The inclusion of caregivers in a holistic care approach represents a basic principle in palliative care. However, many palliative care professionals have a lack of understanding of difficulties or unmet needs among caregivers. To enhance the quality of life of caregivers and the quality of care for patients, healthcare professionals should be better informed about the constructs of caregiver burden. The aim of this study is to synthesize the concept of caregiver burden in palliative care, providing implications for the caregivers and their support systems. This concept analysis study adopts the integrative review approach and the basic text analysis method (ie, word frequency). The PubMed, CINAHL, Embase, and PsycINFO databases are explored for eligible studies.From this literature search, 66 articles from 1998 to 2018 are located. After data collection is completed, the two authors independently evaluate the quality of studies published before 1 September 2018. The caregiver burden is then redefined with its attributes, antecedents, consequences, empirical referents, and facilitators. It is recommended that the multidimensional concept of caregiver burden in palliative care be measured by considering caregiver characteristics and the caregiving context. K E Y W O R D S caregiver burden, concept analysis, integrative review, palliative care, word frequency 1 | BACKGROUND Developments in medical technology and the management of illness have increased the prognosis of terminally ill patients. As a result, caregivers have experienced the increased burden of caring for family members for an extended period of time. 1 Due to the decreasing number of days in hospital stays and the lack of financial support for home care services in palliative care, family caregivers are regarded as hidden patients or second-order patients. 2 Previous studies have reported that family caregivers experience a considerable burden from caregiving, and they become severely depressed and socially isolated from their communities. 3-5 For example, Grunfeld et al 6 and Grant et al 7 identified caregiver burden as one of the factors that most influence anxiety and depression in caregivers and more caregivers suffer from higher levels of perceived burden at the patientsʼ end-of-life than at the start of the palliative care according to their longitudinal studies. This increasing caregiver burden in palliative care can be explained by patientsʼ declining health status, increasing demands for patientsʼ symptom management, and the need for decisions regarding terminal care (ie, enteral tube feeding, advance care planning, and do-not-resuscitate). Nevertheless, numerous family caregivers do not perceive their burden as problematic. De Korte-Verhoef et al, 8 found that even though 66% of family caregivers experienced a severe burden from caregiving, only 25% indicated that their burden had a negative impact on their daily lives. To improve family caregiversʼ quality of life and the quality of care the caregivers can deliver to their patients, the burd...