David Bourget (Western Ontario)
David Chalmers (ANU, NYU)
Rafael De Clercq
Jack Alan Reynolds
Learn more about PhilPapers
Cambridge Quarterly of Healthcare Ethics 6 (03):325- (1997)
A competent patient has the right to refuse treatment necessary to sustain life. However, for many end-of-life decisions, we lack direct access to the wishes of a competent patient. Some treatment decisions near the end of life involve patients with severely diminished mental capacity , some involve patients who are unable to communicate , and some involve patients who are simply unable or unwilling to participate in decisionmaking due to the nature or severity of their illness
|Keywords||No keywords specified (fix it)|
|Categories||categorize this paper)|
Setup an account with your affiliations in order to access resources via your University's proxy server
Configure custom proxy (use this if your affiliation does not provide a proxy)
|Through your library|
References found in this work BETA
No references found.
Citations of this work BETA
No citations found.
Similar books and articles
Christopher Tollefsen (1998). Response to “Reassessing the Reliability of Advance Directives” by Thomas May (CQ Vol. 6, No. 5) Advance Directives and Voluntary Slavery. [REVIEW] Cambridge Quarterly of Healthcare Ethics 7 (4):405-413.
Jim Stone (1994). Advance Directives, Autonomy and Unintended Death. Bioethics 8 (3):223–246.
Leslie Pickering Francis (1993). Advance Directives for Voluntary Euthanasia: A Volatile Combination? Journal of Medicine and Philosophy 18 (3):297-322.
David J. Doukas, Toni Antonucci & Daniel W. Gorenflo (1992). A Multigenerational Study on the Correlation of Values and Advance Directives. Ethics and Behavior 2 (1):51 – 59.
E. Furberg (2012). Advance Directives and Personal Identity: What Is the Problem? Journal of Medicine and Philosophy 37 (1):60-73.
Miguel A. Sanchez-Conzalez (1997). Advance Directives Outside the USA: Are They the Best Solution Everywhere? Theoretical Medicine and Bioethics 18 (3):283-301.
J. Vollmann (2001). Advance Directives in Patients with Alzheimer's Disease; Ethical and Clinical Considerations. Medicine, Health Care and Philosophy 4 (2):161-167.
Chris Hackler, Ray Moseley & Dorothy E. Vawter (eds.) (1989). Advance Directives in Medicine. Praeger.
Christopher Buford (2008). Advancing an Advance Directive Debate. Bioethics 22 (8):423-430.
Stefania Negri (ed.) (2012). Self-Determination, Dignity and End-of-Life Care: Regulating Advance Directives in International and Comparative Perspective. M. Nijhoff Pub..
Violeta Be Irević (2010). End-of-Life Care in the 21st Century: Advance Directives in Universal Rights Discourse. Bioethics 24 (3):105-112.
David J. Doukas, Using the Family Covenant in Planning End-of-Life Care: Obligations and Promises of Patients, Families, and Physicians.
Tolga Guven & Gurkan Sert (2010). Advance Directives in Turkey's Cultural Context: Examining the Potential Benefits for the Implementation of Patient Rights. Bioethics 24 (3):127-133.
Hiroaki Miyata, Hiromi Shiraishi & Ichiro Kai (2006). Survey of the General Public's Attitudes Toward Advance Directives in Japan: How to Respect Patients' Preferences. [REVIEW] BMC Medical Ethics 7 (1):1-9.
Benjamin H. Levi & Michael J. Green (2010). Too Soon to Give Up: Re-Examining the Value of Advance Directives. American Journal of Bioethics 10 (4):3 – 22.
Added to index2010-08-24
Total downloads7 ( #204,162 of 1,413,402 )
Recent downloads (6 months)1 ( #154,345 of 1,413,402 )
How can I increase my downloads?