Publication:
Efficacy of artemether-lumefantrine, the nationally-recommended artemisinin combination for the treatment of uncomplicated falciparum malaria, in southern Laos

dc.contributor.authorMayfong Mayxayen_US
dc.contributor.authorManiphone Khanthavongen_US
dc.contributor.authorOdai Chanthongthipen_US
dc.contributor.authorMallika Imwongen_US
dc.contributor.authorTiengkham Pongvongsaen_US
dc.contributor.authorBouasy Hongvanthongen_US
dc.contributor.authorSamalane Phompidaen_US
dc.contributor.authorViengxay Vanisavethen_US
dc.contributor.authorNicholas J. Whiteen_US
dc.contributor.authorPaul N. Newtonen_US
dc.contributor.otherWellcome Trust-Mahosot Hospital-Oxford University Tropical Medicine Research Collaborationen_US
dc.contributor.otherUniversity of Health Sciencesen_US
dc.contributor.otherUniversity of Oxforden_US
dc.contributor.otherCentre of Malariologyen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherSavannakhet Provincial Malaria Stationen_US
dc.date.accessioned2018-06-11T04:53:09Z
dc.date.available2018-06-11T04:53:09Z
dc.date.issued2012-06-12en_US
dc.description.abstractBackground: The Lao Government changed the national policy for uncomplicated Plasmodium falciparum malaria from chloroquine to artemether-lumefantrine (AL) in 2005. Since then, no information on AL efficacy has been reported. With evidence of resistance to artemisinin derivatives in adjacent Cambodia, there has been a concern as to AL efficacy. Monitoring of AL efficacy would help the Lao Government to make decisions on appropriate malaria treatment. Methods. The efficacy of a three-day, twice daily oral artemether-lumefantrine for the treatment of uncomplicated falciparum malaria in Xepon District, Savannakhet Province, southern Laos was studied over 42days follow-up. This was part of a trial of thiamin supplementation in falciparum malaria. Results: Of 630 patients with P. falciparum enrolled in the trial of thiamin treatment, 549 (87%, 357 children 15years and 192 adults) were included in this study. The per protocol 42-day cure rates were 97% (524/541) [96% (337/352) for children and 99% (187/189) for adults, p=0.042]. By conventional intention-to-treat analysis, the 42-day cure rates adjusted for re-infection, were 97% (532/549) [96% (342/357) in children and 99% (190/192) in adults, p=0.042] . The proportion of patients who remained parasitaemic at day 1 after treatment was significantly higher in children [33% (116/356)] compared to adults [15% (28/192)] (p < 0.001) and only one adult patient had detectable parasitaemia on day 2. There were no serious adverse events. Potential side effects after treatment were reported more commonly in adults (32%) compared to children (15%) (p < 0.001). Patients with recrudescent infections were significantly younger, had longer mean time to fever clearance, and had longer median time to parasite clearance compared to those who were cured. Conclusions: The current nationally-recommended anti-malarial treatment (artemether- lumefantrine) remains highly efficacious for the treatment of uncomplicated falciparum malaria five years after introduction in Laos. Regular monitoring is required in case artemisinin-resistant P. falciparum parasites should appear. Trial registration. ISRCTN85411059. © 2012 Mayxay et al.; licensee BioMed Central Ltd.en_US
dc.identifier.citationMalaria Journal. Vol.11, (2012)en_US
dc.identifier.doi10.1186/1475-2875-11-184en_US
dc.identifier.issn14752875en_US
dc.identifier.other2-s2.0-84861946736en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/14307
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84861946736&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleEfficacy of artemether-lumefantrine, the nationally-recommended artemisinin combination for the treatment of uncomplicated falciparum malaria, in southern Laosen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84861946736&origin=inwarden_US

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