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Author : Santé et Services sociaux Québec
Publisher :
ISBN 13 :
Total Pages : 109 pages
Book Rating : 4.:/5 (927 download)
Download or read book Quebec End-of-Life Palliative Care Policy written by Santé et Services sociaux Québec and published by . This book was released on 2004 with total page 109 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author :
Publisher :
ISBN 13 :
Total Pages : 98 pages
Book Rating : 4.:/5 (671 download)
Download or read book Quebec End-of-life Palliative Care Policy written by and published by . This book was released on 2004 with total page 98 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Pierre Mallia
Publisher : Springer Nature
ISBN 13 : 3030863867
Total Pages : 244 pages
Book Rating : 4.0/5 (38 download)
Download or read book Challenges to the Global Issue of End of Life Care written by Pierre Mallia and published by Springer Nature. This book was released on 2022-02-10 with total page 244 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book addresses the problems faced by people and hospitals dedicated to providing optimal end-of-life care and asks whether ethicists can function as experts on this subject. Though ethics consultation is a growing practice in medical contexts, difficult questions surrounding the role of ethicists in professional decision-making remain. The chapters in this book examine the nature and plausibility of moral expertise, the relationship between character and expertise, the nature and limits of moral authority, the question of how one might become a moral expert, and the trustworthiness of moral testimony. This volume not only engages with the growing literature in the debate on end-of-life care but also offers new perspectives from both academics and practitioners. Such perspectives include ways on how to get together to optimize end-of-life care. This book is of particular interest to bioethicists, clinicians, ethics committees, students of social epistemology, patient groups, and institutions, especially religious, who may not be sufficiently imparting the social teachings of end-of-life care. It also shows how they are indeed stakeholders for what is today called ‘a good death’. These new essays advance discussions and provide practical information on dying as well as acting as a guide to those interested in actively effecting change.
Author : Robert H. Blank
Publisher : Springer Nature
ISBN 13 : 981155840X
Total Pages : 345 pages
Book Rating : 4.8/5 (115 download)
Download or read book Public Policy in ALS/MND Care written by Robert H. Blank and published by Springer Nature. This book was released on 2020 with total page 345 pages. Available in PDF, EPUB and Kindle. Book excerpt: Anyone interested in ALS/MND-physician, patient, or healthcare policy director -should read this book and learn from it. -Walter G. Bradley D.M., F.R.C.P., Professor and Chairman Emeritus, Miller School of Medicine, University of Miami, USA "This book illustrates the inequities in the accessibility of quality neurological care existing globally and which forms a major target for redress by the World Federation of Neurology and the World Health Organisation." -William M Carroll AM, MBBS, MD, FRACP, FRCP(E), President, World Federation of Neurology This book focuses on the public policy and political/ethical dimensions of ALS/MND across a wide selection of countries and argues for the need of a multidisciplinary and international approach. Policy issues addressed include adequacy of funding for research and care, payment policy and regulatory functions of public and private insurers, long-term services and caregiver support, public health and prevention efforts, access to genetic testing and assisted technologies, ensuring a competent and adequate workforce especially for hands-on caregivers, and the challenging issues of providing palliative and hospice care for ALS/MND patients, advance directives and assisted suicide that face policy makers in all political jurisdictions. Robert H. Blank, PhD, (University of Maryland) is an adjunct Professor of Political Science at the University of Canterbury in Christchurch, New Zealand. He has been a frequent guest professor at Aarhus University in Denmark and at National Taiwan University in Taipei, Taiwan, and a Research Scholar at New College Florida. Jerome E. Kurent received his MD from the University of Cincinnati College of Medicine and completed residencies in Neurology and Internal Medicine at the Johns Hopkins Hospital. He completed fellowships in neuromuscular diseases and electromyography at the National Institutes of Health, followed by a Geriatrics Medicine fellowship at Harvard where he also received his MPH. Dr. Kurent joined the Medical University of South Carolina faculty in 1984, and is Professor of Neurology, Medicine and Psychiatry and Behavioral Sciences. David Oliver, MD., recently retired as Consultant Physician in Palliative Medicine at the Wisdom Hospice in Rochester, Kent where he developed an integrated service over 32 years. He is an Honorary Professor at the Tizard Centre at the University of Kent, where he supervises students and is involved in research
Author : Mary Chiarella
Publisher :
ISBN 13 :
Total Pages : 132 pages
Book Rating : 4.3/5 ( download)
Download or read book Policy in End-of-life Care written by Mary Chiarella and published by . This book was released on 2006 with total page 132 pages. Available in PDF, EPUB and Kindle. Book excerpt: This text sets out to provide a review of policy on palliative care. It focuses not only on past and current policy, but also explores a number of major issues that recur in literature on this subject. It is aimed at people working within a spectrum of disciplines but primarily those working in palliative care.
Author :
Publisher :
ISBN 13 :
Total Pages : 0 pages
Book Rating : 4.:/5 (137 download)
Download or read book Quebec end-of-life palliative care policy written by and published by . This book was released on 2004 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: The result of extensive consultations, this policy is aimed at improving the accessibility, continuity, and quality of care and support services we wish to offer our loved ones at the end of life. [...] The third defines the scope of palliative care and the policy. [...] The goal of palliative care is achievement of the best possible quality of life for patients and their families. [...] However, like Canadian and Québec palliative care associations, it also reaffirms certain values intended to guide palliative care services, namely • The intrinsic value of each person as a unique individual, the value of life, and the inescapable nature of death • The necessary participation of patients through their free and informed consent to ensure they are party to decisions in accordance wi [...] The notions of refusing and stopping treatment have been the subject of much jurisprudence12 in Québec, across Canada, and in the U. S. that enshrines the right of patients to refuse any treatment, even if its sole goal is to prolong life.
Author : Attilio Stajano
Publisher : CLAIRVIEW BOOKS
ISBN 13 : 1905570775
Total Pages : 221 pages
Book Rating : 4.9/5 (55 download)
Download or read book Only Love Remains written by Attilio Stajano and published by CLAIRVIEW BOOKS. This book was released on 2015-11-09 with total page 221 pages. Available in PDF, EPUB and Kindle. Book excerpt: What happens to the dying in the final days and weeks of their lives? What emotions come to the surface and what do they want to talk about? Attilio Stajano, a volunteer worker at the palliative care ward of a Brussels hospital, presents a series of deeply-moving personal encounters with seriously-ill patients. The dying, he discovers, have much to teach the living. Whilst their stories are all different, they share one thing in common: in the end, when all is said and done, only love remains... How should we respond to the challenge of death? As a society and as individuals, we can choose to be patient and sensitive, giving dignity to those reaching the end of their lives – even when those lives appear to have no further value. The period leading to death can be full of profound experiences, telling us much about the meaning of life and the abiding nature of love. If we see the terminally-ill as an inconvenience, however, we forego the possibility of finding unexpected resources in ourselves: a tenderness, a touch, a readiness to assist that we did not know we were capable of. Underlying this book is the momentous and very current debate over euthanasia. In a comprehensive appendix, the author reports on the provision of palliative care services and the laws governing euthanasia in European and English-speaking countries around the world, and the implications these have for the way we value and care for the dying.
Author :
Publisher :
ISBN 13 :
Total Pages : 0 pages
Book Rating : 4.:/5 (137 download)
Download or read book Policy brief on hospice palliative care written by and published by . This book was released on 2010 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Our Vision for an Integrated Systems Approach to End-of-Life Care Recognizing that Canadians will continue to die in a variety of settings, Canada urgently needs a systems approach to end-of-life care: one that ensures that high quality care is available in all settings and that all Canadians and their families have the information, resources and support to move from one setting to another based o [...] Care teams have the resources as well as the supportive policies and programs to provide the right care in the right place at the right time. [...] The staff also consults to other hospitals and health facilities in the region, and help support primary care physicians and home care teams provide care for patients at home. [...] The team also consults to all hospitals in the region, and to primary care physicians and home care teams providing end-of-life care at home. [...] The Zone 3 Palliative Care Program was developed to encompass palliative care services within the hospital and in the community, and to promote the use of best practice evidence and consistent standards of care at all care sites (i.e., four hospital sites and four extra-mural units).
Author :
Publisher :
ISBN 13 :
Total Pages : 12 pages
Book Rating : 4.:/5 (821 download)
Download or read book Policy Brief on Hospice Palliative Care written by and published by . This book was released on 2010 with total page 12 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : The Expert Panel Working Group on Advance Requests for MAID
Publisher : Council of Canadian Academies
ISBN 13 : 1926522516
Total Pages : 244 pages
Book Rating : 4.9/5 (265 download)
Download or read book The State of Knowledge on Advance Requests for Medical Assistance in Dying written by The Expert Panel Working Group on Advance Requests for MAID and published by Council of Canadian Academies. This book was released on 2018-12-12 with total page 244 pages. Available in PDF, EPUB and Kindle. Book excerpt: In December 2016, the CCA was asked by then Minister of Health Jane Philpott and Minister of Justice and Attorney General of Canada Jody Wilson-Raybould to undertake independent reviews related to medical assistance in dying (MAID). Specifically, the CCA was tasked with examining three particularly complex types of requests for MAID that were identified for further review and study in the legislation passed by Parliament in 2016: requests by mature minors, advance requests, and requests where a mental disorder is the sole underlying medical condition. On December 12, 2018 the CCA released the three final reports of the Expert Panel, one on each type of request: The State of Knowledge on Medical Assistance in Dying for Mature Minors; The State of Knowledge on Advance Requests for Medical Assistance in Dying; and The State of Knowledge on Medical Assistance in Dying Where a Mental Disorder is the Sole Underlying Medical Condition.
Author : Canada. Parliament. House of Commons
Publisher :
ISBN 13 :
Total Pages : 928 pages
Book Rating : 4.3/5 (555 download)
Download or read book Official Report of the Debates of the House of Commons written by Canada. Parliament. House of Commons and published by . This book was released on 2005-10 with total page 928 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Emmett Macfarlane
Publisher : University of Toronto Press
ISBN 13 : 1487519494
Total Pages : 461 pages
Book Rating : 4.4/5 (875 download)
Download or read book Policy Change, Courts, and the Canadian Constitution written by Emmett Macfarlane and published by University of Toronto Press. This book was released on 2018-11-23 with total page 461 pages. Available in PDF, EPUB and Kindle. Book excerpt: Policy Change, Courts, and the Canadian Constitution aims to further our understanding of judicial policy impact and the role of the courts in shaping policy change. Bringing together a group of political scientists and legal scholars, this volume delves into a diverse set of policy areas, including health care issues, the regulation of elections, criminal justice policy, minority language education, citizenship, refugee policy, human rights legislation, and Indigenous policy. While much of the public law and judicial politics literatures focus on the impact of the constitution and the judicial role, scholarship on courts that makes policy change its central lens of analysis is surprisingly rare. Multidisciplinary in its approach to examining policy issues, this book focuses on specific cases or policy issues through a wide-ranging set of approaches, including the use of interview data, policy analysis, historical and interpretive analysis, and jurisprudential analysis.
Author : Elisha Waldman
Publisher : Oxford University Press
ISBN 13 : 0190066539
Total Pages : 112 pages
Book Rating : 4.1/5 (9 download)
Download or read book A Field Manual for Palliative Care in Humanitarian Crises written by Elisha Waldman and published by Oxford University Press. This book was released on 2019-11-11 with total page 112 pages. Available in PDF, EPUB and Kindle. Book excerpt: As humanitarian aid organizations have evolved, there is a growing recognition that incorporating palliative care into aid efforts is an essential part of providing the best care possible. A Field Manual for Palliative Care in Humanitarian Crises represents the first-ever effort at educating and providing guidance for clinicians not formally trained in palliative care in how to incorporate its principles into their work in crisis situations. Written by a team of international experts, this pocket-sized manual identifies the needs of people affected by natural hazards, political or ethnic conflict, epidemics of life-threatening infections, and other humanitarian crises. Later chapters explore topics including pain management, skin conditions, non-communicable diseases, palliative care emergencies, the law and ethics of end of life care, and more. Concise and highly accessible, this manual is an ideal educational tool pre-deployment or during fieldwork for clinicians involved in planning and providing humanitarian aid, local care providers, and medical trainees.
Author : Marianne Matzo, PhD, APRN-CNP, FPCN, FAAN
Publisher : Springer Publishing Company
ISBN 13 : 0826127193
Total Pages : 725 pages
Book Rating : 4.8/5 (261 download)
Download or read book Palliative Care Nursing written by Marianne Matzo, PhD, APRN-CNP, FPCN, FAAN and published by Springer Publishing Company. This book was released on 2018-06-28 with total page 725 pages. Available in PDF, EPUB and Kindle. Book excerpt: “This 5th edition is an important achievement; it is a symbol of commitment to the field of palliative nursing, where we have been and where we are going.” - Betty Rolling Ferrell, PhD, MA, FAAN, FPCN, CHPN From the Foreword The aging population has only grown since the first edition of this comprehensive and seminal publication nearly 20 years ago. Based on the need to humanize rather than medicalize the illness experience for patients, this text delves into palliative care beyond the specific diseases affecting the patient. Instead, content focuses on the whole person and family. Palliative patients struggle with chronic, debilitating, and painful conditions, and grapple with the fact that life as they knew it has already passed away. Families and friends reciprocally suffer, not knowing how to help and therefore become the secondary victims of the disease. This is not the challenge of a lone nurse, or a single physician, therapist, or social worker. Rather, palliative and hospice care requires the expertise and unique roles of an interprofessional team to help the patient and family strengthen their resilience, continue to find meaning and purpose in life, and cure what can be cured. Palliative Care Nursing, Fifth Edition, delivers advanced empirical, aesthetic, ethical and personal knowledge. This new edition brings an increased focus on outcomes, benchmarking progress, and goals of care. It expounds upon the importance of the cross-disciplinary collaboration introduced in the previous edition. Every chapter in Sections I, II, and III includes content written by a non-nursing member of the interprofessional team. Based on best-evidence and clinical practice guidelines, this text presents comprehensive, targeted interventions responsive to the needs of palliative and hospice patients and family. Each chapter contains compassionate, timely, appropriate, and cost-effective care for diverse populations across the illness trajectory. Key Features The expanded new edition offers current, comprehensive, one-stop source of highly-relevant clinical information on palliative care Life-span approach: age-appropriate nursing considerations (e.g. geriatric, pediatric and family) Includes disease-specific and symptom-specific nursing management chapters Promotes a holistic and interdisciplinary approach to palliative care Offers important legal, ethical and cultural considerations related to death and dying Case Studies with Case Study Conclusion in each clinical chapter New to The Fifth Edition: An expanded chapter on Palliative Care incorporates most up to date scope and standards, information on Basic and Advanced HPNA certification, self-reflection and self-care for nurses. A chapter on Interprofessional Collaboration Instructor Resources: Power points and Test bank
Author : Amy S. Kelley
Publisher : Humana
ISBN 13 : 9781493904068
Total Pages : 0 pages
Book Rating : 4.9/5 (4 download)
Download or read book Meeting the Needs of Older Adults with Serious Illness written by Amy S. Kelley and published by Humana. This book was released on 2014-09-02 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Meeting the Needs of Older Adults with Serious Illness: Challenges and Opportunities in the Age of Health Care Reform provides an introduction to the principles of palliative care; describes current models of delivering palliative care across care settings, and examines opportunities in the setting of healthcare policy reform for palliative care to improve outcomes for patients, families and healthcare institutions. The United States is currently facing a crisis in health care marked by unsustainable spending and quality that is poor relative to international benchmarks. Yet this is also a critical time of opportunity. Because of its focus on quality of care, the Affordable Care Act is poised to expand access to palliative care services for the sickest, most vulnerable, and therefore most costly, 5% of patients- a small group who nonetheless drive about 50% of all healthcare spending. Palliative care is specialized medical care for people with serious illnesses. It focuses on providing patients with relief from the symptoms, pain, and stress of a serious illness—whatever the diagnosis or stage of illness. The goal is to improve quality of life for both the patient and the family. Research has demonstrated palliative care’s positive impact on health care value. Patients (and family caregivers) receiving palliative care experience improved quality of life, better symptom management, lower rates of depression and anxiety, and improved survival. Because patient and family needs are met, crises are prevented, thereby directly reducing need for emergency department and hospital use and their associated costs. An epiphenomenon of better quality of care, the lower costs associated with palliative care have been observed in multiple studies. Meeting the Needs of Older Adults with Serious Illness: Challenges and Opportunities in the Age of Health Care Reform, a roadmap for effective policy and program design, brings together expert clinicians, researchers and policy leaders, who tackle key areas where real-world policy options to improve access to quality palliative care could have a substantial role in improving value.
Author : Dame Cicely M. Saunders
Publisher : Oxford University Press, USA
ISBN 13 :
Total Pages : 84 pages
Book Rating : 4.3/5 (91 download)
Download or read book Living with Dying written by Dame Cicely M. Saunders and published by Oxford University Press, USA. This book was released on 1989 with total page 84 pages. Available in PDF, EPUB and Kindle. Book excerpt: This second edition incorporates the latest developments in the treatment of the terminally ill patient. It tackles the general ethical and medical principles in the care of the dying patient and considers the details of the control of pain and other symptoms, with the hope that doctors and other professionals will support the patient and his family by sharing the truth with them and empathizing with their emotional suffering. Written by internationally renowned authors, this book is an invaluable handbook for family doctors and health professionals and a compassionate source of information for the terminally ill and their relatives.
Author : Robert H. Blank
Publisher : MIT Press
ISBN 13 : 9780262025744
Total Pages : 290 pages
Book Rating : 4.0/5 (257 download)
Download or read book End-of-life Decision Making written by Robert H. Blank and published by MIT Press. This book was released on 2005 with total page 290 pages. Available in PDF, EPUB and Kindle. Book excerpt: Experts analyze death-related issues and policies in twelve countries, discussing health care costs, advance directives, pain management, cultural, social, and religious factors, and other topics.
