Publication:
Population pharmacokinetics of piperaquine after two different treatment regimens with dihydroartemisinm-piperaquine in patients with Plasmodium falciparum malaria in Thailand

dc.contributor.authorJ. Tarningen_US
dc.contributor.authorE. A. Ashleyen_US
dc.contributor.authorN. Lindegardhen_US
dc.contributor.authorK. Stepniewskaen_US
dc.contributor.authorL. Phaiphunen_US
dc.contributor.authorN. P J Dayen_US
dc.contributor.authorR. McGreadyen_US
dc.contributor.authorM. Ashtonen_US
dc.contributor.authorF. Nostenen_US
dc.contributor.authorN. J. Whiteen_US
dc.contributor.otherGoteborg University, Sahlgrenska Academyen_US
dc.contributor.otherShoklo Malaria Research Uniten_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherChurchill Hospitalen_US
dc.contributor.otherEpicentreen_US
dc.date.accessioned2018-07-12T02:46:00Z
dc.date.available2018-07-12T02:46:00Z
dc.date.issued2008-03-01en_US
dc.description.abstractThe population pharmacokinetics of piperaquine in adults and children with uncomplicated Plasmodium falciparum malaria treated with two different dosage regimens of dihydroartemisinin-piperaquine were characterized. Piperaquine pharmacokinetics in 98 Burmese and Karen patients aged 3 to 55 years were described by a two-compartment disposition model with first-order absorption and interindividual random variability on all parameters and were similar with the three- and four-dose regimens. Children had a lower body weight-normalized oral clearance than adults, resulting in longer terminal elimination half-lives and higher total exposure to piperaquine (area under the concentration-time curve from 0 to 63 days [AUCday 0-63]). However, children had lower plasma concentrations in the therapeutically relevant posttreatment prophylactic period (AUCday 3-20) because of smaller body weight-normalized central volumes of distribution and shorter distribution half-lives. Our data lend further support to a simplified once-daily treatment regimen to improve treatment adherence and efficacy and indicate that weight-adjusted piperaquine doses in children may need to be higher than in adults. Copyright © 2008, American Society for Microbiology. All Rights Reserved.en_US
dc.identifier.citationAntimicrobial Agents and Chemotherapy. Vol.52, No.3 (2008), 1052-1061en_US
dc.identifier.doi10.1128/AAC.00955-07en_US
dc.identifier.issn00664804en_US
dc.identifier.other2-s2.0-40549113955en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/19759
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=40549113955&origin=inwarden_US
dc.subjectMedicineen_US
dc.titlePopulation pharmacokinetics of piperaquine after two different treatment regimens with dihydroartemisinm-piperaquine in patients with Plasmodium falciparum malaria in Thailanden_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=40549113955&origin=inwarden_US

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