Movement Disorders (revue)

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Patients', doctors', and caregivers' assessment of disability using the UPDRS‐ADL section: Are these ratings interchangeable?

Identifieur interne : 004006 ( Main/Exploration ); précédent : 004005; suivant : 004007

Patients', doctors', and caregivers' assessment of disability using the UPDRS‐ADL section: Are these ratings interchangeable?

Auteurs : Pablo Martínez-Martín [Espagne] ; Julian Benito-Le N [Espagne] ; Fernando Alonso [Espagne] ; M. José Catalán [Espagne] ; Margarita Pondal [Espagne] ; Aurelio Tobías [Espagne] ; Ivana Zamarbide [Espagne]

Source :

RBID : ISTEX:47C219A6ED629B3849896EAFB10D9A6ADDE11D3A

English descriptors

Abstract

This multicenter study sought to analyze the validity and reliability of the Unified Parkinson's Disease Rating Scale (UPDRS)‐section 2 (Activities of Daily Living, ADL) as applied by patients and caregivers. Sixty pairs of PD patients–caregivers were enrolled for study purposes. Neurologists used a set of scales to determine disease severity and patients' functional state. Patients and caregivers used adapted versions of the UPDRS‐section 2 in tandem with other measures. Wilcoxon and Mann‐Whitney tests, weighted κ, intraclass and Spearman's correlation coefficients, as well as multivariate linear regression models were applied. On the whole, PD patient self‐assessment and caregiver evaluation of patients' disability showed close concordance with neurologists' ratings. Correlation between caregiver ratings and clinical evaluation tended to be slightly lower than that for patient‐based self‐assessment. Depression showed a positive correlation with disability and had a nonsystematic influence on UPDRS‐section 2 (ADL) scores. As expected, there was a significant correlation between perceived disability and health‐related quality of life measures. Caregiver burden did not reduce the level of agreement with neurologists as to the overall rating of any given patient's disability. In PD, UPDRS‐section 2–based assessment of disability by patients themselves and caregivers is a valid and reliable outcome. © 2003 Movement Disorder Society

Url:
DOI: 10.1002/mds.10479


Affiliations:


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Le document en format XML

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<div type="abstract" xml:lang="en">This multicenter study sought to analyze the validity and reliability of the Unified Parkinson's Disease Rating Scale (UPDRS)‐section 2 (Activities of Daily Living, ADL) as applied by patients and caregivers. Sixty pairs of PD patients–caregivers were enrolled for study purposes. Neurologists used a set of scales to determine disease severity and patients' functional state. Patients and caregivers used adapted versions of the UPDRS‐section 2 in tandem with other measures. Wilcoxon and Mann‐Whitney tests, weighted κ, intraclass and Spearman's correlation coefficients, as well as multivariate linear regression models were applied. On the whole, PD patient self‐assessment and caregiver evaluation of patients' disability showed close concordance with neurologists' ratings. Correlation between caregiver ratings and clinical evaluation tended to be slightly lower than that for patient‐based self‐assessment. Depression showed a positive correlation with disability and had a nonsystematic influence on UPDRS‐section 2 (ADL) scores. As expected, there was a significant correlation between perceived disability and health‐related quality of life measures. Caregiver burden did not reduce the level of agreement with neurologists as to the overall rating of any given patient's disability. In PD, UPDRS‐section 2–based assessment of disability by patients themselves and caregivers is a valid and reliable outcome. © 2003 Movement Disorder Society</div>
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