Evaluating the Dissent in State of Oregon v. Ashcroft: Implications for the Patient-Physician Relationship and the Democratic Process

Over the past decade or so, no issue in medical ethics or bioethics law has raised more concerns about federal intervention in the practice of medicine, about judicial attempts to craft health policy, or about the wisdom of public mandates directing specific health care initiatives than the issue of...

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Bibliographic Details
Published inThe Journal of law, medicine & ethics Vol. 33; no. 1; pp. 142 - 153
Main Author Hilliard, Bryan
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 22.03.2005
SAGE Publications
Sage Publications, Inc
Cambridge University Press
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Online AccessGet full text
ISSN1073-1105
1748-720X
DOI10.1111/j.1748-720X.2005.tb00216.x

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Summary:Over the past decade or so, no issue in medical ethics or bioethics law has raised more concerns about federal intervention in the practice of medicine, about judicial attempts to craft health policy, or about the wisdom of public mandates directing specific health care initiatives than the issue of physician-assisted suicide. State voter referenda, lower and federal court cases (including two U.S. Supreme Court decisions), proposed legislation in both houses of Congress, and orders and determinations from agencies within the executive branch of two administrations are representative of the kinds of actions taken in the last ten years implicating medical care at the end of life. Whether the intent was to codify into law physician-assisted suicide, to deny a constitutional right of assisted suicide, or to make “easier” physicians' efforts to alleviate intractable suffering at the risk of hastening death, or to prohibit physician aid in dying altogether, the impact on the patient-doctor relationship and on our understanding of what constitutes dignified and humane care at the end of life is undeniable.
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ISSN:1073-1105
1748-720X
DOI:10.1111/j.1748-720X.2005.tb00216.x