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Mass drug administrations with dihydroartemisinin-piperaquine and single low dose primaquine to eliminate Plasmodium falciparum have only a transient impact on Plasmodium vivax: Findings from randomised controlled trials

dc.contributor.authorKoukeo Phommasoneen_US
dc.contributor.authorFrank van Lethen_US
dc.contributor.authorThomas J. Petoen_US
dc.contributor.authorJordi Landieren_US
dc.contributor.authorThuy Nhien Nguyenen_US
dc.contributor.authorRupam Tripuraen_US
dc.contributor.authorTiengkham Pongvongsaen_US
dc.contributor.authorKhin Maung Lwinen_US
dc.contributor.authorLadda Kajeechiwaen_US
dc.contributor.authorMay Myo Thwinen_US
dc.contributor.authorDaniel M. Parkeren_US
dc.contributor.authorJacher Wiladphaingernen_US
dc.contributor.authorSuphak Nostenen_US
dc.contributor.authorStephane Prouxen_US
dc.contributor.authorChea Nguonen_US
dc.contributor.authorChan Davoeungen_US
dc.contributor.authorHuy Rekolen_US
dc.contributor.authorBipin Adhikarien_US
dc.contributor.authorCholrawee Promnarateen_US
dc.contributor.authorKesinee Chotivanichen_US
dc.contributor.authorBorimas Hanboonkunupakarnen_US
dc.contributor.authorPodjanee Jittmalaen_US
dc.contributor.authorPhaik Yeong Cheahen_US
dc.contributor.authorMehul Dhordaen_US
dc.contributor.authorMallika Imwongen_US
dc.contributor.authorMavuto Mukakaen_US
dc.contributor.authorPimnara Peerawaranunen_US
dc.contributor.authorSasithon Pukrittayakameeen_US
dc.contributor.authorPaul N. Newtonen_US
dc.contributor.authorGuy E. Thwaitesen_US
dc.contributor.authorNicholas P.J. Dayen_US
dc.contributor.authorMayfong Mayxayen_US
dc.contributor.authorTran Tinh Hienen_US
dc.contributor.authorFrancois H. Nostenen_US
dc.contributor.authorFrank Cobelensen_US
dc.contributor.authorArjen M. Dondorpen_US
dc.contributor.authorNicholas J. Whiteen_US
dc.contributor.authorLorenz von Seidleinen_US
dc.contributor.otherAix Marseille Universitéen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherNuffield Department of Clinical Medicineen_US
dc.contributor.otherUniversity of California, Irvineen_US
dc.contributor.otherAmsterdam UMC - University of Amsterdamen_US
dc.contributor.otherOxford University Clinical Research Uniten_US
dc.contributor.otherUniversity of Health Sciencesen_US
dc.contributor.otherAmsterdam Institute for Global Health and Developmenten_US
dc.contributor.otherMahosot Hospitalen_US
dc.contributor.otherSavannakhet Provincial Health Departmenten_US
dc.contributor.otherRoyal Institute of Thailanden_US
dc.contributor.otherNational Center for Parasitology, Entomology and Malaria Controlen_US
dc.contributor.otherProvincial Health Departmenten_US
dc.date.accessioned2020-03-26T04:28:59Z
dc.date.available2020-03-26T04:28:59Z
dc.date.issued2020-01-01en_US
dc.description.abstractCopyright: © 2020 Phommasone et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Background Mass administrations of antimalarial drugs (MDA) have reduced the incidence and prevalence of P. falciparum infections in a trial in the Greater Mekong Subregion. Here we assess the impact of the MDA on P. vivax infections. Methods Between May 2013 and July 2017, four villages in each Myanmar, Vietnam, Cambodia and Lao PDR were selected based on high prevalence of P. falciparum infections. Eight of the 16 villages were randomly assigned to receive MDA consisting of three-monthly rounds of three-day courses of dihydroartemisinin-piperaquine and, except in Cambodia, a single low-dose of primaquine. Cross-sectional surveys were conducted at quarterly intervals to detect Plasmodium infections using ultrasensitive qPCR. The difference in the cumulative incidence between the groups was assessed through a discrete time survival approach, the difference in prevalence through a difference-in-difference analysis, and the difference in the number of participants with a recurrence of P. vivax infection through a mixed-effect logistic regression. Results 3,790 (86%) residents in the intervention villages participated in at least one MDA round, of whom 2,520 (57%) participated in three rounds. The prevalence of P. vivax infections fell from 9.31% to 0.89% at month 3 but rebounded by six months to 5.81%. There was no evidence that the intervention reduced the cumulative incidence of P.vivax infections (95% confidence interval [CI] Odds ratio (OR): 0.29 to 1.36). Similarly, there was no evidence of MDA related reduction in the number of participants with at least one recurrent infection (OR: 0.34; 95% CI: 0.08 to 1.42). Conclusion MDA with schizontocidal drugs had a lasting effect on P. falciparum infections but only a transient effect on the prevalence of P. vivax infections. Radical cure with an 8-aminoquino-line will be needed for the rapid elimination of vivax malaria.en_US
dc.identifier.citationPLoS ONE. Vol.15, No.2 (2020)en_US
dc.identifier.doi10.1371/journal.pone.0228190en_US
dc.identifier.issn19326203en_US
dc.identifier.other2-s2.0-85079070501en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/53544
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85079070501&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMultidisciplinaryen_US
dc.titleMass drug administrations with dihydroartemisinin-piperaquine and single low dose primaquine to eliminate Plasmodium falciparum have only a transient impact on Plasmodium vivax: Findings from randomised controlled trialsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85079070501&origin=inwarden_US

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