AI Article Synopsis

  • Recent studies have shown chloroquine resistance in Brazil and Bolivia, prompting a retrospective analysis of its effectiveness in French Guiana between 2009 and 2015 at Cayenne Hospital.
  • Out of 172 patients studied, 164 responded well to treatment, resulting in a therapeutic efficacy of 95.3%, with only 8 treatment failures identified, including cases of true resistance and low drug concentrations.
  • The study concludes that while current levels of resistance do not necessitate changes in treatment guidelines, increased use of primaquine is recommended to curb resistance, and the development of molecular markers for monitoring is essential.

Article Abstract

In South America, resistance to chloroquine was recently reported in Brazil and Bolivia. The objective of this study was to collect data on chloroquine resistance in French Guiana by associating a retrospective evaluation of therapeutic efficacy with an analysis of recurrent parasitemia from any patients. Patients with infection, confirmed by microscopy and a body temperature of ≥37.5°C, were retrospectively identified at Cayenne Hospital between 2009 and 2015. Follow-up and treatment responses were performed according to the World Health Organization protocol. Parasite resistance was confirmed after dosage of a plasma concentration of chloroquine and microsatellite characterization. The and genes were analyzed for sequence and gene copy number variation. Among the 172 patients followed for 28 days, 164 presented adequate clinical and parasitological responses. Eight cases of treatment failures were identified (4.7%;  = 8/172), all after 14 days. The therapeutic efficacy of chloroquine was estimated at 95.3% (95% confidence interval [CI], 92.5 to 98.1%;  = 164/172). Among the eight failures, five were characterized: two cases were true chloroquine resistance (1.2%; 95% CI, 0 to 2.6%;  = 2/172), and three cases were found with subtherapeutic concentrations of chloroquine. No particular polymorphism in the and genes was identified in the resistant parasites. This identified level of resistance of to chloroquine in French Guiana does not require a change in therapeutic recommendations. However, primaquine should be administered more frequently to limit the spread of resistance, and there is still a need for a reliable molecular marker to facilitate the monitoring of resistance to chloroquine.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6811453PMC
http://dx.doi.org/10.1128/AAC.02116-18DOI Listing

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