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

dc.contributor.authorLandry, Joshua T
dc.contributor.authorPatel, Rakesh
dc.contributor.authorNeilipovitz, David
dc.contributor.authorKyeremanteng, Kwadwo
dc.contributor.authorD’Egidio, Gianni
dc.date.accessioned2019-03-24T04:20:17Z
dc.date.available2019-03-24T04:20:17Z
dc.date.issued2019-03-19
dc.date.updated2019-03-24T04:20:18Z
dc.description.abstractAbstract 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.
dc.identifier.citationBMC Medical Ethics. 2019 Mar 19;20(1):20
dc.identifier.urihttps://doi.org/10.1186/s12910-019-0357-y
dc.identifier.urihttps://doi.org/10.20381/ruor-23167
dc.identifier.urihttp://hdl.handle.net/10393/38917
dc.language.rfc3066en
dc.rights.holderThe Author(s).
dc.titleEthical failings of CPSO policy and the health care consent act: case review
dc.typeJournal Article

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