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

dc.contributor.authorDesclaux, Alice
dc.contributor.authorKy-Zerbo, Odette
dc.contributor.authorSomé, Jean François
dc.contributor.authorMakhlouf-Obermeyer, Carla Makhlouf
dc.contributor.departmentCenter for Research on Population and Health (CRPH)
dc.contributor.facultyFaculty of Health Sciences (FHS)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:17:09Z
dc.date.available2025-01-24T12:17:09Z
dc.date.issued2015
dc.description.abstractBackground: 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. © 2014 Desclaux et al.; licensee BioMed Central Ltd.
dc.identifier.doihttps://doi.org/10.1186/1472-698X-14-27
dc.identifier.eid2-s2.0-84924256772
dc.identifier.pmid25322668
dc.identifier.urihttp://hdl.handle.net/10938/33664
dc.language.isoen
dc.publisherBioMed Central Ltd.
dc.relation.ispartofBMC International Health and Human Rights
dc.sourceScopus
dc.subjectAfrica
dc.subjectBurkina faso
dc.subjectEthics
dc.subjectGlobal norms
dc.subjectHiv
dc.subjectIndividual rights
dc.subjectStigma
dc.subjectTesting campaign
dc.subjectAdult
dc.subjectConfidentiality
dc.subjectCounseling
dc.subjectCulture
dc.subjectFemale
dc.subjectFocus groups
dc.subjectHealth services accessibility
dc.subjectHiv infections
dc.subjectHumans
dc.subjectMale
dc.subjectMass screening
dc.subjectMiddle aged
dc.subjectPerception
dc.subjectPrivacy
dc.subjectQualitative research
dc.subjectSocial norms
dc.subjectYoung adult
dc.subjectArticle
dc.subjectHiv test
dc.subjectHuman
dc.subjectHuman rights
dc.subjectInterview
dc.subjectSocial norm
dc.subjectThematic analysis
dc.subjectWorkplace
dc.subjectCultural anthropology
dc.subjectHealth care delivery
dc.subjectInformation processing
dc.titleEthical considerations of providers and clients on HIV testing campaigns in Burkina Faso
dc.typeArticle

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