Improved rapid diagnostic tests to detect syphilis and yaws: a systematic review and meta-analysis.


Journal

Sexually transmitted infections
ISSN: 1472-3263
Titre abrégé: Sex Transm Infect
Pays: England
ID NLM: 9805554

Informations de publication

Date de publication:
12 2022
Historique:
received: 09 06 2022
accepted: 16 08 2022
pubmed: 1 10 2022
medline: 22 11 2022
entrez: 30 9 2022
Statut: ppublish

Résumé

Current rapid tests for syphilis and yaws can detect treponemal and non-treponemal antibodies. We aimed to critically appraise the literature for rapid diagnostic tests (RDTs) which can better distinguish an active infection of syphilis or yaws. We conducted a systematic review and meta-analysis, searching five databases between January 2010 and October 2021 (with an update in July 2022). A generalised linear mixed model was used to conduct a bivariate meta-analysis for the pooled sensitivity and specificity. Heterogeneity was assessed using the I We included 17 studies for meta-analyses. For syphilis, the pooled sensitivity and specificity of the treponemal component were 0.93 (95% CI: 0.86 to 0.97) and 0.98 (95% CI: 0.96 to 0.99), respectively. For the non-treponemal component, the pooled sensitivity and specificity were 0.90 (95% CI: 0.82 to 0.95) and 0.97 (95% CI: 0.92 to 0.99), respectively. For yaws, the pooled sensitivity and specificity of the treponemal component were 0.86 (95% CI: 0.66 to 0.95) and 0.97 (95% CI: 0.94 to 0.99), respectively. For the non-treponemal component, the pooled sensitivity and specificity were 0.80 (95% CI: 0.55 to 0.93) and 0.96 (95% CI: 0.92 to 0.98), respectively. RDTs that can differentiate between active and previously treated infections could optimise management by providing same-day treatment and reducing unnecessary treatment. CRD42021279587.

Sections du résumé

BACKGROUND
Current rapid tests for syphilis and yaws can detect treponemal and non-treponemal antibodies. We aimed to critically appraise the literature for rapid diagnostic tests (RDTs) which can better distinguish an active infection of syphilis or yaws.
METHODS
We conducted a systematic review and meta-analysis, searching five databases between January 2010 and October 2021 (with an update in July 2022). A generalised linear mixed model was used to conduct a bivariate meta-analysis for the pooled sensitivity and specificity. Heterogeneity was assessed using the I
RESULTS
We included 17 studies for meta-analyses. For syphilis, the pooled sensitivity and specificity of the treponemal component were 0.93 (95% CI: 0.86 to 0.97) and 0.98 (95% CI: 0.96 to 0.99), respectively. For the non-treponemal component, the pooled sensitivity and specificity were 0.90 (95% CI: 0.82 to 0.95) and 0.97 (95% CI: 0.92 to 0.99), respectively. For yaws, the pooled sensitivity and specificity of the treponemal component were 0.86 (95% CI: 0.66 to 0.95) and 0.97 (95% CI: 0.94 to 0.99), respectively. For the non-treponemal component, the pooled sensitivity and specificity were 0.80 (95% CI: 0.55 to 0.93) and 0.96 (95% CI: 0.92 to 0.98), respectively.
CONCLUSIONS
RDTs that can differentiate between active and previously treated infections could optimise management by providing same-day treatment and reducing unnecessary treatment.
PROSPERO REGISTRATION NUMBER
CRD42021279587.

Identifiants

pubmed: 36180209
pii: sextrans-2022-055546
doi: 10.1136/sextrans-2022-055546
pmc: PMC9685714
doi:

Types de publication

Meta-Analysis Systematic Review Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

608-616

Subventions

Organisme : World Health Organization
ID : 001
Pays : International

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Ying Zhang (Y)

School of Public Health, The University of Sydney, Campertown, New South Wales, Australia.

Su Mei Goh (SM)

Melbourne Sexual Health Centre, Melbourne, Victoria, Australia.

Maeve B Mello (MB)

Global HIV, Hepatitis and STI Programmes, WHO, Geneva, Switzerland.

Rachel C Baggaley (RC)

Global HIV, Hepatitis and STI Programmes, WHO, Geneva, Switzerland.

Teodora Wi (T)

Global HIV, Hepatitis and STI Programmes, WHO, Geneva, Switzerland.

Cheryl C Johnson (CC)

Global HIV, Hepatitis and STI Programmes, WHO, Geneva, Switzerland.

Kingsley B Asiedu (KB)

Global HIV, Hepatitis and STI Programmes, WHO, Geneva, Switzerland.

Michael Marks (M)

Clinical Research Department, London School of Hygiene and Tropical Medicine, London, UK.
Hospital for Tropical Diseases, University College London Hospital, London, UK.
Division of Infection and Immunity, University College London, London, UK.

Minh D Pham (MD)

Burnet Institute, Melbourne, Victoria, Australia.
School of Public Health and Preventive Medicine, Monash University Faculty of Medicine, Nursing and Health Sciences, Melbourne, Victoria, Australia.

Christopher K Fairley (CK)

Melbourne Sexual Health Centre, Melbourne, Victoria, Australia.
Central Clinical School, Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Victoria, Australia.

Eric P F Chow (EPF)

Melbourne Sexual Health Centre, Melbourne, Victoria, Australia.
Central Clinical School, Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Victoria, Australia.
Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, Victoria, Australia.

Oriol Mitjà (O)

Fight AIDS and Infectious Diseases Foundation, Catalonia, Spain.

Igor Toskin (I)

Department of Sexual and Reproductive Health and Research, WHO, Geneva, Switzerland.

Ronald C Ballard (RC)

Department of Sexual and Reproductive Health and Research, WHO, Geneva, Switzerland.

Jason J Ong (JJ)

Melbourne Sexual Health Centre, Melbourne, Victoria, Australia jason.ong@monash.edu.
Clinical Research Department, London School of Hygiene and Tropical Medicine, London, UK.
Central Clinical School, Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Victoria, Australia.

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