Overview

Support for the family is a key component of palliative care practice and philosophy, with both patient and family construed as the 'unit of care'. However, there is not always formal acknowledgement of the importance of the family carer role, or that of friends, neighbours and other non-professional, informal carers. Consequently, health and social care professionals find carer support work particularly challenging. Symptom management, personal care, and administering of medications are just some of the tasks taken on by this group of non-professionals, and the impact of this role can have negative emotional, physical, financial and social implications on the care-giver. Furthermore, family carers consistently report unmet needs, and there has been a lack of intervention studies aimed at improving carer support.This book therefore provides an evidence-based, practical guide to enable health and social care professionals to assess and respond to family carer needs. It also explores the wider sociological, policy, and research issues related to family carers and palliative care.

Full Product Details

Author:   Peter Hudson (, Associate Professor and Director, Centre for Palliative Care Education and Research, St Vincent's Hospital and The University of Melbourne, Australia) ,  Sheila Payne (, Professor, Help the Hospices Chair in Hospice Studies, International Observatory on End of Life Care, Lancaster University, UK)
Publisher:   Oxford University Press
Imprint:   Oxford University Press
Dimensions:   Width: 15.60cm , Height: 1.80cm , Length: 23.30cm
Weight:   0.513kg
ISBN:  

9780199216901

ISBN 10:   0199216908
Pages:   336
Publication Date:   23 October 2008
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Paperback
Publisher's Status:   Active
Availability:   To order  
Stock availability from the supplier is unknown. We will order it for you and ship this item to you once it is received by us.

Table of Contents

1: Barbara Monroe and David Oliviere: Communicating with famly carers 2: Allan Kellehear: Understanding the social and cultural dimensions of family caregiving 3: Rosalie Hudson: Responding to family carers' spiritual needs 4: Hilary Arksey and Anne Corden: Policy initiatives for family carers 5: Jennifer Hunt: Family carers in resource poor countries 6: Michael Ashby and Danuta Mendelson: Family carers: ethical and legal issues 7: Kevin Brazil: Assessing family carer satisfaction with health care delivery 8: Betty Ferrell, Tami Borneman and Chan Thai: Family caregiving in hospitals and pallative care units 9: Kelli Stajduhar and Robin Cohen: Family caregiving in the home 10: Mike Nolan and Rosalie Hudson: Family and palliative care in care homes for older people life-threatening illness 11: Sharon De Graves and Jenny Hynson: Family carers of children confronting life-threatening illness 12: Donna Milne and Karen Quinn: Family carers of people with advanced cancer 13: Janice Brown and Julia Addington-Hall: Family carers of people with advanced organ failure and neurodegenerative disorders 14: Sheila Payne and Liz Rolls: Support for bereaved family carers 15: Peter Hudson and Sheila Payne: The future of family caregiving: Research, social policy and clinical pratice

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Author Information

Peter Hudson is associate professor and the Director of the Centre for Palliative Care Education and Research, an academic unit located within St Vincent's Hospital, affiliated with The University of Melbourne (Victoria, Australia). Peter is a member of the Department of Human Services Palliative Care Implementation Advisory Committee (Victoria), Board member of the International Association of Hospice and Palliative Care and co-founder of the International Palliative Care Family Caregiver Research Collaboration. Peter has a significant background in palliative care education and research, and has extensive experience as a palliative care nurse. He leads several competitively funded multi site research studies and has published widely in international journals. Professor Sheila Payne is an applied social scientist with a background in nursing. Over the last twenty years she has been involved in leading and contributing to research and teaching about research methods in palliative care. She has a special interest in end-of-life care for older people, family caregivers and bereavement support. She holds the Help the Hospices Chair in Hospice Studies based at the International Observatory on End of Life Care at Lancaster University, UK. She also co-directs a large five year programme of collaborative research and development called the Cancer Experiences Collaborative. She has published widely in academic and professional journals, and is also Co-director of the Cancer Experiences Collaborative, and Vice President European Association of Palliative Care.

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