We screened for malaria in 594 blood samples from febrile patients who tested negative by a Plasmodium falciparum-specific histidine-rich protein-2-based rapid diagnostic test at 12 health facilities in Zanzibar districts North A and Micheweni, from May to August 2010. Screening was with microscopy, polymerase chain reaction (PCR) targeting the cytochrome b gene (cytbPCR) of the four major human malaria species, and quantitative PCR (qPCR). The prevalence of cytbPCR-detectable malaria infection was 2% (12 of 594), including 8 P. falciparum, 3 Plasmodium malariae, and 1 Plasmodium vivax infections. Microscopy identified 4 of 8 P. falciparum infections. Parasite density as estimated by microscopy or qPCR was > 4,000 parasites/mL in 5 of 8 cytbPCR-detectable P. falciparum infections. The infections that were missed by the rapid diagnostic test represent a particular challenge in malaria elimination settings and highlight the need for more sensitive point-of-care diagnostic tools to improve case detection of all human malaria species in febrile patients. Copyright © 2013 by The American Society of Tropical Medicine and Hygiene.
CITATION STYLE
Baltzell, K. A., Shakely, D., Hsiang, M., Kemere, J., Ali, A. S., Björkman, A., … Greenhouse, B. (2013). Prevalence of PCR detectable malaria infection among febrile patients with a negative plasmodium falciparum specific rapid diagnostic test in Zanzibar. American Journal of Tropical Medicine and Hygiene, 88(2), 289–291. https://doi.org/10.4269/ajtmh.2012.12-0095
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