The rights and interests of First Nations, Metis, and Inuit in debates over deemed consent legislation for deceased organ donation in Canada: calls to action
被引:2
|
作者:
Tait, Caroline L.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Calgary, Fac Social Work, Calgary, AB, Canada
Fac Social Work, 2500 Univ Dr NW Mac Kimmie Tower MT 301, Calgary, AB T2N 1N4, CanadaUniv Calgary, Fac Social Work, Calgary, AB, Canada
Tait, Caroline L.
[1
,2
]
机构:
[1] Univ Calgary, Fac Social Work, Calgary, AB, Canada
[2] Fac Social Work, 2500 Univ Dr NW Mac Kimmie Tower MT 301, Calgary, AB T2N 1N4, Canada
Organ donation;
Transplantation;
Indigenous;
Health equity;
Deemed consent legislation;
Canada;
TRANSPLANTATION;
DIALYSIS;
PEOPLE;
D O I:
10.1016/j.lana.2022.100414
中图分类号:
R19 [保健组织与事业(卫生事业管理)];
学科分类号:
摘要:
Nova Scotia, Canada is the first jurisdiction in North America to pass deemed consent legislation for organ donation. Individuals medically suitable to be deceased organ donors are considered to have authorised post-mortem organ removal for transplantation unless they opt out of the system. While governments do not have a legal duty to consult Indigenous nations before passing health legislation, this does not diminish Indigenous interests and rights in relation to the legislation. This analysis discusses impacts of the legislation, specifically intersectionality with Indigenous rights, trust in the healthcare system, transplant inequities, and distinctions-based health legislation. How governments engage Indigenous groups about the legislation is yet to unfold. Consultation with Indigenous leaders and engagement and education of Indigenous peoples is, however, key to moving forward legislation that respects Indigenous rights and interests. What happens in Canada is being watched globally, as deemed consent is debated as a solution to organ transplant shortages.