TY - JOUR
T1 - Prevalence of PCR detectable malaria infection among febrile patients with a negative plasmodium falciparum specific rapid diagnostic test in Zanzibar
AU - Baltzell, Kimberly A.
AU - Shakely, Deler
AU - Hsiang, Michelle
AU - Kemere, Jordan
AU - Ali, Abdullah Suleiman
AU - Björkman, Anders
AU - Mårtensson, Andreas
AU - Omar, Rahila
AU - Elfving, Kristina
AU - Msellem, Mwinyi
AU - Aydin-Schmidt, Berit
AU - Rosenthal, Philip J.
AU - Greenhouse, Bryan
PY - 2013/2
Y1 - 2013/2
N2 - 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.
AB - 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.
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U2 - 10.4269/ajtmh.2012.12-0095
DO - 10.4269/ajtmh.2012.12-0095
M3 - Article
C2 - 23249688
AN - SCOPUS:84874037214
SN - 0002-9637
VL - 88
SP - 289
EP - 291
JO - American Journal of Tropical Medicine and Hygiene
JF - American Journal of Tropical Medicine and Hygiene
IS - 2
ER -