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


Journal

International journal of STD & AIDS
ISSN: 1758-1052
Titre abrégé: Int J STD AIDS
Pays: England
ID NLM: 9007917

Informations de publication

Date de publication:
04 2021
Historique:
pubmed: 12 2 2021
medline: 18 9 2021
entrez: 11 2 2021
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 33570464
doi: 10.1177/0956462420975639
pmc: PMC8008391
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

453-461

Subventions

Organisme : FIC NIH HHS
ID : D43 TW009610
Pays : United States
Organisme : NIAAA NIH HHS
ID : K01 AA027733
Pays : United States

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Auteurs

Irfaan Maan (I)

Department of Clinical Research, Faculty of Infectious and Tropical Diseases, 218289London School of Hygiene and Tropical Medicine, London, UK.

David S Lawrence (DS)

Department of Clinical Research, Faculty of Infectious and Tropical Diseases, 218289London School of Hygiene and Tropical Medicine, London, UK.
292006Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

Nametso Tlhako (N)

292006Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

Kehumile Ramontshonyana (K)

Botswana University of Pennsylvania Partnership, Gaborone, Botswana.

Aamirah Mussa (A)

292006Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

Adriane Wynn (A)

Division of Infectious Diseases & Global Public Health, 8784University of California, San Diego, USA.

Michael Marks (M)

Department of Clinical Research, Faculty of Infectious and Tropical Diseases, 218289London School of Hygiene and Tropical Medicine, London, UK.
Hospital for Tropical Diseases, London, UK.

Doreen Ramogola-Masire (D)

54547University of Botswana, Gaborone, Botswana.

Chelsea Morroni (C)

292006Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
Botswana University of Pennsylvania Partnership, Gaborone, Botswana.
Department of International Public Health, 9655Liverpool School of Tropical Medicine, Liverpool, UK.

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