David Bourget (Western Ontario)
David Chalmers (ANU, NYU)
Rafael De Clercq
Ezio Di Nucci
Jonathan Jenkins Ichikawa
Jack Alan Reynolds
Learn more about PhilPapers
Cambridge Quarterly of Healthcare Ethics 1 (4):377 (1992)
Historically, patients have deferred to physicians′ judgments about appropriate medical care, thereby limiting patient participation in treatment decisions. In this model of medical decision making, physicians typically decided upon the treatment plan. Communication with patients focused on securing their cooperation in accepting a treatment decision that essentially had already been made
|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
J. Vollmann (2001). Advance Directives in Patients with Alzheimer's Disease; Ethical and Clinical Considerations. Medicine, Health Care and Philosophy 4 (2):161-167.
Leslie Pickering Francis (1993). Advance Directives for Voluntary Euthanasia: A Volatile Combination? Journal of Medicine and Philosophy 18 (3):297-322.
David J. Doukas, Using the Family Covenant in Planning End-of-Life Care: Obligations and Promises of Patients, Families, and Physicians.
Amy M. Bovi (2003). Ethical Guidelines for Use of Electronic Mail Between Patients and Physicians. American Journal of Bioethics 3 (3):43-47.
Jim Stone (1994). Advance Directives, Autonomy and Unintended Death. Bioethics 8 (3):223–246.
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.
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.
David Shaw (2011). A Direct Advance on Advance Directives. Bioethics 26 (5):267-274.
Violeta Be Irević (2010). End-of-Life Care in the 21st Century: Advance Directives in Universal Rights Discourse. Bioethics 24 (3):105-112.
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.
Helga Kuhse (1999). Some Reflections on the Problem of Advance Directives, Personhood, and Personal Identity. Kennedy Institute of Ethics Journal 9 (4):347-364.
Ho Mun Chan (2004). Sharing Death and Dying: Advance Directives, Autonomy and the Family. Bioethics 18 (2):87–103.
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.
Added to index2010-09-13
Total downloads6 ( #498,890 of 1,938,807 )
Recent downloads (6 months)5 ( #125,144 of 1,938,807 )
How can I increase my downloads?