Artemether-lumefantrine versus artemisinin-naphthoquine in Papua New Guinean children with uncomplicated malaria: a six months post-treatment follow-up study
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  • 作者:Moses Laman ; John M Benjamin ; Brioni R Moore ; Mary Salib ; Somoyang Tawat…
  • 关键词:Malaria ; Plasmodium falciparum ; Plasmodium vivax ; Artemisinin combination therapy ; Naphthoquine ; Effectiveness
  • 刊名:Malaria Journal
  • 出版年:2015
  • 出版时间:December 2015
  • 年:2015
  • 卷:14
  • 期:1
  • 全文大小:488 KB
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    14. Laman, M, Moore, BR, Benjamin, J, Padapu, N, Tarongka, N, Siba, P (2014) Comparison of an assumed versus measured leucocyte count in parasite density calculations in Papua New Guinean children with uncomplicated malaria. Malar J 13: pp. 145 CrossRef
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  • 刊物主题:Parasitology; Infectious Diseases; Tropical Medicine;
  • 出版者:BioMed Central
  • ISSN:1475-2875
文摘
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--.033, log rank test). The median (interquartile range) time to first episode of clinical malaria was 64 (50-46) vs 116 (77-30) days, respectively (P--.20). There were no between-group differences in the incidence of first presentation with non-malarial illness (P--.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.

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