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10 岁以下复杂僵硬型先天性脊柱侧凸的两阶段后路截骨术。

Two-staged posterior osteotomy surgery in complex and rigid congenital scoliosis in younger than 10 years old children.

机构信息

Department of Orthopedics, The Second Hospital of Shanxi Medical University, No. 382 Wuyi Road, Shanxi, 030001, Taiyuan, P.R. China.

出版信息

BMC Musculoskelet Disord. 2021 Sep 13;22(1):788. doi: 10.1186/s12891-021-04682-y.

Abstract

BACKGROUND

Congenital scoliosis caused by failure of multiply vertebral segmentation with concave fused rib or unsegmented bar combined with contralateralhemivertebra is usually rigid and produces enormous asymmetric growth. Fusionless techniques have less advantage and come with some complications. Paucity of data was reported for children with complex congenital scoliosis using two-staged osteotomy surgery.

METHODS

From 2006 to 2016, 11 patients less than 10 years old undergoing two staged osteotomy surgery for complex rigid congenital scoliosis were retrospectively reviewed. The analysis included age at initial surgery, second surgery and at the latest follow-up, and complications. Changes in coronal major curve, thoracic kyphosis, lumbar lodorsis, apex vertebra translation, T1-T12 length, T1-S1 length, trunk shift, and SVAwere included in radiological evaluation.

RESULTS

In all, the mean follow-up was 72.5 ± 23.8 (42 to 112) months. The mean flexibility of the spine was 17.4 and 17.8 % before two surgeries. The mean age at the initial surgery was 6.6 ± 2.6 (2.5-10) years. The mean fusion level was 4.6 ± 1.3 (2 to 6) segments. The mean scoliosis improved from 67.4° to 23.7° after initial surgery and was 17.4° at the latest follow-up. The average increase of T1-S1 length was 0.92 cm per year. No patients had neurological complications.

CONCLUSIONS

Two-staged osteotomy surgery including hemivertebrae resection or Y-shaped osteotomy can achieve good radiological and clinical outcomes without severe complications. This procedure can be an option of treatment for complex congenital scoliosis.

摘要

背景

多椎体分节不全伴凹侧融合肋骨或不分节肋骨及对侧半椎体导致的先天性脊柱侧凸通常是僵硬的,会产生巨大的不对称生长。非融合技术优势较小,且存在一些并发症。对于采用两阶段截骨术治疗的复杂先天性脊柱侧凸儿童,相关数据较为缺乏。

方法

回顾性分析 2006 年至 2016 年 11 例年龄小于 10 岁的复杂僵硬先天性脊柱侧凸患者行两阶段截骨术的治疗情况。分析包括初次手术、二次手术及末次随访的年龄、并发症。影像学评估包括冠状面主弯、胸椎后凸、腰椎前凸、顶椎平移、T1-T12 长度、T1-S1 长度、躯干偏移、SVA 的变化。

结果

所有患者的平均随访时间为 72.5±23.8 个月(42-112 个月)。两次手术前脊柱柔韧性平均为 17.4%和 17.8%。初次手术时的平均年龄为 6.6±2.6 岁(2.5-10 岁)。平均融合节段为 4.6±1.3 个(2-6 个)。初次手术后平均侧凸从 67.4°改善至 23.7°,末次随访时为 17.4°。T1-S1 长度的平均年增长为 0.92cm。无患者出现神经并发症。

结论

包括半椎体切除或 Y 形截骨的两阶段截骨术可获得良好的影像学和临床结果,且无严重并发症。该手术可作为复杂先天性脊柱侧凸的治疗选择之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29f/8439016/235555faf193/12891_2021_4682_Fig1_HTML.jpg

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