Caregiving experiences of Korean family caregivers of cancer patients: An integrative literature review

Abstract Objective The purpose of this study was to describe the experiences of Korean family caregivers of patients with cancer by reviewing recent literature. Methods Five electronic databases were searched—MEDLINE, the Cumulative Index to Nursing and Allied Health Literature (CINAHL), and PubMed for English literature, and Korean Information Service System (KISS), and Research Information Sharing Service (RISS) for Korean literature for articles published from January 2010 to March 2020 using the key words cancer, caregiver, and Korean. Twenty‐six articles met the inclusion criteria and remained in the final review. Results No intervention study was found and most of studies were quantitative without theoretical/conceptual framework. All the studies were conducted with Koreans living in Korea. No previous study has been conducted with Koreans living in the U.S. or other countries. Most studies focused on caregivers' quality of life, burden, unmet needs, and resilience/adaptation/post‐traumatic growth. Conclusions Comprehensive intervention studies focused on improving quality of life, burden, and adaptation to their complex roles as caregivers in the context of Korean culture would be helpful. Further research is needed in examining the caregiver‐patient dyad interactions longitudinally to understand the dynamic complicated processes of caregiving.