签、双队列临床试验。

In vivo efficacy of artemether-lumefantrine and artesunate-amodiaquine for the treatment of uncomplicated falciparum malaria in children: a multisite, open-label, two-cohort, clinical trial in Mozambique.

作者信息

Nhama Abel, Bassat Quique, Enosse Sónia, Nhacolo Arsenio, Mutemba Rosália, Carvalho Eva, Naueia Eva, Sevene Esperança, Guinovart Caterina, Warsame Marian, Sanz Sergi, Mussa Abdul, Matsinhe Graça, Alonso Pedro, Tiago Armindo, Macete Eusebio

机构信息

Centro de Investigação em Saúde de Manhiça (CISM), Manhiça, Mozambique.

出版信息

Malar J. 2014 Aug 10;13:309. doi: 10.1186/1475-2875-13-309.

Abstract

BACKGROUND

Mozambique adopted artemisinin-based combination therapy (ACT) for the treatment of uncomplicated Plasmodium falciparum malaria in the year 2006, and since 2009 artemether-lumefantrine (AL) and artesunate-amodiaquine (ASAQ) have been proposed as alternative first-line treatments. A multicentre study was conducted in five sites across the country to assess the in vivo efficacy and tolerability of these two drugs.

METHODS

Children aged six to 59 months with uncomplicated malaria were recruited between June 2011 and January 2012 in five sites across Mozambique (Montepuez, Dondo, Tete, Chokwe, and Manhiça), and treated with AL or ASAQ in a non-randomized study. Follow-up was organized following standard WHO recommendations for in vivo studies, and included daily visits during the three-day-long supervised treatment course, followed by weekly visits up to day 28. The study primary outcome was the day 28 PCR-corrected early treatment failure (ETF), late clinical failure (LCF), late parasitological failure (LPF), and adequate clinical and parasitological response (ACPR). PCR was performed centrally for all cases of recurrent parasitaemia from day 7 onwards to distinguish recrudescence from re-infection.

RESULTS

Four-hundred and thirty-nine (AL cohort; five sites) and 261 (ASAQ cohort, three sites) children were recruited to the study. Day 28 PCR-corrected efficacy for AL was 96.0% (335/339; 95% CI: 93.4-97.8), while for ASAQ it was 99.6% (232/233; 95% CI: 97.6-99.9). The majority of recurring parasitaemia cases throughout follow-up were shown to be re-infections by PCR. Both drugs were well tolerated, with the most frequent adverse event being vomiting (AL 4.5% [20/439]; ASAQ 9.6% [25/261]) and no significant events deemed related to the study drugs.

CONCLUSION

This study confirms that both AL and ASAQ remain highly efficacious and well tolerated for the treatment of uncomplicated malaria in Mozambican children. Studies such as these should be replicated regularly in the selected surveillance sentinel sites to continuously monitor the efficacy of these drugs and to rapidly detect any potential signs of declining efficacy to ACT, the mainstay of malaria treatment.

摘要

背景

莫桑比克于2006年采用以青蒿素为基础的联合疗法(ACT)治疗单纯性恶性疟原虫疟疾,自2009年起,蒿甲醚-本芴醇(AL)和青蒿琥酯-阿莫地喹(ASAQ)被提议作为替代一线治疗药物。在该国五个地点进行了一项多中心研究,以评估这两种药物的体内疗效和耐受性。

方法

2011年6月至2012年1月期间,在莫桑比克的五个地点(蒙特普埃兹、栋多、太特、乔克维和马希卡)招募了6至59个月大的单纯性疟疾患儿,并在一项非随机研究中用AL或ASAQ进行治疗。按照世界卫生组织关于体内研究的标准建议组织随访,包括在为期三天的监督治疗过程中每天访视,随后每周访视直至第28天。研究的主要结局是第28天经PCR校正的早期治疗失败(ETF)、晚期临床失败(LCF)、晚期寄生虫学失败(LPF)以及充分的临床和寄生虫学反应(ACPR)。从第7天起,对所有复发性寄生虫血症病例集中进行PCR检测,以区分复发与再感染。

结果

共有439名(AL队列;五个地点)和261名(ASAQ队列,三个地点)儿童被纳入该研究。AL在第28天经PCR校正的疗效为96.0%(335/339;95%CI:93.4-97.8),而ASAQ为99.6%(232/233;95%CI:97.6-99.9)。通过PCR检测显示,在整个随访期间,大多数复发性寄生虫血症病例为再感染。两种药物耐受性良好,最常见的不良事件是呕吐(AL为4.5%[20/439];ASAQ为9.6%[25/261]),且未发现与研究药物相关的重大不良事件。

结论

本研究证实,AL和ASAQ在治疗莫桑比克儿童单纯性疟疾方面仍然高效且耐受性良好。此类研究应在选定的监测哨点定期重复进行,以持续监测这些药物的疗效,并迅速发现ACT(疟疾治疗的主要手段)疗效下降的任何潜在迹象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4a9/4132202/dd4313c1e2e5/1475-2875-13-309-1.jpg

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