Literature DB >> 15126228

What explains differences between dementia patients' and their caregivers' ratings of patients' quality of life?

Laura P Sands1, Patricia Ferreira, Anita L Stewart, Meryl Brod, Kristine Yaffe.   

Abstract

OBJECTIVE: The authors assessed the magnitude of discrepancy between patients' and caregivers' ratings of the patients' quality of life and sought to determine whether the discrepancies are associated with patient characteristics, caregiver characteristics, or the type of relationship between the patient and caregiver.
METHODS: A sample of 91 patients with mild-to-moderately severe dementia and their primary family caregiver rated five domains of the patients' subjective quality of life.
RESULTS: Agreement between patients and caregivers was low. Caregivers rated patients' quality of life lower than patients rated their own in all five domains. Discrepancies between patients' and caregivers' ratings were not associated with the patients' cognitive performance, level of functioning, nor caregivers' reports of aggressive, attention-seeking, or sexually inappropriate behaviors, nor whether the caregiver lived with or was married to the patient. However, discrepancies were associated with level of caregiver burden and the patients' report of depressive symptoms. Patients with depression reported low quality of life, which matched caregivers' low rating of patients' quality of life. Caregivers who reported higher levels of burden rated patients' quality of life lower than did patients in all five domains of quality of life.
CONCLUSIONS: Discrepancies between dementia patients' and their caregivers' ratings of the patients' quality of life are associated with increased levels of caregiver burden, rather than lower levels of patients' functioning. The results of this study support the direct assessment of mild-to-moderate dementia patients about their subjective quality of life.

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Year:  2004        PMID: 15126228

Source DB:  PubMed          Journal:  Am J Geriatr Psychiatry        ISSN: 1064-7481            Impact factor:   4.105


  40 in total

1.  Utility-based Quality of Life measures in Alzheimer's disease.

Authors:  Gary Naglie; George Tomlinson; Catherine Tansey; Jane Irvine; Paul Ritvo; Sandra E Black; Morris Freedman; Michel Silberfeld; Murray Krahn
Journal:  Qual Life Res       Date:  2006-05       Impact factor: 4.147

2.  Incongruent perceptions of pain and physical function among families living with lung cancer.

Authors:  Lyndsey M Miller; Karen S Lyons; Jill A Bennett
Journal:  Support Care Cancer       Date:  2015-02-12       Impact factor: 3.603

3.  Health status in patients with Alzheimer's disease: an investigation of inter-rater agreement.

Authors:  J L Novella; F Boyer; C Jochum; N Jovenin; I Morrone; D Jolly; S Bakchine; F Blanchard
Journal:  Qual Life Res       Date:  2006-06       Impact factor: 4.147

4.  Perceived mental health status of drug users with HIV: concordance between caregivers and care recipient reports and associations with caregiving burden and reciprocity.

Authors:  Mary M Mitchell; Allysha C Robinson; Jennifer L Wolff; Amy R Knowlton
Journal:  AIDS Behav       Date:  2014-06

5.  Participant-Informant Relationships Affect Quality of Life Ratings in Incipient and Clinical Alzheimer Disease.

Authors:  Amy Lin; Jenny Brook; Joshua D Grill; Edmond Teng
Journal:  Am J Geriatr Psychiatry       Date:  2016-10-13       Impact factor: 4.105

6.  Magnitude and causes of bias among family caregivers rating Alzheimer disease patients.

Authors:  Richard Schulz; Thomas B Cook; Scott R Beach; Jennifer H Lingler; Lynn M Martire; Joan K Monin; Sara J Czaja
Journal:  Am J Geriatr Psychiatry       Date:  2013-01-02       Impact factor: 4.105

7.  Psychometric properties of the EQ-5D in a study of people with mild to moderate dementia.

Authors:  Simone Kunz
Journal:  Qual Life Res       Date:  2010-02-10       Impact factor: 4.147

8.  Care Values in Dementia: Patterns of Perception and Incongruence Among Family Care Dyads.

Authors:  Lyndsey M Miller; Carol J Whitlatch; Christopher S Lee; Michael S Caserta
Journal:  Gerontologist       Date:  2019-05-17

9.  Generic quality of life assessment in dementia patients: a prospective cohort study.

Authors:  Claudia Schiffczyk; Barbara Romero; Christina Jonas; Constanze Lahmeyer; Friedemann Müller; Matthias W Riepe
Journal:  BMC Neurol       Date:  2010-06-20       Impact factor: 2.474

10.  Quality of life as an outcome in Alzheimer's disease and other dementias--obstacles and goals.

Authors:  Matthias W Riepe; Thomas Mittendorf; Hans Förstl; Lutz Frölich; Martin Haupt; Reiner Leidl; Christoph Vauth; Matthias Graf von der Schulenburg
Journal:  BMC Neurol       Date:  2009-08-25       Impact factor: 2.474

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