Putzier Michael, Strube Patrick, Funk Julia F, Gross Christian, Mönig Hans-Joachim, Perka Carsten, Pruss Axel
Klinik für Orthopädie, Centrum für Muskuloskeletale Chirurgie, Charité, Universitätsmedizin Berlin, Charité Campus Mitte, Charitéplatz 1, 10117, Berlin, Germany.
Eur Spine J. 2009 May;18(5):687-95. doi: 10.1007/s00586-008-0875-7. Epub 2009 Jan 16.
The current gold standard in lumbar fusion consists of transpedicular fixation in combination with an interbody interponate of autologous bone from iliac crest. Because of the limited availability of autologous bone as well as the still relevant donor site morbidity after iliac crest grafting the need exists for alternative grafts with a comparable outcome. Forty patients with degenerative spinal disease were treated with a monosegmental spondylodesis (ventrally, 1 PEEK-cage; dorsally, a screw and rod system), and randomly placed in two groups. In group 1, autogenous iliac crest cancellous bone was used as a cage filling. In group 2 the cages were filled with an allogenic cancellous bone graft. Following 3, 6, 9 and 12 months, the clinical outcome was determined on the basis of: the Oswestry Low Back Pain Disability Questionnaire; patient satisfaction; patient willingness to undergo the operation again; and a visual analog scale for pain. The radiological outcome was based on both fusion rate (radiographs, computed tomography), and on the bone mineral density of the grafts. After 6 months, the X-rays of the patients in group 2 had a significantly lower rate of fusion. Aside from this, there were no further significant differences. After 12 months, radiological results showed a similar fusion rate in both groups. Donor site complications consisted of five patients with hematoma, and three patients with persistent pain in group 1. No implant complications were observed. If a bone bank is available for support and accepting the low risk of possible transmission of infectious diseases, freeze-dried allogenic cancellous bone can be used for monosegmental spondylodeses. The results demonstrated an equivalent clinical outcome, as well as similar fusion rates following a 12-month period. This is in despite of a delayed consolidation process.
目前腰椎融合的金标准是椎弓根固定结合取自髂嵴的自体骨椎间植入物。由于自体骨供应有限以及髂嵴植骨后仍存在明显的供区并发症,因此需要有疗效相当的替代移植物。40例退行性脊柱疾病患者接受了单节段脊柱融合术(前路,1个聚醚醚酮椎间融合器;后路,螺钉和棒系统),并随机分为两组。第1组使用自体髂骨松质骨作为椎间融合器填充物。第2组的椎间融合器填充异体松质骨移植物。在3、6、9和12个月后,根据以下指标确定临床疗效:奥斯威斯rey下腰痛残疾问卷;患者满意度;患者再次接受手术的意愿;以及疼痛视觉模拟量表。放射学结果基于融合率(X线片、计算机断层扫描)以及移植物的骨密度。6个月后,第2组患者的X线片融合率明显较低。除此之外,没有进一步的显著差异。12个月后,放射学结果显示两组的融合率相似。第1组供区并发症包括5例血肿患者和3例持续疼痛患者。未观察到植入物并发症。如果有骨库支持并接受可能传播传染病的低风险,冻干异体松质骨可用于单节段脊柱融合术。结果显示,12个月后临床疗效相当,融合率也相似。尽管骨愈合过程有所延迟。