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Laboratory evaluation of the Chembio DPP Syphilis Screen & Confirm point-of-care test on serum and simulated blood samples

JAMMI, ISSN: 2371-0888, Vol: 9, Issue: 2, Page: 82-94
2024
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Article Description

INTRODUCTION: Syphilis infections are increasing in Canada, and traditional serological diagnostics pose barriers for vulnerable and marginalized populations at greatest risk. Point-of-care tests (POCTs) offer solutions, yet none were available in Canada until recently. The Chembio Dual Path Platform (DPP) Syphilis Screen & Confirm (SSC) is one of the first POCTs that helps distinguish active infection from non-infectious syphilis. This study evaluates the reliability of the Chembio DPP SSC to diagnose syphilis infection. METHODS: One hundred clinical samples with known syphilis serology (chemiluminescent microparticle immunoassay [CMIA] and rapid plasma regain [RPR]) results were used to evaluate the Chembio DPP SSC. CMIA–ve (n = 20), CMIA+ve RPR–ve (n = 40), and CMIA+ve RPR+ve (n = 40) samples represented negative, past, and presumed active infection, respectively. Samples were used in two formats: serum and simulated blood. Two laboratory technicians read the test visually, and with the manufacturer’s DPP Micro Reader, in blinded fashion. RESULTS: Overall sensitivity of the Chembio DPP SSC to distinguish presumed active infection from non-infectious syphilis (past infection and no infection) with visual reads were 52.50% (serum) and 55.00% (simulated blood). Sensitivity increased using the DPP Micro Reader to 90.00% (serum) and 97.50% (simulated blood). Specificity with visual reads were 98.33% (serum) and 95.00% (simulated blood) compared to Micro Reader results of 88.30% (serum) and 80.00% (simulated blood). For the non-treponemal portion of the POCT with visual reads, the sensitivity increased with increasing RPR titers. Low RPR titers <1:4 only had a sensitivity of 42.86% (serum) and 14.29% (simulated blood). DISCUSSION: The laboratory evaluation of the Chembio DPP SSC shows promise in detecting active syphilis, particularly in samples with RPR titers >1:4. However, the need for the Micro Reader for more accurate results is a limitation of the POCT, and financial constraints may pose barriers to some users. Further field evaluation is warranted.

Bibliographic Details

Meika Ei Richmond; William Hoang; Michelle Shuel; Raymond S.W. Tsang; Joshua Titus; Paul Van Caeseele; Derek R. Stein

University of Toronto Press Inc. (UTPress)

Medicine

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