Dong Jianwen, Yang Yang, Chen Zihao, Yu Mingzhu, Liu Bin, Wang Qiyou, Xie Peigen, Chen Ruiqiang, Rong Limin
Department of Spine Surgery, the 3rd Affiliated Hospital of Sun Yat-sen University, Guangzhou Guangdong, 510630, P.R.China.
Department of Spine Surgery, the 3rd Affiliated Hospital of Sun Yat-sen University, Guangzhou Guangdong, 510630,
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2019 Jul 15;33(7):814-821. doi: 10.7507/1002-1892.201903112.
To analyze the medium and long-term effectiveness of microendoscope-assisted minimally invasive transforaminal lumbar interbody fusion (MIS-TLIF) for lumbar degenerative diseases in comparison with conventional tubular retractor-assisted MIS-TLIF.
Between November 2008 and March 2013, 53 patients with single segment lumbar degenerative diseases were enrolled. According to the different working channel performed, 28 patients were treated by microendoscope-assisted MIS-TLIF (observation group), while the remaining cases received conventional tubular retractor-assisted MIS-TLIF via Wiltse approach (control group). Preoperative baseline data, including age, gender, body mass index, disease etiology, operated level, the ration for requiring bilateral canal decompression, and preoperative visual analogue scale (VAS) socre of low back pain and leg pain, Japanese Orthopedic Association (JOA) score, Oswestry disability index (ODI) score, showed no significant difference between the two groups ( >0.05). The operation time, intraoperative blood loss, intraoperative fluoroscopy time, postoperative analgesic drug dose, postoperation in-bed time, and perioperative complication incidence were recorded respectively and compared between the two groups. Radiographic evaluation of interbody fusion was performed based on Bridwell grading system at 2 years after operation. VAS scores of low back pain and leg pain, JOA score, and ODI score were assessed before operation, at 2 years after operation, and at last follow-up respectively. Surgical outcome satisfaction was assessed by modified MacNab criteria at last follow-up.
When compared with those in control group, both intraoperative blood loss and postoperative analgesic drug dose were significantly decreased in observation group ( <0.05); similarly, the operation time and intraoperative fluoroscopy time were also significantly increased in observation group ( <0.05). There was no significant difference of postoperative in-bed time between the two groups ( =-0.812, =0.420). Both groups were followed up 6-10.3 years, with an average of 7.9 years. Regarding perioperative complication, its incidence was 14.3% and 20.0% in observation group and control group, respectively, showing no significant difference between both groups ( =0.306, =0.580). Specifically, there were intraspinal hematoma formation in 1 case, incision infection in 1 case, urinary infection in 1 case, transient delirium in 1 case in observation group. By contrast, there were dural tear and cerebrospinal fluid leakage in 1 case, urinary infection in 1 case, pneumonia in 1 case, transient delirium in 2 cases in control group. Bridwell criterion was used to judge the intervertebral fusion at 2 years after operation, the fusion rates of observation group and control group were 92.9% and 92.0%, respectively, showing no significant difference ( =0.162, =0.687). At both 2-year postoperatively and last follow-up, the VAS scores of low back pain and leg pain, JOA score, and ODI score were significantly improved when compared with those before operation ( <0.01), whereas no significant difference between the two groups at either time point was found ( >0.05). At last follow-up, the results of patients' satisfaction with surgery evaluated by modified MacNab criteria, and the excellent and good rates of the observation group and the control group were 96.4% and 92.0%, respectively, showing no significant difference ( =0.485, =0.486).
The medium and long-term effectiveness of microendoscope-assisted MIS-TLIF are similar to those of conventional tubular retractor-assisted MIS-TLIF for lumbar degenerative diseases. The former operation has the additional advantages in terms of more clear surgical site visually, less intraoperative blood loss, and reduced postoperative analgesic dose, all of which seem more feasible to clinical teaching.
比较微型内镜辅助下微创经椎间孔腰椎椎体间融合术(MIS-TLIF)与传统管状牵开器辅助下MIS-TLIF治疗腰椎退变性疾病的中长期疗效。
2008年11月至2013年3月,纳入53例单节段腰椎退变性疾病患者。根据所使用的不同工作通道,28例患者接受微型内镜辅助下MIS-TLIF治疗(观察组),其余患者通过Wiltse入路接受传统管状牵开器辅助下MIS-TLIF治疗(对照组)。术前基线数据,包括年龄、性别、体重指数、疾病病因、手术节段、双侧椎管减压需求比例以及术前腰痛和腿痛的视觉模拟评分(VAS)、日本骨科学会(JOA)评分、Oswestry功能障碍指数(ODI)评分,两组间比较差异无统计学意义(>0.05)。分别记录两组患者的手术时间、术中出血量、术中透视时间、术后镇痛药用量、术后卧床时间及围手术期并发症发生率,并进行比较。术后2年根据Bridwell分级系统对椎间融合情况进行影像学评估。分别于术前、术后2年及末次随访时评估腰痛和腿痛的VAS评分、JOA评分及ODI评分。末次随访时采用改良MacNab标准评估手术疗效满意度。
与对照组相比,观察组术中出血量及术后镇痛药用量均显著减少(<0.05);同样,观察组手术时间及术中透视时间也显著延长(<0.05)。两组术后卧床时间差异无统计学意义(=-0.812,=0.420)。两组均随访6 - 10.3年,平均7.9年。围手术期并发症方面,观察组和对照组发生率分别为14.3%和20.0%,两组间差异无统计学意义(=0.306,=0.580)。具体而言,观察组有1例发生椎管内血肿形成、1例切口感染、1例泌尿系统感染、1例短暂谵妄。相比之下,对照组有1例发生硬脊膜撕裂及脑脊液漏、1例泌尿系统感染、1例肺炎、2例短暂谵妄。术后2年采用Bridwell标准判断椎间融合情况,观察组和对照组融合率分别为92.9%和92.0%,差异无统计学意义(=0.162,=0.687)。术后2年及末次随访时,腰痛和腿痛的VAS评分、JOA评分及ODI评分与术前相比均显著改善(<0.01),但两组在各时间点比较差异无统计学意义(>0.05)。末次随访时采用改良MacNab标准评估患者手术疗效满意度,观察组和对照组优良率分别为96.4%和92.0%,差异无统计学意义(=0.485,=0.486)。
微型内镜辅助下MIS-TLIF治疗腰椎退变性疾病的中长期疗效与传统管状牵开器辅助下MIS-TLIF相似。前者手术在术野更清晰、术中出血量更少及术后镇痛药用量减少方面具有额外优势,对临床教学似乎更可行。