REFERENCES
- Berry, Daniels, Ladin. 2019. Should lack of social support prevent access to organ transplantation? American Journal of Bioethics. 19(11): 13–24.
- Cahn-Fuller, K. L., and B. Parent. 2017. Transplant eligibility for patients with affective and psychotic disorders: A review of practices and a call for justice. BMC Medical Ethics 18(1): 72. doi: 10.1186/s12910-017-0235-4.
- Faden, R., and A. Leplege. 1992. Assessing quality of life. Moral implications for clinical practice. Medical Care 30 (5 Suppl): MS166–MS175. doi: 10.1097/00005650-199205001-00014.
- Ladin, K., Emerson, J. Z. Butt, E. J., et al. 2018. How important is social support in determining patients’ suitability for transplantation? results from a national survey of transplant clinicians. Journal of Medical Ethics 44(10): 666–674. doi: 10.1136/medethics-2017-104695.
- Ladin, K., and D. W. Hanto. 2013. Rationing lung transplants–procedural fairness in allocation and appeals. New England Journal of Medicine 369(7): 599–601. doi: 10.1056/NEJMp1307792.
- Schulz, R., and S. R. Beach. 1999. Caregiving as a risk factor for mortality: The caregiver health effects study. JAMA 282(23): 2215–22159. doi: 10.1001/jama.282.23.2215.
- Wightman, A., A. Goldberg, and D. Diekema. 2018. Fairness, severe intellectual disability, and the special case of transplantation. Pediatric Transplantation 22(5): e13228. doi: 10.1111/petr.13228.
- Young, A. L., I. A. K. Rowe, R. L. Absolom, et al. 2017. The effect of liver transplantation on the quality of life of the recipient's main caregiver—a systematic review. Liver International 37(6): 794–801. doi: 10.1111/liv.13333.