Transplant physicians must respect indecisive patients’ autonomy while continuing to educate them during their progress towards transplantation.

Despite clear donor consent, health professionals must communicate clearly about death to family members to avoid confusion.

Social media platforms and organizational websites that facilitate organ procurement should respect potential donors’ autonomy and confidentiality.

The AMA Code of Medical Ethics’ opinions related to organ donors’ informed, voluntary decisions and equitable distribution of organs and tissues.

Standards for posttransplant graft/survival rates do not reward transplant centers for performing riskier transplants to increase population benefit.

Although organ donation conflicts with self-interest, because donation is vital to the community, interventions to increase it are ethically justified.

Equal access is a goal even when patients present with taboo illnesses. But, the date of a patient’s last drink still matters.

Some technological and policy strategies for increasing organ supplies are ethically and legally proven to work. Consider best next steps for global education efforts to raise organ donation awareness.

Because transplantation for methylmalonic acidaemia prioritizes quality of life over long-term outcomes, justice and utility must be considered.

The Patient- and Family-Centered Care Methodology and Practice follows six steps to improve clinical results and accountability and to reduce costs.