How do patients with Alzheimer disease rate their overall quality of life?

Am J Geriatr Psychiatry. 2005 Jun;13(6):484-90. doi: 10.1176/appi.ajgp.13.6.484.

Abstract

Objective: The authors asked how Alzheimer disease (AD) patients assess their overall quality of life (QOL) and sought to determine the characteristics associated with this assessment.

Methods: The authors performed a cross-sectional survey of 193 persons with mild-to-severe-stage AD in a University Memory Disorders Clinic using a single-item self-assessment of overall QOL.

Results: The 181 of 193 patients (94%) able to complete a single-item QOL self-rating had less severe dementia than patients not able to complete, but some had Mini-Mental State Exam scores as low as 0. Most patients rated their QOL as "good" (35%) or "very good" (36%). Latino patients, patients with less education, and depressed patients were more likely to rate their QOL lower. Among patients able to estimate how they thought their family caregiver would rate their QOL (N=173; 90%), there was moderate agreement between this estimate and their self-ratings.

Conclusion: A single-item global rating of patient QOL could prove useful in assessing QOL of most mild-to-severe-stage AD patients. Affective impairment, more than cognitive or functional impairment, drives this assessment. Screening for and addressing depressive symptoms could improve AD patients' QOL. Despite impairments in insight, patients see a difference in how their caregivers would rate their QOL.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / psychology*
  • Caregivers
  • Cross-Sectional Studies
  • Female
  • Humans
  • Male
  • Middle Aged
  • Mood Disorders / epidemiology
  • Mood Disorders / etiology
  • Mood Disorders / psychology
  • Prevalence
  • Quality of Life / psychology*
  • Severity of Illness Index
  • Surveys and Questionnaires