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Ethical considerations of providers and clients on HIV testing campaigns in Burkina Faso

BACKGROUND: Campaigns have been conducted in a number of low HIV prevalence African settings, as a strategy to expand HIV testing, and it is important to assess the extent to which individual rights and quality of care are protected during campaigns. In this article we investigate provider and clien...

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Autores principales: Desclaux, Alice, Ky-Zerbo, Odette, Somé, Jean-François, Obermeyer, Carla Makhlouf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4211928/
https://www.ncbi.nlm.nih.gov/pubmed/25322668
http://dx.doi.org/10.1186/1472-698X-14-27
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author Desclaux, Alice
Ky-Zerbo, Odette
Somé, Jean-François
Obermeyer, Carla Makhlouf
author_facet Desclaux, Alice
Ky-Zerbo, Odette
Somé, Jean-François
Obermeyer, Carla Makhlouf
author_sort Desclaux, Alice
collection PubMed
description BACKGROUND: Campaigns have been conducted in a number of low HIV prevalence African settings, as a strategy to expand HIV testing, and it is important to assess the extent to which individual rights and quality of care are protected during campaigns. In this article we investigate provider and client perceptions of ethical issues, including whether they think that accessibility of counseling and testing sites during campaigns may hinder confidentiality. METHODS: To examine how campaigns have functioned in Burkina Faso, we undertook a qualitative study based on individual interviews and focus group discussions with 52 people (providers and clients tested during or outside campaigns and individuals never tested). Thematic analysis was performed on discourse about perceptions and experiences of HIV-testing campaigns, quality of care and individual rights. RESULTS: Respondents value testing accessibility and attractiveness during campaigns; clients emphasize convenience, ripple effect, the sense of not being alone, and the anonymity resulting from high attendance. Confronted with numerous clients, providers develop context-specific strategies to ensure consent, counseling, confidentiality and retention in the testing process, and they adapt to workplace arrangements, local resources and social norms. Clients appreciate the quality of care during campaigns. However, new ethical issues arise about confidentiality and accessibility. Confidentiality of HIV-status may be jeopardized due to local social norms that encourage people to share their results with others, when HIV-positive people may not wish to do so. Providers’ ethical concerns are consistent with WHO norms known as the ‘5 Cs,’ though articulated differently. Clients and providers value the accessibility of testing for all during campaigns, and consider it an ethical matter. The study yields insights on the way global norms are adapted or negotiated locally. CONCLUSIONS: Future global recommendations for HIV testing and counseling campaigns should consider accessibility and propose ways for testing services to respond to new ethical issues related to high demand.
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spelling pubmed-42119282014-10-29 Ethical considerations of providers and clients on HIV testing campaigns in Burkina Faso Desclaux, Alice Ky-Zerbo, Odette Somé, Jean-François Obermeyer, Carla Makhlouf BMC Int Health Hum Rights Research Article BACKGROUND: Campaigns have been conducted in a number of low HIV prevalence African settings, as a strategy to expand HIV testing, and it is important to assess the extent to which individual rights and quality of care are protected during campaigns. In this article we investigate provider and client perceptions of ethical issues, including whether they think that accessibility of counseling and testing sites during campaigns may hinder confidentiality. METHODS: To examine how campaigns have functioned in Burkina Faso, we undertook a qualitative study based on individual interviews and focus group discussions with 52 people (providers and clients tested during or outside campaigns and individuals never tested). Thematic analysis was performed on discourse about perceptions and experiences of HIV-testing campaigns, quality of care and individual rights. RESULTS: Respondents value testing accessibility and attractiveness during campaigns; clients emphasize convenience, ripple effect, the sense of not being alone, and the anonymity resulting from high attendance. Confronted with numerous clients, providers develop context-specific strategies to ensure consent, counseling, confidentiality and retention in the testing process, and they adapt to workplace arrangements, local resources and social norms. Clients appreciate the quality of care during campaigns. However, new ethical issues arise about confidentiality and accessibility. Confidentiality of HIV-status may be jeopardized due to local social norms that encourage people to share their results with others, when HIV-positive people may not wish to do so. Providers’ ethical concerns are consistent with WHO norms known as the ‘5 Cs,’ though articulated differently. Clients and providers value the accessibility of testing for all during campaigns, and consider it an ethical matter. The study yields insights on the way global norms are adapted or negotiated locally. CONCLUSIONS: Future global recommendations for HIV testing and counseling campaigns should consider accessibility and propose ways for testing services to respond to new ethical issues related to high demand. BioMed Central 2014-10-16 /pmc/articles/PMC4211928/ /pubmed/25322668 http://dx.doi.org/10.1186/1472-698X-14-27 Text en Copyright © 2014 Desclaux et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Desclaux, Alice
Ky-Zerbo, Odette
Somé, Jean-François
Obermeyer, Carla Makhlouf
Ethical considerations of providers and clients on HIV testing campaigns in Burkina Faso
title Ethical considerations of providers and clients on HIV testing campaigns in Burkina Faso
title_full Ethical considerations of providers and clients on HIV testing campaigns in Burkina Faso
title_fullStr Ethical considerations of providers and clients on HIV testing campaigns in Burkina Faso
title_full_unstemmed Ethical considerations of providers and clients on HIV testing campaigns in Burkina Faso
title_short Ethical considerations of providers and clients on HIV testing campaigns in Burkina Faso
title_sort ethical considerations of providers and clients on hiv testing campaigns in burkina faso
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4211928/
https://www.ncbi.nlm.nih.gov/pubmed/25322668
http://dx.doi.org/10.1186/1472-698X-14-27
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