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dc.contributor.authorKing, D
dc.contributor.authorFarina, Nicolas
dc.contributor.authorBurgon, C
dc.contributor.authorFeeney, Y
dc.contributor.authorBerwald, S
dc.contributor.authorBustard, E
dc.contributor.authorGallaher, L
dc.contributor.authorHabibi, R
dc.contributor.authorWittenberg, R
dc.contributor.authorComas-Herrera, A
dc.contributor.authorKnapp, M
dc.contributor.authorBanerjee, Sube
dc.date.accessioned2022-07-01T15:49:39Z
dc.date.issued2022-05-31
dc.identifier.issn1471-2318
dc.identifier.issn1471-2318
dc.identifier.other469
dc.identifier.urihttp://hdl.handle.net/10026.1/19386
dc.description.abstract

<jats:title>Abstract</jats:title><jats:sec> <jats:title>Background</jats:title> <jats:p>Research to date offers mixed evidence about the relationship between quality of life and severity of cognitive impairment in people with dementia. We aimed to investigate longitudinal changes in patient- and proxy-rated health-related quality of life (HRQL) by severity of dementia and explore factors associated with changes in HRQL over a one-year period. We used data from the MODEM longitudinal cohort study which recruited dyads of persons with clinically diagnosed dementia and their principal carer and interviewed them face-to-face at baseline and again 1 year later.</jats:p> </jats:sec><jats:sec> <jats:title>Methods</jats:title> <jats:p>Quota sampling was used to generate balanced numbers (target <jats:italic>n</jats:italic> = 100 for each severity level) of people with mild cognitive impairment (20+ on the standardised Mini-Mental State Examination (sMMSE)), moderate cognitive impairment (score 10 to 19), and severe cognitive impairment (score 0 to 9). Persons with dementia without an identifiable family carer or other informant (e.g., a formal/professional/paid carer) were excluded from the study. Participants answered a series of questions measuring their HRQL: DEMQOL, DEMQOL-proxy, EQ-5D-3 L, EQ-5D-3L proxy. Multiple regression models were built to understand the effects of baseline demographics and dementia symptoms (cognitive impairment, neuropsychiatric symptoms) on change in HRQL over 1 year.</jats:p> </jats:sec><jats:sec> <jats:title>Results</jats:title> <jats:p>Two hundred and forty-three dyads of people with clinically diagnosed dementia and carers completed baseline and follow-up interviews. Most measures of HRQL remaining relatively stable between time-points, but one index of HRQL, EQ-5D proxy, significantly declined. Depending on the HRQL measure, different factors were associated with change in HRQL. The only factor consistently associated with decline in HRQL (when compared to improvement) was having a diagnosis of a non-Alzheimer’s dementia.</jats:p> </jats:sec><jats:sec> <jats:title>Conclusions</jats:title> <jats:p>Deterioration in HRQL is not an inevitable part of the dementia journey. However, people with non-Alzheimer’s dementias may be more susceptible to HRQL decline. This may indicate that those with non-Alzheimer’s dementia may benefit from specific support focussed on maintaining their quality of life.</jats:p> </jats:sec>

dc.format.extent469-
dc.format.mediumElectronic
dc.languageen
dc.language.isoeng
dc.publisherBioMed Central
dc.subjectQuality of life
dc.subjectDementia
dc.subjectAlzheimer's disease
dc.subjectWellbeing
dc.subjectHealth
dc.subjectCognitive impairment
dc.subjectCaregiver
dc.subjectLongitudinal studies
dc.titleFactors associated with change over time in quality of life of people with dementia: longitudinal analyses from the MODEM cohort study
dc.typejournal-article
dc.typeJournal Article
dc.typeResearch Support, Non-U.S. Gov't
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000803887500003&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue1
plymouth.volume22
plymouth.publication-statusPublished
plymouth.journalBMC Geriatrics
dc.identifier.doi10.1186/s12877-022-03142-z
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/Peninsula Medical School
plymouth.organisational-group/Plymouth/Faculty of Health/Peninsula Medical School/PMS - Manual
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA03 Allied Health Professions, Dentistry, Nursing and Pharmacy
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
plymouth.organisational-group/Plymouth/Users by role/Researchers in ResearchFish submission
dc.publisher.placeEngland
dcterms.dateAccepted2022-03-14
dc.rights.embargodate2022-7-2
dc.identifier.eissn1471-2318
dc.rights.embargoperiodNot known
rioxxterms.funderEconomic and Social Research Council
rioxxterms.identifier.projectComprehensive approach to modelling outcome and cost impacts of interventions for dementia
rioxxterms.versionofrecord10.1186/s12877-022-03142-z
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2022-05-31
rioxxterms.typeJournal Article/Review
plymouth.funderComprehensive approach to modelling outcome and cost impacts of interventions for dementia::Economic and Social Research Council


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