Literature DB >> 17584422

Coping and caring: support for family caregivers of stroke survivors.

Susan K Y Chow1, Frances K Y Wong, Christopher Y F Poon.   

Abstract

AIMS AND
OBJECTIVES: This study examines the physical and emotional burden experienced by caregivers of stroke survivors, compared with caregivers of patients having neurological diseases.
BACKGROUND: Stroke survivors have residual neurological impairment, which requires long-term support and care. Anxiety, depression and poor physical health are common sequelae among family caregivers of stroke survivors. There is a reasonably consistent association between patients' levels of disability and emotional state and the emotional distress of their caregivers.
DESIGN: A convenience sample of 47 families was recruited: of the 47 families, 23 had a member who suffered from stroke and 24 had a member with neurological disease.
METHOD: Two interviews were conducted at three and six months after the occurrence of the index stroke or neurological disease.
RESULTS: When the two groups of caregivers were compared for anxiety, depression and physical health status after care giving, the caregivers of stroke patients demonstrated higher levels of anxiety and depression than their counterparts in the neurological disease group (p < 0.001). However, there was no significant difference in physical health status between the two groups. Educational attainment, patient group and physical and cognitive impairment of the patients were the predictors of anxiety and the depressive status of the caregivers, while their age and level of depression contributed significantly to their physical health status.
CONCLUSION: The physical and emotional well-being of two groups of family caregivers in a neurosurgical unit were compared in the caring context. The caregivers of stroke survivors are at a greater risk of developing poor physical and emotional health than the caregivers of patients having neurological diseases. RELEVANCE TO CLINICAL PRACTICE: The results illustrated that enhanced discharge planning and nurse follow-up sessions are considered essential in maintaining the well-being of the stroke caregivers and bridging the gap between the hospital and the community.

Entities:  

Mesh:

Year:  2007        PMID: 17584422     DOI: 10.1111/j.1365-2702.2006.01711.x

Source DB:  PubMed          Journal:  J Clin Nurs        ISSN: 0962-1067            Impact factor:   3.036


  6 in total

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Authors:  Li Zeng; Xiaoping Zhu; Xianmei Meng; Yafen Mao; Qian Wu; Yan Shi; Lanshu Zhou
Journal:  Int J Clin Exp Med       Date:  2014-07-15

2.  Relationship Consensus and Caregiver Burden in Adults with Cognitive Impairments 6 Months Following Stroke.

Authors:  Chao-Yi Wu; Elizabeth R Skidmore; Juleen Rodakowski
Journal:  PM R       Date:  2019-03-07       Impact factor: 2.298

3.  Dyads affected by chronic heart failure: a randomized study evaluating effects of education and psychosocial support to patients with heart failure and their partners.

Authors:  Susanna Ågren; Lorraine S Evangelista; Carina Hjelm; Anna Strömberg
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4.  Determinants of Health Promotion Behaviors among Family Caregivers of Stroke Survivors.

Authors:  Anna Kavga; Ourania Govina; Petros Galanis; Ioannis Kalemikerakis; Eugenia Vlachou; Nikolaos Fotos; Styliani Tziaferi; Athina Kalokairinou
Journal:  Diseases       Date:  2021-01-22

5.  Perceived Caregiver Strain, 3- and 18-Month Poststroke, in a Cohort of Caregivers from the Life after Stroke Trial (LAST).

Authors:  Birgitta Langhammer; Hege Ihle Hansen; Bent Indredavik; Torunn Askim
Journal:  Nurs Res Pract       Date:  2022-03-31

6.  Disease Acceptance and Eudemonic Well-Being Among Adults With Physical Disabilities: The Mediator Effect of Meaning in Life.

Authors:  Małgorzata Szcześniak; Agata H Świątek; Małgorzata Cieślak; Daria Świdurska
Journal:  Front Psychol       Date:  2020-10-22
  6 in total

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