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先天性脊柱侧凸有哪些新进展?

What's New in Congenital Scoliosis?

作者信息

Pahys Joshua M, Guille James T

机构信息

Shriners Hospitals for Children-Philadelphia, Philadelphia.

Premier Orthopaedics-Brandywine Institute of Orthopaedics Division, Pottstown, PA.

出版信息

J Pediatr Orthop. 2018 Mar;38(3):e172-e179. doi: 10.1097/BPO.0000000000000922.

Abstract

BACKGROUND

Congenital scoliosis is a failure of vertebral formation, segmentation, or a combination of the 2 arising from abnormal vertebral development during weeks 4 to 6 of gestation. The associated spinal deformity can be of varying severity and result in a stable or progressive deformity based on the type and location of the anomalous vertebra(e). Bracing for congenital scoliosis is rarely indicated, while recent reports have demonstrated the utility of serial derotational casting for longer curves with multiple anomalous vertebrae as an effective "time buying strategy" to delay the need for surgery. Earlier hemivertebra excision and short-segment posterior spinal fusion have been advocated to prevent future curve progression of the deformity and/or the development of large compensatory curves. It has been shown in recent long-term follow-up studies that growth rates of the vertebral body and spinal canal are not as dramatically affected by pedicle screw instrumentation at a young age as once thought. Growth friendly surgery with either spine-based or rib-based anchors has demonstrated good results with curve correction while maintaining spinal growth. Rib-based anchors are typically more commonly indicated in the setting of chest wall abnormalities and/or when spinal anatomy precludes placement of spinal instrumentation. Recently, magnetically controlled growing rods have shown promising results in several studies that include a small subset of congenital scoliosis cases.

METHODS

A literature search was performed to identify existing studies related to the treatment of congenital scoliosis published from January 1, 2005 to June 1, 2016. Databases included PubMed, Medline, and the Cochrane Library. The search was limited to English articles and yielded 36 papers. This project was initiated by the Pediatric Orthopaedic Society of North America Publications Committee and was reviewed and approved by the Pediatric Orthopaedic Society of North America Presidential Line.

RESULTS

A total of 36 papers were selected for review based upon new findings. Classic manuscripts on congenital scoliosis are also included to provide sufficient background information.

CONCLUSIONS

Congenital scoliosis represents a wide range of pathology from the simple, stable hemivertebra to the complex, progressive spinal deformity with chest wall abnormalities and associated cardiac, renal, and neural axis anomalies. This paper reviews the natural history and associated anomalies with congenital scoliosis as well as the most up-to-date classification schemes and various treatment options for the care of this challenging patient population.

LEVEL OF EVIDENCE

Level 5.

摘要

背景

先天性脊柱侧凸是指在妊娠第4至6周期间,由于椎体发育异常导致的椎体形成、分节失败或两者兼而有之。相关的脊柱畸形严重程度各异,根据异常椎体的类型和位置,可导致稳定或进展性畸形。先天性脊柱侧凸很少采用支具治疗,而最近的报告表明,对于有多个异常椎体的较长弯曲,连续去旋转石膏固定作为一种有效的“争取时间策略”,可延迟手术需求。早期半椎体切除和短节段后路脊柱融合术已被提倡用于预防畸形未来的曲线进展和/或大的代偿性曲线的发展。最近的长期随访研究表明,年轻时椎弓根螺钉内固定对椎体和椎管生长速度的影响并不像曾经认为的那样显著。基于脊柱或肋骨的锚钉的生长友好型手术在矫正曲线的同时保持脊柱生长方面已显示出良好效果。基于肋骨的锚钉通常更常用于胸壁异常的情况和/或脊柱解剖结构妨碍放置脊柱内固定器械时。最近,在包括一小部分先天性脊柱侧凸病例的多项研究中,磁控生长棒已显示出有前景的结果。

方法

进行文献检索,以确定2005年1月1日至2016年6月1日发表的与先天性脊柱侧凸治疗相关的现有研究。数据库包括PubMed、Medline和Cochrane图书馆。检索限于英文文章,共获得36篇论文。该项目由北美小儿骨科学会出版委员会发起,并经北美小儿骨科学会主席办公室审查和批准。

结果

基于新发现,共选择36篇论文进行综述。还纳入了关于先天性脊柱侧凸的经典手稿,以提供足够的背景信息。

结论

先天性脊柱侧凸代表了从简单、稳定的半椎体到复杂、进展性脊柱畸形伴胸壁异常以及相关心脏、肾脏和神经轴异常的广泛病理情况。本文综述了先天性脊柱侧凸的自然病史和相关异常,以及最新的分类方案和针对这一具有挑战性患者群体的各种治疗选择。

证据水平

5级。

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