双孔通道内镜与显微镜下腰椎间盘切除术治疗腰椎间盘突出症的随机对照试验
Biportal endoscopic versus microscopic discectomy for lumbar herniated disc: a randomized controlled trial.
作者信息
Park Sang-Min, Lee Ho-Jin, Park Hyun-Jin, Choi Jun-Young, Kwon Ohsang, Lee Sanghoon, Kim Ho-Joong, Yeom Jin S
机构信息
Spine Center and Department of Orthopedic Surgery, Seoul National University College of Medicine and Seoul National University Bundang Hospital, Seongnam, Korea.
Department of Orthopaedic Surgery, Chungnam National University School of Medicine, Daejeon, Korea.
出版信息
Spine J. 2023 Jan;23(1):18-26. doi: 10.1016/j.spinee.2022.09.003. Epub 2022 Sep 23.
BACKGROUND CONTEXT
Biportal endoscopic discectomy has been frequently performed in recent years and has shown acceptable clinical outcomes. However, evidence regarding its efficacy and safety remains limited.
PURPOSE
This study aimed to compare the clinical efficacy and safety of biportal endoscopic with that of open microscopic discectomy in patients with single-level herniated lumbar discs.
STUDY DESIGN
Prospective, randomized, multicenter, open-label, assessor-blind, non-inferiority controlled trial.
PATIENT SAMPLE
Sixty-four participants suffering from low back and leg pain with a single-level herniated lumbar disc and required discectomy.
OUTCOME MEASURES
Outcomes were assessed with the use of patient-reported outcome measures (PROMs), visual analog scale (VAS) pain score for surgical site, low back and lower extremity, Oswestry Disability Index (ODI) for lumbar disabilities, European Quality of Life-5 Dimensions value for quality of life, and painDETECT for neuropathic pain. Surgery-related outcomes such as hospital stay, operation time, and opioid usage were collected. Adverse events occurring during the follow-up period were also noted.
METHODS
All participants were randomly assigned in a 1:1 ratio to undergo biportal endoscopic (biportal group) or microscopic discectomy (microscopy group). The primary outcome was the difference in ODI scores at 12-months post surgically based on a modified intention-to-treat strategy, with a non-inferiority margin of 12.8 points. The secondary outcomes included PROMs, surgery-related outcomes, and adverse events.
RESULTS
The ODI score at the 12-month follow-up was 11.97 in the microscopy group and 13.89 in the biportal group (mean difference, 1.92; 95% confidence interval [CI], -3.50 to 7.34), showing the non-inferiority of biportal group. The results for the secondary outcomes were similar to those for the primary outcome. Creatinine phosphokinase ratios were low in the biportal group. Early surgical site pain was slightly lower in the biportal group (mean difference of VAS pain score at 48-hr, -0.98; 95% CI, -1.77 to -0.19). Adverse events including reoperation showed no significant difference between the groups.
CONCLUSION
Biportal endoscopic discectomy was non-inferior to microscopic discectomy over a 12 month period. Biportal endoscopic discectomy is suggested to be a relatively safe and effective surgical technique with the slight advantage of reduced muscle damage. However, the clinical implications of surgical site pain should be carefully considered.
背景
近年来,双孔道内镜下椎间盘切除术已被广泛应用,并显示出可接受的临床效果。然而,关于其疗效和安全性的证据仍然有限。
目的
本研究旨在比较双孔道内镜下椎间盘切除术与开放显微镜下椎间盘切除术治疗单节段腰椎间盘突出症患者的临床疗效和安全性。
研究设计
前瞻性、随机、多中心、开放标签、评估者盲法、非劣效性对照试验。
患者样本
64例患有单节段腰椎间盘突出症且需要进行椎间盘切除术的腰腿痛患者。
观察指标
采用患者报告结局量表(PROMs)、手术部位、腰部和下肢的视觉模拟量表(VAS)疼痛评分、腰椎功能障碍的Oswestry功能障碍指数(ODI)、生活质量的欧洲五维健康量表值以及神经病理性疼痛的疼痛DETECT量表评估结局。收集住院时间、手术时间和阿片类药物使用等手术相关结局。记录随访期间发生的不良事件。
方法
所有参与者按1:1比例随机分配接受双孔道内镜下椎间盘切除术(双孔道组)或显微镜下椎间盘切除术(显微镜组)。主要结局是基于改良意向性分析策略,术后12个月时两组ODI评分的差异,非劣效界值为12.8分。次要结局包括PROMs、手术相关结局和不良事件。
结果
显微镜组术后12个月的ODI评分为11.97,双孔道组为13.89(平均差值为1.92;95%置信区间[CI]为-3.50至7.34),表明双孔道组非劣效。次要结局的结果与主要结局相似。双孔道组的肌酸磷酸激酶比值较低。双孔道组早期手术部位疼痛略低(术后48小时VAS疼痛评分的平均差值为-0.98;95%CI为-1.77至-0.19)。包括再次手术在内的不良事件在两组之间无显著差异。
结论
在12个月的时间里,双孔道内镜下椎间盘切除术不劣于显微镜下椎间盘切除术。双孔道内镜下椎间盘切除术被认为是一种相对安全有效的手术技术,具有减少肌肉损伤的轻微优势。然而,应仔细考虑手术部位疼痛的临床意义。