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Improving generalist end of life care: national consultation with practitioners, commissioners, academics, and service user groups
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 practitioner...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BMJ Publishing Group Ltd.
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2659492/ https://www.ncbi.nlm.nih.gov/pubmed/18829640 http://dx.doi.org/10.1136/bmj.a1720 |
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author | Shipman, Cathy Gysels, Marjolein White, Patrick Worth, Allison Murray, Scott A Barclay, Stephen Forrest, Sarah Shepherd, Jonathan Dale, Jeremy Dewar, Steve Peters, Marilyn White, Suzanne Richardson, Alison Lorenz, Karl Koffman, Jonathan Higginson, Irene J |
author_facet | Shipman, Cathy Gysels, Marjolein White, Patrick Worth, Allison Murray, Scott A Barclay, Stephen Forrest, Sarah Shepherd, Jonathan Dale, Jeremy Dewar, Steve Peters, Marilyn White, Suzanne Richardson, Alison Lorenz, Karl Koffman, Jonathan Higginson, Irene J |
author_sort | Shipman, Cathy |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2659492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BMJ Publishing Group Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-26594922009-03-23 Improving generalist end of life care: national consultation with practitioners, commissioners, academics, and service user groups Shipman, Cathy Gysels, Marjolein White, Patrick Worth, Allison Murray, Scott A Barclay, Stephen Forrest, Sarah Shepherd, Jonathan Dale, Jeremy Dewar, Steve Peters, Marilyn White, Suzanne Richardson, Alison Lorenz, Karl Koffman, Jonathan Higginson, Irene J BMJ Research 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. BMJ Publishing Group Ltd. 2008-10-01 /pmc/articles/PMC2659492/ /pubmed/18829640 http://dx.doi.org/10.1136/bmj.a1720 Text en © Shipman et al 2008 http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Shipman, Cathy Gysels, Marjolein White, Patrick Worth, Allison Murray, Scott A Barclay, Stephen Forrest, Sarah Shepherd, Jonathan Dale, Jeremy Dewar, Steve Peters, Marilyn White, Suzanne Richardson, Alison Lorenz, Karl Koffman, Jonathan Higginson, Irene J Improving generalist end of life care: national consultation with practitioners, commissioners, academics, and service user groups |
title | Improving generalist end of life care: national consultation with practitioners, commissioners, academics, and service user groups |
title_full | Improving generalist end of life care: national consultation with practitioners, commissioners, academics, and service user groups |
title_fullStr | Improving generalist end of life care: national consultation with practitioners, commissioners, academics, and service user groups |
title_full_unstemmed | Improving generalist end of life care: national consultation with practitioners, commissioners, academics, and service user groups |
title_short | Improving generalist end of life care: national consultation with practitioners, commissioners, academics, and service user groups |
title_sort | improving generalist end of life care: national consultation with practitioners, commissioners, academics, and service user groups |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2659492/ https://www.ncbi.nlm.nih.gov/pubmed/18829640 http://dx.doi.org/10.1136/bmj.a1720 |
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