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Palliative Care and Ethics
By Timothy E. Quill (Edited by), Franklin G. Miller (Edited by)

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6 Ratings by Goodreads
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Format
Paperback, 322 pages
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Hardback : $90.95

Published
United States, 5 May 2016

The practice of palliative care and hospice is filled with overt and sometimes covert ethical challenges. These challenges are addressed by leading international palliative care and hospice scholars under three main domains: care delivery systems; addressing the many dimensions of suffering; and difficult decisions near the end of life.


Timothy E. Quill is a Professor of Medicine, Psychiatry, Medical Humanities and Nursing at the University of Rochester School of Medicine where he directs their Palliative Care Division. He is a board member and the immediate past president of the American Academy of Hospice and Palliative Medicine. He was the lead physician plaintiff on a US Supreme Court Case Quill v Vacco testing the legal permissibility of physician assisted death. Quill is a practicing palliative care physician, the previous author/editor of seven books, multiple peer-reviewed articles in major medical journals, and a regular lecturer and commentator on medical decision making, physician patient relationships, palliative care, and end of life issues.; Franklin G. Miller. is a member of the senior faculty in the Department of Bioethics, National Institutes of Health (NIH) and Special Expert, National Institute of Mental Health Intramural Research Program. His principal current research interests are examination of ethical issues in clinical research, death and dying, and the placebo effect. Dr. Miller has co-authored Death, Dying, and Organ Transplantation (with Robert Truog), Oxford University Press (2012), edited five books and written numerous published articles in medical and bioethics journals on the ethics of clinical research, ethical issues concerning death and dying, professional integrity, health policy, pragmatism and bioethics, and the placebo effect.


Section I: Introduction and Overview; Chapter 1: Introduction (Timothy E. Quill and Franklin G. Miller); Chapter 2: Hospice (Charles von Gunten); Chapter 3: Palliative Care (Susan D. Block); Section II. Ethical Challenges within Current Systems of Care; Chapter 4: Emerging Complexities in Pediatric Palliative Care (Renee Boss and Nancy Hutton); Chapter 5: Patient-Centered Ethos in an Era of Cost Control: Palliative Care and Healthcare Reform (Diane E. Meier and Emily Warner); Chapter 6: Palliative Care, Ethics and Interprofessional Teams (Sally A. Norton, Deborah Waldrop, and Robert Gramling); Section III. Addressing Dimensions of Suffering; Chapter 7: Pain Relief and Palliative Care (Nathan Cherny); Chapter 8: Management of Dyspnea (Thomas W. LeBlanc, David C. Currow, Jane L. Phillips, and Amy Abernethy); Chapter 9: Diagnosis and Treatment of Delirium (Maxine De la Cruz and Eduardo Bruera); Chapter 10: Psychosocial and Psychiatric Suffering (Yesne Alici, Kanan Modhwadia, William S. Breitbart); Chapter 11: Capacity and Shared Decision-Making in Serious Illness (Ronald M. Epstein and Vikki Entwistle); Section IV. Difficult Decisions Near the Very End of Life; Chapter 12: Withholding and Withdrawing Life-Sustaining Treatments (Robert D. Truog); Chapter 13: Medical Futility: Content in the Context of Care (Peggy Determeyer and Howard Brody ); Chapter 14: Palliative Sedation (J. Andrew Billings); Chapter 15: Voluntarily Stopping Eating and Drinking (Emily Rubin and James L. Bernat); Chapter 16: Physician Assisted Death (Timothy E. Quill and Franklin Miller); Chapter 17; 17a: Lessons from Legalized Physician Assisted Death in Oregon and Washington: (Linda Ganzini); 17b: Physician Assisted Death in Western Europe: The Legal and Empirical Situation (Heleen Weyers)

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Product Description

The practice of palliative care and hospice is filled with overt and sometimes covert ethical challenges. These challenges are addressed by leading international palliative care and hospice scholars under three main domains: care delivery systems; addressing the many dimensions of suffering; and difficult decisions near the end of life.


Timothy E. Quill is a Professor of Medicine, Psychiatry, Medical Humanities and Nursing at the University of Rochester School of Medicine where he directs their Palliative Care Division. He is a board member and the immediate past president of the American Academy of Hospice and Palliative Medicine. He was the lead physician plaintiff on a US Supreme Court Case Quill v Vacco testing the legal permissibility of physician assisted death. Quill is a practicing palliative care physician, the previous author/editor of seven books, multiple peer-reviewed articles in major medical journals, and a regular lecturer and commentator on medical decision making, physician patient relationships, palliative care, and end of life issues.; Franklin G. Miller. is a member of the senior faculty in the Department of Bioethics, National Institutes of Health (NIH) and Special Expert, National Institute of Mental Health Intramural Research Program. His principal current research interests are examination of ethical issues in clinical research, death and dying, and the placebo effect. Dr. Miller has co-authored Death, Dying, and Organ Transplantation (with Robert Truog), Oxford University Press (2012), edited five books and written numerous published articles in medical and bioethics journals on the ethics of clinical research, ethical issues concerning death and dying, professional integrity, health policy, pragmatism and bioethics, and the placebo effect.


Section I: Introduction and Overview; Chapter 1: Introduction (Timothy E. Quill and Franklin G. Miller); Chapter 2: Hospice (Charles von Gunten); Chapter 3: Palliative Care (Susan D. Block); Section II. Ethical Challenges within Current Systems of Care; Chapter 4: Emerging Complexities in Pediatric Palliative Care (Renee Boss and Nancy Hutton); Chapter 5: Patient-Centered Ethos in an Era of Cost Control: Palliative Care and Healthcare Reform (Diane E. Meier and Emily Warner); Chapter 6: Palliative Care, Ethics and Interprofessional Teams (Sally A. Norton, Deborah Waldrop, and Robert Gramling); Section III. Addressing Dimensions of Suffering; Chapter 7: Pain Relief and Palliative Care (Nathan Cherny); Chapter 8: Management of Dyspnea (Thomas W. LeBlanc, David C. Currow, Jane L. Phillips, and Amy Abernethy); Chapter 9: Diagnosis and Treatment of Delirium (Maxine De la Cruz and Eduardo Bruera); Chapter 10: Psychosocial and Psychiatric Suffering (Yesne Alici, Kanan Modhwadia, William S. Breitbart); Chapter 11: Capacity and Shared Decision-Making in Serious Illness (Ronald M. Epstein and Vikki Entwistle); Section IV. Difficult Decisions Near the Very End of Life; Chapter 12: Withholding and Withdrawing Life-Sustaining Treatments (Robert D. Truog); Chapter 13: Medical Futility: Content in the Context of Care (Peggy Determeyer and Howard Brody ); Chapter 14: Palliative Sedation (J. Andrew Billings); Chapter 15: Voluntarily Stopping Eating and Drinking (Emily Rubin and James L. Bernat); Chapter 16: Physician Assisted Death (Timothy E. Quill and Franklin Miller); Chapter 17; 17a: Lessons from Legalized Physician Assisted Death in Oregon and Washington: (Linda Ganzini); 17b: Physician Assisted Death in Western Europe: The Legal and Empirical Situation (Heleen Weyers)

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Product Details
EAN
9780190604448
ISBN
0190604441
Dimensions
23.1 x 15.5 x 2.5 centimetres (0.41 kg)

Table of Contents

Section I: Introduction and Overview

Chapter 1: Introduction (Timothy E. Quill and Franklin G. Miller)
Chapter 2: Hospice (Charles von Gunten)
Chapter 3: Palliative Care (Susan D. Block)

Section II. Ethical Challenges within Current Systems of Care

Chapter 4: Emerging Complexities in Pediatric Palliative Care (Renee Boss and Nancy Hutton)

Chapter 5: Patient-Centered Ethos in an Era of Cost Control: Palliative Care and Healthcare Reform (Diane E. Meier and Emily Warner)

Chapter 6: Palliative Care, Ethics and Interprofessional Teams (Sally A. Norton, Deborah Waldrop, and Robert Gramling)
Section III. Addressing Dimensions of Suffering
Chapter 7: Pain Relief and Palliative Care (Nathan Cherny)

Chapter 8: Management of Dyspnea (Thomas W. LeBlanc, David C. Currow, Jane L. Phillips, and Amy Abernethy)

Chapter 9: Diagnosis and Treatment of Delirium (Maxine De la Cruz and Eduardo Bruera)

Chapter 10: Psychosocial and Psychiatric Suffering (Yesne Alici, Kanan Modhwadia, William S. Breitbart)

Chapter 11: Capacity and Shared Decision-Making in Serious Illness (Ronald M. Epstein and Vikki Entwistle)

Section IV. Difficult Decisions Near the Very End of Life
Chapter 12: Withholding and Withdrawing Life-Sustaining Treatments (Robert D. Truog)

Chapter 13: Medical Futility: Content in the Context of Care (Peggy Determeyer and Howard Brody )

Chapter 14: Palliative Sedation (J. Andrew Billings)

Chapter 15: Voluntarily Stopping Eating and Drinking (Emily Rubin and James L. Bernat)

Chapter 16: Physician Assisted Death (Timothy E. Quill and Franklin Miller)

Chapter 17
17a: Lessons from Legalized Physician Assisted Death in Oregon and Washington: (Linda Ganzini)
17b: Physician Assisted Death in Western Europe: The Legal and Empirical Situation (Heleen Weyers)

About the Author

Timothy E. Quill is a Professor of Medicine, Psychiatry, Medical Humanities and Nursing at the University of Rochester School of Medicine where he directs their Palliative Care Division. He is a board member and the immediate past president of the American Academy of Hospice and Palliative Medicine. He was the lead physician plaintiff on a US Supreme Court Case Quill v Vacco testing the legal permissibility of physician assisted death. Quill is a practicing
palliative care physician, the previous author/editor of seven books, multiple peer-reviewed articles in major medical journals, and a regular lecturer and commentator on medical decision making, physician
patient relationships, palliative care, and end of life issues.

Franklin G. Miller. is a member of the senior faculty in the Department of Bioethics, National Institutes of Health (NIH) and Special Expert, National Institute of Mental Health Intramural Research Program. His principal current research interests are examination of ethical issues in clinical research, death and dying, and the placebo effect. Dr. Miller has co-authored Death, Dying, and Organ Transplantation (with Robert Truog), Oxford University Press (2012), edited five books and written
numerous published articles in medical and bioethics journals on the ethics of clinical research, ethical issues concerning death and dying, professional integrity, health policy, pragmatism and
bioethics, and the placebo effect.

Reviews

"While there is not a standard format imposed on each chapter, the contributors often use clinical cases to illustrate the related ethical challenges. The attention to both breadth and depth of these issues contributes to the book's relevance. ... In addition to practitioners of palliative care, students in health-related fields or those with an interest in bioethics might find this book relevant." --Doody's Health Sciences Book Review
"This outstanding essay collection, edited by Quill and Miller, provides a survey of the clinical and ethical dilemmas clinicians face in palliative care contexts, mainly, but not exclusively, at life's end. The volume helpfully provides perspectives from the diverse disciplines represented in a contemporary palliative care team, general physicians, psychiatrists, nurses, etc. and the diverse locations in which palliative care takes place, from in-home hospice
to inpatient hospital settings. The book treats the major ethical topics that arise in most clinical contexts; this includes issues related to pediatric cases, and also shared decision making and
substituted judgment. [B]ecause of the clinical chapters, the book is best suited for health sciences libraries and professional programs in medicine and nursing. Highly recommended." --A. W. Klink, CHOICE
"This outstanding essay collection, edited by Quill (Univ. of Rochester) and Miller (National Institutes of Health), provides a survey of the clinical and ethical dilemmas clinicians face in palliative care contexts, mainly, but not exclusively, at life's end. The volume helpfully provides perspectives from the diverse disciplines represented in a contemporary palliative care team, general physicians, psychiatrists, nurses, etc. and the diverse locations in
which palliative care takes place, from in-home hospice to inpatient hospital settings." -- Choice
"This is a very good read, not just for professionals working in the fi eld, but for other disciplines,who would like to know more about the origins of palliative care and its relationship to other disciplines." -The Australian Pain Society Newsletter

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