How clinicians discuss patients’ donor registrations of consent and presumed consent in donor conversations in an opt-out system: a qualitative embedded multiple-case study

BACKGROUND: The Netherlands introduced an opt-out donor system in 2020. While the default in (presumed) consent cases is donation, family involvement adds a crucial layer of influence when applying this default in clinical practice. We explored how clinicians discuss patients’ donor registrations of...

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Detalles Bibliográficos
Autores principales: van Oosterhout, Sanne P. C., van der Niet, Anneke G., Abdo, W. Farid, Boenink, Marianne, Cherpanath, Thomas G. V., Epker, Jelle L., Kotsopoulos, Angela M., van Mook, Walther N. K. A., Sonneveld, Hans P. C., Volbeda, Meint, Olthuis, Gert, van Gurp, Jelle L. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10375668/
https://www.ncbi.nlm.nih.gov/pubmed/37507800
http://dx.doi.org/10.1186/s13054-023-04581-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10375668/
https://www.ncbi.nlm.nih.gov/pubmed/37507800
http://dx.doi.org/10.1186/s13054-023-04581-9

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