Routine feedback of test results to participants in clinic- and survey-based surveillance of HIV

dc.contributor.authorBaggaley, Rachel Clare
dc.contributor.authorJohnson, Cheryl Case
dc.contributor.authorGarcía-Calleja, Jesús Maria
dc.contributor.authorSabin, Keith M.
dc.contributor.authorMakhlouf-Obermeyer, Carla Makhlouf
dc.contributor.authorTaegtmeyer, Miriam M.
dc.contributor.authorZaba, Basia W.
dc.contributor.authorEL HAYEK, Carol
dc.contributor.authorSingh, Jerome Amir
dc.contributor.departmentEpidemiology and Population Health (EPHD)
dc.contributor.facultyFaculty of Health Sciences (FHS)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:34:32Z
dc.date.available2025-01-24T11:34:32Z
dc.date.issued2015
dc.description.abstractSurveillance for human immunodeficiency virus (HIV) in low- and middle-income countries started in the 1980s. However, the questions of whether the results of HIV tests should be given to participants, and if so how, has still not been resolved. In the absence of effective treatment, it was considered acceptable to withhold results from HIV-positive participants. However, when antiretroviral treatment is available, some argue for beneficence – that it is the researcher’s duty to return the test results to all those who provide samples for surveillance. The corollary is that only participants who wish to receive their test results would be eligible to participate in surveys. Others argue for autonomy – that to obtain a more representative result for the general population, surveys should not exclude participants who do not wish to receive their test results. This round table discussion takes a closer look at those two arguments. We believe that the global community should work towards routine feedback of HIV surveillance while ensuring that participants receive and understand their test results. © 2015 World Health Organization. All rights reserved.
dc.identifier.doihttps://doi.org/10.2471/BLT.15.153031
dc.identifier.eid2-s2.0-84928942771
dc.identifier.pmid26229207
dc.identifier.urihttp://hdl.handle.net/10938/28103
dc.language.isoen
dc.publisherWorld Health Organization
dc.relation.ispartofBulletin of the World Health Organization
dc.sourceScopus
dc.subjectAnti-retroviral agents
dc.subjectAttitude of health personnel
dc.subjectFemale
dc.subjectHiv infections
dc.subjectHiv seropositivity
dc.subjectHumans
dc.subjectInformed consent
dc.subjectInterprofessional relations
dc.subjectMale
dc.subjectPatient rights
dc.subjectPhysician-patient relations
dc.subjectPopulation surveillance
dc.subjectUnited nations
dc.subjectHuman immunodeficiency virus
dc.subjectAntiretrovirus agent
dc.subjectDisease treatment
dc.subjectFeedback mechanism
dc.subjectHealth survey
dc.subjectLow income population
dc.subjectParticipatory approach
dc.subjectSpatiotemporal analysis
dc.subjectAcquired immune deficiency syndrome
dc.subjectArticle
dc.subjectDisease eradication
dc.subjectDisease surveillance
dc.subjectFeedback system
dc.subjectHiv test
dc.subjectHuman immunodeficiency virus infection
dc.subjectInfection control
dc.subjectParticipant observation
dc.subjectPoint of care testing
dc.subjectVirus transmission
dc.subjectWorld health organization
dc.subjectDoctor patient relation
dc.subjectEthics
dc.subjectHealth personnel attitude
dc.subjectHuman
dc.subjectPatient right
dc.subjectPsychology
dc.subjectPublic relations
dc.titleRoutine feedback of test results to participants in clinic- and survey-based surveillance of HIV
dc.typeArticle

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