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Understanding why people participate in HIV surveillance
People have argued that the benefits of human immunodeficiency virus (HIV) testing and counselling are so important that participants in HIV surveys must be given their HIV test results and that individuals who decline to receive their test results should be excluded from participation in such surve...
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Published in: | Bulletin of the World Health Organization 2015-05, Vol.93 (5), p.356-357 |
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Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | People have argued that the benefits of human immunodeficiency virus (HIV) testing and counselling are so important that participants in HIV surveys must be given their HIV test results and that individuals who decline to receive their test results should be excluded from participation in such surveys. In African populations with HIV prevalence above 4%, between 30% and 81% of infected men and women have ever been tested for HIV. Those who know they are HIV-positive may be willing to donate blood samples for research purposes but may not want to repeat pre- and post-test counselling. Importantly, the opt-out provisions the authors discuss here align with the general principles of research ethics. They agree that there is public health utility in informing people of their HIV status but they think that this should not override the ethics of respect for individual autonomy. |
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ISSN: | 0042-9686 1564-0604 |
DOI: | 10.2471/BLT.14.135756 |