Operative and non-operative treatment of congenital radio-ulnar synostosis in children: Results from a multicenter study.

IF 1.3 4区 医学 Q3 ORTHOPEDICS
Paola Zarantonello, Giovanni Trisolino, Filippo Maria Senes, Giovanni Luigi Di Gennaro, Diego Antonioli, Nunzio Catena, Annalisa Culmone, Alexandra Stauffer, Laetitia Sophie Chiarella, Sebastian Farr
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引用次数: 0

Abstract

Purpose: Congenital radioulnar synostosis is a congenital disorder affecting the elbow. We aimed to investigate the baseline characteristics and the clinical and functional outcome of a cohort of children with congenital radioulnar synostosis undergoing operative and non-operative treatment.

Methods: This multicenter retrospective study evaluated children with congenital radioulnar synostosis admitted to three European pediatric orthopedic centers from January 1998 to April 2021. Baseline characteristics were extracted from medical records. Operative cases treated with rotational osteotomy were further analyzed. Outcomes were assessed using the Mayo Elbow Performance Score and the Quick-DASH questionnaire.

Results: Ninety-seven patients (122 forearms) were included. Forearm positions were predominantly neutral or excessively pronated. Type 3 Congenital radioulnar synostosis was the most common radiographic finding. A total of 52 patients (66 forearms) underwent proximal derotational osteotomy, achieving a neutral forearm position in 61.9% of cases. Six complications were reported. The mean follow-up was 4.5 ± 3.4 years. MEPS averaged 90.6 points and Quick-DASH 18.5 points. No significant differences were found between operated and non-operated cases. MEPS results were good or excellent in 77.9% of patients, while only 31% reported a Quick-DASH ≤ 7points.

Conclusion: We present the largest case series of pediatric congenital radioulnar synostosis to date. Mild deformities caused minimal disability and required no surgery. For severe malrotation, proximal derotational osteotomy was safe, with low complication rates, restoring a neutral forearm position and yielding outcomes comparable to non-surgical management of mild cases.

儿童先天性桡尺关节闭锁的手术和非手术治疗:来自多中心研究的结果。
目的:先天性尺桡关节闭锁是一种影响肘部的先天性疾病。我们的目的是研究一组接受手术和非手术治疗的先天性尺桡关节闭锁儿童的基线特征、临床和功能结局。方法:这项多中心回顾性研究评估了1998年1月至2021年4月在三家欧洲儿科骨科中心收治的先天性尺桡关节闭锁儿童。从医疗记录中提取基线特征。进一步分析旋转截骨术治疗的手术病例。使用Mayo肘部表现评分和Quick-DASH问卷评估结果。结果:纳入97例患者(122例前臂)。前臂位置主要为中立或过度内旋。3型先天性尺桡关节闭锁是最常见的x线表现。共有52例患者(66例前臂)接受了近端旋转截骨术,61.9%的患者实现了前臂中立位。共报告6例并发症。平均随访时间为4.5±3.4年。MEPS平均90.6分,Quick-DASH平均18.5分。手术组与非手术组无明显差异。77.9%的患者MEPS结果为良或优,而只有31%的患者报告Quick-DASH≤7分。结论:我们提出了迄今为止最大的儿童先天性尺桡关节闭锁病例系列。轻度畸形造成的残疾很小,不需要手术。对于严重的旋转不良,近端旋转截骨术是安全的,并发症发生率低,恢复前臂中立位置,其结果与轻度病例的非手术治疗相当。
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来源期刊
Journal of Childrens Orthopaedics
Journal of Childrens Orthopaedics Medicine-Orthopedics and Sports Medicine
CiteScore
2.70
自引率
14.30%
发文量
61
审稿时长
23 weeks
期刊介绍: Aims & Scope The Journal of Children’s Orthopaedics is the official journal of the European Paediatric Orthopaedic Society (EPOS) and is published by The British Editorial Society of Bone & Joint Surgery. It provides a forum for the advancement of the knowledge and education in paediatric orthopaedics and traumatology across geographical borders. It advocates an increased worldwide involvement in preventing and treating musculoskeletal diseases in children and adolescents. The journal publishes high quality, peer-reviewed articles that focus on clinical practice, diagnosis and treatment of disorders unique to paediatric orthopaedics, as well as on basic and applied research. It aims to help physicians stay abreast of the latest and ever-changing developments in the field of paediatric orthopaedics and traumatology. The journal welcomes original contributions submitted exclusively for review to the journal. This continuously published online journal is fully open access and will publish one print issue each year to coincide with the EPOS Annual Congress, featuring the meeting’s abstracts.
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