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dc.contributor.authorBosboom, P.
dc.contributor.authorAlfonso, Helman
dc.contributor.authorEaton, J.
dc.contributor.authorAlmeida, O.
dc.date.accessioned2017-01-30T15:09:19Z
dc.date.available2017-01-30T15:09:19Z
dc.date.created2015-10-29T04:08:49Z
dc.date.issued2012
dc.identifier.citationBosboom, P. and Alfonso, H. and Eaton, J. and Almeida, O. 2012. Quality of life in Alzheimer's disease: Different factors associated with complementary ratings by patients and family carers. International Psychogeriatrics. 24 (5): pp. 708-721.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/43702
dc.identifier.doi10.1017/S1041610211002493
dc.description.abstract

Background: Quality of life (QoL) in dementia is a complex construct and factors that predict QoL ratings are unclear. We designed this study to determine: (1) the agreement in QoL ratings between community-dwelling patients with mild to moderate dementia and family carers; and (2) the factors associated with self-reported and two types of carer-reported QoL ratings: carer-carer perspective and carer-patient perspective. Methods: A cross-sectional study was carried out of 80 community-dwelling patients with the diagnosis of probable Alzheimer's disease (AD) of mild or moderate severity according to NINCDS-ADRD criteria, and their 80 family carers. The QoL-AD was the primary outcome measure. We collected patients' self-reported QoL ratings and two types of carer-reported QoL ratings: carer-patient and carer-carer perspectives. Explanatory variables included demographics, lifestyle, and clinical information from patients and carers, along with cognition, awareness, psychopathology, burden-of-care, and functionality in daily life. Bland-Altman plots guided the interpretation of agreement by visualizing the distribution of all the ratings. Univariate and multivariate regression analyses were conducted to examine the contribution of candidate explanatory factors. Results: Patients and their carers showed good agreement in their QoL ratings, although the total scores of carers (regardless of perspective) were lower than the scores of patients. Depression, insight and use of anti-dementia agents were associated with QoL self-ratings, whereas cognitive function was directly associated and depression inversely associated with carers' QoL ratings. Conclusion: Mild to moderate community-dwelling AD patients and their carers (with different perspectives) agree within an acceptable range in QoL ratings but the ratings are driven by different factors, and consequently are not interchangeable but complementary. They provide valuable information when used separately, not in a composite score. © International Psychogeriatric Association 2012.

dc.titleQuality of life in Alzheimer's disease: Different factors associated with complementary ratings by patients and family carers
dc.typeJournal Article
dcterms.source.volume24
dcterms.source.number5
dcterms.source.startPage708
dcterms.source.endPage721
dcterms.source.issn1041-6102
dcterms.source.titleInternational Psychogeriatrics
curtin.departmentEpidemiology and Biostatistics
curtin.accessStatusFulltext not available


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