Book Description
Dame Cicely Saunders, founder and president of St. Christopher's Hospice in London (1967), shares her vision of hospice and palliative care, and discusses lessons to be learned from the dying.
Author : Peter Kaye
Publisher :
Page : 436 pages
File Size : 45,31 MB
Release : 1990
Category : Medical
ISBN :
Dame Cicely Saunders, founder and president of St. Christopher's Hospice in London (1967), shares her vision of hospice and palliative care, and discusses lessons to be learned from the dying.
Author : David A. Fleming
Publisher : University of Missouri Press
Page : 172 pages
File Size : 38,23 MB
Release : 2010-04-15
Category : Medical
ISBN : 0826272215
Although the need for improved care for dying patients is widely recognized and frequently discussed, few books address the needs of the physicians, nurses, social workers, therapists, hospice team members, and pastoral counselors involved in care. Care of the Dying Patient contains material not found in other sources, offering advice and solutions to anyone—professional caregiver or family member—confronted with incurable illness and death. Its authors have lectured and published extensively on care of the dying patient and here review a wide range of topics to show that relief of physical suffering is not the only concern in providing care. This collection encompasses diverse aspects of end-of-life care across multiple disciplines, offering a broad perspective on such central issues as control of pain and other symptoms, spirituality, the needs of caregivers, and special concerns regarding the elderly. In its pages, readers will find out how to: effectively utilize palliative-care services and activate timely referral to hospice, arrange for care that takes into account patients’ cultural beliefs, and respond to spiritual and psychological distress, including the loss of hope that often overshadows physical suffering. The authors especially emphasize palliative care and hospice, since some physicians fear that such referrals may be viewed by patients and families as abandonment. They also address ethical and legal risks in pain management and warn that fear of overprescribing pain medication may inadvertently lead to ineffective pain relief and even place the treating team at risk of liability for undertreatment of pain. While physicians have the ability to treat disease, they also help to determine the time and place of death, and they must recognize that end-of-life choices are made more complex than ever before by advances in medicine and at the same time increasingly important. Care of the Dying Patient addresses some of the challenges frequently confronted in terminal care and points the way toward a more compassionate way of death.
Author : Patricia Moyle Wright, PhD, MBA, MSN, CRNP, ACNS-BC, CHPN, CNE, FPCN
Publisher : Springer Publishing Company
Page : 209 pages
File Size : 19,5 MB
Release : 2017-01-28
Category : Medical
ISBN : 0826131999
An on-the-go reference for hospice nurses and those interested in end-of-life care, this practical guide covers the essential elements in the compassionate and holistic care of terminally ill patients and their families. Nurses care for patients facing end-of-life issues in every practice specialty and, as the U.S. population continues to age, the need for proficiency in end-of-life skills will become increasingly important. Fast Facts for the Hospice Nurse: A Concise Guide to End-of-Life Care is an invaluable resource that provides emotional, administrative, and palliative support, whether in a hospice, long-term care facility, or acute care setting. This vital go-to text clearly and concisely lays out not only how to care for patients facing end-of-life issues, but also how to engage in self-care and cope with occupational stress. Beginning with an overview of hospice care, including its history and philosophy, this book offers a timeline of the growth of the hospice movement in the United States. Subsequent sections include up-to-date information on the clinical responsibilities of the hospice nurse in addressing the physical, psychological, and spiritual needs of terminally ill patients and their families in a culturally sensitive way. This book also outlines the administrative duties of the hospice nurse, including hospice documentation, a review of hospice regulations, and quality management. The closing section focuses on occupational stress in hospice nursing and how to engage in self-care. This text can serve as a useful clinical resource and also as a reference for nurses seeking hospice certification from the Hospice and Palliative Credentialing Center. Key Features Organized within the context of the scope and standards of practice of the Hospice and Palliative Nurses Association. Addresses key points about issues unique to hospice nursing and highlights evidence-based interventions Addresses important Medicare regulations and reimbursement Offers numerous clinical resources to assist with hospice nursing practice Serves as a concise study resource for hospice nursing certification
Author : T. M. Marrelli
Publisher : SIGMA Theta Tau International
Page : pages
File Size : 16,86 MB
Release : 2018
Category :
ISBN : 9781945157462
Author : Roger Cole
Publisher :
Page : 26 pages
File Size : 23,17 MB
Release : 1997
Category : Palliative treatment
ISBN : 9780947146023
Author : Ohio Hospice and Palliative Care Organization Staff
Publisher :
Page : 0 pages
File Size : 27,84 MB
Release : 2010-10-21
Category : Hospice care
ISBN : 9780757561849
Author :
Publisher :
Page : 176 pages
File Size : 29,70 MB
Release : 1992
Category : Hospices (Terminal care)
ISBN :
Author :
Publisher : Kendall Hunt
Page : 300 pages
File Size : 36,18 MB
Release : 2002
Category : Medical
ISBN : 9780787293185
Author : Bates D Moses
Publisher : Jones & Bartlett Publishers
Page : 174 pages
File Size : 42,67 MB
Release : 2013-01-07
Category : Medical
ISBN : 1284032000
Tarascon Palliative Medicine Pocketbook is the only shirt pocket-sized, quick reference for guiding those difficult conversations with patients and family members who require palliative and hospice care. Practitioners will find helpful ideas as well as guidance on managing difficult to control symptoms whether practicing in a busy clinic, making home visits or managing the hospitalized patient. Containing communication skill techniques, prognostication tools, symptom management options and ethical issues, this one of a kind, portable guide is an ideal tool for any member of the Palliative Medicine team, including: physicians, nurses, social workers, chaplains, pharmacists and more.
Author : Institute of Medicine
Publisher : National Academies Press
Page : 470 pages
File Size : 16,37 MB
Release : 2015-03-19
Category : Medical
ISBN : 0309303133
For patients and their loved ones, no care decisions are more profound than those made near the end of life. Unfortunately, the experience of dying in the United States is often characterized by fragmented care, inadequate treatment of distressing symptoms, frequent transitions among care settings, and enormous care responsibilities for families. According to this report, the current health care system of rendering more intensive services than are necessary and desired by patients, and the lack of coordination among programs increases risks to patients and creates avoidable burdens on them and their families. Dying in America is a study of the current state of health care for persons of all ages who are nearing the end of life. Death is not a strictly medical event. Ideally, health care for those nearing the end of life harmonizes with social, psychological, and spiritual support. All people with advanced illnesses who may be approaching the end of life are entitled to access to high-quality, compassionate, evidence-based care, consistent with their wishes. Dying in America evaluates strategies to integrate care into a person- and family-centered, team-based framework, and makes recommendations to create a system that coordinates care and supports and respects the choices of patients and their families. The findings and recommendations of this report will address the needs of patients and their families and assist policy makers, clinicians and their educational and credentialing bodies, leaders of health care delivery and financing organizations, researchers, public and private funders, religious and community leaders, advocates of better care, journalists, and the public to provide the best care possible for people nearing the end of life.