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dc.contributor.authorNdase, Patrick
dc.contributor.authorCelum, Connie
dc.contributor.authorKidoguchi, Lara
dc.contributor.authorRonald, Allan
dc.contributor.authorFife, Kenneth H
dc.contributor.authorBukusi, Elizabeth
dc.contributor.authorDonnell, Deborah
dc.contributor.authorBaeten, Jared M.
dc.date.accessioned2015-06-04T06:30:19Z
dc.date.available2015-06-04T06:30:19Z
dc.date.issued2015-04-17
dc.identifier.citationPLoS One. 2015; 10(4): e0123005en_US
dc.identifier.urihttp://hdl.handle.net/11295/84173
dc.description.abstractBackground Rapid HIV assays are the mainstay of HIV testing globally. Delivery of effective biomedical HIV prevention strategies such as antiretroviral pre-exposure prophylaxis (PrEP) requires periodic HIV testing. Because rapid tests have high ( > 95%) but imperfect specificity, they are expected to generate some false positive results. Methods We assessed the frequency of true and false positive rapid results in the Partners PrEP Study, a randomized, placebo-controlled trial of PrEP. HIV testing was performed monthly using 2 rapid tests done in parallel with HIV enzyme immunoassay (EIA) confirmation fol- lowing all positive rapid tests. Results A total of 99,009 monthly HIV tests were performed; 98,743 (99.7%) were dual-rapid HIV negative. Of the 266 visits with 1 positive rapid result, 99 (37.2%) had confirmatory posi- tive EIA results (true positives), 155 (58.3%) had negative EIA results (false positives), anden_US
dc.language.isoenen_US
dc.publisherUniversity of Nairobien_US
dc.titleFrequency of false positive rapid HIV serologic tests in African men and women receiving prep for HIV prevention: implications for programmatic roll-out of biomedical interventionsen_US
dc.typeArticleen_US
dc.type.materialen_USen_US


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