Faundez Antonio A, Taylor Sofia, Kaelin André J
Service de Chirurgie Orthopédique et de Traumatologie de l'Appareil Monteur, University Hospital of Geneva, Geneva, Switzerland.
Eur Spine J. 2006 Oct;15 Suppl 5(Suppl 5):630-5. doi: 10.1007/s00586-006-0162-4. Epub 2006 Jul 25.
In order to avoid the morbidity from autogenous bone harvesting, bone graft substitutes are being used more frequently in spinal surgery. There is indirect radiological evidence that bone graft substitutes are efficacious in humans. The purpose of this four-case study was to visually, manually, and histologically assess the quality of a fusion mass produced by a collagen hydroxyapatite scaffold impregnated with autologous bone marrow aspirate for posterolateral fusion. Four patients sustained an acute thoracolumbar fracture and were treated by short posterior segment fusion using the AO fixateur interne. Autologous bone marrow (iliac crest) impregnated hydroxyapatite-collagen scaffold was laid on the decorticated posterior elements. Routine implant removal was performed after a mean of 15.3 months (12-20). During this second surgery, fusion mass was assessed visually and manually. A bone biopsy was sent for histological analysis of all four cases. Fusion was confirmed in all four patients intraoperatively and sagittal stress testing confirmed mechanical adequacy of the fusion mass. Three out of the four (cases 2-4) had their implants removed between 12 and 15 months after the index surgery. All their histological cuts showed evidence of newly formed bone and presence of active membranous and/or enchondral ossification foci. The last patient (case 1) underwent implant removal at 20 months and his histological cuts showed mature bone, but no active ossification foci. This four-case report suggests that the fusion mass produced by a mineralized collagen matrix graft soaked in aspirated bone marrow is histologically and mechanically adequate in a thoracolumbar fracture model. A larger patient series and/or randomized controlled studies are warranted to confirm these initial results.
为避免自体骨采集带来的发病风险,骨移植替代物在脊柱手术中的应用越来越频繁。有间接影像学证据表明骨移植替代物对人类有效。本四例研究的目的是通过视觉、手动及组织学方法评估一种浸有自体骨髓抽吸物的胶原羟基磷灰石支架用于后外侧融合所产生融合块的质量。四名患者发生急性胸腰椎骨折,采用AO内固定器行短节段后路融合治疗。将浸有自体骨髓(髂嵴)的羟基磷灰石 - 胶原支架置于去皮质的后部结构上。平均15.3个月(12 - 20个月)后进行常规内固定取出。在第二次手术中,对融合块进行视觉和手动评估。对所有四例患者均进行骨活检以进行组织学分析。术中证实所有四名患者均融合良好,矢状面应力测试证实融合块力学性能良好。四例中的三例(病例2 - 4)在初次手术后12至15个月取出内固定。其所有组织学切片均显示有新形成骨的证据以及活跃的膜内和/或软骨内成骨灶。最后一名患者(病例1)在20个月时取出内固定,其组织学切片显示为成熟骨,但无活跃的成骨灶。这份四例报告表明,在胸腰椎骨折模型中,浸有骨髓抽吸物的矿化胶原基质移植物所产生的融合块在组织学和力学方面是足够的。需要更大规模的患者系列研究和/或随机对照研究来证实这些初步结果。