Caring for Patients at the End of Life: Facing an Uncertain Future Together / Edition 1

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Overview

In Caring for Patients at the End of Life: Facing an Uncertain Future Together, Dr. Quill uses his wide range of clinical experience caring for severely ill patients and their families to illustrate the challenges and potential of end-of-life care. Section one utilizes the near death experiences of two patients to explore values underlying medical humanism, and then presents the case of "Diane" to explore the fundamental clinical commitments of partnership and non-abandonment. Section two explores, illustrates, and provides practical guidance for clinicians, patients, and families about critical communication issues including delivering bad news, discussing palliative care, and exploring the wish to die. In section three, difficult ethical and policy challenges inherent in hospice work, including the rule of double effect, terminal sedation, and physician-assisted suicide, are explored using a mix of real cases and an analysis of underlying clinical, ethical, and policy issues. In a final chapter, Dr. Quill discusses the tragic death of his brother which occurred as this book was being completed, and how his family made the most emotionally challenging decisions of their lives.
Dr. Quill exposes readers to an internally consistent and practical way of thinking by simultaneously embracing the potential of palliative care, and also acknowledging that it has limitations. His philosophy of offering forthright discussions with patient and family, mutual decision-making, ensuring medical and palliative care expertise and of committing to see the dying process through to the patient's death is vividly illustrated.

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Editorial Reviews

Doody's Review Service
Reviewer: Lisa Stepp, PhD, RN, APN, AOCN, CRNH (Private Practice)
Description: When providing end of life care, healthcare professionals face numerous problems. As an illness progresses, the patient's suffering increases and care of the patient becomes challenging, both clinically and ethically. Healthcare providers need clear direction to be able to provide the best possible palliative care at this crucial time.
Purpose: The purpose of this book, as defined by the author, is to direct the palliative care provider's attention to the values and assumptions underlying terminal care. There seems to remain a great deal of confusion regarding terminal care. These issues clearly need to be discussed openly and honestly and the author provides a forum for this discussion. Although there are numerous publications that address end of life issues, the author uses personal illustrations to provide a framework to guide conversations between physicians and patients.
Audience: The book is designed for clinicians involved in palliative care. Students would also benefit from having this book in their library. The author speaks form personal experience providing end of life care and provides a comprehensive overview of significant dilemmas in this area of healthcare.
Features: The author addresses medical issues as well as how medical decisions are structured in light of legal and ethical considerations. Illustrations of possible discussions between healthcare professionals and patients are presented in a realistic manner.
Assessment: This book provides a window into one individual's journey as a healthcare professional in end of life care.
Lawrence J. Schneiderman
Caring for Patients at the End of Life provides compelling evidence that Dr Quill's interests and expertise extend beyond this single issue. Rather, he shows that assisting a patient to die when suffering becomes intolerable is only the extreme end of a spectrum of many treatment possibilities.

Most of the chapters are revised versions of coauthored articles published in medical journals. Assembled in this collection, they make a coherent and convenient package of helpful information, which Quill provides with the authority of experience. His case reports and discussions feature both philosophical arguments and practical advice for dealing with the wide variety of end-of-life decisions.
Journal of American Medical Association


3 Stars from Doody
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Product Details

  • ISBN-13: 9780195139402
  • Publisher: Oxford University Press, USA
  • Publication date: 3/28/2001
  • Edition description: New Edition
  • Edition number: 1
  • Pages: 264
  • Sales rank: 1,113,482
  • Product dimensions: 8.90 (w) x 5.80 (h) x 0.70 (d)

Meet the Author

University of Rochester School of Medicine and Dentistry, Rochester, NY
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Table of Contents

I. Underlying Values and Assumptions
1. Same Old Seventeen Dollar Lamps
2. Humanistic End of Life Care
3. Death and Dignity: A Case of Individualized Decision Making
4. Partnership in the Care of the Dying
5. Non-abandonment: A Central Obligation of Physicians
II. The Medical Interview: A Critical Clinical Tool
6. Delivering Bad News
7. Discussing Palliative Care with Patients
8. Palliative Care for Patients with Severe Dementia: A Consensus-Based Approach to Decision-Making
9. Doctor, I want to die! Will you help me?
III. Difficult Clinical and Ethical Issues
10. Hospice and Palliative Care: Clinical, Ethical and Policy Challenges
11. The Rule of Double Effect: A Critique of its Role in End of Life Decision Making
12. Palliative Options of Last Resort: A Comparison of Practices, Justifications, and Safeguards
13. End of Life Care in the Netherlands and the United States: A Comparison of Values, Justifications, and Practices
Epilogue: All About My Brother

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