Department of Neurosurgery, The Johns Hopkins Hospital, Baltimore, MD.
Department of Neurological Surgery, Henry Ford Health System, Detroit, MI.
Clin Spine Surg. 2021 Oct 1;34(8):E439-E449. doi: 10.1097/BSD.0000000000001192.
This was a retrospective clinical series.
The objective of this study was to evaluate radiologic changes in central spinal canal dimensions following minimally invasive transforaminal lumbar interbody fusion (MIS-TLIF) with placement of a static or an expandable interbody device.
MIS-TLIF is used to treat lumbar degenerative diseases and low-grade spondylolisthesis. MIS-TLIF enables direct and indirect decompression of lumbar spinal stenosis, with patients experiencing relief from radiculopathy and neurogenic claudication. However, the effects of MIS-TLIF on the central spinal canal are not well-characterized.
We identified patients who underwent MIS-TLIF for degenerative lumbar spondylolisthesis and concurrent moderate to severe spinal stenosis. We selected patients who had both preoperative and postoperative magnetic resonance imaging (MRI) and upright lateral radiographs of the lumbar spine. Measurements on axial T2-weighted MRI scans include anteroposterior and transverse dimensions of the dural sac and osseous spinal canal. Measurements on radiographs include disk height, neural foraminal height, segmental lordosis, and spondylolisthesis. We made pairwise comparisons between each of the central canal dimensions and lumbar sagittal segmental radiologic outcome measures relative to their corresponding preoperative values. Correlation coefficients were used to quantify the association between changes in lumbar sagittal segmental parameters relative to changes in radiologic outcomes of central canal dimensions. Statistical analysis was performed for "all patients" and further stratified by interbody device subgroups (static and expandable).
Fifty-one patients (age 60.4 y, 68.6% female) who underwent MIS-TLIF at 55 levels (65.5% at L4-L5) were included in the analysis. Expandable interbody devices were used in 45/55 (81.8%) levels. Mean duration from surgery to postoperative MRI scan was 16.5 months (SD 11.9). MIS-TLIF was associated with significant improvements in dural sac dimensions (anteroposterior +0.31 cm, transverse +0.38 cm) and osseous spinal canal dimensions (anteroposterior +0.16 cm, transverse +0.32 cm). Sagittal lumbar segmental parameters of disk height (+0.56 cm), neural foraminal height (+0.35 cm), segmental lordosis (+4.26 degrees), and spondylolisthesis (-7.5%) were also improved following MIS-TLIF. We did not find meaningful associations between the changes in central canal dimensions relative to the corresponding changes in any of the sagittal lumbar segmental parameters. Stratified analysis by interbody device type (static and expandable) revealed similar within-group changes as in the overall cohort and minimal between-group differences.
MIS-TLIF is associated with radiologic decompression of neural foraminal and central spinal canal stenosis. The mechanism for neural foraminal and central canal decompression is likely driven by a combination of direct and indirect corrective techniques.
这是一项回顾性临床研究。
本研究旨在评估微创经椎间孔腰椎体间融合术(MIS-TLIF)中使用静态或可扩张椎间融合器对中央椎管尺寸的放射学变化。
MIS-TLIF 用于治疗腰椎退行性疾病和低度滑脱。MIS-TLIF 可实现腰椎管狭窄的直接和间接减压,患者可缓解神经根病和神经源性跛行。然而,MIS-TLIF 对中央椎管的影响尚未得到很好的描述。
我们确定了因退行性腰椎滑脱和并发中度至重度椎管狭窄而行 MIS-TLIF 的患者。我们选择了术前和术后均有磁共振成像(MRI)和腰椎侧位立位 X 线片的患者。轴向 T2 加权 MRI 扫描的测量包括硬脑膜囊的前后径和横径以及骨性椎管。X 线片的测量包括椎间盘高度、神经孔高度、节段性前凸和滑脱。我们将每个中央椎管尺寸与相应术前值的腰椎矢状节段放射学结果测量值进行了两两比较。使用相关系数来量化腰椎矢状段参数变化与中央椎管尺寸放射学结果变化之间的相关性。对“所有患者”进行了统计分析,并进一步按椎间融合器亚组(静态和可扩张)进行分层。
共纳入 51 例(年龄 60.4 岁,68.6%为女性)患者,共 55 个节段(65.5%为 L4-L5)行 MIS-TLIF。45/55(81.8%)个节段使用了可扩张椎间融合器。从手术到术后 MRI 扫描的平均时间为 16.5 个月(标准差 11.9)。MIS-TLIF 与硬脑膜囊尺寸(前后径增加 0.31cm,横径增加 0.38cm)和骨性椎管尺寸(前后径增加 0.16cm,横径增加 0.32cm)的显著改善相关。MIS-TLIF 后,腰椎节段参数中的椎间盘高度(增加 0.56cm)、神经孔高度(增加 0.35cm)、节段前凸(增加 4.26 度)和滑脱(减少 7.5%)也得到了改善。我们没有发现中央椎管尺寸变化与任何腰椎矢状段参数的相应变化之间有意义的相关性。按椎间融合器类型(静态和可扩张)进行分层分析显示,各亚组内的变化与总队列相似,组间差异最小。
MIS-TLIF 与神经孔和中央椎管狭窄的放射学减压相关。神经孔和中央椎管减压的机制可能是由直接和间接矫正技术的组合驱动的。