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Understanding the barriers to identifying carers of people with advanced illness in primary care: triangulating three data sources
BACKGROUND: Approximately 10% of the UK population have an unpaid caring role for a family member or friend. Many of these carers make a significant contribution to supporting patients at the end of life. Carers can experience poor physical and psychosocial wellbeing, yet they remain largely unsuppo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992158/ https://www.ncbi.nlm.nih.gov/pubmed/24690099 http://dx.doi.org/10.1186/1471-2296-15-48 |
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author | Carduff, Emma Finucane, Anne Kendall, Marilyn Jarvis, Alison Harrison, Nadine Greenacre, Jane Murray, Scott A |
author_facet | Carduff, Emma Finucane, Anne Kendall, Marilyn Jarvis, Alison Harrison, Nadine Greenacre, Jane Murray, Scott A |
author_sort | Carduff, Emma |
collection | PubMed |
description | BACKGROUND: Approximately 10% of the UK population have an unpaid caring role for a family member or friend. Many of these carers make a significant contribution to supporting patients at the end of life. Carers can experience poor physical and psychosocial wellbeing, yet they remain largely unsupported by health and social care services. Despite initiatives for general practices to identify carers and their needs, many remain unidentified. Neither are carers self-identifying and requesting support. This study set out to explore the barriers to, and consider strategies for, identifying carers in primary care. METHODS: We integrated findings from three data sources – a review of the caregiving literature; a workshop with researchers who have undertaken research with those caring at the end of life, and focus groups with carers and health professionals. RESULTS: Three categories of barrier emerged. 1) Taking on the care of another person is often a gradual process, carers did not immediately identify with being a ‘carer’ – preferring to think of themselves in relational terms to the patient e.g. spouse, sibling, son or daughter. Often it was health and social care professionals who encouraged carers to consider themselves as an unpaid carer. 2) As the cared-for person’s condition deteriorated, the caring role often became all-encompassing so that carers were managing competing demands, and felt unable to look after their own needs as well as those of the cared-for person. 3) There was ambiguity about the legitimacy of carer needs and about the role of the primary health care team in supporting carers, from both the perspective of the carers and the health professionals. GPs were thought to be reactive rather than proactive which discouraged carers from asking for help. CONCLUSIONS: The needs of carers have to be legitimised to ensure primary care staff are proactive in their approach and carers are empowered to utilise the support available. Strategies to identify carers have to be sensitive to the complex dynamics of a caring relationship as well as the primary care context. Identification is a key factor in improving support for carers themselves and to enable them to support the patient. |
format | Online Article Text |
id | pubmed-3992158 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39921582014-04-20 Understanding the barriers to identifying carers of people with advanced illness in primary care: triangulating three data sources Carduff, Emma Finucane, Anne Kendall, Marilyn Jarvis, Alison Harrison, Nadine Greenacre, Jane Murray, Scott A BMC Fam Pract Research Article BACKGROUND: Approximately 10% of the UK population have an unpaid caring role for a family member or friend. Many of these carers make a significant contribution to supporting patients at the end of life. Carers can experience poor physical and psychosocial wellbeing, yet they remain largely unsupported by health and social care services. Despite initiatives for general practices to identify carers and their needs, many remain unidentified. Neither are carers self-identifying and requesting support. This study set out to explore the barriers to, and consider strategies for, identifying carers in primary care. METHODS: We integrated findings from three data sources – a review of the caregiving literature; a workshop with researchers who have undertaken research with those caring at the end of life, and focus groups with carers and health professionals. RESULTS: Three categories of barrier emerged. 1) Taking on the care of another person is often a gradual process, carers did not immediately identify with being a ‘carer’ – preferring to think of themselves in relational terms to the patient e.g. spouse, sibling, son or daughter. Often it was health and social care professionals who encouraged carers to consider themselves as an unpaid carer. 2) As the cared-for person’s condition deteriorated, the caring role often became all-encompassing so that carers were managing competing demands, and felt unable to look after their own needs as well as those of the cared-for person. 3) There was ambiguity about the legitimacy of carer needs and about the role of the primary health care team in supporting carers, from both the perspective of the carers and the health professionals. GPs were thought to be reactive rather than proactive which discouraged carers from asking for help. CONCLUSIONS: The needs of carers have to be legitimised to ensure primary care staff are proactive in their approach and carers are empowered to utilise the support available. Strategies to identify carers have to be sensitive to the complex dynamics of a caring relationship as well as the primary care context. Identification is a key factor in improving support for carers themselves and to enable them to support the patient. BioMed Central 2014-04-02 /pmc/articles/PMC3992158/ /pubmed/24690099 http://dx.doi.org/10.1186/1471-2296-15-48 Text en Copyright © 2014 Carduff et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Carduff, Emma Finucane, Anne Kendall, Marilyn Jarvis, Alison Harrison, Nadine Greenacre, Jane Murray, Scott A Understanding the barriers to identifying carers of people with advanced illness in primary care: triangulating three data sources |
title | Understanding the barriers to identifying carers of people with advanced illness in primary care: triangulating three data sources |
title_full | Understanding the barriers to identifying carers of people with advanced illness in primary care: triangulating three data sources |
title_fullStr | Understanding the barriers to identifying carers of people with advanced illness in primary care: triangulating three data sources |
title_full_unstemmed | Understanding the barriers to identifying carers of people with advanced illness in primary care: triangulating three data sources |
title_short | Understanding the barriers to identifying carers of people with advanced illness in primary care: triangulating three data sources |
title_sort | understanding the barriers to identifying carers of people with advanced illness in primary care: triangulating three data sources |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992158/ https://www.ncbi.nlm.nih.gov/pubmed/24690099 http://dx.doi.org/10.1186/1471-2296-15-48 |
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