Shipman, Cathy, Gysels, Marjolein, White, Patrick T., Worth, Allison, Murray, Scott A., Barclay, Stephen, Forrest, S. (Sarah), Shepherd, J., Dale, Jeremy, 1958-, Dewar, Steve, Peters, Marilyn, White, Suzanne, Richardson, Alison, Lorenz, Karl, Koffman, Jonathan and Higginson, Irene J.. (2008) Improving generalist end of life care : national consultation with practitioners, commissioners, academics, and service user groups. British Medical Journal, Vol.337 (No.7674). ISSN 0959-8146

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Abstract

Objective: To identify major concerns of national and local importance in the provision, commissioning, research, and use of generalist end of life care. Design: A national consultation and prioritising exercise using a modified form of the nominal group technique. Participants: Healthcare practitioners, commissioners, academics, and representatives of user and voluntary groups. Setting: Primary and secondary care, specialist palliative care, and academic and voluntary sectors in England and Scotland. Results: 74% of those invited ( 210/ 285) participated. The stage of life to which "end of life care" referred was not understood in a uniform way. Perceptions ranged from a period of more than a year to the last few days of life. Prominent concerns included difficulties in prognosis and the availability of adequate support for patients with advanced non- malignant disease. Generalists in both primary and secondary care were usually caring for only a few patients approaching the end of life at any one time at a point in time. It was therefore challenging to maintain skills and expertise particularly as educational opportunities were often limited. End of life care took place among many other competing and incentivised activities for general practitioners in the community. More needs to be known about models of end of life care and how these can be integrated in a generalist's workload. A greater evidence base is needed about the effectiveness and application of current tools such as the gold standards framework and Liverpool care pathway and about models of palliation in patients with diseases other than cancer. Conclusions: Definitions of end of life care need clarification and standardisation. A greater evidence base is needed to define models of good practice together with a commitment to provide education and training and adequate resources for service provision. More needs to be known about the context of provision and the influence of competing priorities and incentives.

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Item Type:	Journal Article
Subjects:	R Medicine R Medicine > RT Nursing
Divisions:	Faculty of Medicine > Warwick Medical School > Health Sciences Faculty of Medicine > Warwick Medical School
Library of Congress Subject Headings (LCSH):	Terminal care, Palliative treatment, Primary care (Medicine), Terminally ill -- Home care
Journal or Publication Title:	British Medical Journal
Publisher:	BMJ Group
ISSN:	0959-8146
Date:	11 October 2008
Volume:	Vol.337
Number:	No.7674
Number of Pages:	8
Identification Number:	10.1136/bmj.a1720
Status:	Peer Reviewed
Publication Status:	Published
Access rights to Published version:	Restricted or Subscription Access
Funder:	National Institute for Health Research (Great Britain). Service Delivery and Organisation Programme
URI:	http://wrap.warwick.ac.uk/id/eprint/29340

Data sourced from Thomson Reuters' Web of Knowledge

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