100 Questions and Answers about Alchoholism
Author: Charles Herrick
This text addresses these problems and answers the most common 100 questions asked by patients and their family about alcoholism/drug abuse and their treatment. Additionally, there are contributions from actual patients throughout.
Interesting book: Tower of Babble or International Politics on the World Stage
Palliative Ethics of Care: Clinical Wisdom at Life's End
Author: Joseph J Fins
Thid book presents a unique, innovative approach to caring for the terminally ill patient. Using vignettes, the text explains how to develop a set of patient/physician goals for improving quality of life, resolving end of life issues, and generally treating dying patients.
Doody Review Services
Reviewer: David B Cotton, MA; MDiv. (Jersey Shore University Medical Center)
Description: Dr. Fins, in a highly readable, conversational style, presents residents and experienced physicians with a two-part guide to the ethics of caring for patients at the end of life. Part one traces the ethical and legal underpinnings of palliative care, along with some historical context for its appearance on the medical-ethical landscape. Part two is a comprehensive guide for practical application, featuring a specific clinical pathway with goal setting as its guiding principle.
Purpose: The purpose is to educate physicians-in-training regarding the best way to care for the dying. It shares principles and offers relevant information on the skills and strategies necessary for developing a plan of care that meets the patient's needs and respects the patient's goals. In the literature and in the life of the hospital, it is evident that physicians are well prepared for high-tech, aggressive, curative interventions. They are, on the other hand, quite ill prepared to address the complex bundle of issues surrounding death and dying. This book takes direct aim at correcting this imbalance.
Audience: The book is directed specifically to physicians-in-training, especially residents and perhaps fellows. Dr.Fins' wealth of experience and impressive educational credentials combine to make this book worthwhile for practitioners at any level. Reading it is like being on rounds with a master!
Features: The book is divided into two distinct sections. The first chapter addresses the audience directly, stating the case for learning what the book teaches. The following three chapters present the historical, ethical, and legal contexts pertinent to the rise of bioethics consults and the growing emphasis on end-of-life care. The second section builds upon this ethical, historical, and legal framework by presenting a practical guide for bedside care of the dying. This section begins by stressing the importance of the often overlooked step of goal-setting. The need to communicate and formulate a plan of care centered on the patient's and/or family's goals is the most important contribution of the book. The entire application section is centered upon the critical issue of the goal of care as the driver of medical decisions. Fins presents the reader with a Goals of Care Assessment Tool (GCAT) in the book's appendix. It is a terrific answer to the medical-ethical dilemma that presents itself when the physician reaches the point of asking the all-too-familiar question, "Which direction should I go from here with this patient?" Exhausted residents may be tempted to skip the first section and cut right to the practical stuff, but those who hang in there will gain a great deal of wisdom in return for a small sacrifice of time.
Assessment: This is a comprehensive, yet concise, compelling review of the concept, the context, and the content of quality end-of-life care. The emphasis on the need for individual medical decisions to be driven and directed by the goal of care is the book's finest hour and most important contribution. Hopefully it will make the pronouncement, "There's nothing more we can do," obsolete. Dr. Fins encourages and empowers the professional with the idea that competent, compassionate, goal-centered care is every bit as rewarding as cure.
Rating
5 Stars! from Doody
Table of Contents:
Foreword | xi | |
Preface | xv | |
Acknowledgments | xxv | |
Permissions | xxxi | |
Part I | Death and Dying in Context | 1 |
Chapter 1 | Medical Students, Residents, and the Dying Patient | 3 |
The Challenge of Caring for the Dying | 3 | |
Goal-Setting Near the End of Life | 9 | |
How This Book Is Organized | 10 | |
Closing Words | 11 | |
Chapter 2 | The Rise of Bioethics and Palliative Care Movements | 13 |
European Origins of Hospice and Palliative Care | 14 | |
The American Context | 17 | |
The Rise of Self-Determination | 19 | |
Toward an Ethic of Patients' Rights | 22 | |
Chapter 3 | Death, Dying, and the Law | 29 |
The Law and the Rise of Patient Self-Determination | 29 | |
Quinlan and the Right to Die | 30 | |
Quinlan and the Institutionalization of Hospital Ethics Committees | 32 | |
Cruzan and the Patient Self-Determination Act | 34 | |
Advance Care Planning in Theory and Practice | 36 | |
From Self-Determination to Physician-Assisted Suicide | 37 | |
Physician-Assisted Suicide: Laying out the Arguments | 39 | |
Physician-Assisted Suicide in the Courts | 41 | |
A Consensus on Palliative Care | 45 | |
Back to the Future: The Schiavo Case | 48 | |
Epilogue | 52 | |
Chapter 4 | End-of-Life Care in the Hospital | 63 |
Death in the Modern Hospital | 63 | |
Medical Rescue and Intensive Care | 64 | |
Fostering Communication | 70 | |
Communication, Palliation, and the Road Not Taken | 72 | |
Milestones at the End of Life | 73 | |
Ambivalence and Medical Futility | 77 | |
Futility: A Definitional Primer | 79 | |
The Evolution of Futility Disputes | 82 | |
Goal Convergence, Palliative Care, and the Avoidance of Futility Disputes | 85 | |
Part II | Goal-Setting: A Strategy for Effective Palliative Care | 91 |
Chapter 5 | Goals of Care: Triggering the Process | 93 |
Goal-Setting as Differential Diagnosis | 93 | |
Triggering the Process | 95 | |
Concluding Comments | 99 | |
Chapter 6 | Goals of Care: When Death Is Near | 101 |
Introduction | 101 | |
Clinical Perceptions | 101 | |
Patient Perceptions | 104 | |
When a Patient Wants to Die | 106 | |
Surrogate Perceptions | 109 | |
Decision-Making Capacity | 110 | |
Helping Surrogates Decide | 113 | |
Chapter 7 | Goals of Care: End-of-Life Decisions | 119 |
Introduction | 119 | |
Do Not Resuscitate Orders | 121 | |
Advance Care Planning | 125 | |
Working with the Proxy | 129 | |
Withdrawals of Care | 132 | |
Hospice or Palliative Care Referral | 134 | |
Hospice Care | 137 | |
Chapter 8 | Goals of Care: Medical Developments | 145 |
Introduction | 145 | |
A Life-Threatening Illness | 146 | |
Prognosis | 149 | |
Acute Decompensation and the Use of Life-Sustaining Therapies | 153 | |
Consideration of ICU Transfer | 153 | |
Symptoms at the End of Life | 155 | |
The Ethics of Opioid Use | 156 | |
Chapter 9 | Goal-Setting: Gathering Information | 163 |
Introduction | 163 | |
Sources of Information | 163 | |
Demographics and Local Culture | 165 | |
The Power of Diagnosis | 167 | |
Forced Prognostication and Patient Expectations | 169 | |
Assessment of Capacity and the Refusal of Life-Sustaining Therapies | 172 | |
Knowledge of Diagnosis and Prognosis | 174 | |
Constructing a Shared World of Meaning with the Patient and Family | 176 | |
Breaking Bad News | 180 | |
The Therapeutic Exception | 186 | |
DNR in the OR | 189 | |
The Elusive Advance Directive | 192 | |
Family Dynamics | 195 | |
The Symbionic Family | 198 | |
Cultural Issues: Religious Objections to Brain Death | 201 | |
Public Perspectives on Pain and Meaning | 211 | |
Biological Symptom Assessment | 212 | |
Chapter 10 | Formulating the Goals of Care | 225 |
Introduction | 225 | |
Defining Goals | 226 | |
Hospital Resources | 232 | |
Psychiatry Consultation | 233 | |
Pastoral Care/Chaplaincy | 236 | |
Pain Service/Palliative Care Consult/Referral to Palliative Care Unit | 239 | |
Hospice Referral | 241 | |
Social Work | 242 | |
Ethics Committees | 244 | |
The Centrality of Communication and Consensus | 250 | |
Working with Nurses | 252 | |
Involving the Patient and Family | 255 | |
One Good Death | 256 | |
Appendix | The Goals of Care Assessment Tool (GCAT) | 263 |
Index | 267 |
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