Institute of Spinal Deformity, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan.
Department of Orthopaedic Surgery and Orthopaedic Research Institute, West China Hospital, Sichuan University, Chengdu, Sichuan.
Medicine (Baltimore). 2021 Mar 12;100(10):e24030. doi: 10.1097/MD.0000000000024030.
The aim of the study was to determine if multiple intraspinal anomalies increase the risk of scoliosis correction compared to the normal intraspinal condition or 1 or 2 intraspinal anomalies in congenital scoliosis (CS) and whether correction for multiple intraspinal anomalies need to be performed with preliminary neurosurgical intervention before scoliosis correction.A total of 318 consecutive CS patients who underwent corrective surgery without preliminary neurosurgical intervention at a single institution from 2008 to 2016 were retrospectively reviewed, with a minimum of 2 years of follow-up. The patients were divided into 3 groups according to different intraspinal conditions. In the normal group (N group; n = 196), patients did not have intraspinal anomalies. In the abnormal group (A group; n = 93), patients had 1 or 2 intraspinal anomalies. In the multiple anomaly group (M group; n = 29), patients had 3 or more intraspinal anomalies including syringomyelia, split cord malformation [SCM], tethered cord, low conus, intraspinal mass, Chiari malformation or/and arachnoid cyst. The occurrence of complications as well as perioperative and radiographic data were analyzed.The incidence rate of multiple intraspinal anomalies in CS patients was 9.1% (29/318). No significant difference was observed in the perioperative outcomes or radiographic parameters at the final follow-up. There were no significant differences among the 3 groups in the total, major or neurological complication rates (all P > .05). Two patients (1 in the N group and 1 in the A group) experienced transient neurological complications, whereas no patient experienced permanent neurological deficits during surgery or follow-up.To our knowledge, the current study reported the largest cohort of intraspinal anomalies in patients with CS that has been reported in the literature. The results of our study demonstrated that patients with congenital scoliosis associated with intraspinal anomalies, even multiple intraspinal anomalies that coexist with more complex intraspinal pathologies, may safely and effectively achieve scoliosis correction without preliminary neurological intervention. More complex intraspinal pathologies do not seem to increase the risk of neurosurgical complications during corrective surgery.
研究目的在于确定与正常椎管内情况或先天性脊柱侧凸(CS)中的 1 或 2 个椎管内异常相比,多个椎管内异常是否会增加脊柱侧凸矫正的风险,以及在进行脊柱侧凸矫正之前,是否需要进行初步神经外科干预来矫正多个椎管内异常。对 2008 年至 2016 年在一家单机构接受无初步神经外科干预的矫正手术的 318 例连续 CS 患者进行回顾性分析,随访时间至少 2 年。根据不同的椎管内情况将患者分为 3 组。在正常组(N 组;n = 196)中,患者没有椎管内异常。在异常组(A 组;n = 93)中,患者有 1 或 2 个椎管内异常。在多异常组(M 组;n = 29)中,患者有 3 个或更多椎管内异常,包括脊髓空洞症、脊髓分裂畸形[SCM]、脊髓栓系、圆锥低位、椎管内肿块、Chiari 畸形或/和蛛网膜囊肿。分析并发症的发生情况以及围手术期和影像学资料。CS 患者中多个椎管内异常的发生率为 9.1%(29/318)。在最终随访时,围手术期结果或影像学参数无显著差异。3 组之间的总并发症、主要并发症或神经并发症发生率无显著差异(均 P>.05)。2 例患者(N 组 1 例,A 组 1 例)发生一过性神经并发症,而在手术或随访期间无患者发生永久性神经功能缺损。据我们所知,本研究报告了文献中报道的 CS 患者椎管内异常的最大队列。我们的研究结果表明,患有伴有椎管内异常的先天性脊柱侧凸的患者,即使是伴有更复杂椎管内病变的多个椎管内异常,也可以安全有效地进行脊柱侧凸矫正,而无需进行初步神经干预。更复杂的椎管内病变似乎不会增加矫正手术期间神经外科并发症的风险。