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Am. J. Trop. Med. Hyg., 80(3), 2009, pp. 470-474
Copyright © 2009 by The American Society of Tropical Medicine and Hygiene

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Performance of Malaria Rapid Diagnostic Tests as Part of Routine Malaria Case Management in Kenya

Alexandre Macedo de Oliveira*, Jacek Skarbinski, Peter O. Ouma, Simon Kariuki, John W. Barnwell, Kephas Otieno, Phillip Onyona, Louise M. Causer, Kayla F. Laserson, Willis S. Akhwale, Laurence Slutsker, AND Mary Hamel
Malaria Branch, Division of Parasitic Diseases, National Center for Vector-Borne, Zoonotic, and Enteric Diseases, U.S. Centers for Disease Control and Prevention, Atlanta, Georgia; Epidemic Intelligence Service, Office of Workforce and Career Development, U.S. Centers for Disease Control and Prevention, Atlanta, Georgia; Centre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya; Division of Malaria Control, Ministry of Health, Nairobi, Kenya

Data on malaria rapid diagnostic test (RDT) performance under routine program conditions are limited. We assessed the attributes of RDTs performed by study and health facility (HF) staffs as part of routine malaria case management of patients ≥ 5 years of age in Kenya. Expert microscopy was used as our gold standard. A total of 1,827 patients were enrolled; 191 (11.6%) were parasitemic by expert microscopy. Sensitivity and specificity of RDTs performed by study staff were 86.6% (95% confidence interval [CI]: 79.8–93.5%) and 95.4% (95% CI: 93.9–96.9%), respectively. Among tests performed by HF staff, RDTs were 91.7% (95% CI: 80.8–100.0%) sensitive and 96.7% (95% CI: 92.8–100.0%) specific, whereas microscopy was 52.5% (95% CI: 33.2–71.9%) sensitive and 77.0% (95% CI: 67.9–86.2%) specific. Our findings suggest that RDTs perform better than microscopy under routine conditions. Further efforts are needed to maintain this high RDT performance over time.


Received August 5, 2008. Accepted for publication December 4, 2008.

Acknowledgments: We thank the patients who participated in this study and the field staff who collected the data. We also acknowledge the acting director of KEMRI and John Vulule, Director of the Centre for Global Health Research, KEMRI for their support.

Disclaimer: The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the U.S. Centers for Disease Control and Prevention.

* Address correspondence to Alexandre Macedo de Oliveira, Malaria Branch, Centers for Disease Control and Prevention, 4770 Buford Hwy, MS F-22, Atlanta, GA 30341. E-mail: acq7{at}cdc.gov

Authors’ addresses: Alexandre Macedo de Oliveira, Jacek Skarbinski, John W. Barnwell, and Laurence Slutsker, Malaria Branch, Centers for Disease Control and Prevention, 4770 Buford Hwy, MS F-22, Atlanta, GA 30341, Tel: +1-770-488-7747, Fax: +1-770-488-7761. Peter O. Ouma, Simon Kariuki, Kephas Otieno, Philip Onyona, Kayla F. Laserson, and Mary Hamel, Kenya Medical Research Institute and Centers for Disease Control and Prevention, P.O. Box 1578, Kisumu, Kenya, Tel: +254-57-202-2902, Fax: +254-57-202-2981. Louise M. Causer, National Centre in HIV Epidemiology and Clinical Research, University of New South Wales, Level 2, 376 Victoria St, Darlinghurst 2010 NSW, Australia. Willis S. Akhwale, Division of Malaria Control, Ministry of Health, P.O. Box 19882-00202, Nairobi, Kenya, Tel: +254-020-272-7396, Fax: +254-020-271-6935.




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