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Using a dual antibody point-of-care test with visual and digital reads to diagnose syphilis among people living with HIV in Botswana

Syphilis data from low- and middle-income countries are lacking due to limited testing. Point-of-care tests (POCTs) have been promoted to expand testing but previously only included treponemal tests, which cannot distinguish active from past infection. We aimed to assess the feasibility of using a c...

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Autores principales: Maan, Irfaan, Lawrence, David S, Tlhako, Nametso, Ramontshonyana, Kehumile, Mussa, Aamirah, Wynn, Adriane, Marks, Michael, Ramogola-Masire, Doreen, Morroni, Chelsea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008391/
https://www.ncbi.nlm.nih.gov/pubmed/33570464
http://dx.doi.org/10.1177/0956462420975639
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author Maan, Irfaan
Lawrence, David S
Tlhako, Nametso
Ramontshonyana, Kehumile
Mussa, Aamirah
Wynn, Adriane
Marks, Michael
Ramogola-Masire, Doreen
Morroni, Chelsea
author_facet Maan, Irfaan
Lawrence, David S
Tlhako, Nametso
Ramontshonyana, Kehumile
Mussa, Aamirah
Wynn, Adriane
Marks, Michael
Ramogola-Masire, Doreen
Morroni, Chelsea
author_sort Maan, Irfaan
collection PubMed
description Syphilis data from low- and middle-income countries are lacking due to limited testing. Point-of-care tests (POCTs) have been promoted to expand testing but previously only included treponemal tests, which cannot distinguish active from past infection. We aimed to assess the feasibility of using a combined treponemal and non-treponemal POCT in HIV clinic patients in Gaborone, Botswana, and estimate syphilis prevalence in our clinic sample using this approach. We recruited 390 non-pregnant patients. Participants underwent a combined treponemal and non-treponemal POCT (Dual Path Platform (DPP®) Syphilis Screen and Confirm Assay (Chembio Diagnostic Systems)) on finger-prick blood sample and a questionnaire. Median age 45 years, 30% men, median CD4 count 565 cells/μL, and 91% had an HIV viral load <400 copies/mL. Five participants had active syphilis (1.3%, 95% CI 0.5–3.0%) and 64 had previous syphilis (16.4%, 95% CI 13.0–20.4%) using the DPP POCT. There was a reasonable level of agreement between digital and visual reading of the POCT (kappa statistic of 0.81); however, visual reading missed three active infections (60%). The level of active syphilis was similar to local antenatal data. The DPP POCT led to five participants with active syphilis being diagnosed and starting same-day treatment. The digital reader should be used.
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spelling pubmed-80083912021-04-08 Using a dual antibody point-of-care test with visual and digital reads to diagnose syphilis among people living with HIV in Botswana Maan, Irfaan Lawrence, David S Tlhako, Nametso Ramontshonyana, Kehumile Mussa, Aamirah Wynn, Adriane Marks, Michael Ramogola-Masire, Doreen Morroni, Chelsea Int J STD AIDS Original Research Articles Syphilis data from low- and middle-income countries are lacking due to limited testing. Point-of-care tests (POCTs) have been promoted to expand testing but previously only included treponemal tests, which cannot distinguish active from past infection. We aimed to assess the feasibility of using a combined treponemal and non-treponemal POCT in HIV clinic patients in Gaborone, Botswana, and estimate syphilis prevalence in our clinic sample using this approach. We recruited 390 non-pregnant patients. Participants underwent a combined treponemal and non-treponemal POCT (Dual Path Platform (DPP®) Syphilis Screen and Confirm Assay (Chembio Diagnostic Systems)) on finger-prick blood sample and a questionnaire. Median age 45 years, 30% men, median CD4 count 565 cells/μL, and 91% had an HIV viral load <400 copies/mL. Five participants had active syphilis (1.3%, 95% CI 0.5–3.0%) and 64 had previous syphilis (16.4%, 95% CI 13.0–20.4%) using the DPP POCT. There was a reasonable level of agreement between digital and visual reading of the POCT (kappa statistic of 0.81); however, visual reading missed three active infections (60%). The level of active syphilis was similar to local antenatal data. The DPP POCT led to five participants with active syphilis being diagnosed and starting same-day treatment. The digital reader should be used. SAGE Publications 2021-02-11 2021-04 /pmc/articles/PMC8008391/ /pubmed/33570464 http://dx.doi.org/10.1177/0956462420975639 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research Articles
Maan, Irfaan
Lawrence, David S
Tlhako, Nametso
Ramontshonyana, Kehumile
Mussa, Aamirah
Wynn, Adriane
Marks, Michael
Ramogola-Masire, Doreen
Morroni, Chelsea
Using a dual antibody point-of-care test with visual and digital reads to diagnose syphilis among people living with HIV in Botswana
title Using a dual antibody point-of-care test with visual and digital reads to diagnose syphilis among people living with HIV in Botswana
title_full Using a dual antibody point-of-care test with visual and digital reads to diagnose syphilis among people living with HIV in Botswana
title_fullStr Using a dual antibody point-of-care test with visual and digital reads to diagnose syphilis among people living with HIV in Botswana
title_full_unstemmed Using a dual antibody point-of-care test with visual and digital reads to diagnose syphilis among people living with HIV in Botswana
title_short Using a dual antibody point-of-care test with visual and digital reads to diagnose syphilis among people living with HIV in Botswana
title_sort using a dual antibody point-of-care test with visual and digital reads to diagnose syphilis among people living with hiv in botswana
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008391/
https://www.ncbi.nlm.nih.gov/pubmed/33570464
http://dx.doi.org/10.1177/0956462420975639
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