Impact of informal cancer caregiving across the cancer experience: A systematic literature review of quality of life
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CDC STACKS serves as an archival repository of CDC-published products including scientific findings, journal articles, guidelines, recommendations, or other public health information authored or co-authored by CDC or funded partners. As a repository, CDC STACKS retains documents in their original published format to ensure public access to scientific information.
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Impact of informal cancer caregiving across the cancer experience: A systematic literature review of quality of life

Filetype[PDF-832.03 KB]


English

Details:

  • Alternative Title:
    Palliat Support Care
  • Personal Author:
  • Description:
    Objective

    Informal caregiving may likely increase as the number of cancer survivors grows. Caregiving responsibilities can impact caregivers’ quality of life (QoL). Understanding the current state of the science regarding caregiving QoL could help inform future research and intervention development.

    Methods

    A systematic literature review in PubMed/Medline examined research on QoL among informal cancer caregivers and related psychosocial health outcomes. Original research articles in English, published between 2007 and 2017 about caregivers (aged ≥18 years) of adult cancer patients in the United States were included. Abstracted articles were categorized according to caregiving recipient’s phase of survivorship (acute, middle to long-term, end of life/bereavement).

    Results

    Of 920 articles abstracted, 60 met inclusion criteria. Mean caregiver age ranged from 37 to 68 with the majority being female, non-Hispanic white, with at least a high school degree, and middle income. Almost half of the studies focused on caregivers who provided care for survivors from diagnosis through the end of active treatment. Studies examined physical health, spirituality, psychological distress, and social support. Differences in QoL were noted by caregiver age, sex, and employment status.

    Significance of Results

    Additional research include the examination of the needs of diverse cancer caregivers and determine how additional caregiver characteristics (e.g., physical functioning, financial burden, etc.) affect QoL, including studies examining caregiver QoL in the phases following the cessation of active treatment and assessments of health systems, support services, and insurance to determine barriers and facilitators to meeting the immediate and long-term needs of cancer caregivers.

  • Subjects:
  • Source:
  • Pubmed ID:
    31588882
  • Pubmed Central ID:
    PMC8678891
  • Document Type:
  • Funding:
  • Volume:
    18
  • Issue:
    2
  • Collection(s):
  • Main Document Checksum:
  • Download URL:
  • File Type:

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