Clinical manifestations, treatment and prognosis of juvenile idiopathic arthritis with pulmonary involvement in China: a single centre study.

IF 3.4 4区 医学 Q2 RHEUMATOLOGY Clinical and experimental rheumatology Pub Date : 2024-11-01 Epub Date: 2024-09-09 DOI:10.55563/clinexprheumatol/udjbtq
Fengqiao Gao, Junmei Zhang, Jianghong Deng, Weiying Kuang, Xiaohua Tan, Chao Li, Shipeng Li, Xuanyi Liu, Caifeng Li
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Abstract

Objectives: In recent years, the distinct clinical presentations and elevated mortality rates of various subtypes of juvenile idiopathic arthritis (JIA) with pulmonary involvement have garnered significant attention. This study aimed to elucidate the clinical characteristics of pulmonary involvement in patients with JIA to improve clinicians' knowledge.

Methods: This single-centre retrospective study analysed the baseline data, treatment options, follow-up of sixty patients of JIA with pulmonary involvement in China. Patients with interstitial lung disease (ILD) were further classified in accordance with the 2013 American Thoracic Society/European Respiratory Society International multidisciplinary consensus on idiopathic interstitial pneumonia.

Results: Sixty patients (5.03%) with JIA were complicated with pulmonary involvement. The highest subtype was systemic JIA (sJIA, 63.3%), followed by rheumatoid factor (RF)-positive polyarthritis (pJIA, 25.0%). The incidence of macrophage activation syndrome (MAS) was 21.6%. The most common diagnosis was ILD (90%). Respiratory symptoms/signs were initially experienced by 61.7% of the patients, and respiratory support was required by 21.7%. High-resolution CT classification of sJIA revealed non-specific interstitial pneumonia (NSIP) and organising pneumonia. High-resolution CT classification of pJIA was NSIP and usually interstitial pneumonia (UIP). Patients were treated with NSAIDs, along with glucocorticoids, DMARDs, and biological agents. The survival rates after 1 and 5 years were approximately 93.3% and 90.0%, respectively.

Conclusions: Patients with JIA with pulmonary involvement present with early onset, high mortality rate. JIA patients should undergo physical examination thoroughly and high-resolution CT scans, lung function tests for evaluating and monitoring the occurrence and development of pulmonary involvement in early stages to improve prognosis.

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中国肺部受累的幼年特发性关节炎的临床表现、治疗和预后:一项单中心研究。
目的:近年来,各种亚型幼年特发性关节炎(JIA)肺部受累的不同临床表现和较高的死亡率引起了广泛关注。本研究旨在阐明幼年特发性关节炎患者肺部受累的临床特征,以提高临床医生的知识水平:这项单中心回顾性研究分析了中国 60 例肺部受累 JIA 患者的基线数据、治疗方案和随访情况。根据2013年美国胸科学会/欧洲呼吸学会关于特发性间质性肺炎的国际多学科共识,对间质性肺病(ILD)患者进行了进一步分类:60名JIA患者(5.03%)并发肺部受累。发病率最高的亚型是全身性 JIA(sJIA,63.3%),其次是类风湿因子(RF)阳性多关节炎(pJIA,25.0%)。巨噬细胞活化综合征(MAS)的发病率为 21.6%。最常见的诊断是 ILD(90%)。61.7%的患者最初出现呼吸道症状/体征,21.7%的患者需要呼吸支持。sJIA的高分辨率CT分类显示了非特异性间质性肺炎(NSIP)和组织性肺炎。pJIA的高分辨率CT分类为非特异性间质性肺炎(NSIP)和通常的间质性肺炎(UIP)。患者接受非甾体抗炎药、糖皮质激素、DMARDs 和生物制剂治疗。1年和5年后的存活率分别约为93.3%和90.0%:结论:肺部受累的JIA患者发病早,死亡率高。结论:肺部受累的 JIA 患者发病早、死亡率高,JIA 患者应进行全面的体格检查、高分辨率 CT 扫描和肺功能测试,以评估和监测肺部受累的发生和发展,从而改善预后。
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来源期刊
CiteScore
6.10
自引率
18.90%
发文量
377
审稿时长
3-6 weeks
期刊介绍: Clinical and Experimental Rheumatology is a bi-monthly international peer-reviewed journal which has been covering all clinical, experimental and translational aspects of musculoskeletal, arthritic and connective tissue diseases since 1983.
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