Publication: Global extent of chloroquine-resistant Plasmodium vivax: A systematic review and meta-analysis
Issued Date
2014-01-01
Resource Type
ISSN
14744457
14733099
14733099
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2-s2.0-84908134087
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Mahidol University
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SCOPUS
Bibliographic Citation
The Lancet Infectious Diseases. Vol.14, No.10 (2014), 982-991
Suggested Citation
Ric N. Price, Lorenz von Seidlein, Neena Valecha, Francois Nosten, J. Kevin Baird, Nicholas J. White Global extent of chloroquine-resistant Plasmodium vivax: A systematic review and meta-analysis. The Lancet Infectious Diseases. Vol.14, No.10 (2014), 982-991. doi:10.1016/S1473-3099(14)70855-2 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/34833
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Title
Global extent of chloroquine-resistant Plasmodium vivax: A systematic review and meta-analysis
Abstract
© 2014 Price et al. Open Access article distributed under the terms of CC-BY. 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).