Holdsworth, L.M. and King, A.M. (2009) Developing a patient preference questionnaire for place of care when dying: Phase 1 Hospices. Project report. Centre for Health Services Studies, Canterbury
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Abstract
The aim of this study was to develop a staff toolkit for obtaining preferences for place of care and death with palliative care patients. The toolkit was to include guidance and a set of questions acceptable to patients, carers and staff. The objectives were to: 1. Identify issues for collecting preferences from both the perspective of service users (patients and carers) and hospice staff. 2. Create a questionnaire for collecting preferences on place of care and death to be used by hospice staff.
| Item Type: | Monograph (Project report) |
|---|---|
| Uncontrolled keywords: | end of life care, dying, patient preference, place of death |
| Subjects: | H Social Sciences > HQ The family. Marriage. Woman R Medicine > RA Public aspects of medicine > RA0421 Public health. Hygiene. Preventive Medicine |
| Divisions: | Faculties > Social Sciences > School of Social Policy Sociology and Social Research > Centre for Health Services Studies |
| Depositing User: | Tony Rees |
| Date Deposited: | 24 Aug 2010 10:04 |
| Last Modified: | 16 May 2013 14:06 |
| Resource URI: | http://kar.kent.ac.uk/id/eprint/24798 (The current URI for this page, for reference purposes) |
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