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Good outcome and restoration of lordosis after anterior lumbar interbody fusion with additional posterior fixation.

机译:腰椎前路椎体间融合融合后再进行后路固定,效果良好,脊柱前凸恢复。

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STUDY DESIGN: Fifty-two patients with degenerative disc disease underwent single- or double-level anterior lumbar interbody fusion with SynCage and additional posterior fixation as treatment for degenerative disc disease and were prospectively followed for 4 years. OBJECTIVES: To test the clinical performance of anterior lumbar interbody fusion with SynCage, with emphasis on the safety and efficacy of the surgical procedure and the ability to restore anatomy and fuse the motion segment. SUMMARY OF BACKGROUND DATA: Anterior lumbar interbody fusion using femoral allograft and/or autologous bone has a high complication rate. With cage technology, some of these complications can be avoided. The design characteristics of the SynCage offer advantages in restoring and maintaining intervertebral height and restoration of lumbar lordosis. METHODS: Thirty-three patients underwent single-level and 19 patients double-level anterior lumbar interbody fusion with SynCage and additional posterior fixation (translaminar screws, n = 32 or pedicle screws, n = 10). Radiologic and functional results (VAS and Oswestry score) were evaluated. RESULTS: Intervertebral height was corrected from an average of 8.7 to 17.6 mm. Lordosis of the fused segment was significantly increased (average 10.6 degrees for the fused segment and 8 degrees for lumbosacral lordosis). After 2 years, there was radiologic evidence for fusion in 70 of 71 (98.6%) levels. Functional scores showed a significant improvement in pain and function up to the 2-year follow-up observation. At the 4-year follow-up observation, there was some loss of the initial improvement in VAS and Oswestry scores. Despite this loss, they remained significantly better than the preoperative scores. CONCLUSIONS: Anterior lumbar interbody fusion with SynCage and additional posterior fixation is a safe and effective procedure. Intervertebral height is corrected, and lumbosacral lordosis is restored. An initial improvement in VAS and Oswestry scores is partly lost at the 4-year follow-up observation, but 4-year results are still significantly better than the preoperative scores.
机译:研究设计:52例退行性椎间盘疾病患者接受SynCage单级或双级前路腰椎椎间融合术,并采用后路固定治疗退行性椎间盘疾病,预期随访4年。目的:测试SynCage融合前腰椎椎间融合器的临床性能,重点在于手术过程的安全性和有效性以及恢复解剖结构和融合运动节段的能力。背景数据概述:使用股骨同种异体骨和/或自体骨进行前腰椎椎间融合术的并发症发生率很高。使用笼式技术,可以避免其中一些并发症。 SynCage的设计特性在恢复和保持椎间高度以及恢复腰椎前凸方面具有优势。方法:33例患者采用SynCage并附加后路固定(椎板螺钉,n = 32或椎弓根螺钉,n = 10),对单级和19例双级前腰椎椎间融合治疗。评估放射和功能结果(VAS和Oswestry评分)。结果:椎间高度从平均8.7毫米校正为17.6毫米。融合节的Lordosis明显增加(融合节平均10.6度,腰s部前凸平均8度)。两年后,有放射学证据表明融合水平达到了71个(98.6%)中的70个。在两年的随访观察中,功能评分显示疼痛和功能明显改善。在4年的随访观察中,VAS和Oswestry评分的最初改善有些损失。尽管有这种损失,但它们仍显着优于术前评分。结论:前路腰椎椎间融合术与SynCage融合和额外的后路固定术是一种安全有效的方法。矫正椎间高度,恢复腰s脊柱前凸。在4年的随访观察中,VAS和Oswestry评分的最初改善部分失去了,但是4年的结果仍然明显优于术前评分。

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