New themes in palliative care
Series: Facing deathPublication details: Buckingham Open University Press 1997Description: 306; diag.,bibls.; BookFindISBN:- 0335196063
Item type | Home library | Class number | Status | Date due | Barcode | |
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Book | Newcomb Library at Homerton Healthcare Shelves | WB 310 CLA (Browse shelf(Opens below)) | Available | HOM1308 |
Part 1 Policy, ethics, evidence: assessing needs and effectiveness - is palliative care a special case?; cost of palliative care; resource allocation and palliative care; half full or half empty? - impact of health reforms on palliative care services in the UK. Part 2 Services developments: the evolution of the hospice approach; terminal care in South Australia - historical aspects and equity issues; palliative care in India; palliative home care; a Swedish model of home care; rational planning and policy implementation in palliative care; palliative care in Eastern Europe; is hospice a western concept? - a personal view of palliative care in Asia; the WHO cancer pain and palliative care programme. Part 3 Clinical issues: therapeutic innovations; beyond cancer?; teamwork in end-of-life care - a nurse physician perspective on introducing physicians to palliative care concepts; voluntary euthanasia in terminal illness; new approaches in care.
Hardback
Palliative care is moving through an important period of expansion and development, spreading beyond its original hospice base to encompass care in the community, in hospitals, health centres, clinics and nursing homes. It can now be found in over 70 countries of the world. What challenges does this multidisciplinary speciality face as it seeks to combine high grade pain and symptom control with sensitive psychological, spiritual and social care? What are the implications of current constraints on health policy and planning? How do ethical issues about resource allocation and end of life care impinge? Can palliative care be further extended to include conditions other than cancer? ""New Themes in Palliative Care"" addresses these and many related issues in ways which will be readily accessible to students of health and social care as well as to those involved in purchasing or providing palliative care services, and to social scientists interested in chronic illness, death and dying.Its editors are respected experts in the field with backgrounds in the social sciences, nursing and medicine and the book's contributors include leading international figures from a wide range of palliative care and academic disciplines.
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