全椎板切除术联合腰椎椎弓根螺钉固定治疗退行性腰椎管狭窄的老年患者下背部和腿部疼痛:一项自我控制试验的研究方案和初步结果

Chun-Liang Li, Qiang Guo, Feng Qin, Wenqi Yan, Haitao Zhu, Kai Wang
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引用次数: 0

摘要

背景和目的:老年性退行性腰椎管狭窄症的临床典型表现为神经根受压引起的下背部和腿部疼痛。常规全椎板切除术治疗退行性腰椎管狭窄症可迅速缓解患者症状,但由于退行性椎体滑脱引起脊柱不稳定,治疗效果不理想,且有许多不良反应。本研究的目的是探讨全椎板切除术联合腰椎椎弓根螺钉固定治疗老年性退行性腰椎管狭窄症是否能有效减轻神经根压迫引起的下背部和腿部疼痛,增加腰椎稳定性,减少不良反应。设计:前瞻性、单中心、自我控制、干预性试验。方法:在中国青海省人民医院骨科接受治疗的160例老年退行性腰椎管狭窄症患者被纳入本研究。所有患者将行全椎板切除术联合腰椎椎弓根螺钉固定,术后随访3、6、9和12个月。结局指标和初步结果:本研究的主要结局指标是术后12个月日本骨科学会(JOA)评分的恢复率,用于评估患者下背部和腿部疼痛的改善情况。该研究的次要结局指标包括JOA评分、椎管直径、计算机断层扫描图像上腰椎形态的变化以及术后不良事件的发生率。对71例接受相同治疗的老年退行性腰椎管狭窄患者的初步研究结果显示,术后3个月JOA评分和椎管直径均较术前显著升高(P < 0.05)。讨论:本研究结果可能提供临床证据,支持全椎板切除术联合腰椎椎弓根螺钉固定是一种安全可靠的治疗老年性退行性腰椎管狭窄症的方法,因为它可以迅速减轻腰背部和腿部疼痛,并提供脊柱稳定性。伦理与传播:本研究经中国青海省人民医院医学伦理委员会批准(批准号:QHY201602G)。这项研究将严格按照世界医学协会制定的《赫尔辛基宣言》进行。参与者将在参与研究前提供签署的知情同意书。本研究设计于2017年12月。患者招募和数据收集将于2018年8月开始。数据分析将于2019年10月进行。该研究将于2019年12月完成。研究结果将通过在科学会议上的演讲和/或在同行评议的期刊上发表来传播。协议版本:1.0。试验注册:本试验已在中国临床试验注册中心注册(注册号:ChiCTR1800014726)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Total laminectomy combined with lumbar pedicle screw fixation for treatment of lower back and leg pain in older adult patients with degenerative lumbar spinal stenosis: study protocol for a self-control trial and preliminary results
Background and objectives: Senile degenerative lumbar spinal stenosis typically manifests clinically as lower back and leg pain caused by compression of the nerve root. Conventional total laminectomy for degenerative lumbar spinal stenosis can quickly alleviate a patient's symptoms, but produces an unsatisfactory therapeutic effect because of spinal instability caused by degenerative spondylolisthesis, and also has many adverse reactions. The purpose of this study is to investigate whether total laminectomy combined with lumbar pedicle screw fixation for treatment of senile degenerative lumbar spinal stenosis can effectively reduce lower back and leg pain caused by compression of the nerve root, increase lumbar spine stability, and reduce adverse reactions. Design: A prospective, single-center, self-control, interventional trial. Methods: One hundred and sixty older adult patients with degenerative lumbar spinal stenosis who will receive treatment at the Department of Orthopedics, Qinghai Provincial People's Hospital, China will be included in this study. All patients will undergo total laminectomy combined with lumbar pedicle screw fixation, with follow-up at 3, 6, 9, and 12 months post-surgery. Outcome measures and preliminary results: The primary outcome measure of this study is recovery rate in Japanese Orthopedic Society (JOA) score at 12 months post-surgery, which is used to evaluate improvements in patients lower back and leg pain. Secondary outcome measures of this study include changes in JOA score, spinal canal diameter, lumbar spine morphology displayed on computed tomography images, and incidence of adverse events post-surgery. Results of a preliminary study involving 71 older adult patients with degenerative lumbar spinal stenosis who received the same treatment showed that at 3 months post-surgery, JOA score and spinal canal diameter were significantly increased compared with before surgery (P < 0.05). Discussion: Findings from this study may provide clinical evidence supporting that total laminectomy combined with lumbar pedicle screw fixation is a safe and reliable method for treatment of senile degenerative lumbar spinal stenosis because it rapidly alleviates lower back and leg pain and provides spine stability. Ethics and dissemination: This study was approved by Medical Ethics Committee of Qinghai Provincial People's Hospital of China (approval No. QHY201602G). This study will be performed in strict accordance with the Declaration of Helsinki formulated by the World Medical Association. Participants will provide signed informed consent prior to participation in the study. This study was designed in December 2017. Patient recruitment and data collection will begin in August 2018. Data analysis will be performed in October 2019. The study will be completed in December 2019. Results will be disseminated through presentations at scientific meetings and/or by publication in a peer-reviewed journal. Protocol version: 1.0. Trial registration: This trial was registered with the Chinese Clinical Trial Registry (registration number: ChiCTR1800014726).
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