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Just and inclusive end-of-life decision-making for long-term care home residents with dementia: a qualitative study protocol
BACKGROUND: Many people living with dementia eventually require care services and spend the remainder of their lives in long-term care (LTC) homes. Yet, many residents with dementia do not receive coordinated, quality palliative care. The stigma associated with dementia leads to an assumption that p...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684772/ https://www.ncbi.nlm.nih.gov/pubmed/36419147 http://dx.doi.org/10.1186/s12904-022-01097-x |
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author | Sutherland, N. St. Amant, O. Dupuis, S. Kontos, P. Wiersma, E. Brennan, M. |
author_facet | Sutherland, N. St. Amant, O. Dupuis, S. Kontos, P. Wiersma, E. Brennan, M. |
author_sort | Sutherland, N. |
collection | PubMed |
description | BACKGROUND: Many people living with dementia eventually require care services and spend the remainder of their lives in long-term care (LTC) homes. Yet, many residents with dementia do not receive coordinated, quality palliative care. The stigma associated with dementia leads to an assumption that people living in the advanced stages of dementia are unable to express their end-of-life needs. As a result, people with dementia have fewer choices and limited access to palliative care. The purpose of this paper is to describe the protocol for a qualitative study that explores end-of-life decision-making processes for LTC home residents with dementia. METHODS/DESIGN: This study is informed by two theoretical concepts. First, it draws on a relational model of citizenship. The model recognizes the pre-reflective dimensions of agency as fundamental to being human (irrespective of cognitive impairment) and thereby necessitates that we cultivate an environment that supports these dimensions. This study also draws from Smith’s critical feminist lens to foreground the influence of gender relations in decision-making processes towards palliative care goals for people with dementia and reveal the discursive mediums of power that legitimize and sanction social relations. This study employs a critical ethnographic methodology. Through data collection strategies of interview, observation, and document review, this study examines decision-making for LTC home residents with dementia and their paid (LTC home workers) and unpaid (family members) care partners. DISCUSSION: This research will expose the embedded structures and organizational factors that shape relationships and interactions in decision-making. This study may reveal new ways to promote equitable decision-making towards palliative care goals for LTC home residents with dementia and their care partners and help to improve their access to palliative care. |
format | Online Article Text |
id | pubmed-9684772 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-96847722022-11-25 Just and inclusive end-of-life decision-making for long-term care home residents with dementia: a qualitative study protocol Sutherland, N. St. Amant, O. Dupuis, S. Kontos, P. Wiersma, E. Brennan, M. BMC Palliat Care Study Protocol BACKGROUND: Many people living with dementia eventually require care services and spend the remainder of their lives in long-term care (LTC) homes. Yet, many residents with dementia do not receive coordinated, quality palliative care. The stigma associated with dementia leads to an assumption that people living in the advanced stages of dementia are unable to express their end-of-life needs. As a result, people with dementia have fewer choices and limited access to palliative care. The purpose of this paper is to describe the protocol for a qualitative study that explores end-of-life decision-making processes for LTC home residents with dementia. METHODS/DESIGN: This study is informed by two theoretical concepts. First, it draws on a relational model of citizenship. The model recognizes the pre-reflective dimensions of agency as fundamental to being human (irrespective of cognitive impairment) and thereby necessitates that we cultivate an environment that supports these dimensions. This study also draws from Smith’s critical feminist lens to foreground the influence of gender relations in decision-making processes towards palliative care goals for people with dementia and reveal the discursive mediums of power that legitimize and sanction social relations. This study employs a critical ethnographic methodology. Through data collection strategies of interview, observation, and document review, this study examines decision-making for LTC home residents with dementia and their paid (LTC home workers) and unpaid (family members) care partners. DISCUSSION: This research will expose the embedded structures and organizational factors that shape relationships and interactions in decision-making. This study may reveal new ways to promote equitable decision-making towards palliative care goals for LTC home residents with dementia and their care partners and help to improve their access to palliative care. BioMed Central 2022-11-22 /pmc/articles/PMC9684772/ /pubmed/36419147 http://dx.doi.org/10.1186/s12904-022-01097-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Study Protocol Sutherland, N. St. Amant, O. Dupuis, S. Kontos, P. Wiersma, E. Brennan, M. Just and inclusive end-of-life decision-making for long-term care home residents with dementia: a qualitative study protocol |
title | Just and inclusive end-of-life decision-making for long-term care home residents with dementia: a qualitative study protocol |
title_full | Just and inclusive end-of-life decision-making for long-term care home residents with dementia: a qualitative study protocol |
title_fullStr | Just and inclusive end-of-life decision-making for long-term care home residents with dementia: a qualitative study protocol |
title_full_unstemmed | Just and inclusive end-of-life decision-making for long-term care home residents with dementia: a qualitative study protocol |
title_short | Just and inclusive end-of-life decision-making for long-term care home residents with dementia: a qualitative study protocol |
title_sort | just and inclusive end-of-life decision-making for long-term care home residents with dementia: a qualitative study protocol |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684772/ https://www.ncbi.nlm.nih.gov/pubmed/36419147 http://dx.doi.org/10.1186/s12904-022-01097-x |
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