| Literature DB >> 27549633 |
Suiane Negreiros1, Samela Farias1, Giselle Maria Rachid Viana2, Sheila Akinyi Okoth3,4, Stella M Chenet3, Thayna Maria Holanda de Souza1, Paola Marchesini5, Venkatachalam Udhayakumar3, Marinete Marins Povoa2, Ana Carolina Faria E Silva Santelli5, Alexandre Macedo de Oliveira6.
Abstract
We evaluated the efficacy of chloroquine and primaquine on uncomplicated Plasmodium vivax malaria in Cruzeiro do Sul, Brazil, in 2014. Patients ≥ 5 years of age with either fever or history of fever, and laboratory-confirmed P. vivax monoinfection received chloroquine (total dose = 25 mg/kg) and primaquine (total dose = 3.5 mg/kg), and were followed up for 168 days (24 weeks). We used microsatellite genotyping to differentiate recurrent infections caused by heterologous parasites from those caused by homologous ones. No new P. vivax episode occurred by Day 28 among 119 enrolled patients, leading to Day 28, with adequate clinical and parasitological response (ACPR) of 100% (95% confidence interval [CI] = 96.7-100%). Twenty-eight P. vivax episodes occurred by Day 168, with uncorrected ACPR of 69.9% (95% CI = 59.5-79.0%). Fifteen of these episodes were caused by either homologous haplotypes or haplotypes that could not be determined. Excluding the 13 recurrent episodes caused by heterologous parasites, Day 168 microsatellite-corrected ACPR was estimated at 81.2% (95% CI = 71.0-89.1%). Chloroquine and primaquine remain efficacious to treat acute uncomplicated P. vivax infection, but moderate recurrence rates were observed within 24 weeks of follow-up. © The American Society of Tropical Medicine and Hygiene.Entities:
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Year: 2016 PMID: 27549633 PMCID: PMC5094218 DOI: 10.4269/ajtmh.16-0075
Source DB: PubMed Journal: Am J Trop Med Hyg ISSN: 0002-9637 Impact factor: 2.345