Publication:
Lumefantrine and desbutyl-lumefantrine population pharmacokinetic-pharmacodynamic relationships in pregnant women with uncomplicated Plasmodium falciparum malaria on the Thailand-Myanmar border

dc.contributor.authorFrank Kloproggeen_US
dc.contributor.authorRose McGreadyen_US
dc.contributor.authorWarunee Hanpithakpongen_US
dc.contributor.authorDaniel Blessbornen_US
dc.contributor.authorNicholas P.J. Dayen_US
dc.contributor.authorNicholas J. Whiteen_US
dc.contributor.authorFrançois Nostenen_US
dc.contributor.authorJoel Tarningaen_US
dc.contributor.otherNuffield Department of Clinical Medicineen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherWorldWide Antimalarial Resistance Network (WWARN)en_US
dc.date.accessioned2018-11-23T10:34:45Z
dc.date.available2018-11-23T10:34:45Z
dc.date.issued2015-10-01en_US
dc.description.abstractCopyright © 2015, Kloprogge et al. Artemether-lumefantrine is the most widely used antimalarial artemisinin-based combination treatment. Recent studies have suggested that day 7 plasma concentrations of the potent metabolite desbutyl-lumefantrine correlate better with treatment outcomes than those of lumefantrine. Low cure rates have been reported in pregnant women with uncomplicated falciparum malaria treated with artemether-lumefantrine in northwest Thailand. A simultaneous pharmacokinetic drug-metabolite model was developed based on dense venous and sparse capillary lumefantrine and desbutyl-lumefantrine plasma samples from 116 pregnant patients on the Thailand-Myanmar border. The best model was used to evaluate therapeutic outcomes with a time-to-event approach. Lumefantrine and desbutyl-lumefantrine concentrations, implemented in an Emax model, both predicted treatment outcomes, but lumefantrine provided better predictive power. A combined model including both lumefantrine and desbutyllumefantrine did not improve the model further. Simulations suggested that cure rates in pregnant women with falciparum malaria could be increased by prolonging the treatment course. (These trials were registered at controlled-trials.com [ISRCTN 86353884].)en_US
dc.identifier.citationAntimicrobial Agents and Chemotherapy. Vol.59, No.10 (2015), 6375-6384en_US
dc.identifier.doi10.1128/AAC.00267-15en_US
dc.identifier.issn10986596en_US
dc.identifier.issn00664804en_US
dc.identifier.other2-s2.0-84942866303en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/36309
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84942866303&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleLumefantrine and desbutyl-lumefantrine population pharmacokinetic-pharmacodynamic relationships in pregnant women with uncomplicated Plasmodium falciparum malaria on the Thailand-Myanmar borderen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84942866303&origin=inwarden_US

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