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在大鼠后外侧脊柱融合模型中,Accell Evo3和Grafton脱矿骨基质糊剂与自体骨的疗效比较。

Efficacy comparison of Accell Evo3 and Grafton demineralized bone matrix putties against autologous bone in a rat posterolateral spine fusion model.

作者信息

Brecevich Antonio T, Kiely Paul D, Yoon B Victor, Nguyen Joseph T, Cammisa Frank P, Abjornson Celeste

机构信息

Hospital for Special Surgery, 535 East 70th St, New York, NY 10021, USA; Integra® LifeSciences, 103 Morgan Lane, Plainsboro, NJ 08536, USA.

Mater Private Cork, Citygate, Mahon, Cork T12K199, Ireland.

出版信息

Spine J. 2017 Jun;17(6):855-862. doi: 10.1016/j.spinee.2017.01.012. Epub 2017 Jan 23.

Abstract

BACKGROUND CONTEXT

Spinal fusion procedures are intended to stabilize the spinal column for a multitude of disorders including abnormal curvature, traumatic instability, degenerative instability, and damage from infections or tumors. As an aid in the bone healing response, bone graft materials are used to bridge joints for arthrodesis and promote unions in pseudoarthrosis. Currently, the gold standard for stabilizing fusion masses in spinal procedures involves using the osteogenic, osteoinductive, and osteoconductive properties of autologous iliac crest corticocancellous bone. However, considerable morbidity is associated with harvesting the autologous graft. Donor site complications including infection, large hematomas, and pain have been reported at rates as high as 50% (Boden and Jeffrey, 1995). Biologically, the rate of bone repair dictates the rate at which the fusion mass will unite under autologous graft conditions.

PURPOSE

The purpose of this study is to compare the quality and rate of fusion between Accell Evo3 and Grafton demineralized bone matrix (DBM), with the gold standard iliac crest bone graft (ICBG) as the control, in athymic rat posterolateral fusion.

STUDY DESIGN

This study was a randomized, controlled study in a laboratory setting at the Hospital for Special Surgery in New York City. Blinded observations were made, which created an assessment of outcomes for successful fusions between each method.

PATIENT SAMPLE

Forty-eight (48) athymic rats were used in this study and underwent posterolateral lumbar fusion. They were assessed at either 3 weeks or 9 weeks to see the rate and efficacy of fusion.

OUTCOME MEASURES

Outcome measures will be the efficacy of the different bone grafts and their success rates of fusion in the rats.

METHODS

A comparison of the quality and rate of fusion between Accell Evo3® (DBM A) and Grafton (DBM B), with the gold standard iliac crest bone graft (ICBG) as the control, was performed using the established posterolateral intertransverse process on an athymic rat model. Materials were evaluated for fusion by several criteria, including manual palpation, standard and high-resolution radiographic imaging, micro-computed topography, and histologic analysis. Forty-eight (48) athymic rats received a bilateral intertransverse process fusion, using either bone from the iliac crest (control group), Accell Evo3, or Grafton. Twelve (12) rats (four from each group) were sacrificed at 3 weeks postoperatively, whereas the remaining thirty-six (36) were sacrificed at 9 weeks postoperatively. Three blinded observers examined the spines after the rats were euthanized, and they blindly assessed each rat for fusion success.

RESULTS

Manual palpation of the three different groups at 3 weeks postoperatively found successful fusion in 1 of 4 (25%) of the autologous bone graft (ABG) group and 4 of 4 (100%) of both DBM A and B groups. Manual palpation of the remaining animals that were sacrificed at 9 weeks postoperatively showed successful fusion in 4 of 12 (33%) of the ABG group, 8 of 12 (66%) of the DBM A group, and 12 of 12 (100%) of the DBM B group. Radiography found that 9 of 16 (56%) of the ABG group and 16 of 16 (100%) of both DBM Putty A and B groups had fused. Histologic analysis of the ABG group demonstrated less mature and less organized osteoid at both 3 and 9 weeks than the DBM Putty A and B groups. Nondestructive mechanical testing demonstrated increased stiffness in 4-point bending of both DBM A and B compared with ABG.

CONCLUSIONS

Both DBM-treated groups achieved a significantly higher rate of fusion than the ABG-treated group at 9 weeks in this model. Successful fusion was also demonstrated in the DBM-treated groups at 3 weeks.

摘要

背景

脊柱融合手术旨在稳定脊柱,治疗多种病症,包括脊柱侧弯、创伤性不稳定、退行性不稳定以及感染或肿瘤造成的损伤。作为促进骨愈合反应的辅助手段,骨移植材料用于连接关节以实现关节融合,并促进假关节的愈合。目前,脊柱手术中稳定融合块的金标准是使用自体髂嵴皮质松质骨的成骨、骨诱导和骨传导特性。然而,获取自体移植物会带来相当大的发病率。据报道,供体部位并发症,包括感染、大量血肿和疼痛,发生率高达50%(博登和杰弗里,1995年)。从生物学角度来看,骨修复的速度决定了在自体移植物条件下融合块愈合的速度。

目的

本研究的目的是在无胸腺大鼠后外侧融合模型中,将Accell Evo3和Grafton脱矿骨基质(DBM)与金标准髂嵴骨移植(ICBG)进行比较,以评估融合的质量和速度。

研究设计

本研究是在纽约市特种外科医院实验室环境下进行的随机对照研究。进行了盲法观察,以评估每种方法之间成功融合的结果。

患者样本

本研究使用了48只无胸腺大鼠,进行了后外侧腰椎融合手术。在术后3周或9周对它们进行评估,以观察融合的速度和效果。

结果指标

结果指标将是不同骨移植材料在大鼠中的疗效及其融合成功率。

方法

在无胸腺大鼠模型上,采用既定的后外侧横突间方法,将Accell Evo3®(DBM A)和Grafton(DBM B)与金标准髂嵴骨移植(ICBG)进行融合质量和速度的比较。通过多种标准评估材料的融合情况,包括手动触诊、标准和高分辨率放射成像、微计算机断层扫描和组织学分析。48只无胸腺大鼠接受双侧横突间融合手术,使用髂嵴骨(对照组)、Accell Evo3或Grafton。术后3周处死12只大鼠(每组4只),其余36只在术后9周处死。在大鼠安乐死后,由三名盲法观察者检查脊柱,并对每只大鼠的融合成功情况进行盲法评估。

结果

术后3周对三个不同组进行手动触诊发现,自体骨移植(ABG)组4只中有1只(25%)成功融合,DBM A组和DBM B组4只均成功融合(100%)。对术后9周处死的其余动物进行手动触诊发现,ABG组12只中有4只(33%)成功融合,DBM A组12只中有8只(66%)成功融合,DBM B组12只均成功融合(100%)。放射成像发现,ABG组16只中有9只(56%)融合,DBM Putty A组和DBM Putty B组16只均融合(100%)。ABG组的组织学分析表明,在3周和9周时,其类骨质比DBM Putty A组和DBM Putty B组更不成熟且更无组织。非破坏性力学测试表明,与ABG相比,DBM A组和DBM B组在四点弯曲试验中的刚度增加。

结论

在该模型中,9周时两个DBM治疗组的融合率均显著高于ABG治疗组。在3周时,DBM治疗组也显示出成功融合。

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