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间日疟原虫氯喹耐药的全球范围:一项系统评价和荟萃分析

Global extent of chloroquine-resistant Plasmodium vivax: a systematic review and meta-analysis.

作者信息

Price Ric N, von Seidlein Lorenz, Valecha Neena, Nosten Francois, Baird J Kevin, White Nicholas J

机构信息

Worldwide Anti-malarial Resistance Network, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK; Centre for Tropical Medicine, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK; Global Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, NT, Australia.

Global Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, NT, Australia.

出版信息

Lancet Infect Dis. 2014 Oct;14(10):982-91. doi: 10.1016/S1473-3099(14)70855-2. Epub 2014 Sep 8.

Abstract

BACKGROUND

Chloroquine is the first-line treatment for Plasmodium vivax malaria in most endemic countries, but resistance is increasing. Monitoring of antimalarial efficacy is essential, but in P. vivax infections the assessment of treatment efficacy is confounded by relapse from the dormant liver stages. We systematically reviewed P. vivax malaria treatment efficacy studies to establish the global extent of chloroquine resistance.

METHODS

We searched Medline, Web of Science, Embase, and the Cochrane Database of Systematic Reviews to identify studies published in English between Jan 1, 1960, and April 30, 2014, which investigated antimalarial treatment efficacy in P. vivax malaria. We excluded studies that did not include supervised schizonticidal treatment without primaquine. We determined rates of chloroquine resistance according to P. vivax malaria recurrence rates by day 28 whole-blood chloroquine concentrations at the time of recurrence and study enrolment criteria.

FINDINGS

We identified 129 eligible clinical trials involving 21,694 patients at 179 study sites and 26 case reports describing 54 patients. Chloroquine resistance was present in 58 (53%) of 113 assessable study sites, spread across most countries that are endemic for P. vivax. Clearance of parasitaemia assessed by microscopy in 95% of patients by day 2, or all patients by day 3, was 100% predictive of chloroquine sensitivity.

INTERPRETATION

Heterogeneity of study design and analysis has confounded global surveillance of chloroquine-resistant P. vivax, which is now present across most countries endemic for P. vivax. Improved methods for monitoring of drug resistance are needed to inform antimalarial policy in these regions.

FUNDING

Wellcome Trust (UK).

摘要

背景

在大多数疟疾流行国家,氯喹是间日疟原虫疟疾的一线治疗药物,但耐药性正在增加。监测抗疟疗效至关重要,但在间日疟原虫感染中,治疗效果的评估因潜伏在肝脏阶段的复发而变得复杂。我们系统地回顾了间日疟原虫疟疾治疗疗效研究,以确定氯喹耐药的全球范围。

方法

我们检索了医学索引数据库(Medline)、科学引文索引(Web of Science)、荷兰医学文摘数据库(Embase)和考克兰系统评价数据库,以识别1960年1月1日至2014年4月30日期间以英文发表的研究,这些研究调查了间日疟原虫疟疾的抗疟治疗效果。我们排除了未包括无伯氨喹的有监督的裂殖体杀灭治疗的研究。我们根据复发时第28天的全血氯喹浓度和研究纳入标准,根据间日疟原虫疟疾复发率确定氯喹耐药率。

结果

我们确定了129项符合条件的临床试验,涉及179个研究地点的21,694名患者,以及26篇病例报告,描述了54名患者。在113个可评估的研究地点中,有58个(53%)存在氯喹耐药,分布在间日疟原虫流行的大多数国家。第2天通过显微镜检查95%的患者或第3天所有患者的寄生虫血症清除率为100%可预测氯喹敏感性。

解读

研究设计和分析的异质性混淆了对氯喹耐药间日疟原虫的全球监测,目前这种耐药性存在于间日疟原虫流行的大多数国家。需要改进耐药性监测方法,为这些地区的抗疟政策提供依据。

资助

惠康信托基金会(英国)。

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