Factors Associated With the Variability in Caregiver Assessments of the Capacities of Patients With Alzheimer Disease

Abstract

Background:

Several studies have identified certain caregiver factors that can produce variability in their assessments of the capacities of patients with Alzheimer disease (AD).

Objectives:

To identify the caregiver variables associated with variability in their ratings of patients’ capacities.

Methods:

Consecutive sample of 221 outpatients with AD and their family caregivers. The capacities evaluated by caregivers were the degree of functional disability, using the Disability Assessment for Dementia (DAD); psychological and behavioral symptoms, via the Neuropsychiatric Inventory (NPI); anosognosia, with the Anosognosia Questionnaire-Dementia (AQ-D); and quality of life, using the Quality of Life in AD (QOL-AD). The relationship between these measures and caregiver’s gender, burden, depression, and health was analyzed by means of a bivariate analysis, calculating the effect size (Cohen d) and subsequently by a regression analysis, calculating the contribution coefficient (CC).

Results:

The greatest variability in caregiver assessments was observed in relation to patients with early-stage dementia, where caregiver’s burden was the main factor associated with a more negative evaluation (d = 1.02-1.25). Depression in the caregiver was associated with less variability and only in the assessments of patients with moderate dementia (d = 0.38-0.69). In the regression analysis, caregiver factors were associated with greater variance in scores on the NPI (CC = 37.4%) and QOL-AD (CC = 27.2%), and lower variance in AQ-D (CC = 21.6%) and DAD (CC = 10.3%) scores.

Conclusions:

Caregiver’s burden and depression were associated with more negative assessments of patients’ psychological and behavioral symptoms and quality of life.