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Health-related quality of life in partners of persons with MS: a longitudinal 10-year perspective
OBJECTIVES: Multiple sclerosis (MS) impacts the health-related quality of life (HRQL) in partners, but knowledge on the longitudinal perspective is needed. The aim was to analyse HRQL in partners of persons with MS living in Sweden a decade ago and after 10 years. MATERIALS AND METHODS: Partners wer...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4275699/ https://www.ncbi.nlm.nih.gov/pubmed/25515842 http://dx.doi.org/10.1136/bmjopen-2014-006097 |
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author | Gottberg, Kristina Chruzander, C Einarsson, U Fredrikson, S Johansson, S Widén Holmqvist, L |
author_facet | Gottberg, Kristina Chruzander, C Einarsson, U Fredrikson, S Johansson, S Widén Holmqvist, L |
author_sort | Gottberg, Kristina |
collection | PubMed |
description | OBJECTIVES: Multiple sclerosis (MS) impacts the health-related quality of life (HRQL) in partners, but knowledge on the longitudinal perspective is needed. The aim was to analyse HRQL in partners of persons with MS living in Sweden a decade ago and after 10 years. MATERIALS AND METHODS: Partners were identified through a population-based study of persons with MS in Stockholm. Information on HRQL (the Sickness Impact profile), personal factors and disease-specific factors, and measures of functioning of persons with MS was collected at both time points mainly by home visits. RESULTS: Some 64 of 102 identified partners (63%) agreed to participate at baseline, and at 10 years 40 of 54 eligible partners were included (74%). HRQL in partners was worse than in a Swedish, aged-grouped reference population at both baseline and follow-up. Depressive symptoms in persons with MS were independently associated with worse HRQL in partners. CONCLUSIONS: Depressive symptoms in persons with MS were associated with worse HRQL in their partners, and HRQL of partners was continuously impacted in the longitudinal perspective. This knowledge needs to be accounted for in the planning of MS care, together with the development of evidence-based support for depressive symptoms, and engagement in recreational life in both partners and persons with MS. |
format | Online Article Text |
id | pubmed-4275699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-42756992014-12-31 Health-related quality of life in partners of persons with MS: a longitudinal 10-year perspective Gottberg, Kristina Chruzander, C Einarsson, U Fredrikson, S Johansson, S Widén Holmqvist, L BMJ Open Rehabilitation Medicine OBJECTIVES: Multiple sclerosis (MS) impacts the health-related quality of life (HRQL) in partners, but knowledge on the longitudinal perspective is needed. The aim was to analyse HRQL in partners of persons with MS living in Sweden a decade ago and after 10 years. MATERIALS AND METHODS: Partners were identified through a population-based study of persons with MS in Stockholm. Information on HRQL (the Sickness Impact profile), personal factors and disease-specific factors, and measures of functioning of persons with MS was collected at both time points mainly by home visits. RESULTS: Some 64 of 102 identified partners (63%) agreed to participate at baseline, and at 10 years 40 of 54 eligible partners were included (74%). HRQL in partners was worse than in a Swedish, aged-grouped reference population at both baseline and follow-up. Depressive symptoms in persons with MS were independently associated with worse HRQL in partners. CONCLUSIONS: Depressive symptoms in persons with MS were associated with worse HRQL in their partners, and HRQL of partners was continuously impacted in the longitudinal perspective. This knowledge needs to be accounted for in the planning of MS care, together with the development of evidence-based support for depressive symptoms, and engagement in recreational life in both partners and persons with MS. BMJ Publishing Group 2014-12-16 /pmc/articles/PMC4275699/ /pubmed/25515842 http://dx.doi.org/10.1136/bmjopen-2014-006097 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Rehabilitation Medicine Gottberg, Kristina Chruzander, C Einarsson, U Fredrikson, S Johansson, S Widén Holmqvist, L Health-related quality of life in partners of persons with MS: a longitudinal 10-year perspective |
title | Health-related quality of life in partners of persons with MS: a longitudinal 10-year perspective |
title_full | Health-related quality of life in partners of persons with MS: a longitudinal 10-year perspective |
title_fullStr | Health-related quality of life in partners of persons with MS: a longitudinal 10-year perspective |
title_full_unstemmed | Health-related quality of life in partners of persons with MS: a longitudinal 10-year perspective |
title_short | Health-related quality of life in partners of persons with MS: a longitudinal 10-year perspective |
title_sort | health-related quality of life in partners of persons with ms: a longitudinal 10-year perspective |
topic | Rehabilitation Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4275699/ https://www.ncbi.nlm.nih.gov/pubmed/25515842 http://dx.doi.org/10.1136/bmjopen-2014-006097 |
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