Parkinson's disease: Prevalence, diagnosis and impact.
Identifieur interne : 000650 ( PubMed/Corpus ); précédent : 000649; suivant : 000651Parkinson's disease: Prevalence, diagnosis and impact.
Auteurs : Suzy L. Wong ; Heather Gilmour ; Pamela L. Ramage-MorinSource :
- Health reports [ 1209-1367 ] ; 2014.
English descriptors
- KwdEn :
- Age Factors, Aged, Aged, 80 and over, Canada (epidemiology), Caregivers, Cross-Sectional Studies, Female, Health Expenditures, Humans, Interpersonal Relations, Male, Middle Aged, Parkinson Disease (diagnosis), Parkinson Disease (economics), Parkinson Disease (epidemiology), Prevalence, Sex Factors, Time Factors, Time-to-Treatment.
- MESH :
- diagnosis : Parkinson Disease.
- economics : Parkinson Disease.
- epidemiology : Canada, Parkinson Disease.
- Age Factors, Aged, Aged, 80 and over, Caregivers, Cross-Sectional Studies, Female, Health Expenditures, Humans, Interpersonal Relations, Male, Middle Aged, Prevalence, Sex Factors, Time Factors, Time-to-Treatment.
Abstract
This article provides information on Parkinson's disease, using the 2010/2011 Canadian Community Health Survey, the 2011/2012 Survey of Neurological Conditions in Institutions in Canada, and the 2011 Survey of Living with Neurological Conditions in Canada. An estimated 0.2% of Canadian adults in private households (55,000), and 4.9% of those in residential institutions (12,500), had Parkinson's disease. Younger age at symptom onset was associated with a longer period to disease diagnosis. As a result of the condition, 58% reported that social interactions were negatively affected, 61% reported out-of-pocket expenses, and 56% reported receiving assistance with activities such as housework, transportation or personal care. Among those receiving assistance, 84% relied at least in part on family, friends or neighbours. The primary informal caregiver tended to be a spouse (64%), female (62%), live in the same household (72%), and provide assistance on a daily basis (76%).
PubMed: 25408491
Links to Exploration step
pubmed:25408491Le document en format XML
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<author><name sortKey="Gilmour, Heather" sort="Gilmour, Heather" uniqKey="Gilmour H" first="Heather" last="Gilmour">Heather Gilmour</name>
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<author><name sortKey="Ramage Morin, Pamela L" sort="Ramage Morin, Pamela L" uniqKey="Ramage Morin P" first="Pamela L" last="Ramage-Morin">Pamela L. Ramage-Morin</name>
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<term>Health Expenditures</term>
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<front><div type="abstract" xml:lang="en">This article provides information on Parkinson's disease, using the 2010/2011 Canadian Community Health Survey, the 2011/2012 Survey of Neurological Conditions in Institutions in Canada, and the 2011 Survey of Living with Neurological Conditions in Canada. An estimated 0.2% of Canadian adults in private households (55,000), and 4.9% of those in residential institutions (12,500), had Parkinson's disease. Younger age at symptom onset was associated with a longer period to disease diagnosis. As a result of the condition, 58% reported that social interactions were negatively affected, 61% reported out-of-pocket expenses, and 56% reported receiving assistance with activities such as housework, transportation or personal care. Among those receiving assistance, 84% relied at least in part on family, friends or neighbours. The primary informal caregiver tended to be a spouse (64%), female (62%), live in the same household (72%), and provide assistance on a daily basis (76%).</div>
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<Abstract><AbstractText>This article provides information on Parkinson's disease, using the 2010/2011 Canadian Community Health Survey, the 2011/2012 Survey of Neurological Conditions in Institutions in Canada, and the 2011 Survey of Living with Neurological Conditions in Canada. An estimated 0.2% of Canadian adults in private households (55,000), and 4.9% of those in residential institutions (12,500), had Parkinson's disease. Younger age at symptom onset was associated with a longer period to disease diagnosis. As a result of the condition, 58% reported that social interactions were negatively affected, 61% reported out-of-pocket expenses, and 56% reported receiving assistance with activities such as housework, transportation or personal care. Among those receiving assistance, 84% relied at least in part on family, friends or neighbours. The primary informal caregiver tended to be a spouse (64%), female (62%), live in the same household (72%), and provide assistance on a daily basis (76%).</AbstractText>
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