用三角形固定柄假体固定的超短残余股骨近端初级稳定性:基于锯骨模型的生物力学比较研究。

IF 4.3 3区 工程技术 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Frontiers in Bioengineering and Biotechnology Pub Date : 2024-10-14 eCollection Date: 2024-01-01 DOI:10.3389/fbioe.2024.1493738
Ziwei Hou, Kai Zheng, Ming Xu, Xiuchun Yu
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引用次数: 0

摘要

背景:股骨近端附近的肿瘤切除和股骨远端假体翻修手术可能会导致股骨近端残留非常短的骨段,即超短残余股骨近端(URPF)。在这项研究中,我们提出了一种三角形固定柄(TFS)假体,以改善 URPF 的固定。本研究的目的是通过体外生物力学实验研究 TFS 假体的生物力学特性,并将其与传统干(CS)假体进行比较,为 URPF 的假体固定提供初步的生物力学证据:方法:使用锯骨进行生物力学研究,以探索初始稳定性。使用 12 块锯骨创建骨缺损模型,并设计和制造假体以模拟 TFS 固定和 CS 固定结构。使用机械试验机对固定模型进行轴向压缩和水平扭转实验,记录最大位移、最大扭矩和股骨应变情况:在 2800 N 的轴向压缩载荷下,TFS 组的整体位移为 3.33 ± 0.58 mm,明显小于 CS 组(4.03 ± 0.32 mm,P = 0.029)。TFS组的股骨样本显示,内侧2、3、5、6点和外侧10点的应变值变化明显小于传统骨干组(P < 0.05)。在1°、3°和5°水平的扭转负荷下,TFS组的扭矩分别为3.86±0.69 Nm、3.90±1.26 Nm和4.39±1.67 Nm,均明显大于CS组(分别为1.82±0.82 Nm,P < 0.001;2.05±0.89 Nm,P = 0.016;1.96±0.50 Nm,P = 0.015):结论:TFS假体提高了固定强度,减少了股骨近端表面的应变。结论:TFS假体提高了固定强度,减少了股骨近端表面的应变,与CS固定相比,它具有更好的抗压缩性和抗旋转性,并提高了初始稳定性。
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The primary stability of ultrashort residual proximal femur fixed with triangular fixation stem prosthesis: a comparative biomechanical study based on sawbones models.

Background: Tumor resection near the proximal end of the femur and revision surgery of the distal femoral prosthesis may result in a very short bone segment remaining at the proximal end of the femur, known as ultrashort residual proximal femur (URPF). In this study, we propose a triangular fixation stem (TFS) prosthesis to improve the fixation of URPF. The aim of this research is to investigate the biomechanical properties of the TFS prosthesis and compare it with the conventional stem (CS) prosthesis through in vitro biomechanical experiments, providing preliminary biomechanical evidence for prosthetic fixation of URPF.

Methods: A biomechanical study was conducted using Sawbones to explore initial stability. Twelve Sawbones were used to create a bone defect model, and prostheses were designed and fabricated to emulate TFS fixation and CS fixation structures. Axial compression and horizontal torsion experiments were performed on the fixed models using a mechanical testing machine, recording maximum displacement, maximum torque, and femoral strain conditions.

Results: Under an axial compressive load of 2800 N, the overall displacement of the TFS group was 3.33 ± 0.58 mm, which was significantly smaller than that of the CS group (4.03 ± 0.32 mm, P = 0.029). The femoral samples of the TFS group demonstrated that the strain value alterations at the medial points 2, 3, 5, 6 and the lateral point 10 were conspicuously smaller than those of the conventional stem group (P < 0.05). Under torsional loads at levels of 1°, 3°, and 5°, the torques of the TFS group were 3.86 ± 0.69 Nm, 3.90 ± 1.26 Nm, and 4.39 ± 1.67 Nm respectively, all of which were significantly greater than those of the CS group (1.82 ± 0.82 Nm, P < 0.001; 2.05 ± 0.89 Nm, P = 0.016; 1.96 ± 0.50 Nm, P = 0.015 respectively).

Conclusion: The TFS prosthesis improves fixation strength and reduces strain on the femur's proximal surface. Compared to CS fixation, it offers better resistance to compression and rotation, as well as improved initial stability.

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来源期刊
Frontiers in Bioengineering and Biotechnology
Frontiers in Bioengineering and Biotechnology Chemical Engineering-Bioengineering
CiteScore
8.30
自引率
5.30%
发文量
2270
审稿时长
12 weeks
期刊介绍: The translation of new discoveries in medicine to clinical routine has never been easy. During the second half of the last century, thanks to the progress in chemistry, biochemistry and pharmacology, we have seen the development and the application of a large number of drugs and devices aimed at the treatment of symptoms, blocking unwanted pathways and, in the case of infectious diseases, fighting the micro-organisms responsible. However, we are facing, today, a dramatic change in the therapeutic approach to pathologies and diseases. Indeed, the challenge of the present and the next decade is to fully restore the physiological status of the diseased organism and to completely regenerate tissue and organs when they are so seriously affected that treatments cannot be limited to the repression of symptoms or to the repair of damage. This is being made possible thanks to the major developments made in basic cell and molecular biology, including stem cell science, growth factor delivery, gene isolation and transfection, the advances in bioengineering and nanotechnology, including development of new biomaterials, biofabrication technologies and use of bioreactors, and the big improvements in diagnostic tools and imaging of cells, tissues and organs. In today`s world, an enhancement of communication between multidisciplinary experts, together with the promotion of joint projects and close collaborations among scientists, engineers, industry people, regulatory agencies and physicians are absolute requirements for the success of any attempt to develop and clinically apply a new biological therapy or an innovative device involving the collective use of biomaterials, cells and/or bioactive molecules. “Frontiers in Bioengineering and Biotechnology” aspires to be a forum for all people involved in the process by bridging the gap too often existing between a discovery in the basic sciences and its clinical application.
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