| Literature DB >> 27549635 |
Baba Dieye1, Muna Affara2, Lassana Sangare3, Fatou Joof2, Yaye D Ndiaye1, Jules F Gomis1, Mouhamadou Ndiaye1, Aminata Mbaye1, Mouhamadou Diakite3, Ngayo Sy1, Babacar Mbengue1, Awa B Deme1, Rachel Daniels4, Ambroise D Ahouidi1, Tandakha Dieye1, Ahmad Abdullahi2, Seydou Doumbia3, Jean L Ndiaye1, Ayouba Diarra3, Abubakar Ismaela2, Mamadou Coulibaly3, Clint Welty5, Alfred Amambua Ngwa2, Jeffrey Shaffer5, Umberto D'Alessandro2,6,7, Sarah K Volkman4,8,9, Dyann F Wirth4,8, Donald J Krogstad5, Ousmane Koita3, Davis Nwakanma2, Daouda Ndiaye10.
Abstract
In 2006, artemether-lumefantrine (AL) became the first-line treatment of uncomplicated malaria in Senegal, Mali, and the Gambia. To monitor its efficacy, between August 2011 and November 2014, children with uncomplicated Plasmodium falciparum malaria were treated with AL and followed up for 42 days. A total of 463 subjects were enrolled in three sites (246 in Senegal, 97 in Mali, and 120 in Gambia). No early treatment failure was observed and malaria infection cleared in all patients by day 3. Polymerase chain reaction (PCR)-adjusted adequate clinical and parasitological response (ACPR) was 100% in Mali, and the Gambia, and 98.8% in Senegal. However, without PCR adjustment, ACPR was 89.4% overall; 91.5% in Mali, 98.8% in Senegal, and 64.3% in the Gambia (the lower value in the Gambia attributed to poor compliance of the full antimalarial course). However, pfmdr1 mutations were prevalent in Senegal and a decrease in parasite sensitivity to artesunate and lumefantrine (as measured by ex vivo drug assay) was observed at all sites. Recrudescent parasites did not show Kelch 13 (K13) mutations and AL remains highly efficacious in these west African sites. © The American Society of Tropical Medicine and Hygiene.Entities:
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Year: 2016 PMID: 27549635 PMCID: PMC5094217 DOI: 10.4269/ajtmh.16-0053
Source DB: PubMed Journal: Am J Trop Med Hyg ISSN: 0002-9637 Impact factor: 2.345