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不建议对 2-3 岁 Tönnis 分级为 III 度发育性髋关节发育不良的儿童行股骨截骨术。

Femoral osteotomy is not recommended for children aged 2-3 years with Tönnis grade III developmental dysplasia of the hip.

机构信息

Department of Orthopaedic Surgery, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu Province, China.

出版信息

J Pediatr Orthop B. 2022 May 1;31(3):242-246. doi: 10.1097/BPB.0000000000000860.

Abstract

The objective of this study was to compare outcomes following open reduction with and without femoral shortening when treating patients aged 2-3 years with Tönnis grade III developmental dysplasia of the hip (DDH). In this prospective study, 78 patients (6 boys and 72 girls; mean age: 27.8 months; age range: 24-35 months) with Tönnis grade III DDH at our hospital from January 2014 to August 2017 were included. There were 34 hips in the without femoral shortening group and 44 hips in the femoral shortening group. Clinical outcomes were rated using the modified McKay criteria, and the hips were graded using the Severin score. Avascular necrosis (AVN) and redislocation were assessed. Mean follow-up was 26.5 months (range 17-32 months). In the without femoral shortening group (n = 34), there were five patients with AVN (14.7%), and 30 scored excellent and 4 scored good results per the modified McKay criteria. Further, 28 excellent and six good results were obtained using the Severin scale; no patient had redislocation. In the femoral shortening group(n = 44), there were seven patients with AVN (15.9%), and 38 scored excellent and six scored good results per the modified McKay criteria. Further, 31 excellent and 13 good results were obtained using the Severin scale; no patient had redislocation. Additionally, there were no statistically significant differences based on Modified McKay criteria, Severin score and AVN rate. Femoral shortening is not required for children aged 2-3 years with Tönnis grade III DDH.

摘要

本研究旨在比较治疗 2-3 岁 Tönnis Ⅲ型发育性髋关节发育不良(DDH)患者时,切开复位并股骨短缩与单纯切开复位的疗效。本前瞻性研究纳入 2014 年 1 月至 2017 年 8 月我院收治的 Tönnis Ⅲ型 DDH 患儿 78 例(男 6 例,女 72 例;平均年龄 27.8 个月;年龄范围 24-35 个月)。其中无股骨短缩组 34 髋,股骨短缩组 44 髋。采用改良 McKay 标准评定临床疗效,采用 Severin 评分评估髋关节分级。评估有无发生股骨头坏死(AVN)和再脱位。平均随访 26.5 个月(17-32 个月)。无股骨短缩组(n=34)中,发生 AVN 5 髋(14.7%),改良 McKay 标准评估结果为优 30 髋,良 4 髋;Severin 评分评估结果为优 28 髋,良 6 髋;无一髋再脱位。股骨短缩组(n=44)中,发生 AVN 7 髋(15.9%),改良 McKay 标准评估结果为优 38 髋,良 6 髋;Severin 评分评估结果为优 31 髋,良 13 髋;无一髋再脱位。两组改良 McKay 标准、Severin 评分及 AVN 发生率差异均无统计学意义。对于 Tönnis Ⅲ型 DDH 患儿,2-3 岁时无需行股骨短缩。

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