Association between quality of end-of-life care and possible complicated grief among bereaved family members

J Palliat Med. 2014 Sep;17(9):1025-31. doi: 10.1089/jpm.2013.0552. Epub 2014 Jul 22.

Abstract

Background: Little is known about the association between quality of end-of-life care of a patient and complicated grief among bereaved family members.

Objective: This study aims to examine the impact of quality of end-of-life care on complicated grief among bereaved family members in a Japanese general population sample.

Methods: A mail-based cross-sectional questionnaire survey was used. A total of 641 individuals aged 40 to 79 years in the general population who lost their loved one within the period between 6 months and 10 years were enrolled. Complicated grief was assessed using the Brief Grief Questionnaire, and the bereaved family members' perceptions on quality of end-of-life care were assessed using the Care Evaluation Scale and the Good Death Inventory. Logistic regression analysis was used to identify the variables that associated with possible complicated grief.

Results: Possible complicated grief was observed in 24.5% of the participants. Three components of quality of end-of-life care, namely, dissatisfaction with the explanation to the family about the patient's expected outcome, unreasonable cost of care, and family's perception that the deceased person had not achieved a sense of completion about his or her life, were significantly associated with possible complicated grief. Spousal relationship, primary caregiver, and high psychological distress also had significant association.

Conclusions: Perceptions on quality of end-of-life care were significantly associated with complicated grief. Providing sufficient information to patients' family about expected outcome and enhancing patients' sense of completion about their life may prevent bereaved family members from developing complicated grief.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Bereavement*
  • Cross-Sectional Studies
  • Family / psychology*
  • Humans
  • Japan
  • Middle Aged
  • Quality of Health Care*
  • Surveys and Questionnaires
  • Terminal Care / standards*