Abstract
Background: Stroke survivors experience long-term physical, psychosocial and cognitive impairment that are formidable challenges to caregivers because caring for stroke survivors needs explicit knowledge and caregivers have to endure the stressfulness as a result of caring. In addition, little is known about perceived benefits of the stroke care giving experience.Objectives: This study was aimed to determine the caregivers’ burden and challenges as reported by caregivers of stroke survivors.Materials and Methods: This was a cross-sectional study involving 18 stroke caregivers. The data were collected from November 2015 to June 2016 at a conveniently selected community rehabilitation centre in Kuching, Sarawak.Results: The qualitative data analysis revealed that the burden was aggravated by financial problems, multiple responsibilities hold by the caregivers, behavioural changes of the stroke survivors and lack of social support during care giving.Conclusion: This study highlighted the experiences by the caregivers in caring for the stroke survivors that focused on the different needs of the caregivers. Understanding these experiences may help the service providers to provide better support and resources for caregivers in caring for stroke survivors.Bangladesh Journal of Medical Science Vol.17(4) 2018 p.593-599
Highlights
The operational definition of stroke was a rapidly developing sign of focal disturbance of cerebral function lasting more than 24 hours with no apparent non-vascular cause[1]
Another limitation was that the caregivers were asked to recall their experiences of only stroke survivors, which may be influenced by recall bias
This study focused on the caring experiences of caregivers of stroke survivors with different complications
Summary
The operational definition of stroke was a rapidly developing sign of focal disturbance of cerebral function lasting more than 24 hours with no apparent non-vascular cause[1]. Stroke is the third most common cause of death in developed countries, after coronary heart diseases and cancers. Objectives: This study was aimed to determine the caregivers’ burden and challenges as reported by caregivers of stroke survivors. Results: The qualitative data analysis revealed that the burden was aggravated by financial problems, multiple responsibilities hold by the caregivers, behavioural changes of the stroke survivors and lack of social support during care giving. Conclusion: This study highlighted the experiences by the caregivers in caring for the stroke survivors that focused on the different needs of the caregivers. Understanding these experiences may help the service providers to provide better support and resources for caregivers in caring for stroke survivors
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