Ethics of organ procurement from the unrepresented patient population.

Ethics of organ procurement from the unrepresented patient population.

Raho, Joseph A;Brown-Saltzman, Katherine;Korenman, Stanley G;Weiss, Fredda;Orentlicher, David;Lin, James A;Moreno, Elisa A;Nuri-Robins, Kikanza;Stein, Andrea;Schnell, Karen E;Diamant, Allison L;Weiss, Irwin K;
Journal of medical ethics 2019
339
raho2019ethicsjournal

Abstract

The shortage of organs for transplantation by its nature prompts ethical dilemmas. For example, although there is an imperative to save human life and reduce suffering by maximising the supply of vital organs, there is an equally important obligation to ensure that the process by which we increase the supply respects the rights of all stakeholders. In a relatively unexamined practice in the USA, organs are procured from unrepresented decedents without their express consent. Unrepresented decedents have no known healthcare wishes or advance care planning document; they also lack a surrogate. The Revised Uniform Anatomical Gift Act (RUAGA) of 2006 sends a mixed message about the procurement of organs from this patient population and there are hospitals that authorise donation. In addition, in adopting the RUAGA, some states included provisions that clearly allow organ procurement from unrepresented decedents. An important unanswered question is whether this practice meets the canons of ethical permissibility. The current Brief Report presents two principled approaches to the topic as a way of highlighting some of the complexities involved. Concluding remarks offer suggestions for future research and discussion.

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