Publication:
Artemether-lumefantrine treatment of uncomplicated Plasmodium falciparum malaria: A systematic review and meta-analysis of day 7 lumefantrine concentrations and therapeutic response using individual patient data

dc.contributor.authorElizabeth A. Ashleyen_US
dc.contributor.authorFrancesca Aweekaen_US
dc.contributor.authorKaren I. Barnesen_US
dc.contributor.authorQuique Bassaten_US
dc.contributor.authorSteffen Borrmannen_US
dc.contributor.authorPrabin Dahalen_US
dc.contributor.authorTimothy M.E. Davisen_US
dc.contributor.authorMey Bouth Denisen_US
dc.contributor.authorAbdoulaye A. Djimdeen_US
dc.contributor.authorJean François Faucheren_US
dc.contributor.authorBlaise Gentonen_US
dc.contributor.authorPhilippe J. Guérinen_US
dc.contributor.authorKamal Hameden_US
dc.contributor.authorEva Maria Hodelen_US
dc.contributor.authorLiusheng Huangen_US
dc.contributor.authorVincent Jullienen_US
dc.contributor.authorHarin A. Karunajeewaen_US
dc.contributor.authorJean René Kiechelen_US
dc.contributor.authorPoul Erik Kofoeden_US
dc.contributor.authorGilbert Lefèvreen_US
dc.contributor.authorNiklas Lindegardh Lindegardhen_US
dc.contributor.authorAndreas Mårtenssonen_US
dc.contributor.authorMayfong Mayxayen_US
dc.contributor.authorRose Mcgreadyen_US
dc.contributor.authorClarissa Moreiraen_US
dc.contributor.authorPaul N. Newtonen_US
dc.contributor.authorBilly E. Ngasalaen_US
dc.contributor.authorFrancois Nostenen_US
dc.contributor.authorChristian Nsanzabanaen_US
dc.contributor.authorSunil Parikhen_US
dc.contributor.authorPatrice Piolaen_US
dc.contributor.authorRic N. Priceen_US
dc.contributor.authorPascal Ringwalden_US
dc.contributor.authorLars Romboen_US
dc.contributor.authorBirgit Schrammen_US
dc.contributor.authorCarol Hopkins Sibleyen_US
dc.contributor.authorKasia Stepniewskaen_US
dc.contributor.authorJoel Tarningen_US
dc.contributor.authorJohan Ursingen_US
dc.contributor.authorMichele Van Vugten_US
dc.contributor.authorNicholas J. Whiteen_US
dc.contributor.authorLesley J. Workmanen_US
dc.contributor.authorPhilippe Deloronen_US
dc.contributor.authorKevin Marshen_US
dc.contributor.otherShoklo Malaria Research Uniten_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherUniversity of California, San Franciscoen_US
dc.contributor.otherWorldWide Antimalarial Resistance Network (WWARN)en_US
dc.contributor.otherUniversity of Cape Townen_US
dc.contributor.otherInstituto de Salud Global de Barcelonaen_US
dc.contributor.otherCentro de Investigação em Saúde de Manhiça (CISM)en_US
dc.contributor.otherWellcome Trust Research Laboratories Nairobien_US
dc.contributor.otherUniversitat Tubingenen_US
dc.contributor.otherNuffield Department of Clinical Medicineen_US
dc.contributor.otherUniversity of Western Australiaen_US
dc.contributor.otherIRD Institut de Recherche pour le Developpementen_US
dc.contributor.otherUniversite Paris Descartesen_US
dc.contributor.otherNational Center for Parasitologyen_US
dc.contributor.otherOrganisation Mondiale de la Santeen_US
dc.contributor.otherUniversity of Bamako Faculty of Medicine, Pharmacy and Odonto-Stomatologyen_US
dc.contributor.otherHopital Jean Minjozen_US
dc.contributor.otherSwiss Tropical and Public Health Institute (Swiss TPH)en_US
dc.contributor.otherCentre Hospitalier Universitaire Vaudoisen_US
dc.contributor.otherNovartis Pharmaceuticals Corporationen_US
dc.contributor.otherLiverpool School of Tropical Medicineen_US
dc.contributor.otherDrugs for Neglected Diseases Initiativeen_US
dc.contributor.otherSyddansk Universiteten_US
dc.contributor.otherKolding Sygehusen_US
dc.contributor.otherNovartis International AGen_US
dc.contributor.otherKenya Medical Research Instituteen_US
dc.contributor.otherKarolinska Instituteten_US
dc.contributor.otherWellcome Trusten_US
dc.contributor.otherMuhimbili University of Health and Allied Sciencesen_US
dc.contributor.otherYale Schools of Public Health and Medicineen_US
dc.contributor.otherDepartment of Clinical Pharmacologyen_US
dc.contributor.otherInstitut Pasteur de Madagascaren_US
dc.contributor.otherMenzies School of Health Researchen_US
dc.contributor.otherUppsala Universiteten_US
dc.contributor.otherEpicentreen_US
dc.contributor.otherUniversity of Washington, Seattleen_US
dc.contributor.otherUniversity of Amsterdamen_US
dc.date.accessioned2018-11-23T10:36:04Z
dc.date.available2018-11-23T10:36:04Z
dc.date.issued2015-09-18en_US
dc.description.abstract© 2015 WorldWide Antimalarial Resistance Network (WWARN) Lumefantrine PK/PD Study Group. Background: Achieving adequate antimalarial drug exposure is essential for curing malaria. Day 7 blood or plasma lumefantrine concentrations provide a simple measure of drug exposure that correlates well with artemether-lumefantrine efficacy. However, the 'therapeutic' day 7 lumefantrine concentration threshold needs to be defined better, particularly for important patient and parasite sub-populations. Methods: The WorldWide Antimalarial Resistance Network (WWARN) conducted a large pooled analysis of individual pharmacokinetic-pharmacodynamic data from patients treated with artemether-lumefantrine for uncomplicated Plasmodium falciparum malaria, to define therapeutic day 7 lumefantrine concentrations and identify patient factors that substantially alter these concentrations. A systematic review of PubMed, Embase, Google Scholar, ClinicalTrials.gov and conference proceedings identified all relevant studies. Risk of bias in individual studies was evaluated based on study design, methodology and missing data. Results: Of 31 studies identified through a systematic review, 26 studies were shared with WWARN and 21 studies with 2,787 patients were included. Recrudescence was associated with low day 7 lumefantrine concentrations (HR 1.59 (95 % CI 1.36 to 1.85) per halving of day 7 concentrations) and high baseline parasitemia (HR 1.87 (95 % CI 1.22 to 2.87) per 10-fold increase). Adjusted for mg/kg dose, day 7 concentrations were lowest in very young children (<3 years), among whom underweight-for-age children had 23 % (95 % CI -1 to 41 %) lower concentrations than adequately nourished children of the same age and 53 % (95 % CI 37 to 65 %) lower concentrations than adults. Day 7 lumefantrine concentrations were 44 % (95 % CI 38 to 49 %) lower following unsupervised treatment. The highest risk of recrudescence was observed in areas of emerging artemisinin resistance and very low transmission intensity. For all other populations studied, day 7 concentrations ≥200 ng/ml were associated with >98 % cure rates (if parasitemia <135,000/μL). Conclusions: Current artemether-lumefantrine dosing recommendations achieve day 7 lumefantrine concentrations ≥200 ng/ml and high cure rates in most uncomplicated malaria patients. Three groups are at increased risk of treatment failure: very young children (particularly those underweight-for-age); patients with high parasitemias; and patients in very low transmission intensity areas with emerging parasite resistance. In these groups, adherence and treatment response should be monitored closely. Higher, more frequent, or prolonged dosage regimens should now be evaluated in very young children, particularly if malnourished, and in patients with hyperparasitemia.en_US
dc.identifier.citationBMC Medicine. Vol.13, No.1 (2015)en_US
dc.identifier.doi10.1186/s12916-015-0456-7en_US
dc.identifier.issn17417015en_US
dc.identifier.other2-s2.0-84942087456en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/36324
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84942087456&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleArtemether-lumefantrine treatment of uncomplicated Plasmodium falciparum malaria: A systematic review and meta-analysis of day 7 lumefantrine concentrations and therapeutic response using individual patient dataen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84942087456&origin=inwarden_US

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