Abstract
This article reviews recent studies (published in 2010 and 2011) dealing with cancer caregivers' needs. The studies are organized by the phase of the illness trajectory studied and the association with demographic characteristics and quality-of-life outcomes.
The findings indicate that the major issues faced were: caregivers' needs for managing the psychological concerns of the patient as well as their own concerns, managing the patients' medical symptoms and side effects, and obtaining help with daily tasks. These needs vary across the patient's illness trajectory. Although fairly consistently mentioned during the end-of-life and bereavement phases, spiritual concerns caregivers are facing in cancer care were not systematically documented in other phases of survivorship. The caregivers' needs were often not satisfactorily met. Caregivers who are younger and lack social resources appear to report greater unmet needs and poorer quality of life. Caregivers' unmet needs are strong and consistent predictors of poor mental health.
The findings suggest that programs must be developed for caregivers who are younger and lack social resources and who report greater unmet needs and poorer quality of life. Also, future efforts need to include longitudinal studies that bridge survivorship and bereavement phases.
