Ethical failings of CPSO policy and the health care consent act: case review

Abstract End-of-life disputes in Ontario are currently overwhelmingly assessed through the singular lens of patient autonomy. The current dispute resolution mechanism(s) does not adequately consider evidence-based medical guidelines, standards of care, the patient’s best interests, expert opinion, o...

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Main Authors: Joshua T. Landry, Rakesh Patel, David Neilipovitz, Kwadwo Kyeremanteng, Gianni D’Egidio
Format: Article
Language:English
Published: BMC 2019-03-01
Series:BMC Medical Ethics
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12910-019-0357-y
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spelling doaj-9cec6846c02249deb7ac7504162395982020-11-25T03:59:17ZengBMCBMC Medical Ethics1472-69392019-03-012011510.1186/s12910-019-0357-yEthical failings of CPSO policy and the health care consent act: case reviewJoshua T. Landry0Rakesh Patel1David Neilipovitz2Kwadwo Kyeremanteng3Gianni D’Egidio4Ontario Shores Centre for Mental Health SciencesUniversity of OttawaUniversity of OttawaUniversity of OttawaUniversity of OttawaAbstract End-of-life disputes in Ontario are currently overwhelmingly assessed through the singular lens of patient autonomy. The current dispute resolution mechanism(s) does not adequately consider evidence-based medical guidelines, standards of care, the patient’s best interests, expert opinion, or distributive justice. We discuss two cases adjudicated by the Consent and Capacity board of Ontario that demonstrate the over emphasis on patient autonomy. Current health care policy and the Health Care Consent Act also place emphasis on patient autonomy without considering other ethically defensible factors. We argue that current policy and legislation require amendment, and unless there are measures undertaken to modify them, both the quality of care provided and the long-term capabilities of the health care system to remain publicly-funded, comprehensive and equitable, are at stake.http://link.springer.com/article/10.1186/s12910-019-0357-yEnd-of-lifeAutonomyMedical consentPalliative careQuality of lifeEthical responsibility
collection DOAJ
language English
format Article
sources DOAJ
author Joshua T. Landry
Rakesh Patel
David Neilipovitz
Kwadwo Kyeremanteng
Gianni D’Egidio
spellingShingle Joshua T. Landry
Rakesh Patel
David Neilipovitz
Kwadwo Kyeremanteng
Gianni D’Egidio
Ethical failings of CPSO policy and the health care consent act: case review
BMC Medical Ethics
End-of-life
Autonomy
Medical consent
Palliative care
Quality of life
Ethical responsibility
author_facet Joshua T. Landry
Rakesh Patel
David Neilipovitz
Kwadwo Kyeremanteng
Gianni D’Egidio
author_sort Joshua T. Landry
title Ethical failings of CPSO policy and the health care consent act: case review
title_short Ethical failings of CPSO policy and the health care consent act: case review
title_full Ethical failings of CPSO policy and the health care consent act: case review
title_fullStr Ethical failings of CPSO policy and the health care consent act: case review
title_full_unstemmed Ethical failings of CPSO policy and the health care consent act: case review
title_sort ethical failings of cpso policy and the health care consent act: case review
publisher BMC
series BMC Medical Ethics
issn 1472-6939
publishDate 2019-03-01
description Abstract End-of-life disputes in Ontario are currently overwhelmingly assessed through the singular lens of patient autonomy. The current dispute resolution mechanism(s) does not adequately consider evidence-based medical guidelines, standards of care, the patient’s best interests, expert opinion, or distributive justice. We discuss two cases adjudicated by the Consent and Capacity board of Ontario that demonstrate the over emphasis on patient autonomy. Current health care policy and the Health Care Consent Act also place emphasis on patient autonomy without considering other ethically defensible factors. We argue that current policy and legislation require amendment, and unless there are measures undertaken to modify them, both the quality of care provided and the long-term capabilities of the health care system to remain publicly-funded, comprehensive and equitable, are at stake.
topic End-of-life
Autonomy
Medical consent
Palliative care
Quality of life
Ethical responsibility
url http://link.springer.com/article/10.1186/s12910-019-0357-y
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