Palliative care support needs of family caregivers of patients with non-malignant disease
Smith, P., Sque, M. and Davies, M. (2006) Palliative care support needs of family caregivers of patients with non-malignant disease. Palliative Medicine, 20, (2), p.133. (doi:10.1191/0269216306pm1141xx).
Full text not available from this repository.
Background: There are increasing calls for patients with non-malignant disease and their carers to have access to general and Specialist Palliative Care Services (SPCS). However, it is unclear how patients and their carers’ access and view such services.
Aim: To explore the experience of family caregivers’ caring for a patient with a non-malignant condition with palliative care needs.
|Digital Object Identifier (DOI):||doi:10.1191/0269216306pm1141xx|
|Additional Information:||Delivered at the 6th Palliative Care Congress, University of Sheffield, UK, 5-7 April 2006|
|Subjects:||H Social Sciences > HQ The family. Marriage. Woman
R Medicine > RT Nursing
|Divisions :||University Structure - Pre August 2011 > Superseded (SONM) > Superseded (CPE)
|Accepted Date and Publication Date:||
|Date Deposited:||19 Jan 2007|
|Last Modified:||31 Mar 2016 12:15|
|RDF:||RDF+N-Triples, RDF+N3, RDF+XML, Browse.|
Actions (login required)