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Published on: August 22, 2012
Public Health
Claire Godard-Sebillotte1, Sanjna Navani1, Wang Xia1
1McGill University, Montreal, QC, Canada.
Introduction:
Burgeoning literature reports inequities in dementia diagnosis and care; evidence from a universal health care system using a comprehensive set of indicators and an intersectional approach is lacking.
Methods:
We conducted a repeated yearly cohort study of community-dwelling people in Quebec with incident dementia (2000-2017). We described dementia diagnosis and 23 indicators of health service use and mortality across levels of material deprivation, derived from a validated ecological index based on the average income, employment, and education of residential neighborhoods. We then conducted preliminary description of patterns of primary care use across material deprivation and a neighborhood racialization index, derived from a census question around self-identification as visible minority.
Results:
Of the 193,834 community-dwelling people with a new diagnosis of dementia, around 20% belonged to each material deprivation category. Age-standardised rates of 15/23 indicators differed across SES. People from most deprived areas had more hospitalisations, emergency department visits, potentially inappropriate medication prescriptions, and higher 1-year mortality, though they had higher care continuity. Conversely, rates were comparable across groups for the prescription of dementia-specific medications, and primary care visits. Patterns of primary care use varied across material deprivation and neighborhood racialization; with higher use in wealthiest neighborhoods, the highest use being in the most racialized ones.
Discussion:
Despite global findings of higher dementia incidence in lower SES, we found similar incidence across SES. These findings indicate that there is likely severe under-diagnosis of dementia in more materially deprived neighborhoods. Stark differences across SES in service use by people with dementia may indicate different health needs and/or allude to pervasive health inequities. An intersectional lens allows for a nuanced description of inequalities. These results can inform policies to offer equitable, appropriate, and needs-based care to all people living with dementia.
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