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What does it mean to be the main caregiver to a terminally ill family member in Lithuania?: A qualitative study
INTRODUCTION: Family caregivers are a great resource for providing dignified end-of-life care for terminally ill patients. Framed from the perspective of role theory and the relational nature of providing and receiving care, study objectives were as follows: (1) to capture caregivers’ understanding...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098011/ https://www.ncbi.nlm.nih.gov/pubmed/35551302 http://dx.doi.org/10.1371/journal.pone.0265165 |
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author | Kuznecovienė, Jolanta Butkevičienė, Rūta Harrison, W. David Peičius, Eimantas Urbonas, Gvidas Astromskė, Kristina |
author_facet | Kuznecovienė, Jolanta Butkevičienė, Rūta Harrison, W. David Peičius, Eimantas Urbonas, Gvidas Astromskė, Kristina |
author_sort | Kuznecovienė, Jolanta |
collection | PubMed |
description | INTRODUCTION: Family caregivers are a great resource for providing dignified end-of-life care for terminally ill patients. Framed from the perspective of role theory and the relational nature of providing and receiving care, study objectives were as follows: (1) to capture caregivers’ understanding of the process of taking on the role of main caregiver, (2) to conceptualize their understanding of the functions that they assume while being the main caregivers, and (3) to understand how they experienced the consequences they confronted. METHODS: The research team employed the methodological strategy of descriptive thematic analysis using a semi-structured interview guide. The sample consisting of 33 family caregivers was recruited using purposeful and snowball sampling strategies in 2020. Interview data was analyzed using content-driven inductive thematic analysis. RESULTS: The data analysis revealed four main themes that structure the process of becoming the main care giver of a terminally ill family member and the meaning of the caregiver role: (1) inaccessibility and mistrust of public care services for persons with terminal illness, (2) moral obligations and responsibilities of immediate family and friends, (3) cultural traditions, (4) the caregiver feels responsible for everything. The themes describe the social role of family caregiver in social context, address the process of taking on the role of caregiver and living with systemic corruption. CONCLUSIONS: Recognition of caregiving experiences is essential in planning better systems, in direct practice and in confronting corruption. The study suggests the need for open communication, accessibility of quality services, and the recognition of caregivers as care-team members. The larger implication is that the increasing numbers of distressed caregivers and aging populations can be considered as public health populations, and thus addressable through public health methods. |
format | Online Article Text |
id | pubmed-9098011 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-90980112022-05-13 What does it mean to be the main caregiver to a terminally ill family member in Lithuania?: A qualitative study Kuznecovienė, Jolanta Butkevičienė, Rūta Harrison, W. David Peičius, Eimantas Urbonas, Gvidas Astromskė, Kristina PLoS One Research Article INTRODUCTION: Family caregivers are a great resource for providing dignified end-of-life care for terminally ill patients. Framed from the perspective of role theory and the relational nature of providing and receiving care, study objectives were as follows: (1) to capture caregivers’ understanding of the process of taking on the role of main caregiver, (2) to conceptualize their understanding of the functions that they assume while being the main caregivers, and (3) to understand how they experienced the consequences they confronted. METHODS: The research team employed the methodological strategy of descriptive thematic analysis using a semi-structured interview guide. The sample consisting of 33 family caregivers was recruited using purposeful and snowball sampling strategies in 2020. Interview data was analyzed using content-driven inductive thematic analysis. RESULTS: The data analysis revealed four main themes that structure the process of becoming the main care giver of a terminally ill family member and the meaning of the caregiver role: (1) inaccessibility and mistrust of public care services for persons with terminal illness, (2) moral obligations and responsibilities of immediate family and friends, (3) cultural traditions, (4) the caregiver feels responsible for everything. The themes describe the social role of family caregiver in social context, address the process of taking on the role of caregiver and living with systemic corruption. CONCLUSIONS: Recognition of caregiving experiences is essential in planning better systems, in direct practice and in confronting corruption. The study suggests the need for open communication, accessibility of quality services, and the recognition of caregivers as care-team members. The larger implication is that the increasing numbers of distressed caregivers and aging populations can be considered as public health populations, and thus addressable through public health methods. Public Library of Science 2022-05-12 /pmc/articles/PMC9098011/ /pubmed/35551302 http://dx.doi.org/10.1371/journal.pone.0265165 Text en © 2022 Kuznecovienė et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kuznecovienė, Jolanta Butkevičienė, Rūta Harrison, W. David Peičius, Eimantas Urbonas, Gvidas Astromskė, Kristina What does it mean to be the main caregiver to a terminally ill family member in Lithuania?: A qualitative study |
title | What does it mean to be the main caregiver to a terminally ill family member in Lithuania?: A qualitative study |
title_full | What does it mean to be the main caregiver to a terminally ill family member in Lithuania?: A qualitative study |
title_fullStr | What does it mean to be the main caregiver to a terminally ill family member in Lithuania?: A qualitative study |
title_full_unstemmed | What does it mean to be the main caregiver to a terminally ill family member in Lithuania?: A qualitative study |
title_short | What does it mean to be the main caregiver to a terminally ill family member in Lithuania?: A qualitative study |
title_sort | what does it mean to be the main caregiver to a terminally ill family member in lithuania?: a qualitative study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098011/ https://www.ncbi.nlm.nih.gov/pubmed/35551302 http://dx.doi.org/10.1371/journal.pone.0265165 |
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