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dc.contributor.authorLaman, M.
dc.contributor.authorBenjamin, J.
dc.contributor.authorMoore, Brioni
dc.contributor.authorSalib, M.
dc.contributor.authorTawat, S.
dc.contributor.authorDavis, W.
dc.contributor.authorSiba, P.
dc.contributor.authorRobinson, L.
dc.contributor.authorDavis, T.
dc.date.accessioned2017-01-30T13:36:47Z
dc.date.available2017-01-30T13:36:47Z
dc.date.created2016-11-03T19:30:25Z
dc.date.issued2015
dc.identifier.citationLaman, M. and Benjamin, J. and Moore, B. and Salib, M. and Tawat, S. and Davis, W. and Siba, P. et al. 2015. Artemether-lumefantrine versus artemisinin-naphthoquine in Papua New Guinean children with uncomplicated malaria: A six months post-treatment follow-up study. Malaria Journal. 14 (1).
dc.identifier.urihttp://hdl.handle.net/20.500.11937/33377
dc.identifier.doi10.1186/s12936-015-0624-4
dc.description.abstract

Background: In a recent trial of artemisinin-naphthoquine (artemisinin-NQ) and artemether-lumefantrine (AM-LM) therapy in young children from Papua New Guinea (PNG), there were no treatment failures in artemisinin-NQ-treated children with Plasmodium falciparum or Plasmodium vivax compared with 2.2% and 30.0%, respectively, in AM-LM-treated children during 42 days of follow-up. To determine whether, consistent with the long elimination half-life of NQ, this difference in efficacy would be more durable, clinical episodes of malaria were assessed in a subset of trial patients followed for six months post-treatment. Methods: For children completing trial procedures and who were assessable at six months, all within-trial and subsequent clinical malaria episodes were ascertained, the latter by clinic attendances and/or review of hand-held health records. Presentations with non-malarial illness were also recorded. Differences between allocated treatments for pre-specified endpoints were determined using Kaplan-Meier survival analysis. Results: Of 247 children who were followed to Day 42, 176 (71.3%) were included in the present sub-study, 87 allocated to AM-LM and 89 to artemisinin-NQ. Twenty children in the AM-LM group (32.8%) had a first episode of clinical malaria within six months compared with 10 (16.4%) in the artemisinin-NQ group (P=0.033, log rank test). The median (interquartile range) time to first episode of clinical malaria was 64 (50-146) vs 116 (77-130) days, respectively (P=0.20). There were no between-group differences in the incidence of first presentation with non-malarial illness (P=0.31). Conclusions: The greater effectiveness of artemisinin-NQ over conventional AM-LM extends to at least six months post-treatment for clinical malaria but not non-malarial illness. Trial registration: Australian New Zealand Clinical Trials Registry ACTRN12610000913077.

dc.publisherBioMed Central
dc.titleArtemether-lumefantrine versus artemisinin-naphthoquine in Papua New Guinean children with uncomplicated malaria: A six months post-treatment follow-up study
dc.typeJournal Article
dcterms.source.volume14
dcterms.source.number1
dcterms.source.titleMalaria Journal
curtin.note

This open access article is distributed under the Creative Commons license https://creativecommons.org/licenses/by/4.0/

curtin.departmentSchool of Pharmacy
curtin.accessStatusOpen access


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