Kim Jin Wook, Park Hyung Chun, Yoon Seung Hwan, Oh Seong Hoon, Roh Sung Woo, Rim Dae Cheol, Kim Tae Sung
Department of Neurosurgery , Inha University, College of Medicine, Incheon, Korea.
J Korean Neurosurg Soc. 2007 Oct;42(4):251-7. doi: 10.3340/jkns.2007.42.4.251. Epub 2007 Oct 20.
This multi-center clinical study was designed to determine the long-term results of patients who received a one-level posterior lumbar interbody fusion with expandable cage (Tyche(R) cage) for degenerative spinal diseases during the same period in each hospital.
Fifty-seven patients with low back pain who had a one-level posterior lumbar interbody fusion using a newly designed expandable cage were enrolled in this study at five centers from June 2003 to December 2004 and followed up for 24 months. Pain improvement was checked with a Visual Analogue Scale (VAS) and their disability was evaluated with the Oswestry Disability Index. Radiographs were obtained before and after surgery. At the final follow-up, dynamic stability, quality of bone fusion, interveretebral disc height, and lumbar lordosis were assessed. In some cases, a lumbar computed tomography scan was also obtained.
The mean VAS score of back pain was improved from 6.44 points preoperatively to 0.44 at the final visit and the score of sciatica was reduced from 4.84 to 0.26. Also, the Oswestry Disability Index was improved from 32.62 points preoperatively to 18.25 at the final visit. The fusion rate was 92.5%. Intervertebral disc height, recorded as 9.94+/-2.69 mm before surgery was increased to 12.23+/-3.31 mm at postoperative 1 month and was stabilized at 11.43+/-2.23 mm on final visit. The segmental angle of lordosis was changed significantly from 3.54+/-3.70 degrees before surgery to 6.37+/-3.97 degrees by 24 months postoperative, and total lumbar lordosis was 20.37+/-11.30 degrees preoperatively and 24.71+/-11.70 degrees at 24 months postoperative.
There have been no special complications regarding the expandable cage during the follow-up period and the results of this study demonstrates a high fusion rate and clinical success.
本多中心临床研究旨在确定同期在各医院接受单节段后路腰椎椎间融合术并使用可扩张椎间融合器(Tyche®椎间融合器)治疗退行性脊柱疾病患者的长期疗效。
2003年6月至2004年12月期间,来自五个中心的57例因腰痛接受了使用新设计的可扩张椎间融合器的单节段后路腰椎椎间融合术的患者被纳入本研究,并进行了24个月的随访。使用视觉模拟量表(VAS)检查疼痛改善情况,并用Oswestry功能障碍指数评估其功能障碍程度。在手术前后拍摄X光片。在最后一次随访时,评估动态稳定性、骨融合质量、椎间隙高度和腰椎前凸。在某些情况下,还进行了腰椎计算机断层扫描。
背痛的平均VAS评分从术前的6.44分改善至最后一次随访时的0.44分,坐骨神经痛评分从4.84分降至0.26分。此外,Oswestry功能障碍指数从术前的32.62分改善至最后一次随访时的18.25分。融合率为92.5%。术前记录的椎间隙高度为9.94±2.69mm,术后1个月增加至12.23±3.31mm,并在最后一次随访时稳定在11.43±2.23mm。脊柱前凸节段角度从术前的3.54±3.70度显著变化至术后24个月时的6.37±3.97度,术前总腰椎前凸为20.37±11.30度,术后24个月时为24.71±11.70度。
随访期间,可扩张椎间融合器未出现特殊并发症,本研究结果显示融合率高且临床效果良好。