Development and validation of a Pediatric Internationally agreed UltraSound Hip synovitis protocol (PIUS-hip), by the PReS imaging working party.

IF 2.3 3区 医学 Q1 PEDIATRICS
Daniel Windschall, Ralf Trauzeddel, Silvia Magni-Manzoni, Hatice Adiguzel-Dundar, Sven Hardt, Manuela Krumrey-Langkammerer, Lampros Fotis, Rainer Berendes, Sebastian Schua, Maria Haller, Ferhat Demir, Betul Sözeri, Faekah Gohar
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引用次数: 0

Abstract

Background: Whilst musculoskeletal ultrasound (MSUS) normal values for examination of the hip joint have been established for healthy children, equivalent values for patients with juvenile idiopathic arthritis (JIA), as well as internationally validated MSUS protocols for the optimal evaluation of synovitis are lacking. This study aimed to develop and validate the most sensitive MSUS protocol for the detection of hip synovitis in JIA.

Methods: In consecutive JIA patients with ≥ 1 clinically affected hip joint, affected and unaffected hips underwent MSUS. Disease, demographic and clinical findings were recorded. Synovitis was graded using the pediatric OMERACT score for B-Mode (BM) and power-Doppler Mode (PD) in the longitudinal and transverse scans and the sensitivity and specificity was analyzed. Additionally anterior recess size (bone to capsula distance), capsula thickness and femoral head cartilage thickness (transverse view) were measured. Published data provided further control data for anterior recess size (children without JIA). Interobserver reliability of BM and PD was tested using Fleiss-Kappa.

Results: 60 patients were enrolled who had 76 hips with and 32 without clinical arthritis. BM was positive (grade ≥ 1) in 74/76 of hips with clinical arthritis (97%, sensitivity 0.97 (0.93-1.0), specificity 0.85 (0.74-0.97) versus 2/32 (6%) in hips without arthritis. PD positivity frequency was 6 (8%) in hips with arthritis versus 0 in hips without. Anterior recess size (mean ± SD) was significantly wider in patients with clinical arthritis (9.9 ± 2.5 vs 5.5 ± 1.3, p-value 0.001). Use of the cut-off of ≥ 7.2 mm resulted in an area under the curve of at least 95%, with a sensitivity of 86% and specificity of 94%. Articular capsula and femoral head cartilage thickness did not differ between patients with and without arthritis. Recess size was comparable in the internal and external control groups (n = 449). Interobserver reliability of BM and PD positivity showed excellent agreement (kappa = 0.85).

Conclusions: The Pediatric internationally agreed UltraSound hip synovitis protocol (PIUS-hip) could be limited to one longitudinal scan including B-Mode scoring plus measurement of anterior recess size for maximal sensitivity and specificity for synovitis.

由PReS成像工作组制定和验证儿科国际商定的超声髋关节滑膜炎方案(PIUS-hip)。
背景:虽然健康儿童髋关节检查的肌肉骨骼超声(MSUS)正常值已经建立,但青少年特发性关节炎(JIA)患者的正常值以及国际上验证的滑膜炎最佳评估MSUS方案都缺乏。本研究旨在开发和验证最敏感的MSUS方案,以检测JIA患者的髋关节滑膜炎。方法:在连续的JIA患者中,临床上有≥1个髋关节受影响,受影响和未受影响的髋关节进行MSUS。记录疾病、人口统计学和临床结果。采用儿童纵向和横向扫描的b模式(BM)和功率多普勒模式(PD)的OMERACT评分对滑膜炎进行分级,并分析其敏感性和特异性。此外,测量前隐窝大小(骨到囊的距离)、囊厚度和股骨头软骨厚度(横切面)。已发表的数据为前隐窝大小(无JIA的儿童)提供了进一步的对照数据。采用Fleiss-Kappa测试BM和PD的观察者间信度。结果:60例患者入组,其中76例髋关节有临床关节炎,32例无临床关节炎。在74/76的临床关节炎髋部,BM阳性(分级≥1)(97%,敏感性0.97(0.93-1.0),特异性0.85(0.74-0.97),而在无关节炎髋部,BM阳性(6%)为2/32。有关节炎髋部PD阳性频率为6(8%),无关节炎髋部PD阳性频率为0。临床关节炎患者的前隐窝大小(平均±SD)明显变宽(9.9±2.5 vs 5.5±1.3,p值0.001)。使用≥7.2 mm的截止值,曲线下面积至少为95%,灵敏度为86%,特异性为94%。关节囊和股骨头软骨厚度在关节炎患者和非关节炎患者之间没有差异。内部对照组和外部对照组的隐窝大小相当(n = 449)。BM和PD阳性的观察者间信度表现出极好的一致性(kappa = 0.85)。结论:国际公认的儿科超声髋关节滑膜炎方案(PIUS-hip)可以限制为一次纵向扫描,包括b模式评分加上前隐窝大小的测量,以获得滑膜炎的最大敏感性和特异性。
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来源期刊
Pediatric Rheumatology
Pediatric Rheumatology PEDIATRICS-RHEUMATOLOGY
CiteScore
4.10
自引率
8.00%
发文量
95
审稿时长
>12 weeks
期刊介绍: Pediatric Rheumatology is an open access, peer-reviewed, online journal encompassing all aspects of clinical and basic research related to pediatric rheumatology and allied subjects. The journal’s scope of diseases and syndromes include musculoskeletal pain syndromes, rheumatic fever and post-streptococcal syndromes, juvenile idiopathic arthritis, systemic lupus erythematosus, juvenile dermatomyositis, local and systemic scleroderma, Kawasaki disease, Henoch-Schonlein purpura and other vasculitides, sarcoidosis, inherited musculoskeletal syndromes, autoinflammatory syndromes, and others.
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