Literature DB >> 21447466

Increased residual disability among poststroke survivors and the repercussions for the lives of informal caregivers.

Michèle Baumann1, Katia Lurbe-Puerto, Kazem Alzahouri, Pierre Aïach.   

Abstract

PURPOSE: To analyze the associations between increased residual disability among poststroke survivors and the repercussions for their informal caregivers' lives, taking into account the latter's gender and education level.
METHODS: 215 stroke survivors (64.5 years; 55.8% men) were recruited by one neurologist from each of the 22 French regions. Katz Index of Independence in Activities of Daily Living (Katz ADL) was mean 9.3, and 54% still had impairments in "more than two of the six neurological domains" of the American Heart Association Stroke Outcome Classification (AHA.SOC): motor, sensory, vision, affect, cognition, and language. The 215 caregivers (57.8 years; 72.1% women) completed a face-to-face questionnaire concerning their social (8 items), material (4 items), and emotional (8 items) repercussions.
RESULTS: Katz ADL and AHA.SOC were significantly related to social repercussions for caregivers. Lack of autonomy among stroke survivors (low Katz ADL) was associated with the material difficulties of most concern to caregivers: "I needed to move house" (odds ratio [OR] 1.16; 95% CI, 1.07-1.27) and "I cannot go out anymore" (OR 1.29; 95% CI, 1.16-1.44). Being a male caregiver was strongly associated with a feeling of injustice (OR 2.53; 95% CI, 1.07-6.00). A low educational level was linked to an increased feeling of fear (OR 2.61; 95% CI, 1.05-6.51) and a greater feeling of isolation (OR 6.49; 95% CI, 1.20-35.02).
CONCLUSION: Increased dependency post stroke leads to impoverishment in the caregiver's social relationships. Evaluating the emotional repercussions, particularly for men, is an important aspect of enabling survivors to continue to live at home. Innovative accompaniment and counseling services should be considered.

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Mesh:

Year:  2011        PMID: 21447466     DOI: 10.1310/tsr1802-162

Source DB:  PubMed          Journal:  Top Stroke Rehabil        ISSN: 1074-9357            Impact factor:   2.119


  6 in total

1.  Lifestyle as a health risk for family caregivers with least life satisfaction, in home-based post-stroke caring.

Authors:  Michèle Baumann; Barbara Bucki
Journal:  Healthc Policy       Date:  2013-10

2.  Caregiver burden and coping strategies in caregivers of older patients with stroke.

Authors:  Azar Kazemi; Jalil Azimian; Maryam Mafi; Kelly-Ann Allen; Seyedeh Ameneh Motalebi
Journal:  BMC Psychol       Date:  2021-04-01

3.  Relationships between care burden, resilience, and depressive symptoms among the main family caregivers of stroke patients: A cross-sectional study.

Authors:  Linlin Fang; Mengyuan Dong; Wenbo Fang; Jin Zheng
Journal:  Front Psychiatry       Date:  2022-09-20       Impact factor: 5.435

4.  Life satisfaction two-years after stroke onset: the effects of gender, sex occupational status, memory function and quality of life among stroke patients (Newsqol) and their family caregivers (Whoqol-bref) in Luxembourg.

Authors:  Michèle Baumann; Sophie Couffignal; Etienne Le Bihan; Nearkasen Chau
Journal:  BMC Neurol       Date:  2012-09-25       Impact factor: 2.474

5.  Associations between quality of life and socioeconomic factors, functional impairments and dissatisfaction with received information and home-care services among survivors living at home two years after stroke onset.

Authors:  Michèle Baumann; Etienne Le Bihan; Kénora Chau; Nearkasen Chau
Journal:  BMC Neurol       Date:  2014-04-28       Impact factor: 2.474

6.  A Canadian qualitative study exploring the diversity of the experience of family caregivers of older adults with multiple chronic conditions using a social location perspective.

Authors:  Allison Williams; Bharati Sethi; Wendy Duggleby; Jenny Ploeg; Maureen Markle-Reid; Shelley Peacock; Sunita Ghosh
Journal:  Int J Equity Health       Date:  2016-03-02
  6 in total

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