Gao Mingxuan, Liu Xingyan, Zhen Ping, Xue Yun, Tian Qi
Department of Orthopaedics and Trauma, Center of Orthopedic Surgery, General Hospital of Lanzhou Military Area Command of Chinese PLA, Lanzhou Gansu 730050, PR China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2009 Aug;23(8):904-8.
To evaluate the therapeutic effects of expandable pedicle screw (EPS) combined with interbody fusion cage on lumbar spondylolisthesis.
From June 2004 to March 2008, 23 patients with lumbar spondylolisthesis were treated, including 9 males and 14 females aged 24-72 years old (average 48.7 years old). The course of the disease varied from 6 months to 6 years (average 30.4 months). There were 18 cases of degenerative spondylolisthesis and 5 of isthmic spondylolisthesis, including 1 case at L3,4 level, 14 at L4,5 level, and 8 at L5 and S1 levels. There were 17 cases of grade I, 4 of grade II, and 2 of grade III (including 1 case of recurrent L5 spondylolysis) according to Meyerding classification system. Posterior lumbar interbody fusion was performed using 48 PLIVIOS interbody fusion cages, and spondylolisthesis reduction and internal fixation were conducted using 84 pieces of EPS. The indications for use of EPS were initial operation with bone mass reduction or osteoporosis, reoperation of previous pedicle instrumentation, intraoperative screw relocation, sacral anchoring, and construct reinforcement. Clinical outcomes, radiographic reduction of spondylolisthesis and bone fusion of lumbar interbody were evaluated based on JOA score, Boxall index, and Cook criteria.
The incision healed by first intension in all cases except for one revision case that suffered from postoperative cerebrospinal fluid leakage and obtained delayed-healing without infection 23 days after operation using conservative treatment. No operative complications such as nerve and organ injuries were found. All cases were followed up for 12-39 months (average 17.8 months). X-ray exams of spine AP, lateral, fully extended position and fully flexed position view showed all 84 EPS were fully expanded within vertebral body. The improvement rate of JOA at the final follow-up visit was markedly effective in 14 cases, and effective in 5 cases, and noneffective in 4 cases, with a total effective rate of 82.61%. Anatomic reduction was achieved in 14 cases, improvement was obtained in 6 cases, no improvement was observed in 3 cases, and the reduction rate was 86.69%. Lumber interbody fusion was achieved in 20 cases, fixation was achieved in 2 cases, failure was observed in 1 cases, and the fusion rate was 86.69%.
EPS in complex with interbody fusion cage provides effective reduction, internal fixation and interbody fusion for the reconstruction of lumbar spondylolisthesis.
评估可扩张椎弓根螺钉(EPS)联合椎间融合器治疗腰椎滑脱症的疗效。
2004年6月至2008年3月,对23例腰椎滑脱症患者进行治疗,其中男性9例,女性14例,年龄24 - 72岁(平均48.7岁)。病程6个月至6年(平均30.4个月)。退行性腰椎滑脱症18例,峡部裂性腰椎滑脱症5例,其中L3、4节段1例,L4、5节段14例,L5与S1节段8例。根据Meyerding分级系统,I级17例,II级4例,III级2例(包括1例复发性L5椎弓根峡部裂)。采用48枚PLIVIOS椎间融合器行后路腰椎椎间融合术,使用84枚EPS进行腰椎滑脱复位及内固定。EPS的使用指征为初次手术伴骨质减少或骨质疏松、既往椎弓根内固定翻修手术、术中螺钉重新定位、骶骨锚固及加强内固定结构。根据JOA评分、Boxall指数和Cook标准评估临床疗效、腰椎滑脱的影像学复位情况及腰椎椎间融合情况。
除1例翻修病例术后出现脑脊液漏,经保守治疗术后23天延迟愈合且无感染外,所有病例切口均一期愈合。未发现神经及器官损伤等手术并发症。所有病例随访12 - 39个月(平均17.8个月)。脊柱正位、侧位、过伸位及过屈位X线检查显示,84枚EPS在椎体内均完全扩张。末次随访时JOA改善率:显效14例,有效5例,无效4例,总有效率82.61%。解剖复位14例,改善6例,未改善3例,复位率86.69%。腰椎椎间融合20例,固定2例,失败1例,融合率86.69%。
EPS联合椎间融合器可为腰椎滑脱症的重建提供有效的复位、内固定及椎间融合。