Patient data and patient rights: Swiss healthcare stakeholders’ ethical awareness regarding large patient data sets – a qualitative study

BACKGROUND: There is a growing interest in aggregating more biomedical and patient data into large health data sets for research and public benefits. However, collecting and processing patient data raises new ethical issues regarding patient’s rights, social justice and trust in public institutions....

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Detalles Bibliográficos
Autores principales: Mouton Dorey, Corine, Baumann, Holger, Biller-Andorno, Nikola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5842517/
https://www.ncbi.nlm.nih.gov/pubmed/29514635
http://dx.doi.org/10.1186/s12910-018-0261-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5842517/
https://www.ncbi.nlm.nih.gov/pubmed/29514635
http://dx.doi.org/10.1186/s12910-018-0261-x

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