Publication:
Population pharmacokinetic and pharmacodynamic properties of intramuscular quinine in tanzanian children with severe falciparum malaria

dc.contributor.authorIlse C E Hendriksenen_US
dc.contributor.authorDeogratius Maigen_US
dc.contributor.authorMartha M. Lemngeen_US
dc.contributor.authorGeorge Mtoveen_US
dc.contributor.authorSamwel Gesasen_US
dc.contributor.authorHugh Reyburnen_US
dc.contributor.authorNiklas Lindegardhen_US
dc.contributor.authorNicholas P J Dayen_US
dc.contributor.authorLorenz Von Seidleinen_US
dc.contributor.authorArjen M. Dondorpen_US
dc.contributor.authorJoel Tarningen_US
dc.contributor.authorNicholas J. Whiteen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherUniversity of Oxforden_US
dc.contributor.otherNational Institute for Medical Research Tangaen_US
dc.contributor.otherLondon School of Hygiene & Tropical Medicineen_US
dc.contributor.otherMenzies School of Health Researchen_US
dc.date.accessioned2018-10-19T05:33:54Z
dc.date.available2018-10-19T05:33:54Z
dc.date.issued2013-02-01en_US
dc.description.abstractAlthough artesunate is clearly superior, parenteral quinine is still used widely for the treatment of severe malaria.A loading-dose regimen has been recommended for 30 years but is still often not used.A population pharmacokinetic study was conducted with 75 Tanzanian children aged 4 months to 8 years with severe malaria who received quinine intramuscularly; 69 patients received a loading dose of 20 mg quinine dihydrochloride (salt)/kg of body weight.Twenty-one patients had plasma quinine concentrations detectable at baseline.A zero-order absorption model with one-compartment disposition pharmacokinetics described the data adequately.Body weight was the only significant covariate and was implemented as an allometric function on clearance and volume parameters.Population pharmacokinetic parameter estimates (and percent relative standard errors [%RSE]) of elimination clearance, central volume of distribution, and duration of zero-order absorption were 0.977 liters/h (6.50%), 16.7 liters (6.39%), and 1.42 h (21.5%), respectively, for a typical patient weighing 11 kg.Quinine exposure was reduced at lower body weights after standard weight-based dosing; there was 18% less exposure over 24 h in patients weighing 5 kg than in those weighing 25 kg.Maximum plasma concentrations after the loading dose were unaffected by body weight.There was no evidence of dose-related drug toxicity with the loading dosing regimen.Intramuscular quinine is rapidly and reliably absorbed in children with severe falciparum malaria.Based on these pharmacokinetic data, a loading dose of 20 mg salt/kg is recommended, provided that no loading dose was administered within 24 h and no routine dose was administered within 12 h of admission.(This study has been registered with Current Controlled Trials under registration number ISRCTN 50258054.).Copyright © 2013, American Society for Microbiology.All Rights Reserved.en_US
dc.identifier.citationAntimicrobial Agents and Chemotherapy. Vol.57, No.2 (2013), 775-783en_US
dc.identifier.doi10.1128/AAC.01349-12en_US
dc.identifier.issn10986596en_US
dc.identifier.issn00664804en_US
dc.identifier.other2-s2.0-84872867551en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/32560
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84872867551&origin=inwarden_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titlePopulation pharmacokinetic and pharmacodynamic properties of intramuscular quinine in tanzanian children with severe falciparum malariaen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84872867551&origin=inwarden_US

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