A New Classification System for Forearm Deformities Caused by Hereditary Multiple Osteochondromas.

IF 2.1 2区 医学 Q2 ORTHOPEDICS Journal of Hand Surgery-American Volume Pub Date : 2024-08-22 DOI:10.1016/j.jhsa.2024.07.010
Chloe Xiaoyun Chan, Jun Song, Chin Yee Woo, Kai Yet Lam, Mark Edward Puhaindran, Bo Ning, Hoi Po James Hui
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Abstract

Purpose: The objective of this study was to evaluate the Masada and Jo classifications for clinical use in patients with forearm deformity caused by hereditary multiple osteochondroma and propose a new classification system that is all-inclusive and can guide clinical management.

Methods: A retrospective review of 275 forearms was performed. A split-sample approach was used, where 138 forearms were analyzed to create a new classification, which was then validated on the remaining 137 forearms. Radiographs were reviewed to determine the number and location of osteochondromas and the presence of radial head dislocation (RHD) and to measure radiographic parameters. Multivariable logistic regression analysis was performed to identify radiological parameters associated with RHD.

Results: According to the Masada and Jo classifications, 95 of 275 forearms (34.5%) were unclassifiable. Analyses of the split group (n = 138) revealed 42 forearms with RHD. All these had distal ulna lesions, qualifying as the greatest associated factor for RHD. Further subgroup multivariable logistic regression analysis of forearms with distal ulna lesions identified radiological parameter proportional ulna length as a statistically significant association of RHD, qualifying as "at-risk" criteria. The area under the receiver operating characteristic curve for proportional ulna length was 0.89, with a receiver operating characteristic-derived ideal value of ≤ 0.95 (sensitivity 0.86 and specificity 0.86).

Conclusions: We proposed a new classification system stratified into three groups-high, moderate, and low-risk of RHD-based on the identified factors associated with RHD. Type 1 comprises forearms with distal ulna osteochondromas-subdivided into type 1A (high-risk), where forearms meet the at-risk criteria for RHD and type 1B (moderate-risk), where forearms do not meet the at-risk criteria. Type 2 (low-risk) comprises forearms without distal ulna osteochondromas.

Clinical relevance: Our classification system addresses the limitations of existing classifications by risk stratifying forearms into three groups-high, moderate, and low-risk of RHD.

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遗传性多发性骨软骨瘤导致前臂畸形的新分类系统
目的:本研究的目的是评估 Masada 和 Jo 分类法在遗传性多发性骨软骨瘤导致的前臂畸形患者中的临床应用,并提出一种新的分类系统,该系统包罗万象,可指导临床治疗:方法:对 275 例前臂进行了回顾性研究。方法:对 275 个前臂进行了回顾性审查,采用了分割样本的方法,对 138 个前臂进行了分析,以创建新的分类,然后对其余 137 个前臂进行了验证。对X光片进行复查,以确定骨软骨瘤的数量和位置、是否存在桡骨头脱位(RHD),并测量X光片参数。进行了多变量逻辑回归分析,以确定与RHD相关的放射学参数:根据 Masada 和 Jo 的分类,275 个前臂中有 95 个(34.5%)无法分类。对分离组(n = 138)的分析显示,有 42 个前臂患有 RHD。所有这些前臂都有尺骨远端病变,这是导致 RHD 的最大相关因素。对有尺骨远端病变的前臂进一步进行分组多变量逻辑回归分析,发现放射学参数尺骨长度比例与 RHD 有显著的统计学关联,符合 "高危 "标准。尺骨比例长度的接收器操作特征曲线下面积为 0.89,接收器操作特征的理想值≤ 0.95(灵敏度 0.86,特异性 0.86):我们提出了一种新的分类系统,根据已确定的 RHD 相关因素,将 RHD 分为高、中、低三类。1型包括前臂尺骨远端骨软骨瘤,又分为1A型(高风险)和1B型(中度风险),前臂尺骨远端骨软骨瘤符合RHD高风险标准,前臂尺骨远端骨软骨瘤不符合高风险标准。2型(低风险)包括没有尺骨远端骨软骨瘤的前臂:我们的分类系统解决了现有分类的局限性,将前臂的风险分为三类--RHD的高风险、中度风险和低风险。
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来源期刊
CiteScore
3.20
自引率
10.50%
发文量
402
审稿时长
12 weeks
期刊介绍: The Journal of Hand Surgery publishes original, peer-reviewed articles related to the pathophysiology, diagnosis, and treatment of diseases and conditions of the upper extremity; these include both clinical and basic science studies, along with case reports. Special features include Review Articles (including Current Concepts and The Hand Surgery Landscape), Reviews of Books and Media, and Letters to the Editor.
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