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Exploring preferences for place of death with terminally ill patients: qualitative study of experiences of general practitioners and community nurses in England

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Munday, Dan, Petrova, M. and Dale, Jeremy, 1958-. (2009) Exploring preferences for place of death with terminally ill patients: qualitative study of experiences of general practitioners and community nurses in England. BMJ, Vol.339 . Article:b2391. ISSN 0959-535X

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Official URL: http://dx.doi.org/10.1136/bmj.b2391

Abstract

Objective To explore the experiences and perceptions of general practitioners and community nurses in discussing preferences for place of death with terminally ill patients. Design Qualitative study using semistructured interviews and thematic analysis. Participants 17 general practitioners and 19 nurses (16 district nurses, three clinical nurse specialists). Setting 15 general practices participating in the Gold Standards Framework for palliative care from three areas in central England with differing socio-geography. Practices were selected on the basis of size and level of adoption of the standards framework. Results All interviewees bar one had experience of discussing preferred place of death with terminally ill patients. They reported that preferences for place of death frequently changed over time and were often ill defined or poorly formed in patients’ minds. Preferences were often described as being co-created in discussion with the patient or, conversely, inferred by the health professional without direct questioning or receiving a definitive answer from the patient. This inherent uncertainty challenged the practicability, usefulness, and value of recording a definitive preference. The extent to which the assessment of enabling such preferences can be used as a proxy for the effectiveness of palliative care delivery is also limited by this uncertainty. Generally, interviewees did not find discussing preferred place of death an easy area of practice, unless the patient broached the subject or led the discussions. Conclusions Further research is needed to enable development of appropriate training and support for primary care professionals. Better understanding of the importance of place of death to patients and their carers is also needed.

Item Type: Journal Article
Subjects: R Medicine > R Medicine (General)
Divisions: Faculty of Medicine > Warwick Medical School > Health Sciences
Faculty of Medicine > Warwick Medical School
Library of Congress Subject Headings (LCSH): Terminally ill -- Psychology, Terminal care -- Social aspects, Place (Philosophy), Palliative treatment -- Great Britain
Journal or Publication Title: BMJ
Publisher: BMJ Group
ISSN: 0959-535X
Date: 15 July 2009
Volume: Vol.339
Number of Pages: 9
Page Range: Article:b2391
Identification Number: 10.1136/bmj.b2391
Status: Peer Reviewed
Access rights to Published version: Open Access
Funder: Macmillan Cancer Support (Great Britain) (MCS)
References: 1 Department of Health. Endof LifeCareStrategy. London: Department of Health, 2008. 2 Murray S, Sheikh A, Thomas K. Advance care planning in primary care. BMJ 2006;333:868-9. 3 Munday D, Maher E. Informed consent and palliative chemotherapy. BMJ 2008;337:a868. 4 Glare P, Virik K, Jones M, et al. A systematic review of physicians’ survival predictions in terminally ill cancer patients. BMJ 2003;327:195-201. 5 Fox E, Landrum-McNiff K, Zhong Z, Dawson NV, Wu AW, Lynn J. Evaluation of prognostic criteria for determining hospice eligibility in patients with advanced lung, heart, or liver disease. JAMA 1999;282:1638-45. 6 Earle CC, Neville BA, Landrum M, Ayanian JZ, Block SD, Weeks JC. Trends in the aggressiveness of cancer care near the end of life. J Clin Oncol 2004;22:315-21. 7 Higginson I, Sen-Gupta. Place of care in advanced cancer: A qualitative systematic literature review of patient preferences. J Palliat Med 2000;3:287-300. 8 Munday D, Shipman C. Introduction: concepts, scope and models of continuity in palliative care. In: Munday D, Shipman C, editors. Continuity in palliative care: key issues and perspectives. London: RCGP, 2007. 9 Hinton J. Can home care maintain an acceptable quality of life for patients with terminal cancer and their relatives? Palliat Med 1994;8:183-96. 10 Townsend J, Frank A, Fermont D, Dyer S, Karran O, Walgrove A, et al. Terminal cancer care and patients’ preference for place of death: a prospective study. BMJ 1990;301:415-7. 11 Thomas C, Morris S, Clark D. Place of death: preferences among cancer patients and their carers. Soc Sci Med 2004;58:2431-44. 12 Murray S, Boyd K, Sheikh A, Thomas K, Higginson I. Developing primary palliative care. BMJ 2004;329:1056-7. 13 Storey L, Pemberton C, Howard A, O’Donnell L. Place of death: Hobson’s choice or patient choice. Cancer Nursing Practice 2003;2:33-7. 14 Munday D, Dale J. Palliative care in the community. BMJ 2007;334:809-10. 15 Wood J, Storey L, Clark D. Preferred place of care: an analysis of the ‘first 100’ patient assessments. Palliat Med 2007;21(5):449-50. 16 Dale J, PetrovaM, Munday D, Koistinen-Harris J, Lall R, Thomas K. A national facilitation project to improve primary palliative care: impact of the Gold Standards Framework on process and self-ratings of quality. Qual Saf Health Care 2009;18:174-80. 17 The Gold Standards Framework: A programme for community palliative care. www.goldstandardsframework.nhs.uk. 18 Department of Health. Quality and Outcomes Framework. London: Department of Health, 2006. http://www.bma.org.uk/images/Quality%20and% 20outcomes%20framework%20guidance%20-%20Feb% 202006_tcm41-37124.pdf (accessed 12 February 2009). 19 The Information Centre for Health and Social Care. National Quality and Outcomes Framework Statistics for 2006/2007. London: The Information Centre for Health and Social Care, 2007. http://www.ic.nhs.uk/webfiles/QOF/2006-07/QOF% 202006-07%20Statistical%20Bulletin.pdf (accessed 12 February 2009). 20 Munday D, Dale J, Murray S. Choice and place of death: individual preferences, uncertainty, and the availability of care. J R SocMed 2007;100:211-5. 21 Munday D, Mahmood K, Dale J, King N. Facilitating good process in primary palliative care: does the Gold Standards Framework enable quality performance? Fam Pract 2007;24:486-94. 22 Mahmood-Yousuf K, Munday D, Dale J, King N. Interprofessional relationships and communication in primary palliative care: impact of the Gold Standards Framework. Br J Gen Pract 2008;58:256-63. 23 Mays N, Pope C. Qualitative research in health care: assessing quality in qualitative research. BMJ 2000;320:50-2. 24 Pope C, Ziebland S, Mays N. Qualitative research in health care: Analysing qualitative data. BMJ 2000;320:114-6. 25 Gomes B, Higginson I. Factors influencing death at home in terminally ill patients with cancer: systematic review. BMJ 2006;332:515-21. 26 Hinton J. Which patients with terminal cancer are admitted from home care? Palliat Med 1994;8:197-210. 27 Barritt P. Care of the dying in one practice. J R CollGen Pract 1984;34:446-8. 28 Rhodes P, Shaw S. Informal care and terminal illness. Health Soc Care Community 1999;7:39-50. 29 Faulkner A. ABC of palliative care: Communication with patients, families, and other professionals. BMJ 1998;316:130-2. 30 Wenrich MD, Curtis J, Shannon SE, Carline JD, Ambrozy DM, Ramsey PG. Communicating with dying patients within the spectrum ofmedical care fromterminal diagnosis to death. Arch Intern Med 2001;161:868-74. 31 Barclay S, Todd CJ, Grande G, Lipscombe J. How common is medical training in palliative care? A postal survey of general practitioners. Br J Gen Pract 1997;47:800-5. 32 Barclay S,Wyatt P, Shore S, Finlay I, Grande G, Todd C. Caring for the dying: how well prepared are general practitioners? A questionnaire study in Wales. Palliat Med 2003;17:27-39. 33 Lloyd-WilliamsM, Carter Y. General practice vocational training in the UK: what teaching is given in palliative care? Palliat Med 2003;17:616-20. 34 Shipman C, Addington-Hall J, Barclay S, Briggs J, Cox I, Daniels L, et al. Educational opportunities in palliative care: what do general practitioners want? Palliat Med 2001;15:191-6. 35 Goodman C, Knight D, Machen I, Hunt B. Emphasizing terminal care as district nurse work: a helpful strategy in a purchasing environment. J Adv Nurs 1998;28:491-8. 36 Seale C. Community nurses and the care of the dying. Soc Sci Med 1992;34:375-82. 37 Mcilfactrick S, Curran C. District nurses’ perception of palliative care services: part 2. Int Journal Palliat Nurs 2000;6(1):32-8. 38 ShipmanC, Burt J, ReamE, BeynonT, RichardsonA, Addington-Hall J. Improving district nurses’ confidence and knowledge in the principles and practice of palliative care. J Adv Nurs 2008;63:494-505. 39 Grande G, Farquhar M, Barclay S, Todd C. Valued aspects of primary palliative care: content analysis of bereaved carers’ descriptions. Br J Gen Pract 2004;54:772-8. 40 KendallM, BoydK, Campbell C,CormieP,FifeS, ThomasK, etal.How do people with cancer wish to be cared for in primary care? Serial discussion groups of patients and carers. Fam Pract 2006;23:644-50. 41 Lecouturier J, Jacoby A, Bradshaw C, Lovel T, Eccles M. Lay carers’ satisfaction with community palliative care: results of a postal survey. Palliat Med 1999;13:275-83. 42 Ingleton C, Morgan J, Hughes P, Noble B, Evans A, Clark D. Carer satisfaction with end-of-life care in Powys, Wales: a cross-sectional survey. Health Soc Care Community 2003;12:43-52. 43 Hanratty B. Palliative care provided by GPs: the carer’s viewpoint. Br J Gen Pract 2000;50:653-4. 44 Kelly B, Varghese F, Burnett P, Turner J, Robertson M, Kelly P, et al. General practitioners’ experiences of the psychological aspects of the care of a dying patient. Palliat Support Care 2008;6:125-31. 45 Grande G, Barclay S, Todd CJ. Difficulty of symptom control and general practitioners’ knowledge of patients’ symptoms. Pall Med 1997;11:399-406. 46 Hebert RS, Schulz R, Copeland V, Arnold RM.What questions do family caregivers want to discuss with health care providers in order to prepare for the death of a loved one? An ethnographic study of caregivers of patients at end of life. J Palliat Med 2008;11:476-83. 47 Steinhauser KE, Christakis NA, Clipp EC, McNeilly M, McIntyre L, Tulsky JA. Factors considered important at the end of life by patients, family, physicians, and other care providers. JAMA 2000;284:2476-82. 48 Worth A, Irshad T, Bhopal R, BrownD, Lawton J,Grant E, et al. Vulnerability and access to care for South Asian Sikh and Muslim patients with life limiting illness in Scotland: prospective longitudinal qualitative study. BMJ 2009;338:b183.
URI: http://wrap.warwick.ac.uk/id/eprint/2153

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