Palliative Care: Transforming the Care of Serious Illness / Edition 1

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Overview

This book is intended as an introduction and guide to palliative care, and more broadly, the medical care of the seriously ill. Although concerns about the suffering and pain that seriously ill people and their families endure is not new-the hospice movement in the United States can be dated to the mid-1960s and Elizabeth Kubler-Ross's seminal book, On Death and Dying, appeared in 1969-it was during the 1980s and 1990s that the American public began to pay serious attention. This attention has, if anything, increased during 2000s. In the late 1970s and early 1980s the field of palliative care did not exist. More often than not, a very sick or dying patient was viewed as a failure-a failure of technology and know-how to cure disease, or at least to extend life In response, the new field of medicine called palliative care came into existence -from the Latin palliare, to clothe. Palliative care focuses on the relief of suffering for patients with serious and complex illness, and tries to ensure the best possible quality of life for them and their family members. This book examines this new and significant field. Transforming Palliative Care begins with a comprehensive review of the field, written by editor Diane Meier, recipient of a Macarthur grant. What follows are twenty-five of the most important or influential articles in the field, written by its leading practitioners and analysts. These articles cover Care of the Seriously Ill: Why Is It an Important Issue?; Efforts to Cope with Death and Provide Care for the Dying; Research into End-of-Life Care; and Palliative Care: Pain and Medical Decision-making, Issues and Perspectives, and Caregiving.

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Product Details

Meet the Author

Diane E. Meier, M.D., is director of the Center to AdvancePalliative Care and director of the Lilian and Benjamin HertzbergPalliative Care Institute, Professor of Geriatrics and InternalMedicine, and Catherine Gaisman Professor of Medical Ethics atMount Sinai School of Medicine in New York City.

Stephen L. Isaacs, J.D., is a partner in Isaacs/Jellinek, a SanFrancisco-based consulting firm.

Robert G. Hughes, Ph.D., is vice president and chief learningofficer at the Robert Wood Johnson Foundation.

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Table of Contents

Foreword (Risa Lavizzo-Mourey Editors').

Introduction (Diane E. Meier, Stephen L. Isaacs, and Robert G.Hughes).

Acknowledgments.

Part I Review of the Palliative Care Field: OriginalArticle.

1. The Development, Status, and Future of Palliative Care (DianeE. Meier).

Reprints of Key Articles and Book Chapters.

Part II Care of the Seriously Ill: Why Is It an ImportantIssue? Approaching Death: Improving Care at the End of Life(Marilyn J. Field and Christine K. Cassel, editors, for theCommittee on Care at the End of Life, Institute ofMedicine).

3. Decisions Near the End of Life.

Council on Ethical and Judicial Affairs, American MedicalAssociation.

Part III Efforts to Cope with Death and Provide Care for theDying.

4. Hope (Elisabeth Kübler-Ross).

5. The Nature of Suffering and the Goals of Medicine (Eric J.Cassell).

6. The Nature of Suffering and the Goals of Nursing (Betty R.Ferrell and Nessa Coyle).

7. Death: “The Distinguished Thing” (DanielCallahan).

8. The Philosophy of Terminal Care (Cicely Saunders).

9. Access to Hospice Care: Expanding Boundaries, OvercomingBarriers

(Bruce Jennings, True Ryndes, Carol D’Onofrio, and MaryAnn Baily).

Part IV Social, Legal, and Ethical Issues.

10. The Health Care Proxy and the Living Will (George J.Annas).

11. Terri Schiavo: A Tragedy Compounded (Timothy E. Quill).

Part V Research into End-of-Life Care.

12. A Controlled Trial to Improve Care for Seriously IllHospitalized Patients: The Study to Understand Prognoses andPreferences for Outcomes and Risks of Treatments (SUPPORT)

SUPPORT Principal Investigators.

13. Factors Considered Important at the End of Life by Patients,Family, Physicians, and Other Care Providers (Karen E. Steinhauser,Nicholas A. Christakis, Elizabeth C. Clipp, Maya McNeilly, LaurenMcIntyre, and James A Tulsky).

14. Use of Hospitals, Physician Visits, and Hospice Care DuringLast Six Months of Life Among Cohorts Loyal to Highly RespectedHospitals in the United States (John E. Wennberg, Elliott S.Fisher, Thérèse A. Stukel, Jonathan S. Skinner, Sandra M.Sharp, and Kristen K. Bronner).

15. Family Perspectives on End-of-Life Care at the Last Place ofCare (Joan M. Teno, Brian R. Clarridge, Virginia Casey, Lisa C.Welch, Terrie Wetle, Renee Shield, and Vincent Mor).

Part VI Palliative Care.

16. The Treatment of Cancer Pain (Kathleen M. Foley).

17. Responding to Intractable Terminal Suffering: The Role ofTerminal Sedation and Voluntary Refusal of Food and Fluids (TimothyE. Quill and Ira R. Byock, for the ACP-ASIM End-of-Life CareConsensus Panel).

18. Response to Quill and Byock, “Responding toIntractable Suffering” (Daniel P. Sulmasy, Wayne A. Ury,Judith C. Ahronheim, Mark Siegler, Leon Kass, John Lantos, RobertA. Burt, Kathleen Foley, Richard Payne, Carlos Gomez, Thomas J.Krizek, Edmund D. Pellegrino, and Russell K. Portenoy).

19. Challenges in Palliative Care: Four Clinical Areas ThatConfront and Challenge Hospice Practitioners (Balfour M.Mount).

20. Outcomes from a National Multispecialty Palliative CareCurriculum Development Project (David E. Weissman, Bruce Ambuel,Charles F. von Gunten, Susan Block, Eric Warm, James Hallenbeck,Robert Milch, Karen Brasel, and Patricia B. Mullan).

21. Negotiating Cross-Cultural Issues at the End of Life:“You Got to Go Where He Lives” (Marjorie Kagawa-Singerand Leslie J. Blackhall).

22. Variability in Access to Hospital Palliative Care in theUnited States (Benjamin Goldsmith, Jessica Dietrich, Qingling Du,and R. Sean Morrison).

23. Do Palliative Care Consultations Improve Patient Outcomes(David Casarett, Amy Pickard, F. Amos Bailey, Christine Ritchie,Christian Furman, Ken Rosenfeld, Scott Shreve, Zhen Chen, Judy A.Shea)?

24. Cost Savings Associated with U.S. Hospital Palliative CareConsultation Programs (R. Sean Morrison, Joan D. Penrod, J. BrianCassel, Melissa Caust-Ellenbogen, Ann Litke, Lynn Spragens, DianeE. Meier, for the Pallative Care Leadership Centers' OutcomesGroup).

25. The Loneliness of the Long-Term Care Giver (CarolLevine).

26. Understanding Economic and Other Burdens of TerminalIllness: The Experience of Patients and Their Caregivers (EzekielJ. Emanuel, Diane L. Fairclough, Julia Slutsman, Linda L.Emanuel).

Part VII The Ends of Medicine and Society.

27. Finding Our Way: Perspectives on Care at the Close of Life(Stephen J. McPhee, Michael W. Rabow, Steven Z. Pantilat, Amy J.Markowitz, and Margaret A. Winker).

The Editors.

Name Index.

Subject Index.

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