Switch to: Citations

Add references

You must login to add references.
  1. Cultural Engagement in Clinical Ethics: A Model for Ethics Consultation.Michele A. Carter & Craig M. Klugman - 2001 - Cambridge Quarterly of Healthcare Ethics 10 (1):16-33.
    In the rapidly evolving healthcare environment, perhaps no role is in greater flux and redefinition than that of the clinical bioethicist. The discussion of ethics consultation in the bioethics literature has moved from an ambiguous concern regarding its proper place in the clinical milieu to the more provocative question of which methods and theories should best characterize the intellectual and practical work it claims to do. The American Society for Bioethics and Humanities addressed these concerns in its 1998 report, CoreCompetenciesforHealthCareEthicsConsultation. (...)
    Direct download (6 more)  
     
    Export citation  
     
    Bookmark   6 citations  
  • Health Care Ethics Consultation: An Update on Core Competencies and Emerging Standards From the American Society for Bioethics and Humanities' Core Competencies Update Task Force.Anita Tarzian - 2013 - American Journal of Bioethics 13 (2):3-13.
    Ethics consultation has become an integral part of the fabric of U.S. health care delivery. This article summarizes the second edition of the Core Competencies for Health Care Ethics Consultation report of the American Society for Bioethics and Humanities. The core knowledge and skills competencies identified in the first edition of Core Competencies have been adopted by various ethics consultation services and education programs, providing evidence of their endorsement as health care ethics consultation standards. This revised report was prompted by (...)
    Direct download (3 more)  
     
    Export citation  
     
    Bookmark   33 citations  
  • Damage Compounded: Disparities, Distrust, and Disparate Impact in End-of-Life Conflict Resolution Policies.Mary Ellen Wojtasiewicz - 2006 - American Journal of Bioethics 6 (5):8 – 12.
    For a little more than a decade, professional organizations and healthcare institutions have attempted to develop guidelines and policies to deal with seemingly intractable conflicts that arise between clinicians and patients (or their proxies) over appropriate use of aggressive life-sustaining therapies in the face of low expectations of medical benefit. This article suggests that, although such efforts at conflict resolution are commendable on many levels, inadequate attention has been given to their potential negative effects upon particular groups of patients/proxies. Based (...)
    Direct download (3 more)  
     
    Export citation  
     
    Bookmark   21 citations  
  • Caring for Patients in Cross‐Cultural Settings.Nancy S. Jecker, Joseph A. Carrese & Robert A. Pearlman - 1995 - Hastings Center Report 25 (1):6-14.
  • Case Study: Mistrust, Racism, and End-of-Life Treatment.Eric L. Krakauer & Robert D. Truog - 1997 - Hastings Center Report 27 (3):23.
  • Writing at the Margin Discourse Between Anthropology and Medicine.Arthur Kleinman - 1995