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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...

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Autores principales: Johansson, Helena, Berterö, Carina, Jonasson, Lise-Lotte, Berg, Katarina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
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.
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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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