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Textbook of Palliative Medicine and Supportive Care
"the thoroughness of the text has to be admired. It is an excellent starting point for students of palliative care which makes an important contribution to any library."-British Journal of Hospital Medicine" covers a plethora of topics ranging from the development of palliative medicine in different countries to clinical topics and bioethics an
Research methods in palliative care
Palliative and end of life care are concerned with the physical, social, psychological and spiritual care of people with advanced disease. It currently has a poorly developed research base, but the need to improve this is increasingly recognised. One of the reasons for the lack of research - and the variable quality of the research that is undertaken - is the difficulty of conducting research with very ill and bereaved people. Standard and well-established research methods may need to be adapted to work in this context. This means that existing research methods textbooks may be of limited use to palliative care practitioners seeking to do research for the first time, or to more experienced r...
Textbook of Palliative Medicine
Textbook of Palliative Medicine provides an alternative, truly international approach to this rapidly growing specialty. This textbook fills a niche with its evidence-based, multi-professional approach and global perspective ensured by the international team of editors and contributing authors. In the absence of an international curriculum for the study of palliative medicine, this textbook provides essential guidance for those both embarking upon a career in palliative medicine or already established in the field, and the structure and content have been constructed very much with this in mind. With an emphasis on providing a service anywhere in the world, including the important issue of palliative care in the developing nations, Textbook of Palliative Medicine offers a genuine alternative to the narrative approach of its competitors, and is an ideal complement to them. It is essential reading for all palliative care physicians in training and in practice, as well as palliative care nurses and other health professionals in the palliative care team
Palliative Care in Terminal Illness
Many people find incurable illness difficult to deal with, and subconsciously erect a barrier. This work demonstrates a deep understanding and empathic approach, providing an introduction to palliative care.
Public Health in the Context of Life-Limiting Illnesses: Patient-Centered Care in Advanced and Life-Limiting Illnesses
It is estimated that at least 60% of persons dying have a prolonged advanced illness. The need for palliative and end-of-life care will increase due to the rapidly aging world population and the increase of multiple long-term conditions. For these reasons, palliative care is an integral part of public health and public health strategies. Palliative care as holistic person-centered care and has played a critical role in the recent public health emergency of the COVID-19 pandemic. There is a close association between public health, health promotion, and palliative care, and this research topic will highlight this association. Through a series of multi-disciplinary articles, we will explore public health in the context of life-limiting illnesses contributing to shaping person-centered care, including palliative, end-of-life, and rehabilitation. This research topic will discuss advanced and life-limiting illness as a public health challenge and explore the role of palliative and end-of-life care including rehabilitation in shaping person-centered care.
Quality of Life
The way we think about health and health care is changing. Two factors driving this change are that we recognise the importance of the social consequences of disease and secondly, we acknowledge that health care aims to increase both the quantity and quality of survival. For these reasons, health care focusses more and more on 'quality of life'. Measuring quality of life brings many challenges. What do we mean by 'quality of life'? Who should measure it? How can we measure it? What can we use the information for? This book provides an accessible but up to date and authoritative overview of the measurement of quality of life in health care. It brings together the work of authors from Medicine, Palliative Care, Nursing, Ethics, Dentistry, Assistive Technology, Sociology, Epidemiology and Statistics.
ThirdWay
Monthly current affairs magazine from a Christian perspective with a focus on politics, society, economics and culture.
Helping People at the End of Their Lives
A comprehensive analysis of today's situation of palliative care in Europe is provided, including previously unidentified statistics and standardised profiles of 16 European countries. The analysis contains demographics, the history of hospice and palliative care, the number of current services, funding, education and training of professional staff and the role of volunteers, with an in-depth case portrayal of particular services.
Palliative Care for Non-cancer Patients
The specialty of palliative care has traditionally grown out of oncology and there has been little research into the needs of patients dying from causes other than cancer. Few non-cancer patients receive hospice in-patient, home care or day care although a good proportion of hospices say that their services are available to non-cancer patients. As a result, the importance of palliative care for non-cancer patients is now being increasingly recognized internationally, and in the UK a committee reporting to the Department of Health recommended that palliative care should be accessible to all patients who need such care. Palliative Care for Non-Cancer Patients considers the needs and experiences of patients dying from, for example, stroke, heart disease or dementia by,drawing on a range of disciplines and specialties in medicine. The provision of palliative care for patients dying from causes other than cancer raises a number of important questions for policy makers and purchasers. This book summarizes what is known about the needs of and appropriate service provision for people dying of causes other than cancer and begins to set a research agenda.
