Recommendations for improving the end-of-life care system for homeless populations: A qualitative study of the views of Canadian health and social services professionals

<p>Abstract</p> <p>Background</p> <p>Homeless populations have complex and diverse end-of-life care needs. However, they typically die outside of the end-of-life care system. To date, few studies have explored barriers to the end-of-life care system for homeless populat...

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Main Authors: McNeil Ryan, Guirguis-Younger Manal, Dilley Laura B
Format: Article
Language:English
Published: BMC 2012-09-01
Series:BMC Palliative Care
Online Access:http://www.biomedcentral.com/1472-684X/11/14
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spelling doaj-5a0070fa38a74ab9aa2f94ee5c205e362020-11-25T00:20:20ZengBMCBMC Palliative Care1472-684X2012-09-011111410.1186/1472-684X-11-14Recommendations for improving the end-of-life care system for homeless populations: A qualitative study of the views of Canadian health and social services professionalsMcNeil RyanGuirguis-Younger ManalDilley Laura B<p>Abstract</p> <p>Background</p> <p>Homeless populations have complex and diverse end-of-life care needs. However, they typically die outside of the end-of-life care system. To date, few studies have explored barriers to the end-of-life care system for homeless populations. This qualitative study involving health and social services professionals from across Canada sought to identify barriers to the end-of-life care system for homeless populations and generate recommendations to improve their access to end-of-life care.</p> <p>Methods</p> <p>Semi-structured qualitative interviews were conducted with 54 health and social services professionals involved in end-of-life care services delivery to homeless persons in six Canadian cities (Halifax, Hamilton, Ottawa, Thunder Bay, Toronto and Winnipeg). Participants included health administrators, physicians, nurses, social workers, harm reduction specialists, and outreach workers. Interviews were audio-recorded, transcribed verbatim and analysed thematically.</p> <p>Results</p> <p>Participants identified key barriers to end-of-life care services for homeless persons, including: (1) insufficient availability of end-of-life care services; (2) exclusionary operating procedures; and, (3) poor continuity of care. Participants identified recommendations that they felt had the potential to minimize these barriers, including: (1) adopting low-threshold strategies (e.g. flexible behavioural policies and harm reduction strategies); (2) linking with population-specific health and social care providers (e.g. emergency shelters); and, (3) strengthening population-specific training.</p> <p>Conclusions</p> <p>Homeless persons may be underserved by the end-of-life care system as a result of barriers that they face to accessing end-of-life care services. Changes in the rules and regulations that reflect the health needs and circumstances of homeless persons and measures to improve continuity of care have the potential to increase equity in the end-of-life care system for this underserved population.</p> http://www.biomedcentral.com/1472-684X/11/14
collection DOAJ
language English
format Article
sources DOAJ
author McNeil Ryan
Guirguis-Younger Manal
Dilley Laura B
spellingShingle McNeil Ryan
Guirguis-Younger Manal
Dilley Laura B
Recommendations for improving the end-of-life care system for homeless populations: A qualitative study of the views of Canadian health and social services professionals
BMC Palliative Care
author_facet McNeil Ryan
Guirguis-Younger Manal
Dilley Laura B
author_sort McNeil Ryan
title Recommendations for improving the end-of-life care system for homeless populations: A qualitative study of the views of Canadian health and social services professionals
title_short Recommendations for improving the end-of-life care system for homeless populations: A qualitative study of the views of Canadian health and social services professionals
title_full Recommendations for improving the end-of-life care system for homeless populations: A qualitative study of the views of Canadian health and social services professionals
title_fullStr Recommendations for improving the end-of-life care system for homeless populations: A qualitative study of the views of Canadian health and social services professionals
title_full_unstemmed Recommendations for improving the end-of-life care system for homeless populations: A qualitative study of the views of Canadian health and social services professionals
title_sort recommendations for improving the end-of-life care system for homeless populations: a qualitative study of the views of canadian health and social services professionals
publisher BMC
series BMC Palliative Care
issn 1472-684X
publishDate 2012-09-01
description <p>Abstract</p> <p>Background</p> <p>Homeless populations have complex and diverse end-of-life care needs. However, they typically die outside of the end-of-life care system. To date, few studies have explored barriers to the end-of-life care system for homeless populations. This qualitative study involving health and social services professionals from across Canada sought to identify barriers to the end-of-life care system for homeless populations and generate recommendations to improve their access to end-of-life care.</p> <p>Methods</p> <p>Semi-structured qualitative interviews were conducted with 54 health and social services professionals involved in end-of-life care services delivery to homeless persons in six Canadian cities (Halifax, Hamilton, Ottawa, Thunder Bay, Toronto and Winnipeg). Participants included health administrators, physicians, nurses, social workers, harm reduction specialists, and outreach workers. Interviews were audio-recorded, transcribed verbatim and analysed thematically.</p> <p>Results</p> <p>Participants identified key barriers to end-of-life care services for homeless persons, including: (1) insufficient availability of end-of-life care services; (2) exclusionary operating procedures; and, (3) poor continuity of care. Participants identified recommendations that they felt had the potential to minimize these barriers, including: (1) adopting low-threshold strategies (e.g. flexible behavioural policies and harm reduction strategies); (2) linking with population-specific health and social care providers (e.g. emergency shelters); and, (3) strengthening population-specific training.</p> <p>Conclusions</p> <p>Homeless persons may be underserved by the end-of-life care system as a result of barriers that they face to accessing end-of-life care services. Changes in the rules and regulations that reflect the health needs and circumstances of homeless persons and measures to improve continuity of care have the potential to increase equity in the end-of-life care system for this underserved population.</p>
url http://www.biomedcentral.com/1472-684X/11/14
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