Family caregivers’ subjective caregiving burden, quality of life, and depressive symptoms are associated with terminally ill cancer patients’ distinct patterns of conjoint symptom distress and functional impairment in their last 6 months of life

Family caregivers constitute a critical component of the end-of-life (EOL) care system with considerable cost to themselves. However, the joint association of terminally ill cancer patients' symptom distress and functional impairment with caregivers' subjective caregiving burden, quality of life (QOL), and depressive symptoms remains unknown.

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