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논문 기본 정보

자료유형
학술저널
저자정보
김선영 (화순전남대학교병원) 김재민 (전남대학교) 김성완 (전남대학교) 강희주 (전남대학교) 이주연 (전남대학교) 신일선 (전남대학교) 심현정 (전남대학교) 윤진상
저널정보
대한생물치료정신의학회 생물치료정신의학 생물치료정신의학 제20권 제3호
발행연도
2014.12
수록면
227 - 237 (11page)

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Objectives:The primary purpose of the present study was to assess the factors associated with quality of life(QoL) of the family caregivers of terminally ill cancer patients.
Methods:A broad range of factors related to the patient-family caregiver dyad was investigated in a palliative care setting using a cross-sectional design. Caregiver QoL was assessed by the EuroQoL-5 dimensions-visual analog scale (EQ-VAS). The independent variables included patient- and caregiver-related sociodemographic and psychological factors such as depressive symptoms, subjective burden, and coping style. The clinical data of the patients were also obtained from their medical charts or gathered using measurements on face-to face interview. Multivariate linear regression analyses were conducted to identify the influences of individual factors on caregiver QoL.
Results:Of 304 analyzed dyads, multivariate analyses revealed that the psychological factors of the caregivers were significantly related to their QoL. Greater levels of depressive symptoms and subjective burden in the caregiver were significantly associated with a lower QoL, but an active coping style was associated with a higher QoL. Caregivers with a physical illness reported a lower QoL than those without an illness. However, patient-related factors were not related to caregiver QoL.
Conclusions:Caregiver’s psychological factors rather than patient’s factors are significantly related with caregiver’s QoL. Providing psychiatric screening and intervention for depression and caregiver support programs for burden and coping style are recommended for enhancing QoL in caregivers of terminally ill cancer patients.

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UCI(KEPA) : I410-ECN-0101-2016-513-001023846