Factors affecting health‐related quality of life amongst Asian patients with Parkinson’s disease
Identifieur interne : 000E02 ( Main/Exploration ); précédent : 000E01; suivant : 000E03Factors affecting health‐related quality of life amongst Asian patients with Parkinson’s disease
Auteurs : Y. J. Zhao [Singapour] ; L. C. S. Tan [Singapour] ; P. N. Lau [Singapour] ; W. L. Au [Singapour] ; S. C. Li [Australie] ; N. Luo [Singapour]Source :
- European Journal of Neurology [ 1351-5101 ] ; 2008-07.
English descriptors
Abstract
Background and purpose: This cross‐sectional study was carried out to identify factors predicting health‐related quality of life (HRQoL) amongst Asian patients with Parkinson’s disease (PD). Methods: A total of 183 PD patients (mean age: 61 years, male: 68.9%) attending a tertiary neuroscience clinic in Singapore completed the English or Chinese version of the 8‐item Parkinson’s Disease Questionnaire (PDQ‐8). Patients’ socio‐demographic characteristics and their clinical variables were analysed to identify factors influencing the PDQ‐8 Summary Index and responses to its eight dimensions. Results: In the multiple linear regression model, the use of Chinese survey, higher motor score and longer duration of PD were associated with poorer overall HRQoL. The multiple logistic regression analyses showed that female patients and patients with higher Hoehn and Yahr stage were more probably to report worse emotional well‐being; patients who completed Chinese survey reported more problems with mobility, cognition and stigma; patients with higher motor scores were more probably to report problems with activities of daily living; patients with longer duration of PD were more probably to report problems with mobility, social support, communication and stigma. Conclusion: Both socio‐demographic factors and disease‐specific variables influence HRQoL in PD patients; the effects of culture‐related factors on HRQoL should not be overlooked when assessing HRQoL in multi‐cultural settings.
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DOI: 10.1111/j.1468-1331.2008.02178.x
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Li</name><affiliation wicri:level="1"><country xml:lang="fr">Australie</country><wicri:regionArea>Discipline of Pharmacy & Experimental Pharmacology, School of Biomedical Sciences, University of Newcastle</wicri:regionArea><wicri:noRegion>University of Newcastle</wicri:noRegion></affiliation></author><author><name sortKey="Luo, N" sort="Luo, N" uniqKey="Luo N" first="N." last="Luo">N. 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Methods: A total of 183 PD patients (mean age: 61 years, male: 68.9%) attending a tertiary neuroscience clinic in Singapore completed the English or Chinese version of the 8‐item Parkinson’s Disease Questionnaire (PDQ‐8). Patients’ socio‐demographic characteristics and their clinical variables were analysed to identify factors influencing the PDQ‐8 Summary Index and responses to its eight dimensions. Results: In the multiple linear regression model, the use of Chinese survey, higher motor score and longer duration of PD were associated with poorer overall HRQoL. The multiple logistic regression analyses showed that female patients and patients with higher Hoehn and Yahr stage were more probably to report worse emotional well‐being; patients who completed Chinese survey reported more problems with mobility, cognition and stigma; patients with higher motor scores were more probably to report problems with activities of daily living; patients with longer duration of PD were more probably to report problems with mobility, social support, communication and stigma. 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