Living-Donor Organ Donation: Impact of Expansion of Genetic Relationship

2019 ◽  
Vol 17 (Suppl 1) ◽  
pp. 1-5
Author(s):  
Saleh Hammad ◽  
◽  
Abdel-Hadi Albreizat
1998 ◽  
Vol 5 (1) ◽  
pp. 19-44 ◽  
Author(s):  
◽  

AbstractHard choices confront societies generally as well as clinicians individually in the face of escalating organ supply requirements for transplantation within Europe. Living organ donation is an important supplement to cadaveric sources of supply, at least in the short to medium term. However, all acceptable therapeutic transplantation strategies require a proper legal regulatory framework to facilitate their use and to encompass central ethical principles and standards. Living donor organ transplantation has typically lacked such a framework, creating vagueness and both doubt and scepticism as to its status and practice.


2003 ◽  
Vol 35 (3) ◽  
pp. 1185
Author(s):  
L. Pączek ◽  
B. Ciszek ◽  
M. Lao ◽  
G. Thiel ◽  
P. Neuhaus ◽  
...  

2003 ◽  
Vol 12 (1) ◽  
pp. 116-118 ◽  
Author(s):  
Aaron Spital

In their recent article, Glannon and Ross remind us that family members have obligations to help each other that strangers do not have. They argue, I believe correctly, that what creates moral obligations within families is not genetic relationship but rather a sharing of intimacy. For no one are these obligations stronger than they are for parents of young children. This observation leads the authors to the logical conclusion that organ donation by a parent to her child is not optional but rather a prima facie duty. However, Glannon and Ross go a step further by suggesting that because parent-to-child organ donation is a duty, it cannot be altruistic. They assert that “altruistic acts are optional, nonobligatory…supererogatory…. Given that altruism consists in purely optional actions presupposing no duty to aid others, any parental act that counts as meeting a child's needs cannot be altruistic.” Here I think the authors go too far.


2014 ◽  
Vol 24 (1) ◽  
pp. 76-81 ◽  
Author(s):  
Patricia H. Warren ◽  
Kimberly A. Gifford ◽  
Barry A. Hong ◽  
Robert M. Merion ◽  
Akinlolu O. Ojo

2017 ◽  
Vol 101 ◽  
pp. S63
Author(s):  
Prasad Herath ◽  
M.H.P. Godakandage ◽  
W.A.N.N. Peries ◽  
L.P. Dilrukshi ◽  
T.D.S. Gunasekera ◽  
...  

2021 ◽  
pp. 002436392110381
Author(s):  
Thomas A. Cavanaugh

In “Double Effect Donation,” Camosy and Vukov argue that “there are circumstances in which it is morally permissible for a healthy individual to donate their organs even though their death is a foreseeable outcome”. They propose that a living donor could ethically donate an entire, singular, vital organ while knowing that this act would result in death. In reply, I argue that it is not ethical for a living person to donate an entire, singular, vital organ. Moreover, mutatis mutandis, it is not ethical for surgeons and others to perform such a deadly operation. For to do so is “intentionally to cause the death of the donor in disposing of his organs”. Such an act violates the dead donor rule which holds that an entire, singular, vital organ may be taken only from a corpse. Contrary to Camosy and Vukov’s claims, double-effect reasoning does not endorse such organ donation.


2020 ◽  
pp. medethics-2019-105999
Author(s):  
Annet Glas

Given the dramatic shortage of transplantable organs, demand cannot be met by established and envisioned organ procurement policies targeting postmortem donation. Live organ donation (LOD) is a medically attractive option, and ethically permissible if informed consent is given and donor beneficence balances recipient non-maleficence. Only a few legal and regulatory frameworks incentivise LOD, with the key exception of Israel’s Organ Transplant Law, which has produced significant improvements in organ donation rates. Therefore, I propose an organ procurement system that incentivises LOD by allocating additional priority points to the living donor on any transplant waiting list. I outline benefits and challenges for potential recipients, donors and society at large, and suggest measures to ensure medical protection of marginalised patient groups.


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