The ethics of feedback of HIV test results in population-based surveys of HIV infection
Population-based disease prevalence surveys raise ethical questions, including whether participants should be routinely told their test results. Ethical guidelines call for informing survey participants of any clinically relevant finding to enable appropriate management. However, in anonymous survey...
Saved in:
Main Author: | Dermot Maher (Author) |
---|---|
Format: | Book |
Published: |
The World Health Organization,
2013-12-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Routine feedback of test results to participants in clinic- and survey-based surveillance of HIV
by: Rachel Baggaley, et al.
Published: (2015) -
Concurrent sexual partnerships and associated factors: a cross-sectional population-based survey in a rural community in Africa with a generalised HIV epidemic
by: Karabarinde Alex, et al.
Published: (2011) -
Feedback on research results to healthcare professionals in the context of HIV
by: Iací Proença Palmeira, et al. -
Mortality and its predictors among antiretroviral therapy naïve HIV-infected individuals with CD4 cell count ≥350 cells/mm3 compared to the general population: data from a population-based prospective HIV cohort in Uganda
by: Ben Masiira, et al.
Published: (2014) -
Determinants of knowledge of HIV status in South Africa: results from a population-based HIV survey
by: Peltzer Karl, et al.
Published: (2009)