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Palliative Care and Ethics
Contributor(s): Quill, Timothy E. (Author)
ISBN: 0190604441     ISBN-13: 9780190604448
Publisher: Oxford University Press, USA
OUR PRICE:   $60.80  
Product Type: Paperback - Other Formats
Published: March 2016
Qty:
Additional Information
BISAC Categories:
- Philosophy | Ethics & Moral Philosophy
- Medical | Ethics
- Medical | Terminal Care
Dewey: 179.7
Physical Information: 1" H x 6.1" W x 9.1" (1.05 lbs) 322 pages
Themes:
- Topical - Death/Dying
 
Descriptions, Reviews, Etc.
Publisher Description:
Hospice is the premiere end of life program in the United States, but its requirement that patients forgo disease-directed therapies and that they have a prognosis of 6 months or less means that it serves less than half of dying patients and often for very short periods of time. Palliative
care offers careful attention to pain and symptom management, added support for patients and families, and assistance with difficult medical decision making alongside any and all desired medical treatments, but it does not include a comprehensive system of care as is provided by hospice. The
practice of palliative care and hospice is filled with sometimes overt (requests for hastened death in an environment where such acts are legally prohibited) and other times covert (the delay in palliative care referral because the health care team believes it will undermine disease directed
treatment) ethical issues.

The contributors to this volume use a series of case presentations within each chapter to illustrate some of the palliative care and hospice challenges with significant ethical dimensions across the three overarching domains: 1) care delivery systems; 2) addressing the many dimensions of suffering;
and 3) difficult decisions near the end of life. The contributors are among the most experienced palliative care, hospice and ethics scholars in North America and Western Europe. Each has been given relatively free reign to address what they feel are the most pressing ethical challenges within
their domain, so a wide range of positions and vantage points are represented. As a result, the volume provides a very diverse ethical exploration of this relatively young field that can deepen, stretch, and at times confront any simple notion of the challenges facing patients, their families,
professional caregivers, and policy makers.