首页> 美国卫生研究院文献>other >Anterior Lumbar Interbody Fusion for Degenerative Discogenic Low Back Pain
【2h】

Anterior Lumbar Interbody Fusion for Degenerative Discogenic Low Back Pain

机译:前腰椎椎间融合治疗退行性椎间盘源性腰痛

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The treatment of degenerative discogenic pain is controversial, and anterior lumbar fusion for the treatment of degenerative discogenic low back pain has also been a controversial topic for over a generation.The aim of this systematic review was to evaluate the outcome of different anterior lumbar fusion levels for degenerative discogenic low back pain.In this study, we performed a clinical outcome subgroup analysis. The outcomes of 84 consecutive patients who underwent anterior lumbar interbody fusion from 2004 to 2009 were reviewed. The operative time, intraoperative blood loss, hospital stay, Oswestry Disability Index (ODI), visual analog scale (VAS) results, and complication rate were recorded separately.Medical indications were degenerative disc disease (73.8%), postdiscectomy disc disease (16.1%), and disc herniation (9.5%). Patients with severe spondylolysis or disc degeneration, with more than 3 or multilevel lesions, were excluded.The mean operative time was 124.5 ± 10.9 min (range 51–248 min), the mean intraoperative blood loss was 242.1 ± 27.7 mL (range 50–2700 mL), the mean hospital stay was 3.9 ± 1.1 days (range 3–6 days), the mean preoperative VAS score was 7.5 ± 1.4, and the mean preoperative ODI score was 60.0 ± 5.7. At the 1-year follow-up, the mean postoperative VAS score was 3.3 ± 1.3 and the mean postoperative ODI score was 13.6 ± 3.4 (P < 0.05). L4–L5 disc fusion led to better clinical results than 2-level L4–L5/L5–S1 disc fusion. Additionally, the 2-level fusion of L4–L5/L5–S1 had better clinical results than the L5–S1 disc fusion at both the 1 and 2-year postoperative follow-ups regarding the VAS score and the ODI score. The rate of complications was more frequent in the 2-level L4–L5/L5–S1 group (27.3%) (group C) than in the L4–L5 group (9.1%) (group A) and the L5–S1 group (12.5%) (group B). There was no difference between the L4–L5 group (9.1%) and the L5–S1 group (12.5%). A venous tear occurred during surgery and was successfully repaired in 6 of the 84 patients. Also, out of the 84 patients, 6 were found with pseudarthrosis during the follow-up, and these patients underwent a spinal fusion with instrumentation, with a posterior approach after a mean of 1 year. The complications secondary to the surgical approach were persistent abdominal pain (1/84, 1.2%) and wound dehiscence (1/84, 1.2%).Anterior lumbar interbody fusion for L4–L5 had better clinical results than the 2-segmental L4–L5/L5–S1 disc fusion, and the 2-segmental L4–L5/L5–S1 disc fusion had better clinical results than the L5–S1 disc fusion. Also, the 2-segmental L4–L5/L5–S1 disc fusion had a higher complication rate (27.3%), but there was no difference between the L4–L5 group (9.1%) and the L5–S1 group (12.5%).
机译:退行性椎间盘源性疼痛的治疗是有争议的,前腰椎融合术治疗退行性椎间盘源性下腰痛也已经是一个多世纪以来的有争议的话题。该系统评价的目的是评估不同的前路腰椎融合水平的结果在研究中,我们进行了临床结局亚组分析。回顾了2004年至2009年连续进行的84例前腰椎椎间融合术的患者的结局。分别记录手术时间,术中失血量,住院时间,Oswestry残疾指数(ODI),视觉模拟量表(VAS)结果和并发症发生率,其中医学指征为退行性椎间盘疾病(73.8%),椎间盘切除术后椎间盘疾病(16.1%) )和椎间盘突出症(9.5%)。严重椎体峡部裂或椎间盘退变并有3个以上或多级病变的患者被排除在外。平均手术时间为124.5±10.9 min(范围为51–248 min),平均术中失血量为242.1±27.7(mL(范围为50– 2700 mL),平均住院时间为3.9±1.1天(范围3–6天),术前VAS评分为7.5±1.4,平均ODI评分为60.0±5.7。术后1年的平均VAS评分为3.3±±1.3,术后ODI评分为13.6±3.4(P <0.05)。 L2–L5椎间盘融合术比2级L4–L5 / L5–S1椎间盘融合术产生更好的临床效果。此外,在术后1年和2年随访中,就VAS评分和ODI评分而言,L4–L5 / L5–S1的2级融合比L5–S1椎间盘融合具有更好的临床效果。 2级L4–L5 / L5–S1组(27.3%)(C组)的并发症发生率高于L4–L5组(9.1%)(A组)和L5–S1组( 12.5%)(B组)。 L4–L5组(9.1%)和L5–S1组(12.5%)之间没有差异。手术期间发生静脉撕裂,成功修复了84例患者中的6例。另外,在这84例患者中,有6例在随访期间发现假关节,这些患者在平均1年后接受了器械后路脊柱融合术。手术方法继发的并发症是持续性腹痛(1 / 84,1.2%)和伤口裂开(1 / 84,1.2%)。L4-L5的前路腰椎椎间融合比二段式L4- L5 / L5-S1椎间盘融合和2段L4-L5 / L5-S1椎间盘融合比L5-S1椎间盘融合具有更好的临床效果。同样,两段式L4–L5 / L5–S1椎间盘融合术的并发症发生率更高(27.3%),但L4–L5组(9.1%)和L5–S1组(12.5%)之间没有差异。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号