Current Validated Clinical and Patient Reported Disease Outcome Measures in Juvenile Idiopathic Arthritis.

IF 1.7 Q3 RHEUMATOLOGY
Open Access Rheumatology-Research and Reviews Pub Date : 2023-10-09 eCollection Date: 2023-01-01 DOI:10.2147/OARRR.S261773
Erin Balay-Dustrude, Susan Shenoi
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Abstract

Juvenile idiopathic arthritis (JIA) is a common chronic illness in childhood and comprises seven categories based on the International League of Associations for Rheumatology (ILAR) criteria. Accurate assessment and measurement of the clinical, functional, and quality of life outcomes of patients with JIA are paramount for understanding the disease course and formulating effective treatment strategies. Interest in the development and use of outcome measurements specifically focused on rheumatologic conditions has greatly expanded over the last two decades, adding to and improving upon the established disease measures. Furthermore, many of these measures have been validated using the widely accepted Outcome Measures in Rheumatology (OMERACT) core principles of instrument validation, allowing researchers and clinicians to gain confidence in these tools. This review summarizes the current validated disease outcome measures in JIA, including clinical, imaging, patient-reported, and functional outcome measurement tools, and highlights ongoing work that continues to refine and improve upon the available tools. The clinical disease outcome measures discussed in this review include physician global assessment (PhGA), American College of Rheumatology (ACR, Wallace) criteria for clinical inactive disease and clinical remission, juvenile arthritis disease activity scores (JADAS), juvenile spondyloarthritis disease activity index (JSPaDA), juvenile arthritis damage index (JADAI), and the ACR pediatric response scores. The imaging outcome measures discussed include the Dijkstra composite scores, childhood arthritis radiographic score of the hip (CARSH), and Poznanski Score. The patient-reported disease outcome measures discussed include patient global assessment (PtGA), patient-reported outcome measurement information system for JIA (PROMIS), juvenile arthritis parent/child centered disease assessment index (JAPAI, JACAI), juvenile arthritis multidimensional assessment report (JAMAR), and the Pediatric quality of life inventory rheumatology module (PedsQL). The functional outcome tools discussed include the Childhood Health Assessment Questionnaire (CHAQ), juvenile arthritis functionality scale and index (JAFS and JASI), and Juvenile Arthritis Functional Assessment Report and Scale (JAFAS and JAFAR).

Abstract Image

青少年特发性关节炎目前已验证的临床和患者报告的疾病结果指标。
青少年特发性关节炎(JIA)是一种常见的儿童慢性疾病,根据国际风湿病协会联盟(ILAR)的标准分为七类。准确评估和测量JIA患者的临床、功能和生活质量结果对于了解病程和制定有效的治疗策略至关重要。在过去的二十年里,人们对开发和使用专门针对风湿病学条件的结果测量的兴趣大大增加,增加并改进了既定的疾病测量。此外,这些测量中的许多已经使用广泛接受的风湿病结果测量(OMERACT)仪器验证的核心原则进行了验证,使研究人员和临床医生能够对这些工具充满信心。这篇综述总结了目前在JIA中验证的疾病结果测量,包括临床、成像、患者报告和功能结果测量工具,并强调了正在进行的工作,这些工作将继续完善和改进现有的工具。本综述中讨论的临床疾病结果指标包括医师全球评估(PhGA)、美国风湿病学会(ACR,Wallace)临床非活动性疾病和临床缓解标准、青少年关节炎疾病活动评分(JADAS)、青少年脊椎关节炎疾病活动指数(JSPaDA)、,以及ACR儿科反应评分。所讨论的影像学结果指标包括Dijkstra综合评分、儿童关节炎髋关节影像学评分(CARSH)和Poznanski评分。讨论的患者报告的疾病结果指标包括患者总体评估(PtGA)、患者报告的JIA结果测量信息系统(PROMIS)、以青少年关节炎父母/儿童为中心的疾病评估指数(JAPAI,JACAI)、青少年关节炎多维评估报告(JAMAR)和儿科生活质量清单风湿病模块(PedsQL)。讨论的功能结果工具包括儿童健康评估问卷(CHAQ)、青少年关节炎功能量表和指数(JAFS和JASI)以及青少年关节炎能力评估报告和量表(JAFAS和JAFAR)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.80
自引率
0.00%
发文量
34
审稿时长
16 weeks
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