Preferred place of care: an analysis of the 'first 100' patient assessments

Wood, J., Storey, L. and Clark, D. (2007) Preferred place of care: an analysis of the 'first 100' patient assessments. Palliative Medicine, 21(5), pp. 449-450. (doi:10.1177/0269216307078294)

Full text not currently available from Enlighten.

Abstract

The ‘preferred place of care’ (PPC)<sup>1</sup> patient assessment tool, recently renamed ‘preferred priorities for care’, is one of three interventions promoted within the National Health Service (NHS) End of Life Care Initiative. PPC offers patients, their carers and healthcare professionals the opportunity to consider, discuss, express and record priorities for care at the end of life. Department of Health guidance highlights how ‘available evidence suggests that whilst over 50% of all patients wish to spend their final days at home, less than 20% in practice are actually able to do so’.<sup>2</sup> Nationally, the proportion of home deaths for patients with cancer is falling, from 27% in 1994 to 22% in 2003.<sup>3</sup> Choice over care is a fundamental tenet of government policy. A retrospective quantitative and spatial analysis of the first 100 PPC assessments identified patients’ and carers’ preferences for care and place of death at the end of life, and highlights issues for the development of PPC.

Item Type:Articles (Letter)
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Clark, Professor David
Authors: Wood, J., Storey, L., and Clark, D.
College/School:College of Social Sciences > School of Interdisciplinary Studies
Journal Name:Palliative Medicine
Journal Abbr.:Palliat Med
Publisher:Sage Publications Ltd.
ISSN:0269-2163
ISSN (Online):1477-030X

University Staff: Request a correction | Enlighten Editors: Update this record