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ABSTRACT: Background
Rapid dual treponemal/non-treponemal (lipoidal antigen) tests could improve syphilis detection strategies among people living with HIV (PLHIV). The World Health Organization (WHO) recommends minimum performance targets for syphilis point-of-care tests: sensitivity >80% for the treponemal component, >95% for the non-treponemal component, and specificity >90% for both. We evaluated the diagnostic accuracy of a dual treponemal/non-treponemal test in PLHIV.Methods
Cross-sectional study using stored serum samples donated by PLHIV who had been previously enrolled in a study conducted in Cali, Colombia. The index test was the Dual Path Platform® Syphilis Screen & Confirm Assay (DPP-SSCA, Chembio Diagnostic Systems, Inc.). A combination of Treponema pallidum haemagglutin
SUBMITTER: Fuertes-Bucheli JF
PROVIDER: S-EPMC12917955 | biostudies-literature | 2025 Dec
REPOSITORIES: biostudies-literature