Pain Management and Improving End-of-life Care
Author: United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions
Publisher:
Published: 1999
Total Pages: 140
ISBN-13:
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Author: United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions
Publisher:
Published: 1999
Total Pages: 140
ISBN-13:
DOWNLOAD EBOOKAuthor: James M. Jeffords
Publisher:
Published: 2001-07-01
Total Pages: 136
ISBN-13: 9780756712761
DOWNLOAD EBOOKWitnesses: Walter R. Hunter, M.D., Assoc. National Medical Dir., VistaCare Hospice; Samira K. Beckwith, CHE, LCSW, pres. and CEO, Hope Hospice and Palliative Care; Dr. Yank D. Coble, on behalf of the Amer. Medical Assoc.; Dr. Gerald Holman, on behalf of the National Hospice Org.; Dr. James P. Rathmell, dir., Pain Management Center, Dept. of Anesthesiology, Univ. of VT, on behalf of the Amer. Soc. of Anesthesiologists; David E. Joranson, Pain and Policy Studies Group, Comprehensive Cancer Center, Univ. of Wisconsin; and prepared statements by Pain Care Coalition, Amer. for Better Care of the Dying, Amer. Pharmaceut. Assoc., and Amer. Soc. of Health-System Pharmacists.
Author: Shaun Kinghorn
Publisher: Elsevier Health Sciences
Published: 2007-11-14
Total Pages: 298
ISBN-13: 0702028169
DOWNLOAD EBOOKThis title is directed primarily towards health care professionals outside of the United States. Content has been thoroughly revised and updated in line with changes in practice and policy both locally and internationally, particularly the UK NICE guidance on Supportive and palliative care for people with cancer and the Care of the Dying Pathway. It reflects the rapid development of palliative nursing as an emerging specialty. It helps in the process of defining palliative nursing and how it interfaces with other disciplines within the specialty. The text is divided into three sections and comprehensively, yet sensitively, covers all aspects of palliative nursing. Key themes covered include pain control, symptom control, loss and grief, and handling loss. . A strong emphasis is placed on the integration of theory and practice and evidence based care. . Reconciliation of the theory and practice is achieved by the use of case studies. . It addresses malignant and non-malignant palliative care. . Research and extensive literature support each chapter. Content has been thoroughly revised and updated in line with changes in practice and policy both locally and internationally, particularly the UK NICE guidance on Supportive and palliative care for people with cancer and the Care of the Dying Pathway . Three new chapters on: . Sexuality . Care of the Dying Pathway . Changing roles of the nurse in palliative care . New appendix on North American drug names equivalents for the international market
Author: Committee on Care at the End of Life
Publisher: National Academies Press
Published: 1997-10-30
Total Pages: 457
ISBN-13: 0309518253
DOWNLOAD EBOOKWhen the end of life makes its inevitable appearance, people should be able to expect reliable, humane, and effective caregiving. Yet too many dying people suffer unnecessarily. While an "overtreated" dying is feared, untreated pain or emotional abandonment are equally frightening. Approaching Death reflects a wide-ranging effort to understand what we know about care at the end of life, what we have yet to learn, and what we know but do not adequately apply. It seeks to build understanding of what constitutes good care for the dying and offers recommendations to decisionmakers that address specific barriers to achieving good care. This volume offers a profile of when, where, and how Americans die. It examines the dimensions of caring at the end of life: Determining diagnosis and prognosis and communicating these to patient and family. Establishing clinical and personal goals. Matching physical, psychological, spiritual, and practical care strategies to the patient's values and circumstances. Approaching Death considers the dying experience in hospitals, nursing homes, and other settings and the role of interdisciplinary teams and managed care. It offers perspectives on quality measurement and improvement, the role of practice guidelines, cost concerns, and legal issues such as assisted suicide. The book proposes how health professionals can become better prepared to care well for those who are dying and to understand that these are not patients for whom "nothing can be done."
Author: Sushma Bhatnagar
Publisher: Lippincott Williams & Wilkins
Published: 2018-06-29
Total Pages: 241
ISBN-13: 1975103106
DOWNLOAD EBOOKPublisher's Note: Products purchased from 3rd Party sellers are not guaranteed by the Publisher for quality, authenticity, or access to any online entitlements included with the product. A Comprehensive Handbook of Cancer Pain Management in Developing Countries Written by an international panel of expert pain physicians, A Comprehensive Handbook of Cancer Pain Management in Developing Countries addresses this challenging and vital topic with reference to the latest body of evidence relating to cancer pain. It thoroughly covers pain management in the developing world, explaining the benefit of psychological, interventional, and complementary therapies in cancer pain management, as well as the importance of identifying and overcoming regulatory and educational barriers.
Author: United States. Congress. Senate. Special Committee on Aging
Publisher:
Published: 2000
Total Pages: 106
ISBN-13:
DOWNLOAD EBOOKAuthor: National Research Council
Publisher: National Academies Press
Published: 2001-10-19
Total Pages: 344
ISBN-13: 0309074029
DOWNLOAD EBOOKIn our society's aggressive pursuit of cures for cancer, we have neglected symptom control and comfort care. Less than one percent of the National Cancer Institute's budget is spent on any aspect of palliative care research or education, despite the half million people who die of cancer each year and the larger number living with cancer and its symptoms. Improving Palliative Care for Cancer examines the barriersâ€"scientific, policy, and socialâ€"that keep those in need from getting good palliative care. It goes on to recommend public- and private-sector actions that would lead to the development of more effective palliative interventions; better information about currently used interventions; and greater knowledge about, and access to, palliative care for all those with cancer who would benefit from it.
Author: Joanne Lynn M.D.
Publisher: Oxford University Press
Published: 2007-02-08
Total Pages: 273
ISBN-13: 0199748330
DOWNLOAD EBOOKImproving care for the patients who are in the last phase of their lives has been a field that most health care providers have struggled with during last few years. Having worked with hundreds of providers throughout the country, these experienced authors know what providers need when it comes to implementing a quality improvement project. This guide will provide user-friendly, step-by-step instructions on how to implement a quality improvement project in the full range of care settings. The instructions will be brought to life with specific examples from actual successful projects and key information on the best practices in the industry. Readers will also be pointed to resources available online and elsewhere, with information on how to access them. The guide will be written in an informal, maximally helpful style, with checklists, tables, and boxed information. Answering 80% of the questions in less than half the space, The Common Sense Guide is the perfect portable companion to Dr. Lynn's desk reference, Improving Care for the End of Life. The book will be of great interest to all health care professionals involved in the care of those with serious chronic illness -- doctors, nurses, social workers, chaplains, clinic administrators, quality improvement experts, and so forth.
Author: Joanne Lynn
Publisher: Oxford University Press
Published: 2008
Total Pages: 464
ISBN-13: 019531042X
DOWNLOAD EBOOKHealth care professionals seeking to improve the quality of life for those living with serious illness and nearing the end of life will find exactly what their organization needs in the second edition of this acclaimed book by Dr. Joanne Lynn and her colleagues. Improving Care for the End of Life provides expert guidance on how to make significant improvements now, at all levels of the health care system from the bedside and the hospital to the health care policy and legislative arenas by using the rapid-cycle breakthrough approach to change. The ideas are proven, and the stories of teams that have put them to use will inspire and enlighten.New to the second edition: DT New chapters to address issues of growing interest such as continuity of care, and the special needs of dementia patients and their loved ones. DT Details on trajectories of care and how these affect decisions at the end of life DT Updated and expanded information on pain management, advance care planning, ventilator withdrawal, depression and delirium, advanced heart and lung disease, and more DT Scores of new insights, measurement approaches, and tips based on the experiences of hundreds of improvement teams nationwide DT Thoroughly updated referencesThe sourcebook speaks to all managers of health care systems serving people with serious illnesses, including doctors in offices, nurse managers on hospital units, social workers in long-term care facilities, administrators of home care and hospice agencies, hospital chaplains, directors of volunteer services, and others.
Author: Sarah Gehlert
Publisher: John Wiley & Sons
Published: 2006-03-20
Total Pages: 769
ISBN-13: 0471758884
DOWNLOAD EBOOKThe Handbook of Health Social Work provides a comprehensive and evidence-based overview of contemporary social work practice in health care. Written from a wellness perspective, the chapters cover the spectrum of health social work settings with contributions from a wide range of experts. The resulting resource offers both a foundation for social work practice in health care and a guide for strategy, policy, and program development in proactive and actionable terms. Three sections present the material: The Foundations of Social Work in Health Care provides information that is basic and central to the operations of social workers in health care, including conceptual underpinnings; the development of the profession; the wide array of roles performed by social workers in health care settings; ethical issues and decision - making in a variety of arenas; public health and social work; health policy and social work; and the understanding of community factors in health social work. Health Social Work Practice: A Spectrum of Critical Considerations delves into critical practice issues such as theories of health behavior; assessment; effective communication with both clients and other members of health care teams; intersections between health and mental health; the effects of religion and spirituality on health care; family and health; sexuality in health care; and substance abuse. Health Social Work: Selected Areas of Practice presents a range of examples of social work practice, including settings that involve older adults; nephrology; oncology; chronic diseases such as diabetes, heart disease, and HIV/AIDS; genetics; end of life care; pain management and palliative care; and alternative treatments and traditional healers. The first book of its kind to unite the entire body of health social work knowledge, the Handbook of Health Social Work is a must-read for social work educators, administrators, students, and practitioners.