Zhe Lu, Li-Wen Tan, Hong Xu, Zheng-Kun Xia, Xiao-Yun Jiang, Xiao-Chuan Wu, Fang Wang, Xiao-Rong Liu, Cheng-Guang Zhao, Xiao-Zhong Li, Jian-Hua Mao, Xiao-Wen Wang, Wen-Yan Huang, Xiao-Shan Shao, Jian-Jiang Zhang, Shi-Pin Feng, Jun Yang, Qiu Li, Ai-Hua Zhang, Mo Wang
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In this study, we introduced an updated algorithm based on the European Medicines Agency (EMA) algorithm in conjunction with the American College of Rheumatology (ACR)/European Alliance of Associations for Rheumatology (EULAR) criteria. This new approach aims to resolve the issue of duplicate classification present in the 2022 ACR/EULAR criteria and to refine the existing EMA algorithm.</p><p><strong>Methods: </strong>This study included 179 pediatric patients diagnosed with AAV across 17 centers in China. Patients were classified using the EMA algorithm, the ACR/EULAR criteria, and the EMA-ACR/EULAR algorithm. The Kappa value and Net Reclassification Index (NRI) were used to evaluate the classification performance of these criteria.</p><p><strong>Results: </strong>According to the EMA algorithm, 136 (76.0%) patients were classified with microscopic polyangiitis (MPA) and 14 (7.8%) with granulomatosis with polyangiitis (GPA), while 29 (16.2%) remained unclassifiable. According to the ACR/EULAR criteria, 145 (81.0%) patients were classified with MPA, 14 (7.8%) with GPA, 2 (1.1%) with eosinophilic granulomatosis with polyangiitis (EGPA), and 4 (2.2%) with both MPA and GPA, while 14 (7.8%) remained unclassifiable. The EMA-ACR/EULAR algorithm classified 124 patients (69.3%) as MPA, 26 (14.5%) as GPA, and 2 (1.1%) as EGPA, while 27 (15.1%) were unclassified. The Kappa values between the EMA algorithm and ACR/EULAR criteria for GPA and MPA were 0.225 [95% confidence interval (CI) 0.000-0.456, P = 0.003] and 0.357 (95% CI 0.196-0.518, P < 0.001). 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引用次数: 0
摘要
背景:抗中性粒细胞细胞质抗体相关性血管炎(AAV)是一种预后较差的坏死性血管炎,在儿童中更为严重。对AAV患者进行分类有助于诊断和治疗。然而,目前儿科AAV的分类标准主要是基于成人制定的,在临床实践中存在局限性。在这项研究中,我们结合美国风湿病学会(ACR)/欧洲风湿病协会联盟(EULAR)的标准,介绍了一种基于欧洲药品管理局(EMA)算法的更新算法。这种新方法旨在解决2022年ACR/EULAR标准中存在的重复分类问题,并改进现有的EMA算法。方法:本研究纳入中国17个中心诊断为AAV的179例儿科患者。采用EMA算法、ACR/EULAR标准和EMA-ACR/EULAR算法对患者进行分类。采用Kappa值和净重分类指数(NRI)评价各指标的分类效果。结果:根据EMA算法,136例(76.0%)患者被分类为显微多血管炎(MPA), 14例(7.8%)患者被分类为肉芽肿病合并多血管炎(GPA), 29例(16.2%)患者无法分类。根据ACR/EULAR标准,145例(81.0%)患者为MPA, 14例(7.8%)为GPA, 2例(1.1%)为嗜酸性肉芽肿病合并多血管炎(EGPA), 4例(2.2%)为MPA和GPA, 14例(7.8%)仍无法分类。EMA-ACR/EULAR算法将124例(69.3%)患者分类为MPA, 26例(14.5%)为GPA, 2例(1.1%)为EGPA, 27例(15.1%)未分类。EMA算法与ACR/EULAR标准的GPA和MPA Kappa值分别为0.225和0.357[95%置信区间(CI) 0.2000 -0.456, P = 0.003]和0.357 (95% CI 0.196-0.518, P)。结论:EMA-ACR/EULAR算法解决了EMA框架内1990年ACR标准的局限性,解决了2022年ACR/EULAR标准中重复分类的问题。然而,EMA-ACR/EULAR算法在小儿AAV患者临床分型中的优越性有待进一步研究验证。
Performance of EMA algorithm, 2022 ACR/EULAR criteria, and EMA-ACR/EULAR algorithm in classifying pediatric ANCA-associated vasculitis: a national cohort study in China.
Background: Anti-neutrophil cytoplasmic antibody-associated vasculitis (AAV) is a type of necrotizing vasculitis with poor prognosis, which is more severe in children. Classifying AAV patients may be helpful for diagnosis and management. However, present classification criteria for pediatric AAV are developed mainly based on adults, which have limitations in clinical practice. In this study, we introduced an updated algorithm based on the European Medicines Agency (EMA) algorithm in conjunction with the American College of Rheumatology (ACR)/European Alliance of Associations for Rheumatology (EULAR) criteria. This new approach aims to resolve the issue of duplicate classification present in the 2022 ACR/EULAR criteria and to refine the existing EMA algorithm.
Methods: This study included 179 pediatric patients diagnosed with AAV across 17 centers in China. Patients were classified using the EMA algorithm, the ACR/EULAR criteria, and the EMA-ACR/EULAR algorithm. The Kappa value and Net Reclassification Index (NRI) were used to evaluate the classification performance of these criteria.
Results: According to the EMA algorithm, 136 (76.0%) patients were classified with microscopic polyangiitis (MPA) and 14 (7.8%) with granulomatosis with polyangiitis (GPA), while 29 (16.2%) remained unclassifiable. According to the ACR/EULAR criteria, 145 (81.0%) patients were classified with MPA, 14 (7.8%) with GPA, 2 (1.1%) with eosinophilic granulomatosis with polyangiitis (EGPA), and 4 (2.2%) with both MPA and GPA, while 14 (7.8%) remained unclassifiable. The EMA-ACR/EULAR algorithm classified 124 patients (69.3%) as MPA, 26 (14.5%) as GPA, and 2 (1.1%) as EGPA, while 27 (15.1%) were unclassified. The Kappa values between the EMA algorithm and ACR/EULAR criteria for GPA and MPA were 0.225 [95% confidence interval (CI) 0.000-0.456, P = 0.003] and 0.357 (95% CI 0.196-0.518, P < 0.001). Compared to these two criteria, the EMA-ACR/EULAR algorithm demonstrated positive NRIs in the classification of both GPA (0.702, 95% CI 0.258-1.146, P = 0.002; 0.547 95% CI 0.150-0.944, P = 0.007) and MPA (0.425, 95% CI 0.209-0.642, P < 0.001; 0.519, 95% CI 0.305-0.733, P < 0.001).
Conclusions: The EMA-ACR/EULAR algorithm addresses the limitations of the 1990 ACR criteria within the EMA framework and resolves the issue of duplicate classification in the 2022 ACR/EULAR criteria. However, further research is necessary to validate the superiority of the EMA-ACR/EULAR algorithm in the clinical classification of pediatric AAV patients.
期刊介绍:
The World Journal of Pediatrics, a monthly publication, is dedicated to disseminating peer-reviewed original papers, reviews, and special reports focusing on clinical practice and research in pediatrics.
We welcome contributions from pediatricians worldwide on new developments across all areas of pediatrics, including pediatric surgery, preventive healthcare, pharmacology, stomatology, and biomedicine. The journal also covers basic sciences and experimental work, serving as a comprehensive academic platform for the international exchange of medical findings.