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在退变性腰椎疾病的后路腰椎椎间融合术中,大肠杆菌衍生的重组人骨形态发生蛋白-2与自体局部骨移植相比的融合率

Fusion rate of Escherichia coli-derived recombinant human bone morphogenetic protein-2 compared with local bone autograft in posterior lumbar interbody fusion for degenerative lumbar disorders.

作者信息

Park Sangman, Jeong Yeong Ha, Ha Byeong Jin, Yoo Beom Seok, Kim Soo-Heon, Lee Chang Kyu, Yi Seong, Ha Yoon, Kim Keung Nyun, Shin Dong Ah

机构信息

Department of Neurosurgery, Spine and Spinal Cord Institute, Severance Hospital, Yonsei University College of Medicine, 50-1, Yonsei-ro, Seodaemun-gu, Seoul, Republic of Korea.

Department of Neurosurgery, Spine and Spinal Cord Institute, Severance Hospital, Yonsei University College of Medicine, 50-1, Yonsei-ro, Seodaemun-gu, Seoul, Republic of Korea.

出版信息

Spine J. 2023 Dec;23(12):1877-1885. doi: 10.1016/j.spinee.2023.07.017. Epub 2023 Jul 27.

Abstract

BACKGROUND CONTEXT

The use of recombinant human bone morphogenetic proteins-2 (rhBMP-2) for spinal fusion has been reported to be effective. However, most studies have focused on posterolateral and anterior lumbar interbody fusion, and few have investigated posterior lumbar interbody fusion (PLIF).

PURPOSE

This study aimed to determine the effectiveness and safety of the delivery of Escherichia coli-derived rhBMP-2 (E.BMP-2) with hydroxyapatite (HA) and β-tricalcium phosphate (β-TCP) poloxamer hydrogel composite carriers for PLIF.

STUDY DESIGN

A retrospective study.

PATIENT SAMPLE

Patients who underwent 1 to 3 levels of PLIF for lumbar degenerative disc disorders between 2015 and 2020 with a follow-up of ≥1 year were enrolled. In total, 254 patients (357 levels) were included in the analysis. The evaluation was performed at each segment level. In the E.BMP-2 group, 160 patients (221 levels) received autologous local bone with E.BMP-2 (maximum 0.5 mg/level), and in the control group, 94 patients (136 levels) received only local bone graft.

OUTCOME MEASURES

The primary outcome of this study was to compare the X-ray and CT fusion rates between the two groups. Secondary outcomes included analysis of the patients' clinical outcomes and postoperative complications on CT scans.

METHODS

Clinical evaluations were performed using a visual analog scale for back pain, the Oswestry Disability Index for disability, and physical and mental component summaries of the Short Form 36-Item Form Health Survey to assess functional effects and quality of life. The fusion was evaluated using radiography and CT. On radiography, solid fusion was defined when the difference between extension and flexion was less than 5°. On CT, solid fusion was defined when the upper and lower vertebral bodies were connected by the trabecular bone (bone bridge formation). In addition, complications such as osteolysis, cage subsidence, and screw loosening were investigated using CT.

RESULTS

All clinical results for low back pain, disability, and quality of life in both groups were excellent and showed statistically significant improvements compared with baseline (p<.0001). According to the X-ray evaluations, fusion was achieved in 92.31% (204/221) of the patients in the E.BMP-2 group and 82.35% (112/136) of the patients in the control group (p=.0041). According to the CT evaluations, the fusion rates were 93.21% (206/221) and 88.24% (120/136) in the E.BMP-2 and control groups (p=.1048), respectively. Except for screw loosening, which had a significantly higher incidence in the control group (p=.0014), the rates of most postoperative complications were not significantly different between the groups.

CONCLUSIONS

This study demonstrated that the adjunctive use of a low dose of E.BMP-2 with HA and β-TCP hydrogel can effectively promote bone fusion, making it a promising option for patients with limited autograft availability or compromised bone quality in PLIF.

摘要

背景

据报道,重组人骨形态发生蛋白-2(rhBMP-2)用于脊柱融合术是有效的。然而,大多数研究集中在后外侧和前路腰椎椎间融合术,很少有研究调查后路腰椎椎间融合术(PLIF)。

目的

本研究旨在确定将大肠杆菌衍生的rhBMP-2(E.BMP-2)与羟基磷灰石(HA)和β-磷酸三钙(β-TCP)泊洛沙姆水凝胶复合载体用于PLIF的有效性和安全性。

研究设计

一项回顾性研究。

患者样本

纳入2015年至2020年间因腰椎间盘退变疾病接受1至3节段PLIF且随访≥1年的患者。总共254例患者(357节段)纳入分析。在每个节段水平进行评估。在E.BMP-2组,160例患者(221节段)接受自体局部骨加E.BMP-2(最大0.5mg/节段),对照组94例患者(136节段)仅接受局部骨移植。

观察指标

本研究的主要观察指标是比较两组之间的X线和CT融合率。次要观察指标包括分析患者的临床结局以及CT扫描上的术后并发症。

方法

使用视觉模拟量表评估背痛、Oswestry功能障碍指数评估功能障碍,以及简短健康调查问卷36项版本的生理和心理成分总结来评估功能影响和生活质量。使用X线摄影和CT评估融合情况。在X线摄影中,当伸展和屈曲之间的差异小于5°时定义为牢固融合。在CT上,当上、下椎体通过小梁骨连接(骨桥形成)时定义为牢固融合。此外,使用CT调查诸如骨质溶解、椎间融合器下沉和螺钉松动等并发症。

结果

两组中所有关于下腰痛、功能障碍和生活质量的临床结果均极佳,与基线相比有统计学意义的改善(p<0.0001)。根据X线评估,E.BMP-2组92.31%(204/221)的患者实现融合,对照组82.35%(112/136)的患者实现融合(p=0.0041)。根据CT评估,E.BMP-2组和对照组的融合率分别为93.21%(206/221)和88.24%(120/136)(p=0.1048)。除了对照组螺钉松动发生率显著更高(p=0.0014)外,两组间大多数术后并发症的发生率无显著差异。

结论

本研究表明,低剂量E.BMP-2与HA和β-TCP水凝胶联合使用可有效促进骨融合,使其成为PLIF中自体骨可用性有限或骨质受损患者的一个有前景的选择。

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