Department of Orthopaedics, The Second Affiliated Xinqiao Hospital of Army Medical University, Chongqing 400037, China.
Biomed Res Int. 2019 Jan 10;2019:6509409. doi: 10.1155/2019/6509409. eCollection 2019.
There is a steep learning curve with traditional percutaneous endoscopic lumbar discectomy (PELD). The aim of this study is to assess the safety and efficacy of PELD assisted by O-arm-based navigation for treating lumbar disc herniation (LDH).
From September of 2017 to January of 2018, 118 patients with symptomatic LDH were enrolled in the prospective cohort study. The patients undergoing PELD with O-arm-based navigation technique were defined as group A (58 cases), and those undergoing traditional X-ray fluoroscopy method were defined as group B (60 cases). We recorded the operation time, cannula placement time, radiation exposure time, visual analog scale (VAS), Oswestry Disability Index (ODI), and Macnab criteria score of the 2 groups.
The average operation time (95.21 ± 19.05 mins) and the cannula placement time (36.38 ± 14.67 mins) in group A were significantly reduced compared with group B (operation time, 113.83 ± 22.01 mins, P<0.001; cannula placement time, 52.63 ± 17.94 mins, P<0.001). The learning curve of PELD in group A was steeper than that in group B and was lower in the relatively flat region of the end. There were significant differences of the clinical parameters at different time points (VAS of low back, P < 0.001; VAS of leg, P < 0.001; and ODI, P < 0.001). The VAS scores for low back pain and leg pain improved significantly in both groups after surgery and gradually improved as time went by. No serious complication was observed in any patients in either group.
The study indicated that PELD assisted by O-arm navigation is safe, accurate, and efficient for the treatment of lumbar intervertebral disc herniation. It reshaped the learning curve of PELD, reduced the difficulty of surgery, and minimized radiation exposure to surgeons. This study was registered at Chinese Clinical Trail Registry (Registration Number: ChiCTR1800019586).
传统经皮内窥镜腰椎间盘切除术(PELD)的学习曲线陡峭。本研究旨在评估基于 O 臂导航的 PELD 治疗腰椎间盘突出症(LDH)的安全性和疗效。
本前瞻性队列研究纳入 2017 年 9 月至 2018 年 1 月的 118 例症状性 LDH 患者。采用基于 O 臂导航技术的 PELD 治疗的患者为 A 组(58 例),采用传统 X 射线透视法的患者为 B 组(60 例)。记录两组患者的手术时间、套管放置时间、辐射暴露时间、视觉模拟量表(VAS)评分、Oswestry 残疾指数(ODI)和 Macnab 标准评分。
A 组的平均手术时间(95.21±19.05min)和套管放置时间(36.38±14.67min)明显短于 B 组(手术时间:113.83±22.01min,P<0.001;套管放置时间:52.63±17.94min,P<0.001)。A 组的 PELD 学习曲线比 B 组陡峭,在相对平坦的区域较低。两组患者在不同时间点的临床参数均有显著差异(VAS 腰痛,P<0.001;VAS 腿痛,P<0.001;ODI,P<0.001)。两组患者术后腰痛和腿痛的 VAS 评分均显著改善,且随时间推移逐渐改善。两组患者均未发生严重并发症。
基于 O 臂导航的 PELD 治疗腰椎间盘突出症安全、准确、有效。它重塑了 PELD 的学习曲线,降低了手术难度,最大限度地减少了术者的辐射暴露。本研究在中国临床试验注册中心注册(注册号:ChiCTR1800019586)。