A review of the measurement of caregiver and family burden in palliative care

J Palliat Care. 1998 Summer;14(2):37-45.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Caregivers* / psychology
  • Cost of Illness*
  • Family* / psychology
  • Health Services Needs and Demand
  • Humans
  • Psychometrics
  • Quality of Life
  • Reproducibility of Results
  • Surveys and Questionnaires / standards*
  • Terminal Care* / economics
  • Terminal Care* / psychology