Dual rapid test for HIV and syphilis: A laboratory evaluation of the diagnostic accuracy of the Standard Q HIV/Syphilis Combo Test

dc.date.accessioned2019-03-05T15:25:03Z
dc.date.available2019-03-05T15:25:03Z
dc.date.created2019-03-05T15:25:03Z
dc.date.issued2018
dc.identifierhttps://hdl.handle.net/20.500.12866/5937
dc.identifierhttps://doi.org/10.1016/j.diagmicrobio.2018.11.018
dc.description.abstractWe evaluated the Standard Q HIV/Syphilis Combo Test (SD Biosensor, South Korea), a dual rapid test using stored sera (N = 400) in a laboratory setting in Lima, Peru. The sensitivity and specificity for HIV antibody detection was 100.0% (95% CI: 98.2–100.0%) and 99.5% (95% CI: 97.2–100.0%), respectively. For treponemal antibody detection the sensitivity and specificity was 97.5% (95%CI:94.3–99.2%) and 100.0% (95%CI:98.2–100.0%), respectively.
dc.languageeng
dc.publisherElsevier
dc.relationDiagnostic Microbiology and Infectious Disease
dc.relation1879-0070
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectantibody detection
dc.subjectArticle
dc.subjectcohort analysis
dc.subjectcontrolled study
dc.subjectDiagnosis
dc.subjectdiagnostic accuracy
dc.subjectdiagnostic test accuracy study
dc.subjectDual test
dc.subjectenzyme immunoassay
dc.subjectfemale
dc.subjectHIV
dc.subjecthuman
dc.subjectHuman immunodeficiency virus infection
dc.subjectimmunoreactivity
dc.subjectmajor clinical study
dc.subjectPeru
dc.subjectpriority journal
dc.subjectRapid test
dc.subjectsensitivity and specificity
dc.subjectsyphilis
dc.subjectTreponema pallidum
dc.subjectTreponema pallidum hemagglutination test
dc.titleDual rapid test for HIV and syphilis: A laboratory evaluation of the diagnostic accuracy of the Standard Q HIV/Syphilis Combo Test
dc.typeinfo:eu-repo/semantics/article


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