Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/104116
Title: Diagnosing dengue at the point-of-care : utility of a rapid combined diagnostic kit in Singapore
Authors: Gan, Victor C.
Tan, Li-Kiang
Lye, David C.
Pok, Kwoon-Yong
Mok, Shi-Qi
Chua, Rachel Choon-Rong
Leo, Yee-Sin
Ng, Lee-Ching
Keywords: DRNTU::Science::Medicine
Issue Date: 2014
Source: Gan, V. C., Tan, L.-K., Lye, D. C., Pok, K.-Y., Mok, S.-Q., Chua, R. C.-R., et al. (2014). Diagnosing Dengue at the Point-of-Care: Utility of a Rapid Combined Diagnostic Kit in Singapore. PLoS ONE, 9(3), e90037-.
Series/Report no.: PLoS ONE
Abstract: WHO recommendations for dengue diagnosis require laboratory facilities. Antibody-based rapid diagnostic tests (RDTs) have performed poorly, and clinical diagnosis remains the mainstay in dengue-endemic countries. We evaluated a combination antigen-antibody RDT for point-of-care testing in a high-prevalence setting. In this prospective cohort study, adults were enrolled from a tertiary infectious disease centre for evaluation of undifferentiated febrile illness from October 2011 to May 2012. SD Bioline Dengue Duo was evaluated at point-of-care against a WHO-based reference standard of viral isolation, RT-PCR, NS1-, IgM-, and IgG-ELISA. 246 adults were enrolled (median age 34 years, range 18–69), of which 197 could be confirmed definitively as either dengue or non-dengue. DENV-2 was the predominant serotype (79.5%) and the ratio of primary to secondary cases was 1:1.1. There were no test failures and minimal interobserver variation with a Fleiss’ kappa of 0.983 (95% CI 0.827–1.00). Overall sensitivity and specificity were 93.9% (95% CI 88.8–96.8%) and 92.0% (95% CI 81.2–96.9%) respectively. Using WHO clinical criteria alone for diagnosis had similar sensitivities (95.9%, 95% CI 91.4–98.1%) and lower specificities (20.0%, 95% CI 11.2–33.0%). No significant difference in performance was found when testing early versus late presenters, primary versus secondary cases, or DENV-1 versus DENV-2 infections. The use of a combination RDT fulfills WHO ASSURED criteria for point-of-care testing and can enhance dengue diagnosis in an endemic setting. This has the potential to markedly improve clinical management of dengue in the field.
URI: https://hdl.handle.net/10356/104116
http://hdl.handle.net/10220/19516
ISSN: 1932-6203
DOI: 10.1371/journal.pone.0090037
Rights: © 2014 Gan et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Fulltext Permission: open
Fulltext Availability: With Fulltext
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