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The experience of caregiver burden when being next of kin to a person with severe chronic obstructive pulmonary disease: A qualitative study
BACKGROUND: Chronic obstructive pulmonary disease (COPD) is an inflammatory and irreversible lung disease. For next of kin caregiver burden can be a consequence of the situation of being close to a person affected by a chronic disease and in need of help. When there is an imbalance between stressors...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107968/ https://www.ncbi.nlm.nih.gov/pubmed/37042067 http://dx.doi.org/10.1177/14799731231168897 |
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author | Johansson, Helena Berterö, Carina Jonasson, Lise-Lotte Berg, Katarina |
author_facet | Johansson, Helena Berterö, Carina Jonasson, Lise-Lotte Berg, Katarina |
author_sort | Johansson, Helena |
collection | PubMed |
description | BACKGROUND: Chronic obstructive pulmonary disease (COPD) is an inflammatory and irreversible lung disease. For next of kin caregiver burden can be a consequence of the situation of being close to a person affected by a chronic disease and in need of help. When there is an imbalance between stressors and resources to cope with the situation, caregiver burden emerges. Knowledge is sparse about how the caregiver burden is experienced by the next of kin. Therefore, the aim of this study is to identify and describe the caregiver burden experienced by next of kin of persons with severe COPD. METHOD: Qualitative interviews with 21 next of kin were conducted. Thematic analysis was used in accordance with the six steps of Braun and Clarke. RESULTS: The next of kin experience caregiver burden as 1) changed roles in daily life 2) putting life on hold 3) to stand aside. The next of kin are in need of support to manage daily life. CONCLUSIONS: The caregiver burden affect the next of kin physically and emotionally. To prevent advance consequences, person-centered care can be used to support the next of kin in the situation. |
format | Online Article Text |
id | pubmed-10107968 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-101079682023-04-18 The experience of caregiver burden when being next of kin to a person with severe chronic obstructive pulmonary disease: A qualitative study Johansson, Helena Berterö, Carina Jonasson, Lise-Lotte Berg, Katarina Chron Respir Dis Original Paper BACKGROUND: Chronic obstructive pulmonary disease (COPD) is an inflammatory and irreversible lung disease. For next of kin caregiver burden can be a consequence of the situation of being close to a person affected by a chronic disease and in need of help. When there is an imbalance between stressors and resources to cope with the situation, caregiver burden emerges. Knowledge is sparse about how the caregiver burden is experienced by the next of kin. Therefore, the aim of this study is to identify and describe the caregiver burden experienced by next of kin of persons with severe COPD. METHOD: Qualitative interviews with 21 next of kin were conducted. Thematic analysis was used in accordance with the six steps of Braun and Clarke. RESULTS: The next of kin experience caregiver burden as 1) changed roles in daily life 2) putting life on hold 3) to stand aside. The next of kin are in need of support to manage daily life. CONCLUSIONS: The caregiver burden affect the next of kin physically and emotionally. To prevent advance consequences, person-centered care can be used to support the next of kin in the situation. SAGE Publications 2023-04-11 /pmc/articles/PMC10107968/ /pubmed/37042067 http://dx.doi.org/10.1177/14799731231168897 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Paper Johansson, Helena Berterö, Carina Jonasson, Lise-Lotte Berg, Katarina The experience of caregiver burden when being next of kin to a person with severe chronic obstructive pulmonary disease: A qualitative study |
title | The experience of caregiver burden when being next of kin to a person
with severe chronic obstructive pulmonary disease: A qualitative
study |
title_full | The experience of caregiver burden when being next of kin to a person
with severe chronic obstructive pulmonary disease: A qualitative
study |
title_fullStr | The experience of caregiver burden when being next of kin to a person
with severe chronic obstructive pulmonary disease: A qualitative
study |
title_full_unstemmed | The experience of caregiver burden when being next of kin to a person
with severe chronic obstructive pulmonary disease: A qualitative
study |
title_short | The experience of caregiver burden when being next of kin to a person
with severe chronic obstructive pulmonary disease: A qualitative
study |
title_sort | experience of caregiver burden when being next of kin to a person
with severe chronic obstructive pulmonary disease: a qualitative
study |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107968/ https://www.ncbi.nlm.nih.gov/pubmed/37042067 http://dx.doi.org/10.1177/14799731231168897 |
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