The Measurement Performance of the Parkinson's Disease Activities of Daily Living, Interference, and Dependence Instrument

被引:2
|
作者
Deal, Linda S. [1 ]
Andrae, David A. [2 ]
Myers, Daniela E. [3 ]
Johnson, Nathan [4 ]
Foster, Brandon [2 ]
Evans, Christopher J. [2 ]
机构
[1] Pfizer Inc, Patient Ctr Outcomes Assessment, New York, NY 10017 USA
[2] Endpoint Outcomes, Outcomes Res, Boston, MA USA
[3] Pfizer Inc, Hlth Econ & Outcomes Res, Collegeville, PA USA
[4] Endpoint Outcomes, Outcomes Res, Long Beach, CA USA
来源
FRONTIERS IN NEUROLOGY | 2022年 / 13卷
关键词
Parkinson's disease; patient-reported outcomes; activities of daily living; reliability; validity;
D O I
10.3389/fneur.2022.760174
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Parkinson's disease is a neurodegenerative disease that can be associated with motor fluctuations that result in substantial negative impact to an individual's activities of daily living. Understanding the patient's perspective about the impact of Parkinson's disease therapies is an important part of drug development and shared treatment decision-making. The objective of this research was to examine the structure, scoring, internal consistency, test-retest reliability, and concurrent and known groups validity of the Parkinson's Disease Activities of Daily Living, Interference and Dependence (PD-AID) instrument, a new, patient-reported outcomes instrument, developed to assess the clinical benefit of Parkinson's disease treatment from the patient's perspective. This was a non-interventional study among persons with mild-to-moderate Parkinson's disease currently using and responding to L-Dopa. The structure of the measure was confirmed applying item response theory to data from baseline, supporting 4 candidate scores. Baseline Patient Global Impression of Severity ratings facilitated known-groups analysis. Data from all participants were used to estimate test-retest reliability. Concurrent validity was assessed using correlations with related measures. Participants (n = 94) were mean age 69 years (mean time since diagnosis 6.9 years); 34 experienced L-Dopa-related dyskinesia. Psychometric models supported 4 candidate scoring regimes for the PD-AID. All exhibited adequate reliability and validity characteristics and strong internal consistency. Correlations with reference measures were in the expected direction and range of magnitude. Analyses supported the PD-AID as fit-for-purpose, producing psychometrically sound scores. Further research to confirm the measurement properties of the PD-AID in an expanded sample and to establish thresholds for meaningful score changes is recommended.
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页数:9
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