1Department of Orthopedics, Luhe People's Hospital of Nanjing; and.
2Spine Surgery, the Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
J Neurosurg Spine. 2019 Apr 5;31(1):40-45. doi: 10.3171/2019.1.SPINE181205. Print 2019 Jul 1.
Intraspinal anomalies associated with congenital scoliosis (CS) complicate the decision-making process for spinal correction surgery in CS patients. Recently, deformity correction surgery without prior prophylactic neurological intervention has been recognized to be safe in CS patients with intact or stable neurological status. However, no case-control study has identified the surgical outcomes and risks of spinal correction surgery in this patient population. The authors sought to investigate the safety and efficacy of spinal correction surgery for CS associated with untreated intraspinal anomalies (split cord malformation [SCM], tethered cord, and/or syringomyelia) with intact or stable neurological status.
A group of CS patients with intraspinal anomalies (CS+IA) and another group of CS patients without intraspinal anomalies (CS-IA) undergoing 1-stage posterior correction surgery were retrospectively reviewed. The radiographic and clinical outcomes and postoperative complications were compared between the 2 groups.
There were 57 patients in the CS+IA group and 184 patients in the CS-IA group. No significant difference was observed in age, sex, spinal curve pattern, main Cobb angle, and flexibility of the main curve between the 2 groups (p > 0.05 for all). The postoperative correction rates of the major curve were comparable between the 2 groups (53.5% vs 55.7% for the CS+IA and CS-IA groups, respectively, p > 0.05). No significant difference was observed in the incidence of either implant-related or neurological complications between 2 groups. No patients in the CS+IA group developed neurological complications, whereas 1 patient in the CS-IA group experienced transient weakness of the left lower extremity after surgery.
Coexisting intraspinal anomalies (SCM, tethered cord, and/or syringomyelia) in CS patients with normal or stable neurological status do not significantly increase the risk of neurological complications of correction surgery. Prophylactic neurosurgical intervention for intraspinal anomalies before correction surgery might be unnecessary for these patients.
先天性脊柱侧凸(CS)伴发的椎管内异常使 CS 患者脊柱矫正手术的决策复杂化。最近,对于神经功能完整或稳定的 CS 患者,人们已经认识到,无需进行预防性神经干预即可安全地进行畸形矫正手术。然而,尚无病例对照研究确定该患者人群脊柱矫正手术的手术结果和风险。作者旨在研究脊柱矫正手术治疗伴有未治疗的椎管内异常(脊髓分裂畸形[SCM]、脊髓栓系和/或脊髓空洞症)但神经功能完整或稳定的 CS 患者的安全性和有效性。
回顾性分析了一组接受 1 期后路矫正手术的伴有椎管内异常的 CS 患者(CS+IA 组)和另一组无椎管内异常的 CS 患者(CS-IA 组)。比较了两组的影像学和临床结果以及术后并发症。
CS+IA 组有 57 例患者,CS-IA 组有 184 例患者。两组间年龄、性别、脊柱曲线类型、主弯 Cobb 角和主弯柔韧性无显著差异(p > 0.05 均)。两组间主要曲线的术后矫正率相当(CS+IA 组和 CS-IA 组分别为 53.5%和 55.7%,p > 0.05)。两组间植入物相关或神经并发症的发生率无显著差异。CS+IA 组无患者发生神经并发症,而 CS-IA 组有 1 例患者术后出现左下肢短暂无力。
神经功能完整或稳定的 CS 患者伴有椎管内异常(SCM、脊髓栓系和/或脊髓空洞症)并不会显著增加矫正手术神经并发症的风险。对于这些患者,在矫正手术前对椎管内异常进行预防性神经外科干预可能是不必要的。