Individuals and families face challenges at the end of life that can vary significantly depending on social and cultural contexts, yet more than ever is now known about the needs that cut across the great diversity of experiences in the face of dying and death. A number of behavioural interventions and clinical approaches to addressing these needs have been developed and are available to help providers care for clients and assist them in achieving their goals. Perspectives on Palliative and End-of-Life Care: Disease, Social and Cultural Contexts explores how these interventions can be used to address a range of issues across social and cultural contexts for those in need of end of life care.
With perspectives from experienced clinicians, providers, and caregivers from around the world, the book offers a strong foundation in contemporary evidence-based practice alongside seasoned practice insights from the field and explores interventions for people as diverse as HIV caregivers in Africa and individuals dying with dementia. In addition, readers will learn about the process of caring for individuals with chronic illnesses including severe mental illness; weigh the impact of policy regulations on the availability of and access to palliative care and interventions; and be able to compare the different issues experienced by family caregivers and formal caregivers.
As the companion volume to Perspectives on Behavioural Interventions in Palliative and End-of-Life Care, this book will be of interest to a wide variety of individuals, such as academics, researchers and postgraduates in the fields of mental health, medicine, psychology and social work. It will also be essential reading for healthcare providers and trainees from psychosocial and palliative medicine, social work and nursing.
1. The International Context of Behavioural Palliative and End-of-Life Care Revisited by Allen, Carpenter, & Eichorst
Section 1: Specific Populations and Palliative and EOL Care
2. Living and Dying Well with HIV/AIDS by Parker, Csikai, & Payne Foster (USA)
3. Serious Mental Illness and Palliative Care by Kasl-Godley and Hiroto (USA)
4. Person-Centered End-of-Life Care for Individuals Living with Dementia in the United Kingdom by Chatterjee and Downs (UK)
Section 2: Social and Cultural Contexts Including Ethics, Bereavement, and Policy Issues
5.Ethical Issues in Palliative and End-of-Life Care by Halli-Tierney, Albright, Dragan, Lippe, & Allen (USA)
6. Diversity in Family Bereavement by Matthews et al. (USA)
7. Policy and practice on psychosocial care in palliative care programs by Guldin and Payne (Europe)
8. Synthesis and the Future of Palliative and End-of-Life Care by Carpenter, Eichorst, Dorman, & Allen
In the 21st century, the world’s aging population is growing more rapidly than ever before. This is driving the international research agenda to help older people live better for longer, and to find the causes and cures for chronic diseases, such as dementia. This series provides a forum for the rapidly expanding field by investigating the relationship between the aging process and mental health. It compares and contrasts scientific and service developments across a range of settings, including the mental changes associated with normal and abnormal or pathological aging, as well as the psychological and psychiatric problems of the aging population.
The series encourages an integrated approach between biopsychosocial models and etiological factors to promote better strategies, therapies and services for older people. This will create a strong alliance between the theoretical, experimental and applied sciences to provide an original and dynamic focus, integrating the normal and abnormal aspects of mental health in aging so that theoretical issues can be set in the context of important new practical developments in this field.