A cohort study of the impact of COVID-19 on the quality of life of people newly diagnosed with dementia and their family carers.
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Authors
Read, Sanna
Hu, Bo
Wittenberg, Raphael
Grahamslaw, Amanda
Karim, Anomita
Martin, Evelyn
Nuzum, Eleanor
Reichental, Jacob
Russell, Alice
Siddle, Elaine
Storey, Bryony
Tipping, Eva
Baxter, Kate
Birks, Yvonne
Brayne, Carol
Brimblecombe, Nicola
Dangoor, Margaret
Dixon, Josie
Gridley, Kate
Harris, Peter R
Knapp, Martin
Miles, Eleanor
Perach, Rotem
Robinson, Louise
Rusted, Jennifer
Stewart, Rob
Thomas, Alan J
Banerjee, Sube
Publication Date
2022Journal Title
Alzheimers Dement (N Y)
ISSN
2352-8737
Publisher
Wiley
Language
eng
Type
Article
This Version
VoR
Metadata
Show full item recordCitation
Hicks, B., Read, S., Hu, B., Wittenberg, R., Grahamslaw, A., Karim, A., Martin, E., et al. (2022). A cohort study of the impact of COVID-19 on the quality of life of people newly diagnosed with dementia and their family carers.. Alzheimers Dement (N Y) https://doi.org/10.1002/trc2.12236
Abstract
INTRODUCTION: COVID-19 has impacted people with dementia and their family carers, yet little is known about effects on overall quality of life. METHODS: In a UK cohort study, pre- and post-pandemic data were collected from 114 carers and 93 recently diagnosed people with dementia. Latent growth curve modeling examined change in quality of life. RESULTS: Carers reported significant decline in quality of life, although no change was demonstrated by people with dementia. In multivariable analyses, higher levels of cognitive impairment, deprivation, study site, and lower number of memory clinic contacts were associated with greater decline in carer quality of life. DISCUSSION: Maintaining life quality for people with dementia during the pandemic appears to have come at the expense of their family carers. This inequity has fallen hardest on those caring for people with more severe dementia, in deprived areas, and with least support from memory services. These effects may be prevented or reversed by post-diagnostic care.
Keywords
COVID‐19, cohort study, dementia, inequalities, inequities, post‐diagnostic care, quality of life
Identifiers
35509503, PMC9060551
External DOI: https://doi.org/10.1002/trc2.12236
This record's URL: https://www.repository.cam.ac.uk/handle/1810/337819
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