|
|
|
|
김금순 ( Kim Keum-Soon ) - 서울대학교 간호대학
최명애 ( Choe Myoung-Ae ) - 서울대학교 간호대학
하양숙 ( Hah Yang-Sook ) - 서울대학교 간호대학
이명선 ( Yi Myung-Sun ) - 서울대학교 간호대학
김복자 ( Kim Bok-Ja ) - 울산대학교 의과대학
김성렬 ( Kim Sung-Reul ) - 서울아산병원 간호본부
김경희 ( Kim Kyung-Hee ) - 중앙대학교 의과대학 간호학과
권소희 ( Kwon So-Hi ) - 서울대학교 간호대학
황영란 ( Hwang Young-Ran ) - 서울대학교 간호대학
|
|
Abstract
|
|
|
|
|
ression and quality of life of family caregivers of patients with Parkinson’s disease(PD).
Methods: A cross-sectional descriptive study was conducted in one neurology outpatient clinic in Seoul, Korea from March to June, 2006. Sixty eight family caregivers of PD patients were participated to the study, using CES-D and SF-36.
Results: Mean scores of depression were 16.18±8.39 (range: 0-48) and it was a little lower than caregiver’s who took care of Dementia patients and were higher than primary caregivers of the patients with Stroke. Time for caregiving, perceived severity, duration of PD were significantly related with depression respectively. Higher ADL scores which mean greater motor disabilities were related to higher caregiver depression. Lower income and greater medical expenditure were closely related with the depression of family caregivers respectively. The mean scores of total QOL were 435.5±96.5 and the mean scores of PF, SF, RE and MH were lower than general population. Time for caregiving, depression, patients’ ADL scores were significantly associated with QOL respectively. People who were older and had lower educational background showed lower QOL scores respectively.
Conclusion: Healthcare professionals should pay more attention to emotional aspects of caregivers who take care of PD patients, and develop comprehensive management strategies both for patients and their caregivers.
|
|
|
KeyWords
|
|
파킨슨병, 우울, 삶의 질, 가족, 간호제공자
Parkinson disease, Depression, Quality of life, Caregivers
|
|
|
원문 및 링크아웃 정보
|
|
|
|
|
|
등재저널 정보
|
|
 
|
|
|
|
|