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Laboratory Evaluation of a Dual-Path Platform Assay for Rapid Point-of-Care HIV and Syphilis Testing

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dc.contributor.author Leon, S. R.
dc.contributor.author Ramos, L. B.
dc.contributor.author Vargas, S. K.
dc.contributor.author Kojima, N.
dc.contributor.author Perez, D. G.
dc.contributor.author Caceres, C. F.
dc.contributor.author Klausner, J. D.
dc.date.accessioned 2019-02-06T14:52:38Z
dc.date.available 2019-02-06T14:52:38Z
dc.date.issued 2016
dc.identifier.uri https://hdl.handle.net/20.500.12866/5340
dc.description.abstract We assessed the laboratory performance of the Chembio dual-path platform HIV-syphilis rapid immunodiagnostic test and electronic reader for detection of HIV and Treponema pallidum antibodies in 450 previously characterized serum specimens. For visual or electronic reader HIV antibody detection, the sensitivity was 100% and the specificity was 98.7%. For visual T. pallidum antibody detection, the test sensitivity was 94.7% and the specificity was 100.0%; with the electronic reader, the sensitivity was 94.7% and the specificity was 99.7%. en_US
dc.language.iso eng
dc.publisher American Society for Microbiology
dc.relation.ispartof urn:issn:1098-660X
dc.rights info:eu-repo/semantics/restrictedAccess
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.subject Humans en_US
dc.subject Sensitivity and Specificity en_US
dc.subject Reproducibility of Results en_US
dc.subject Point-of-Care Systems en_US
dc.subject HIV Infections/diagnosis en_US
dc.subject Syphilis/diagnosis en_US
dc.subject Coinfection en_US
dc.subject Immunologic Tests/methods/standards en_US
dc.subject Antigens, Bacterial/immunology en_US
dc.subject HIV Antibodies/immunology en_US
dc.subject HIV Core Protein p24/immunology en_US
dc.title Laboratory Evaluation of a Dual-Path Platform Assay for Rapid Point-of-Care HIV and Syphilis Testing en_US
dc.type info:eu-repo/semantics/article
dc.identifier.doi https://doi.org/10.1128/JCM.03152-15
dc.subject.ocde https://purl.org/pe-repo/ocde/ford#3.02.00 es_PE


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