Department of Anatomy and Neurobiology, Northeast Ohio Medical University, Rootstown, OH.
Clin J Pain. 2013 Nov;29(11):939-43. doi: 10.1097/AJP.0b013e31827fb803.
The aim of this report was to evaluate the long-term effectiveness and safety of mild lumbar decompression for the treatment of neurogenic claudication associated with lumbar spinal stenosis. This technique uses a percutaneous dorsal approach to remove small portions of ligament and lamina, thereby restoring space and decompressing the spinal canal.
Two-year data are reported for 45 patients treated with mild decompression at 11 US sites. Outcome measures included the Visual Analog Scale (VAS), Oswestry Disability Index, and Zurich Claudication Questionnaire. Safety was monitored throughout the procedural and follow-up period for all patients. Interim data are included for these patients at 1 week, 6 months, and 1-year follow-up.
Seventy-one percent of patients reported improvement in VAS at the end of the reporting period. At 2 years, patients demonstrated a statistically significant reduction of pain as measured by VAS, and improvement in physical function and mobility was significant as measured by Zurich Claudication Questionnaire and Oswestry Disability Index. Tukey honestly significant different test found significant improvement in all outcome measures from baseline to each follow-up interval. Further, major improvement occurred by 1-week follow-up and showed no difference between each subsequent follow-up, signifying considerable stability and durability of the initial result over time. No major device or intraprocedural adverse events were reported.
In this report of 2-year follow-up on 45 patients treated with mild percutaneous lumbar decompression, patients experienced statistically significant pain relief and improved functionality.
本报告旨在评估轻度腰椎减压治疗腰椎管狭窄症相关神经源性跛行的长期疗效和安全性。该技术采用经皮背侧入路切除小部分韧带和椎板,从而恢复空间并减压椎管。
在 11 个美国站点,对 45 名接受轻度减压治疗的患者进行了为期 2 年的数据报告。结果测量包括视觉模拟量表(VAS)、Oswestry 残疾指数和苏黎世跛行问卷。在整个手术和随访期间,对所有患者的安全性进行了监测。这些患者的临时数据包括 1 周、6 个月和 1 年的随访。
71%的患者在报告期末报告 VAS 改善。2 年后,患者的 VAS 测量疼痛明显减轻,苏黎世跛行问卷和 Oswestry 残疾指数测量的身体功能和活动能力明显改善。Tukey 诚实显著差异检验发现,所有结果测量值均从基线到每个随访间隔均有显著改善。此外,主要改善发生在 1 周随访时,且随后每个随访间隔无差异,表明初始结果具有相当大的稳定性和耐久性。未报告重大设备或手术内不良事件。
在对 45 名接受轻度经皮腰椎减压治疗的患者进行的 2 年随访报告中,患者经历了统计学上显著的疼痛缓解和功能改善。