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.

Communication End-of-life decision-making Intensive care Medical ethics Opt-out consent Organ donation Professional-family relations Qualitative research

Journal

Critical care (London, England)
ISSN: 1466-609X
Titre abrégé: Crit Care
Pays: England
ID NLM: 9801902

Informations de publication

Date de publication:
28 07 2023
Historique:
received: 26 05 2023
accepted: 13 07 2023
medline: 31 7 2023
pubmed: 29 7 2023
entrez: 28 7 2023
Statut: epublish

Résumé

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 (presumed) consent in donor conversations in the first years of the opt-out system. A qualitative embedded multiple-case study in eight Dutch hospitals. We performed a thematic analysis based on audio recordings and direct observations of donor conversations (n = 15, 7 consent and 8 presumed consent) and interviews with the clinicians involved (n = 16). Clinicians' personal considerations, their prior experiences with the family and contextual factors in the clinicians' profession defined their points of departure for the conversations. Four routes to discuss patients' donor registrations were constructed. In the Consent route (A), clinicians followed patients' explicit donation wishes. With presumed consent, increased uncertainty in interpreting the donation wish appeared and prompted clinicians to refer to "the law" as a conversation starter and verify patients' wishes multiple times with the family. In the Presumed consent route (B), clinicians followed the law intending to effectuate donation, which was more easily achieved when families recognised and agreed with the registration. In the Consensus route (C), clinicians provided families some participation in decision-making, while in the Family consent route (D), families were given full decisional capacity to pursue optimal grief processing. Donor conversations in an opt-out system are a complex interplay between seemingly straightforward donor registrations and clinician-family interactions. When clinicians are left with concerns regarding patients' consent or families' coping, families are given a larger role in the decision. A strict uniform application of the opt-out system is unfeasible. We suggest incorporating the four previously described routes in clinical training, stimulating discussions across cases, and encouraging public conversations about donation.

Sections du résumé

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 (presumed) consent in donor conversations in the first years of the opt-out system.
METHODS
A qualitative embedded multiple-case study in eight Dutch hospitals. We performed a thematic analysis based on audio recordings and direct observations of donor conversations (n = 15, 7 consent and 8 presumed consent) and interviews with the clinicians involved (n = 16).
RESULTS
Clinicians' personal considerations, their prior experiences with the family and contextual factors in the clinicians' profession defined their points of departure for the conversations. Four routes to discuss patients' donor registrations were constructed. In the Consent route (A), clinicians followed patients' explicit donation wishes. With presumed consent, increased uncertainty in interpreting the donation wish appeared and prompted clinicians to refer to "the law" as a conversation starter and verify patients' wishes multiple times with the family. In the Presumed consent route (B), clinicians followed the law intending to effectuate donation, which was more easily achieved when families recognised and agreed with the registration. In the Consensus route (C), clinicians provided families some participation in decision-making, while in the Family consent route (D), families were given full decisional capacity to pursue optimal grief processing.
CONCLUSION
Donor conversations in an opt-out system are a complex interplay between seemingly straightforward donor registrations and clinician-family interactions. When clinicians are left with concerns regarding patients' consent or families' coping, families are given a larger role in the decision. A strict uniform application of the opt-out system is unfeasible. We suggest incorporating the four previously described routes in clinical training, stimulating discussions across cases, and encouraging public conversations about donation.

Identifiants

pubmed: 37507800
doi: 10.1186/s13054-023-04581-9
pii: 10.1186/s13054-023-04581-9
pmc: PMC10375668
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

299

Informations de copyright

© 2023. The Author(s).

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Auteurs

Sanne P C van Oosterhout (SPC)

Department of IQ Healthcare, Radboud Institute for Health Sciences, Radboud University Medical Center, Kapittelweg 54, 6525 EP, Nijmegen, The Netherlands. Sanne.vanOosterhout@radboudumc.nl.

Anneke G van der Niet (AG)

Department of IQ Healthcare, Radboud Institute for Health Sciences, Radboud University Medical Center, Kapittelweg 54, 6525 EP, Nijmegen, The Netherlands.

W Farid Abdo (WF)

Department of Intensive Care Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.

Marianne Boenink (M)

Department of IQ Healthcare, Radboud Institute for Health Sciences, Radboud University Medical Center, Kapittelweg 54, 6525 EP, Nijmegen, The Netherlands.

Thomas G V Cherpanath (TGV)

Department of Intensive Care Medicine, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

Jelle L Epker (JL)

Department of Intensive Care Medicine, Erasmus Medical Center, Rotterdam, The Netherlands.

Angela M Kotsopoulos (AM)

Department of Intensive Care, Elisabeth Tweesteden Hospital, Tilburg, The Netherlands.

Walther N K A van Mook (WNKA)

Department of Intensive Care Medicine, Maastricht University Medical Center, Maastricht, The Netherlands.

Hans P C Sonneveld (HPC)

Department of Intensive Care Medicine, Isala Hospital, Zwolle, The Netherlands.

Meint Volbeda (M)

Department of Critical Care, University of Groningen, University Medical Center, Groningen, The Netherlands.

Gert Olthuis (G)

Department of IQ Healthcare, Radboud Institute for Health Sciences, Radboud University Medical Center, Kapittelweg 54, 6525 EP, Nijmegen, The Netherlands.

Jelle L P van Gurp (JLP)

Department of IQ Healthcare, Radboud Institute for Health Sciences, Radboud University Medical Center, Kapittelweg 54, 6525 EP, Nijmegen, The Netherlands.

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