Physician's global assessment of disease activity in juvenile idiopathic arthritis: consensus-based recommendations from an international task force

医学 工作队 投票 协商一致会议 关节炎 多数决原则 物理疗法 疾病 家庭医学 病理 内科学 人工智能 计算机科学 法学 政治 政治学 公共行政
作者
Veronika Rypdal,Hermine I. Brunner,Brian M. Feldman,Nicolino Ruperto,Amita Aggarwal,Sheila T. Angeles‐Han,Maria Bäckström,Erin Balay‐Dustrude,Claudia Bracaglia,Fabrizio De Benedetti,Pavla Doležalová,Marco Garrone,Jaime Guzmán,Daniel B. Horton,Ronald M. Laxer,Daniel J. Lovell,Tonje Løvli,Silvia Magni‐Manzoni,Francesca Minoia,Esi M. Morgan
出处
期刊:Annals of the Rheumatic Diseases [BMJ]
卷期号:84 (8): 1425-1436 被引量:4
标识
DOI:10.1016/j.ard.2025.01.013
摘要

To develop consensus-based recommendations for physician's global assessment of disease activity (PhGA) scoring and to standardise definitions of disease activity. An international task force of 34 members was assembled, and recommendations were developed in 3 phases: (1) 2 preliminary surveys of paediatric rheumatologists and a literature review; (2) 14 videoconference meetings, informed by multicriteria decision analysis and formal anonymous voting; and (3) a 2-day in-person consensus conference using structured nominal group technique discussions and formal voting. The threshold for achieving consensus was ≥78% of voting task force members. Agreement with the final statements was rated using a numerical rating scale from 0, strongly disagree, to 10, strongly agree. Eighteen points to consider were agreed upon. All statements achieved consensus (≥78%), with a level of agreement ≥9.2. Points included the definition of disease activity in juvenile idiopathic arthritis (JIA), factors to assess in nonsystemic JIA and systemic JIA, consideration of available imaging and laboratory tests, the role of extra-articular manifestations, the evaluation of treatment, and the timing of PhGA scoring. The task force developed consensus-based recommendations when scoring the PhGA in nonsystemic and systemic JIA. These recommendations will lead to more reliable scoring of disease activity in patients with JIA.

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