Transplant Recipient Preferences Regarding Organ Donor Research: Their Role in Consent and use of Their Data

Author:

Lucas Amanda1ORCID,Strachan Patricia H.1,D’Aragon Frederick2ORCID,Sarti Aimee J.3,Meade Maureen O.1

Affiliation:

1. McMaster University, Hamilton, Ontario, Canada

2. Universite de Sherbrooke, Sherbrooke, Quebec, Canada

3. University of Ottawa, Ottawa, Canada

Abstract

Research on deceased organ donors has been hindered by concerns related to seeking research consent from transplant recipients. We undertook this qualitative study to elucidate solid organ transplant recipients views on organ donor research, their role in the consent for such research, and their preferences related to providing their data. We conducted interviews with 18 participants and three themes emerged from the data. The first centered around participant research literacy. The second described practical preferences of participating in research, and the third related to the connection between donor and recipient. We concluded that previously held views about the requirement for transplant recipients to have a consenting role in donor research is not always suitable.

Funder

Canadian Donation and Transplantation Research Program (CDTRP)/Astellas Research Innovation Grant

Publisher

SAGE Publications

Subject

Communication,Education,Social Psychology

Reference23 articles.

1. Organ Donor Research: It Is Time for Much Needed Clarity

2. Canadian Institute for Healthcare Innovation (2014). Deceased organ donor potential in Canada report. https://secure.cihi.ca/free_products/OrganDonorReport_ENweb.pdf. Accessed March 14, 2022

3. Examining consent for interventional research in potential deceased organ donors: a narrative review

4. Canada-DONATE study protocol: a prospective national observational study of the medical management of deceased organ donors

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