"It was difficult to offer same day results": evaluation of community-based point-of-care testing for sexually transmitted infections among youth using the GeneXpert platform in Zimbabwe.


Journal

BMC health services research
ISSN: 1472-6963
Titre abrégé: BMC Health Serv Res
Pays: England
ID NLM: 101088677

Informations de publication

Date de publication:
10 Feb 2022
Historique:
received: 02 09 2021
accepted: 27 01 2022
entrez: 11 2 2022
pubmed: 12 2 2022
medline: 15 2 2022
Statut: epublish

Résumé

Point-of-care testing for sexually transmitted infections (STIs) may improve diagnosis and treatment of STIs in low- and middle-income counties. We explored the facilitators and barriers to point-of-care testing for Chlamydia trachomatis (CT) and Neisseria gonorrhoea (NG) for youth in community-based settings in Zimbabwe. This study was nested within a cluster randomised trial of community-based delivery of integrated HIV and sexual and reproductive health services for youth aged 16 to 24 years. On-site CT/NG testing on urine samples using the Xpert® CT/NG test was piloted in four intervention clusters, with testing performed by service providers. On-site testing was defined as sample processing on the same day and site as sample collection. Outcomes included proportion of tests processed on-site, time between sample collection and collection of results, and proportion of clients receiving treatment. In-depth interviews were conducted with nine service providers and three staff members providing study co-ordination or laboratory support to explore facilitators and barriers to providing on-site CT/NG testing. Of 847 Xpert tests, 296 (35.0%) were performed on-site. Of these, 61 (20.6%) were positive for CT/NG; one (1.6%) received same day aetiological treatment; 33 (54.1%) presented later for treatment; and 5 (8.2%) were treated as a part of syndromic management. There was no difference in the proportion of clients who were treated whether their sample was processed on or off-site (64% (39/61) vs 60% (66/110); p = 0.61). The median (IQR) number of days between sample collection and collection of positive results was 14 (7-35) and 14 (7-52.5) for samples processed on and off-site, respectively, The interviews revealed four themes related to the provision of on-site testing associated with the i) diagnostic device ii) environment, iii) provider, and iv) clients. Some of the specific barriers identified included insufficient testing capacity, inadequate space, as well as reluctance of clients to wait for their results. In addition to research to optimise the implementation of point-of-care tests for STIs in resource-limited settings, the development of new platforms to reduce analytic time will be necessary to scale up STI testing and reduce the attrition between testing and treatment. Registered in clinical trials.gov ( NCT03719521 ).

Sections du résumé

BACKGROUND BACKGROUND
Point-of-care testing for sexually transmitted infections (STIs) may improve diagnosis and treatment of STIs in low- and middle-income counties. We explored the facilitators and barriers to point-of-care testing for Chlamydia trachomatis (CT) and Neisseria gonorrhoea (NG) for youth in community-based settings in Zimbabwe.
METHODS METHODS
This study was nested within a cluster randomised trial of community-based delivery of integrated HIV and sexual and reproductive health services for youth aged 16 to 24 years. On-site CT/NG testing on urine samples using the Xpert® CT/NG test was piloted in four intervention clusters, with testing performed by service providers. On-site testing was defined as sample processing on the same day and site as sample collection. Outcomes included proportion of tests processed on-site, time between sample collection and collection of results, and proportion of clients receiving treatment. In-depth interviews were conducted with nine service providers and three staff members providing study co-ordination or laboratory support to explore facilitators and barriers to providing on-site CT/NG testing.
RESULTS RESULTS
Of 847 Xpert tests, 296 (35.0%) were performed on-site. Of these, 61 (20.6%) were positive for CT/NG; one (1.6%) received same day aetiological treatment; 33 (54.1%) presented later for treatment; and 5 (8.2%) were treated as a part of syndromic management. There was no difference in the proportion of clients who were treated whether their sample was processed on or off-site (64% (39/61) vs 60% (66/110); p = 0.61). The median (IQR) number of days between sample collection and collection of positive results was 14 (7-35) and 14 (7-52.5) for samples processed on and off-site, respectively, The interviews revealed four themes related to the provision of on-site testing associated with the i) diagnostic device ii) environment, iii) provider, and iv) clients. Some of the specific barriers identified included insufficient testing capacity, inadequate space, as well as reluctance of clients to wait for their results.
CONCLUSIONS CONCLUSIONS
In addition to research to optimise the implementation of point-of-care tests for STIs in resource-limited settings, the development of new platforms to reduce analytic time will be necessary to scale up STI testing and reduce the attrition between testing and treatment.
TRIAL REGISTRATION BACKGROUND
Registered in clinical trials.gov ( NCT03719521 ).

Identifiants

pubmed: 35144602
doi: 10.1186/s12913-022-07557-7
pii: 10.1186/s12913-022-07557-7
pmc: PMC8830017
doi:

Banques de données

ClinicalTrials.gov
['NCT03719521']

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

171

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 206316/Z/17/Z
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/T040327/1
Pays : United Kingdom

Informations de copyright

© 2022. The Author(s).

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Auteurs

Kevin Martin (K)

Department of Global Health and Infection, Brighton and Sussex Medical School, Brighton, UK. kevinmartin@doctors.org.uk.
Clinical Research Department, London School of Hygiene & Tropical Medicine, London, WC1E 7HT, UK. kevinmartin@doctors.org.uk.

Chido Dziva Chikwari (C)

Clinical Research Department, London School of Hygiene & Tropical Medicine, London, WC1E 7HT, UK.
Biomedical Research and Training Institute, Harare, Zimbabwe.

Constance R S Mackworth-Young (CRS)

Clinical Research Department, London School of Hygiene & Tropical Medicine, London, WC1E 7HT, UK.

Mutsawashe Chisenga (M)

Biomedical Research and Training Institute, Harare, Zimbabwe.

Tsitsi Bandason (T)

Biomedical Research and Training Institute, Harare, Zimbabwe.

Ethel Dauya (E)

Biomedical Research and Training Institute, Harare, Zimbabwe.

Ioana D Olaru (ID)

Clinical Research Department, London School of Hygiene & Tropical Medicine, London, WC1E 7HT, UK.
Biomedical Research and Training Institute, Harare, Zimbabwe.

Suzanna C Francis (SC)

Department of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK.

Constancia Mavodza (C)

Department of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK.
Department of Public Health and Policy, London School of Hygiene & Tropical Medicine, London, UK.

Portia Nzombe (P)

Biomedical Research and Training Institute, Harare, Zimbabwe.

Rangarirayi Nyamwanza (R)

Biomedical Research and Training Institute, Harare, Zimbabwe.

Fadzanai Hove (F)

Biomedical Research and Training Institute, Harare, Zimbabwe.

Maureen Tshuma (M)

Biomedical Research and Training Institute, Harare, Zimbabwe.

Anna Machiha (A)

AIDS and TB Unit, Ministry of Health and Child Care, Harare, Zimbabwe.

Katharina Kranzer (K)

Clinical Research Department, London School of Hygiene & Tropical Medicine, London, WC1E 7HT, UK.
Biomedical Research and Training Institute, Harare, Zimbabwe.
Division of Infectious and Tropical Medicine, Medical Centre of the University of Munich, Munich, Germany.

Rashida A Ferrand (RA)

Clinical Research Department, London School of Hygiene & Tropical Medicine, London, WC1E 7HT, UK.
Biomedical Research and Training Institute, Harare, Zimbabwe.

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