dc.date.accessioned2022-01-04T20:31:44Z
dc.date.available2022-01-04T20:31:44Z
dc.date.created2022-01-04T20:31:44Z
dc.date.issued2013
dc.identifierhttps://hdl.handle.net/20.500.12866/10581
dc.identifierhttps://doi.org/10.1309/LMUY1PHAC0S0DMJR
dc.description.abstractThe aim of this study was to validate and compare 4 point-of-care (POC) devices for the detection of antibodies to human immunodeficiency virus 1 (HIV-1) and/or HIV-2 in cryopreserved serum specimens. We analyzed 99 specimens that had tested positive for antibodies to HIV-1/HIV-2 by Western blot and 101 samples with negative test results. All the samples were analyzed by each of the 4 rapid tests. The POC devices assessed in this study use lateral flow immunochemistry technology and provided results within 15 to 20 minutes. We obtained an average sensitivity of 97.57%, specificity of 98.77%, positive predictive value of 98.52%, and negative predictive value of 97.82%. The among-test correlation was 97.57%, and the kappa index was 0.96. Assessment of the performance of new rapid HIV tests must be regularly practiced where regular enzyme immunoassay (EIA) tests are not widely available. All 4 rapid HIV tests assessed in this study performed with acceptable accuracy.
dc.languageeng
dc.publisherOxford University Press
dc.relationLaboratory Medicine
dc.relation1943-7730
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectHIV rapid test
dc.subjectPOC
dc.subjectsensitivity and specificity
dc.subjectPeru
dc.titleDiagnostic accuracy among 4 point-of-care tests for the screening of HIV infection
dc.typeinfo:eu-repo/semantics/article


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