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김동원 ( Kim Dong-Won ) - 동아대학교 간호학과
배은숙 ( Bae Eun-Sook ) - 동의대학교 간호학과
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Abstract
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Purpose: Depression is a common sign of suffering among the patients with Parkinson’s disease (PD). Frequent and severe neuropsychiatric symptoms lead to high levels of distress in patients and their caregivers, which results in the high levels of caregiver burden. The aim of this study was to determine the predictors of caregiver burden in caregivers of the patients with Parkinson’s disease (PD).
Methods: The study included 183 consecutive PD patients and their caregivers. Patients were assessed using the Hoehn and Yahr scale, Mini Mental State Examination (MMSE), Beck Depression Inventory (BDI), and Schwab and England Activities of Daily Living Scale. Caregivers’ depressive symptoms were evaluated using the Caregiver Burden Inventor (CBI), BDI, and World Health Organization Quality of Life Scale.
Results: All of the patients reported one or more neuropsychiatric symptoms. Patients’ and caregivers’ depressive symptoms, caregivers’ age and education, time for caregiving, and quality of life were significantly associated with the increased caregiver burden. After controlling the level of education as a potential confounding variable, depression in both patients and caregivers, time for caregiving, and quality of life explained 45.6% of the variance in caregiver burden.
Conclusion: Substantial attention needs to be given to the early identification of depression in PD patients and their caregivers to improve caregivers’ quality of life and burden.
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KeyWords
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파킨슨병, 부양자, 우울, 삶의 질, 부담
Parkinson’s disease, Caregivers, Depression, Quality of life, Burden
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원문 및 링크아웃 정보
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등재저널 정보
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