Volume 21, Issue 1 pp. 50-56
Research Article

Dementia patients caregivers quality of life: the PIXEL study

Philippe Thomas

Corresponding Author

Philippe Thomas

University Department of Psychogeriatrics & Memory Clinic CH Limoges, France

University Department of Psychogeriatrics, 15 rue du Dr Marcland, CH Esquirol, 87025, Limoges, France.Search for more papers by this author
Fabrice Lalloué

Fabrice Lalloué

University Department of Psychogeriatrics & Memory Clinic CH Limoges, France

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Pierre-Marie Preux

Pierre-Marie Preux

Functional Unit of Biostatistics and Clinic Research, CHU Limoges, France

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Cyril Hazif-Thomas

Cyril Hazif-Thomas

CHG Psychiatric Unit, Quimperlé, France

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Sylvie Pariel

Sylvie Pariel

Geriatrics Unit, Ivry Hospital Center, Ivry, France

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Robcis Inscale

Robcis Inscale

Geriatrics Unit, Ivry Hospital Center, Ivry, France

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Joël Belmin

Joël Belmin

Geriatrics Unit, Ivry Hospital Center, Ivry, France

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Jean-Pierre Clément

Jean-Pierre Clément

University Department of Psychogeriatrics & Memory Clinic CH Limoges, France

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First published: 02 December 2005
Citations: 156

Abstract

Background

Alzheimer's disease and related syndromes have heavy social and human consequences for the patient and his family. Beyond the neuropsychiatric effects of specific therapies for dementia, one of today's challenges is the quality of life for both patients and their informal caregivers.

Objectives

This survey tends to determine parameters influencing caregivers' quality of life, and its possible link with patients' quality of life.

Methods

A scale measuring caregivers' quality of life, developed from data from previous PIXEL studies was used. It is a questionnaire composed of 20 items. The scale was related to the socio-demographic data of both patients and their main caregivers, to the ADRQL scale (Alzheimer Disease Related Quality Life) of Rabins for the QoL of dementia patients, to the patients medical and therapeutic data, specially a neuropsychological inventory: Folstein's cognition test, Cornell's depression scale, the fast battery of frontal assessment, Katz's dependence index, Cummings' neuropsychiatric inventory for behavioral and psychological symptoms of dementia and to a physician evaluation of caregiver's depression.

Results

One hundred patients diagnosed with dementia who live at home with their principal caregivers were recruited for this survey. Patients were 80.2 ± 6.8 years old and caregivers were 65.7 ± 12.8 years old. The caregivers' quality of life was correlated to the quality of life of the patients they cared for, the importance of behavioral disorders, and the duration of dementia evolution. Women caregivers had a worse quality of life and were more depressive than men.

Discussion

Caregivers' and patients' quality of life are related and both share a community of distress. Copyright © 2005 John Wiley & Sons, Ltd.

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