American Journal of Clinical Pathology · 2011 · 20 citations · 12 references
MedicineDiagnostic SciencesInfectious DiseasesDiagnostic AssessmentEarly DetectionMolecular DiagnosticsAnalytical ValidationAntigen Detection AssaysAssay ValidationBioanalytical Method ValidationDiagnostic EvaluationDiagnostic Test EvaluationDirect Fluorescent Antibody TestingHeat InactivationIndirect Fluorescent Antibody AssayPerformance PrecisionPrecisionSyphilis DiagnosticsSyphilis ScreeningValidation Of Diagnostic Tests
We evaluated analytic performances of an automated treponemal test and compared this test with the Venereal Disease Research Laboratory test (VDRL) and fluorescent treponemal antibody absorption test (FTA-ABS). Precision performance of the Architect Syphilis TP assay (TP; Abbott Japan, Tokyo, Japan) was assessed, and 150 serum samples were assayed with the TP before and after heat inactivation to estimate the effect of heat inactivation. A total of 616 specimens were tested with the FTA-ABS and TP, and 400 were examined with the VDRL. The TP showed good precision performance with total imprecision of less than a 10% coefficient of variation. An excellent linear relationship between results before and after heat inactivation was observed (R(2) = 0.9961). The FTA-ABS and TP agreed well with a κ coefficient of 0.981. The concordance rate between the FTA-ABS and TP was the highest (99.0%), followed by the rates between FTA-ABS and VDRL (85.0%) and between TP and VDRL (83.8%). The automated TP assay may be adequate for screening for syphilis in a large volume of samples and can be an alternative to FTA-ABS.
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Karina A. Orle, Cynthia A. Gates, David H. Martin et al. · Journal of Clinical Microbiology · 1996 · 319 citations · Full text
Guidelines for serological testing for syphilis
H Young · Sexually Transmitted Infections · 2000 · 99 citations · Full text
Medicine, Nephrology, Pathology +17