Dimar John R, Glassman Steven D, Burkus J Kenneth, Pryor Philip W, Hardacker James W, Carreon Leah Y
Leatherman Spine Center, 210 East Gray Street, Suite 900, Louisville, KY 40202, USA.
J Bone Joint Surg Am. 2009 Jun;91(6):1377-86. doi: 10.2106/JBJS.H.00200.
Previous studies have demonstrated the ability of recombinant human bone morphogenetic protein to achieve a solid fusion in anterior lumbar interbody arthrodesis. The purpose of this study was to compare iliac crest bone graft and recombinant human bone morphogenetic protein-2, combined with a carrier consisting of bovine collagen and beta-tricalcium phosphate-hydroxyapatite to create a compression-resistant matrix, for instrumented single-level posterolateral arthrodesis.
Four hundred and sixty-three patients with symptomatic single-level lumbosacral degenerative disease with no greater than grade-1 spondylolisthesis were treated with single-level instrumented posterolateral arthrodesis through an open midline approach. Patients were randomly assigned to either the recombinant human bone morphogenetic protein-2 matrix group (239 patients) or the autogenous iliac crest bone-graft group (224 patients). The Oswestry Disability Index, Short Form-36, and back and leg pain scores were determined preoperatively and at 1.5, three, six, twelve, and twenty-four months postoperatively. Radiographs and computed tomography scans were made at six, twelve, and twenty-four months postoperatively to evaluate for fusion.
The mean operative time and mean blood loss in the recombinant human bone morphogenetic protein-2 matrix group (2.5 hours and 343.1 mL, respectively) were significantly less than those in the iliac crest bone-graft group (2.9 hours and 448.6 mL). Both groups showed similar improvements in clinical outcomes and reduced pain. At twenty-four months, 60% of the iliac crest bone-graft group reported donor-site pain. At twenty-four months, fusion was evident in 96% of the patients in the recombinant human bone morphogenetic protein-2 matrix group compared with 89% in the iliac crest bone-graft group (p = 0.014). There was a significant difference (p = 0.011) in the rate of failures because of nonunion (eighteen patients with an iliac crest bone graft compared with six patients with the recombinant human bone morphogenetic protein-2 matrix). Also, the number of patients requiring second surgeries was significantly higher in the iliac crest bone-graft group (thirty-six patients) compared with the recombinant human bone morphogenetic protein-2 matrix group (twenty patients) (p = 0.015).
The use of recombinant human bone morphogenetic protein-2 in instrumented posterolateral lumbar arthrodesis decreases operative time and blood loss and produces earlier and higher fusion rates than does iliac crest bone graft. Clinical outcomes are similar to those with iliac crest bone graft. Thus, the need for harvesting iliac crest bone is eliminated along with the morbidities associated with the harvest procedure.
既往研究已证实重组人骨形态发生蛋白在前路腰椎椎间融合术中实现牢固融合的能力。本研究的目的是比较髂骨植骨与重组人骨形态发生蛋白-2,联合由牛胶原蛋白和β-磷酸三钙-羟基磷灰石组成的载体以创建抗压基质,用于器械辅助单节段后外侧融合术。
463例有症状的单节段腰骶部退行性疾病且滑脱不超过Ⅰ度的患者,通过开放中线入路接受单节段器械辅助后外侧融合术。患者被随机分为重组人骨形态发生蛋白-2基质组(239例患者)或自体髂骨植骨组(224例患者)。术前及术后1.5、3、6、12和24个月测定Oswestry功能障碍指数、简明健康状况调查量表以及腰腿痛评分。术后6、12和24个月进行X线片及计算机断层扫描以评估融合情况。
重组人骨形态发生蛋白-2基质组的平均手术时间和平均失血量(分别为2.5小时和343.1 mL)显著少于髂骨植骨组(2.9小时和448.6 mL)。两组在临床结局改善和疼痛减轻方面表现相似。在24个月时,髂骨植骨组60%的患者报告供区疼痛。在24个月时,重组人骨形态发生蛋白-2基质组96%的患者出现明显融合,而髂骨植骨组为89%(p = 0.014)。因不愈合导致的失败率存在显著差异(p = 0.011)(髂骨植骨组18例患者,重组人骨形态发生蛋白-2基质组6例患者)。此外,髂骨植骨组需要二次手术的患者数量(36例患者)显著高于重组人骨形态发生蛋白-2基质组(20例患者)(p = 0.015)。
在器械辅助下的腰椎后外侧融合术中使用重组人骨形态发生蛋白-2可减少手术时间和失血量,且比髂骨植骨产生更早、更高的融合率。临床结局与髂骨植骨相似。因此,消除了获取髂骨的需求以及与获取过程相关的并发症。