Improving the organ donor card system in Switzerland
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Published on: March 12, 2018
1University of Basel, SWITZERLAND; davidmartinshaw@gmail.com.
Insights
Switzerland
Area of Science:
- Medical Ethics
- Public Health Policy
- Transplantation Medicine
Background:
- Switzerland faces low deceased organ donation rates.
- The current organ donor card system may contribute to this issue.
- Understanding systemic problems is crucial for improving donation rates.
Purpose of the Study:
- To analyze Switzerland's organ donor card system.
- To identify specific problems hindering deceased organ donation.
- To propose solutions for increasing organ donation rates.
Main Methods:
- Analysis of the current organ donor card system in Switzerland.
- Identification of systemic issues within the donation process.
- Review of Swisstransplant's information dissemination and consent procedures.
Main Results:
- Five problems identified: understated benefits on Swisstransplant's website, questionable informed consent, lack of a central donor registry, high likelihood of family veto, and failure to inform potential donors of these issues.
- These issues likely contribute to low deceased organ donation rates.
Conclusions:
- Improving donation rates requires addressing identified systemic flaws.
- Recommendations include providing accurate donation benefits information, establishing a central donor registry, and prohibiting family vetoes.
Abstract:
This paper analyses the current organ donor card system in Switzerland and identifies five problems that may be partially responsible for the country's low deceased organ donation rates. There are two minor issues concerning the process of obtaining a donor card: the Swisstransplant website understates the prospective benefits of donation, and the ease with which donor cards can be obtained raises questions regarding whether any consent to donation provided is truly informed. Furthermore, there are two major practical problems that might affect those who carry an organ donor card: the lack of a central donor registry increases the likelihood that donors' wishes will be "lost", and there is a high probability that family members will veto organ donation. The fact that these two practical problems are not mentioned to potential donors by Swisstransplant constitutes the fifth problem. Donation rates would probably improve if more accurate information about the benefits of donation were provided to potential donors, a central donor registry were created, and families were not permitted to veto donation from those on the registry.
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