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评价传统和椎板间全内镜减压术治疗腰椎管狭窄症的疗效和安全性(ENDO-F 试验):一项前瞻性、随机、多中心试验的方案。

Evaluation of the efficacy and safety of conventional and interlaminar full-endoscopic decompressive laminectomy to treat lumbar spinal stenosis (ENDO-F trial): Protocol for a prospective, randomized, multicenter trial.

机构信息

Department of Neurosurgery, Seoul St Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.

Department of Neurosurgery, Chungdam Wooridul Spine Hospital, Seoul, Korea.

出版信息

PLoS One. 2023 Apr 5;18(4):e0283924. doi: 10.1371/journal.pone.0283924. eCollection 2023.

Abstract

Lumbar spinal stenosis is a common spinal degenerative condition. Minimally invasive interlaminar full-endoscopic decompressive laminectomy provides greater patient satisfaction and faster recovery than open decompressive laminectomy. The aim of our randomized controlled trial will be to compare the safety and efficacy of interlaminar full-endoscopic laminectomy and open decompressive laminectomy. Our trial will include 120 participants (60 per group) who will undergo surgical treatment for lumbar spinal stenosis. The primary outcome will be the Oswestry Disability Index measured at 12 months postoperatively. Secondary patient-reported outcomes will include back and radicular leg pain measured via a visual analog scale; the Oswestry Disability Index; the Euro-QOL-5 Dimensions score measured at 2 weeks and at 3, 6, and 12 months postoperatively; and patient satisfaction. The functional measures will include time to return to daily activities postoperatively and walking distance/time. The surgical outcomes will include postoperative drainage, operation time, duration of hospital stay, postoperative creatine kinase (an indicator of muscle injury) level, and postoperative surgical scarring. Magnetic resonance and computed tomography images and simple radiographs will be obtained for all patients. The safety outcomes will include surgery-related complications and adverse effects. All evaluations will be performed by a single assessor at each participating hospital who will be blinded to group allocation. The evaluations will be conducted preoperatively and at 2 weeks and 3, 6, and 12 months postoperatively. The randomized, multicenter design of the trial, blinding, and justification of the sample size will reduce the risk of bias in our trial. The results of the trial will provide data regarding the use of interlaminar full-endoscopic laminectomy as an alternative to open decompressive laminectomy that results in similar surgical findings with less invasiveness. Trial registration: This trial is registered at cris.nih.go.kr. (KCT0006198; protocol version 1; 27 May 2021).

摘要

腰椎管狭窄症是一种常见的脊柱退行性疾病。微创经椎间孔全内镜减压性椎板切除术比开放性减压性椎板切除术更能提高患者满意度和加快康复速度。我们的随机对照试验旨在比较经椎间孔全内镜椎板切除术和开放性减压性椎板切除术的安全性和疗效。我们的试验将纳入 120 名(每组 60 名)接受腰椎管狭窄症手术治疗的参与者。主要结局将是术后 12 个月时的 Oswestry 残疾指数。次要的患者报告结果将包括通过视觉模拟量表测量的腰背和神经根性腿痛;Oswestry 残疾指数;术后 2 周以及 3、6 和 12 个月时的 Euro-QOL-5 维度评分;以及患者满意度。功能测量将包括术后恢复日常活动的时间和行走距离/时间。手术结果将包括术后引流、手术时间、住院时间、术后肌酸激酶(肌肉损伤的指标)水平和术后手术瘢痕。所有患者都将获得磁共振和计算机断层扫描图像和简单的 X 光片。安全性结果将包括与手术相关的并发症和不良反应。每个参与医院的一名评估员将进行所有评估,评估员将对分组分配情况保持盲态。评估将在术前以及术后 2 周和 3、6 和 12 个月时进行。该试验的随机、多中心设计、盲法和样本量的合理性将降低试验偏倚的风险。该试验的结果将提供关于经椎间孔全内镜椎板切除术作为开放性减压性椎板切除术替代方法的使用数据,该方法具有相似的手术结果,但侵入性更小。试验注册:该试验在 cris.nih.go.kr 注册(KCT0006198;方案版本 1;2021 年 5 月 27 日)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e22e/10075401/c46c13cbea65/pone.0283924.g001.jpg

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