Clinical Audit In Palliative Care
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Author | : |
Publisher | : Radcliffe Publishing |
Total Pages | : 208 |
Release | : 2002 |
Genre | : Medical |
ISBN | : 9781857759761 |
Clinical audit is at the heart of clinical governance. Provides the mechanisms for reviewing the quality of everyday care provided to patients with common conditions like asthma or diabetes. Builds on a long history of doctors, nurses and other healthcare professionals reviewing case notes and seeking ways to serve their patients better. Addresses the quality issues systematically and explicitly, providing reliable information. Can confirm the quality of clinical services and highlight the need for improvement. Provides clear statements of principle about clinical audit in the NHS.
Author | : Irene Higginson |
Publisher | : |
Total Pages | : 224 |
Release | : 1993 |
Genre | : Hospice care |
ISBN | : |
Clinical audit is now an integral part of the practice of doctors, nurses, social workers and others who work in hospitals or the community. However, in palliative care, where quality is paramount, audit has been hampered by the lack of sensitive methods and measures. This study brings together methods and experiences in practising audit from the United Kingdom, Ireland and Canada to show how audit in this crucial area of care can be provided.
Author | : OECD |
Publisher | : OECD Publishing |
Total Pages | : 447 |
Release | : 2019-10-17 |
Genre | : |
ISBN | : 9264805907 |
This volume, developed by the Observatory together with OECD, provides an overall conceptual framework for understanding and applying strategies aimed at improving quality of care. Crucially, it summarizes available evidence on different quality strategies and provides recommendations for their implementation. This book is intended to help policy-makers to understand concepts of quality and to support them to evaluate single strategies and combinations of strategies.
Author | : World Health Organization |
Publisher | : World Health Organization |
Total Pages | : 74 |
Release | : 1996 |
Genre | : Medical |
ISBN | : 9789241544825 |
The second edition of a guide, which introduced a simple, yet highly effective method for the relief of cancer pain. Thoroughly revised and updated, the new edition further refines the WHO method, which advocates the use of a small number of relatively inexpensive drugs, including morphine. Revisions draw on experiences with millions of patients around the world as well as new knowledge about the specific pain syndromes unique to cancer. Completely new are chapters describing the international system by which morphine and other opioids are made available for medical purposes. The book has two parts. Part one provides a practical guide to the relief of cancer pain, concentrating on drug treatment as the mainstay of pain management. The most extensive section sets out detailed guidelines for the selection and prescribing of non-opioid analgesics, opioid analgesics, drugs for neuropathic pain, and adjuvant drugs for the treatment of adverse effects, the enhancement of pain relief and the management of concomitant psychological disturbances. Information ranges from explanations of how specific drugs work, through the precautions to take in the presence of certain disorders, to a list of factors that influence the effectiveness of opioids. Concerning the use of opioids, readers are reminded that psychological dependence does not occur in cancer patients and that the only correct dose of morphine is the one that relieves the pain. Part two provides a guide to opioid availability. A discussion of the reasons why opioids continue to be underprescribed or difficult to obtain is followed by an explanation of the Single Convention on Narcotic Drugs.
Author | : Institute of Medicine |
Publisher | : National Academies Press |
Total Pages | : 470 |
Release | : 2015-03-19 |
Genre | : 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.
Author | : Russell K. Portenoy |
Publisher | : |
Total Pages | : 316 |
Release | : 1997 |
Genre | : Analgesia |
ISBN | : 9780195132199 |
Author | : Karen Hertz |
Publisher | : Springer |
Total Pages | : 169 |
Release | : 2018-06-15 |
Genre | : Medical |
ISBN | : 3319766813 |
This open access book aims to provide a comprehensive but practical overview of the knowledge required for the assessment and management of the older adult with or at risk of fragility fracture. It considers this from the perspectives of all of the settings in which this group of patients receive nursing care. Globally, a fragility fracture is estimated to occur every 3 seconds. This amounts to 25 000 fractures per day or 9 million per year. The financial costs are reported to be: 32 billion EUR per year in Europe and 20 billon USD in the United States. As the population of China ages, the cost of hip fracture care there is likely to reach 1.25 billion USD by 2020 and 265 billion by 2050 (International Osteoporosis Foundation 2016). Consequently, the need for nursing for patients with fragility fracture across the world is immense. Fragility fracture is one of the foremost challenges for health care providers, and the impact of each one of those expected 9 million hip fractures is significant pain, disability, reduced quality of life, loss of independence and decreased life expectancy. There is a need for coordinated, multi-disciplinary models of care for secondary fracture prevention based on the increasing evidence that such models make a difference. There is also a need to promote and facilitate high quality, evidence-based effective care to those who suffer a fragility fracture with a focus on the best outcomes for recovery, rehabilitation and secondary prevention of further fracture. The care community has to understand better the experience of fragility fracture from the perspective of the patient so that direct improvements in care can be based on the perspectives of the users. This book supports these needs by providing a comprehensive approach to nursing practice in fragility fracture care.
Author | : Julia M Addington-Hall |
Publisher | : Oxford University Press |
Total Pages | : 328 |
Release | : 2007-06-07 |
Genre | : Medical |
ISBN | : 0198530250 |
The research base for palliative care must improve as it continues to develop in increasingly evidence-based health care systems, and to provide the needs of patients and families. This is the first research methods textbook focusing on the unique needs of palliative care, aimed at improving current research and stimulating new research in the field.
Author | : Elaine Stevens |
Publisher | : Scion Publishing Ltd |
Total Pages | : 469 |
Release | : 2008-09-15 |
Genre | : Medical |
ISBN | : 1906052409 |
Editors’ Preface Introduction 1. Introduction to palliative care 2. Essential concepts 3. Generic assessment in palliative care 4. Anxiety and depression 5. Breathlessness 6. Fatigue 7. Pain 8. Quality improvement Glossary Abbreviations
Author | : Sara Booth |
Publisher | : Oxford University Press |
Total Pages | : 184 |
Release | : 2010 |
Genre | : Medical |
ISBN | : 0199238928 |
Based on the extensive experience of three clinicians in the area, this book provides those setting up palliative care services in hospitals with practical guidance and down to earth advice on the range of problems they might encounter.