Publication:
Efficacy of artemether-lumefantrine for the treatment of uncomplicated falciparum malaria in northwest Cambodia

dc.contributor.authorMey Bouth Denisen_US
dc.contributor.authorReiko Tsuyuokaen_US
dc.contributor.authorPharath Limen_US
dc.contributor.authorNiklas Lindegardhen_US
dc.contributor.authorPoravuth Yien_US
dc.contributor.authorSophoan Narann Topen_US
dc.contributor.authorDuong Socheaten_US
dc.contributor.authorThierry Fandeuren_US
dc.contributor.authorAnna Annerbergen_US
dc.contributor.authorEva Maria Christophelen_US
dc.contributor.authorPascal Ringwalden_US
dc.contributor.otherOrganisation Mondiale de la Santeen_US
dc.contributor.otherNational Center for Parasitology, Entomology and Malaria Controlen_US
dc.contributor.otherInstitut Pasteur du Cambodgeen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherChurchill Hospitalen_US
dc.date.accessioned2018-08-20T06:59:50Z
dc.date.available2018-08-20T06:59:50Z
dc.date.issued2006-12-01en_US
dc.description.abstractObjective: To determine the efficacy of artemether-lumefantrine malaria treatment, as an alternative to artesunate + mefloquine, which is becoming ineffective in some areas of the Thai-Cambodian border. Methods: Two studies were conducted to monitor the efficacy of artemether-lumefantrine in Sampov Lun referral hospital, Battambang Province, in 2002 and 2003, and one study was conducted to assess the efficacy of mefloquine + artesunate in 2003 for comparison. The studies were performed according to the WHO standardized protocol with a follow-up of 28 days. The therapeutic efficacy tests were complemented with in vitro tests and in 2003, with the measurement of lumefantrine plasma concentration at day 7 for the patients treated with artemether-lumefantrine. Results: A total of 190 patients were included: 55 were treated with artemether-lumefantrine in 2002 (AL2002), 80 with artemether-lumefantrine and food supplementation in 2003 (AL2003) and 55 with artesunate + mefloquine in 2003 (AM2003). With the per-protocol analysis, the cure rate was 71.1% in study AL2002, 86.5% in study AL2003 and 92.4% in study AM2003. All the data were PCR corrected. The artemether-lumefantrine cure rate was unexpectedly low in 2002, but it increased with food supplementation in 2003. There was a significant difference (P = 0.02) in lumefantrine plasma concentrations between adequate clinical and parasitological responses and treatment failure cases. In vitro susceptibility to lumefantrine was reduced for isolates sampled from patients presenting with treatment failure, but the difference was not statistically different from isolates sampled from patients who were successfully treated. Conclusion: Treatment failure cases of artemether-lumefantrine are most probably because of low levels of lumefantrine blood concentration. Further investigations are necessary to determine whether resistance of Plasmodium falciparum isolates to lumefantrine is present in the region. © 2006 Blackwell Publishing Ltd.en_US
dc.identifier.citationTropical Medicine and International Health. Vol.11, No.12 (2006), 1800-1807en_US
dc.identifier.doi10.1111/j.1365-3156.2006.01739.xen_US
dc.identifier.issn13653156en_US
dc.identifier.issn13602276en_US
dc.identifier.other2-s2.0-33751354768en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/23281
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33751354768&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleEfficacy of artemether-lumefantrine for the treatment of uncomplicated falciparum malaria in northwest Cambodiaen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33751354768&origin=inwarden_US

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