儿科残疾评估量表--患者报告结果的心理计量特性:一种可用于认知的功能表现测量方法。

IF 3.8 2区 医学 Q1 CLINICAL NEUROLOGY Developmental Medicine and Child Neurology Pub Date : 2024-11-04 DOI:10.1111/dmcn.16117
Jessica M Kramer, Pengsheng Ni, Beth Pfeiffer, Andrew Persch, Fiorella Guerrero Calle, Ariel Schwartz, Elizabeth Barbour, Daniel K Davies
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引用次数: 0

摘要

目的:评估儿科残疾评估量表--患者报告结果(PEDI-PRO)的结构有效性、内部可靠性和测量不变性:这是一项横断面研究,共有306名14至22岁(平均18岁10个月,标准差2岁5个月)的发育障碍青少年(43.1%仅患有自闭症谱系障碍,23.9%患有智力障碍,17.6%患有其他残疾,11.4%同时患有自闭症谱系障碍和智力障碍,3.9%下落不明)完成了PEDI-PRO。根据基于共识的健康测量工具选择标准(COSMIN),我们进行了确认性因素分析,应用了Rasch评分量表模型,检验了克朗巴赫α、Rasch人信度和分离系数以及差异项目功能(DIF):日常活动和行动领域的结构效度良好,社会/认知领域的结构效度可以接受。李克特三点反应量表的功能符合预期。所有领域在所有标准上的内部一致性均可接受。每个领域都有一两个项目出现了 DIF,但对所有领域得分的影响均小于 1.0 临界值:易于认知的设计和创新性的概念测量框架可能是得出这些令人鼓舞的结果的原因。PEDI-PRO填补了高质量患者报告结果测量的空白,可评估发育障碍青少年的优先结果。
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Psychometric properties of the Pediatric Evaluation of Disability Inventory - Patient Reported Outcome: A cognitively accessible measure of functional performance.

Aim: To evaluate the structural validity, internal reliability, and measurement invariance of the Pediatric Evaluation of Disability Inventory - Patient Reported Outcome (PEDI-PRO), a measure of functional performance of discrete tasks required to participate in everyday life situations important for adulthood.

Method: This was a cross-sectional study with 306 young people aged 14 to 22 years (mean 18 years 10 months, SD 2 years 5 months) with developmental disabilities (43.1% autism spectrum disorder only, 23.9% intellectual disability, 17.6% other disability, 11.4% both autism spectrum disorder and intellectual disability, 3.9% missing) completed the PEDI-PRO. Following COnsensus-based Standards for selection of health Measurement INstruments (COSMIN) criteria, we conducted a confirmatory factor analysis, applied a Rasch rating-scale model, examined Cronbach's alpha, Rasch person reliability and separation coefficients, and differential item functioning (DIF).

Results: Structural validity was good for the daily activities and mobility domains, and acceptable for the social/cognitive domain. The 3-point Likert response scale functioned as intended. All domains demonstrated acceptable internal consistency on all criteria. One or two items in each domain demonstrated DIF, but the impact on all domain scores was less than 1.0 threshold.

Interpretation: The cognitively accessible design and innovative conceptual measurement framework probably contributed to these promising findings. The PEDI-PRO addresses a gap in high-quality patient-reported outcome measures that assess priority outcomes for young people with developmental disabilities.

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来源期刊
CiteScore
7.80
自引率
13.20%
发文量
338
审稿时长
3-6 weeks
期刊介绍: Wiley-Blackwell is pleased to publish Developmental Medicine & Child Neurology (DMCN), a Mac Keith Press publication and official journal of the American Academy for Cerebral Palsy and Developmental Medicine (AACPDM) and the British Paediatric Neurology Association (BPNA). For over 50 years, DMCN has defined the field of paediatric neurology and neurodisability and is one of the world’s leading journals in the whole field of paediatrics. DMCN disseminates a range of information worldwide to improve the lives of disabled children and their families. The high quality of published articles is maintained by expert review, including independent statistical assessment, before acceptance.
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