Do people have an ethical obligation to share their health information? Comparing narratives of altruism and health information sharing in a nationally representative sample

BACKGROUND: With the emergence of new health information technologies, health information can be shared across networks, with or without patients’ awareness and/or their consent. It is often argued that there can be an ethical obligation to participate in biomedical research, motivated by altruism,...

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Detalles Bibliográficos
Autores principales: Raj, Minakshi, De Vries, Raymond, Nong, Paige, Kardia, Sharon L. R., Platt, Jodyn E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7774955/
https://www.ncbi.nlm.nih.gov/pubmed/33382835
http://dx.doi.org/10.1371/journal.pone.0244767

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7774955/
https://www.ncbi.nlm.nih.gov/pubmed/33382835
http://dx.doi.org/10.1371/journal.pone.0244767

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