Shriners Hospitals for Children-Philadelphia, 3551 N Broad St, Philadelphia, PA, 19140, USA.
Children's Hospital of Philadelphia, 34th & Civic Center Blvd, Philadelphia, PA, 19140, USA.
Spinal Cord Ser Cases. 2021 Apr 20;7(1):33. doi: 10.1038/s41394-021-00386-6.
The incidence of neurologic complications with spinal surgery for adolescent idiopathic scoliosis (AIS) has been reported to be 0.69%. This rare complication typically occurs during surgery or immediately postoperatively. We report the occurrence of a delayed neurologic deficit that presented 36 h after the initial surgery of a staged posterior spinal fusion for severe AIS.
A 12-year-old girl with severe thoracolumbar AIS of 125° underwent attempted posterior spinal fusion from T2-L4. The case was complicated by a transient loss of transcutaneous motor evoked potentials (TcMEP) that resolved with an increase in the mean arterial pressure (MAP) and relaxation of curve correction with rod removal. The patient awoke with normal neurologic function. She had a transient decrease in MAP 36 h post-op and awoke on postoperative day #2 with nearly complete lower extremity paraplegia (American Spinal Injury Association [ASIA] Impairment Scale B). Emergent exploration and removal of the concave apical pedicles resulted in improvement of TcMEPs and return of function.
Delayed postoperative neurologic deficit is a very rare phenomenon, with only a few case reports in the literature to date. The delayed neurologic decline of our patient was likely secondary to a transient episode of postoperative hypotension combined with spinal cord compression by the apical concave pedicles. Close monitoring and support of spinal cord perfusion as well as emergent decompression are imperative in the setting of a delayed neurologic deficit. Further multicenter study on this rare occurrence is underway to identify potential causes and improve treatment.
青少年特发性脊柱侧凸(AIS)脊柱手术后神经系统并发症的发生率为 0.69%。这种罕见的并发症通常发生在手术过程中或术后即刻。我们报告了一例在 AIS 严重患者分阶段后路脊柱融合术后 36 小时发生的迟发性神经功能缺损。
一名 12 岁女孩患有严重的胸腰椎 AIS,角度为 125°,行 T2-L4 后路脊柱融合术。该病例并发一过性经皮运动诱发电位(TcMEP)丢失,经增加平均动脉压(MAP)和放松矫正棒后缓解。患者术后苏醒时神经功能正常。术后 36 小时 MAP 一过性下降,术后第 2 天苏醒时出现下肢几乎完全截瘫(美国脊髓损伤协会 [ASIA] 损伤分级 B)。紧急探查并切除凹侧顶椎椎弓根,TcMEP 改善,功能恢复。
术后迟发性神经功能缺损是一种非常罕见的现象,迄今为止文献中仅有少数病例报告。我们患者的迟发性神经功能下降可能是术后短暂性低血压与顶椎凹侧椎弓根压迫脊髓共同作用的结果。在迟发性神经功能缺损的情况下,必须密切监测和支持脊髓灌注,并紧急减压。正在进行进一步的多中心研究以确定潜在的原因并改善治疗方法。