He Li-Ming, Li Jia-Rui, Wu Hao-Ran, Chang Qiang, Guan Xiao-Ming, Ma Zhuo, Feng Hao-Yu
Department of Orthopaedic Surgery, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Taiyuan, China.
Department of Orthopaedic Surgery, Third Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.
Front Surg. 2022 May 25;9:915522. doi: 10.3389/fsurg.2022.915522. eCollection 2022.
Endoscopic lumbar interbody fusion is a new technology that is mostly used for single-segment and unilateral lumbar spine surgery. The purpose of this study is to introduce percutaneous endoscopic posterior lumbar interbody fusion (PE-PLIF) with unilateral laminotomy for bilateral decompression (ULBD) for lumbar spondylolisthesis and evaluate the efficacy by comparing it with open posterior lumbar interbody fusion (PLIF).
Twenty-eight patients were enrolled in PE-PLIF with the ULBD group and the open PLIF group. The perioperative data of the two groups were compared to evaluate the safety of PE-PLIF with ULBD. The visual analog scale (VAS) back pain, VAS leg pain, and Oswestry Disability Index (ODI) scores of the two groups preoperatively and postoperatively were compared to evaluate clinical efficacy. Preoperative and postoperative imaging data were collected to evaluate the effectiveness of the operation.
No differences in baseline data were found between the two groups ( > 0.05). The operation time in PE-PLIF with the ULBD group (221.2 ± 32.9 min) was significantly longer than that in the PLIF group (138.4 ± 25.7 min) ( < 0.05), and the estimated blood loss and postoperative hospitalization were lower than those of the PLIF group ( < 0.05). The postoperative VAS and ODI scores were significantly improved in both groups ( < 0.05), but the postoperative VAS back pain score in the PE-PLIF group was significantly lower than that in the PLIF group ( < 0.05). The excellent and good rates in both groups were 96.4% according to MacNab's criteria. The disc height and cross-sectional area of the spinal canal were significantly improved in the two groups after surgery ( < 0.05), with no difference between the groups ( > 0.05). The fusion rates in PE-PLIF with the ULBD group and the PLIF group were 89.3% and 92.9% ( > 0.05), respectively, the cage subsidence rates were 14.3% and 17.9% ( > 0.05), respectively, and the lumbar spondylolisthesis reduction rates were 92.72 ± 6.39% and 93.54 ± 5.21%, respectively ( > 0.05).
The results from this study indicate that ULBD can be successfully performed during PE-PLIF, and the combined procedure is a safe and reliable treatment method for lumbar spondylolisthesis.
内镜下腰椎椎间融合术是一项主要用于单节段和单侧腰椎手术的新技术。本研究的目的是介绍用于腰椎滑脱症的经皮内镜下后路腰椎椎间融合术(PE-PLIF)联合单侧椎板切开双侧减压术(ULBD),并通过与开放后路腰椎椎间融合术(PLIF)比较来评估其疗效。
将28例患者纳入PE-PLIF联合ULBD组和开放PLIF组。比较两组的围手术期数据以评估PE-PLIF联合ULBD的安全性。比较两组术前和术后的视觉模拟量表(VAS)背痛评分、VAS腿痛评分和Oswestry功能障碍指数(ODI)评分以评估临床疗效。收集术前和术后的影像学数据以评估手术效果。
两组间基线数据无差异(>0.05)。PE-PLIF联合ULBD组的手术时间(221.2±32.9分钟)显著长于PLIF组(138.4±25.7分钟)(<0.05),估计失血量和术后住院时间低于PLIF组(<0.05)。两组术后VAS和ODI评分均显著改善(<0.05),但PE-PLIF组术后VAS背痛评分显著低于PLIF组(<0.05)。根据MacNab标准,两组的优良率均为96.4%。两组术后椎间盘高度和椎管横截面积均显著改善(<0.05),组间无差异(>0.05)。PE-PLIF联合ULBD组和PLIF组的融合率分别为89.3%和92.9%(>0.05),椎间融合器下沉率分别为14.3%和17.9%(>0.05),腰椎滑脱复位率分别为92.72±6.39%和93.54±5.21%(>0.05)。
本研究结果表明,在PE-PLIF过程中可成功实施ULBD,该联合手术是治疗腰椎滑脱症的一种安全可靠的治疗方法。