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翻修手术中取出钢板的失效分析与设计改进

Failure analysis and design improvement of retrieved plates from revision surgery.

作者信息

Zhang Ning-Ze, Shui Yang-Yang, Zhang Qi-Da, Zhang Yuan-Tao, Su Jian, Qin Ling, Cheng Cheng-Kung

机构信息

Musculoskeletal Research Laboratory, Department of Orthopaedics & Traumatology, The Chinese University of Hong Kong, Hong Kong SAR, 999077, China.

Key Laboratory of Biomechanics and Mechanobiology, Ministry of Education, Beijing Advanced Innovation Center for Biomedical Engineering, School of Biological Science and Medical Engineering, Beihang University, Beijing, 100083, China.

出版信息

J Orthop Translat. 2024 Sep 27;49:1-10. doi: 10.1016/j.jot.2024.08.011. eCollection 2024 Nov.

Abstract

BACKGROUND

The fracture of bone plate can cause considerable pain for the patient and increase the burden on the public finances. This study aims to explore the failure mechanism of 49 plates retrieved from revision surgery and introduce pure magnesium (Mg) block to improve the biomechanical performance of the plate via decreasing the stiffness and to stimulate the biological response of the plate potentially by the degradation of Mg block.

METHODS

The morphological analysis and component analysis of the plates were conducted to determine the fracture reason of the plates combining the clinical data. According to the structural feature, the 49 retrieved plates were divided into: traditional plate (TP), asymmetrical plate (AP), reconstructive plate (RP) and central enhancement plate (CEP), and their structure features are normalized in a commercial plate, respectively. The biomechanical performance of the plates was evaluated using a validated femoral finite element model. A block of pure Mg with a thickness of 1 mm, 1.5 mm and 2 mm was also incorporated into the CEP to be assessed.

RESULTS

The results indicated that the retrieved plates mainly failed due to fatigue fracture induced by delayed union or nonunion (44/49), and using pure titanium plates in weight-bearing areas increased the risk of fracture compared with Ti alloy plates when the delayed union or nonunion occurred. The TP demonstrated the highest compression resistance and bending resistance, while CEP had the highest rotational resistance. As the thickness of the Mg block was increased, the stress on the plate in compression decreased, but the stress in rotation increased. The plate with a 1.5 mm Mg block demonstrated excellent compression resistance, bending resistance and rotational resistance.

CONCLUSION

Fatigue fracture resulting from the delayed union or nonunion is the primary failure reason of plates in clinic. The incorporation of Mg block into plate improves the biomechanical performance and has the potential to promote bone healing. The plate with a 1.5 mm Mg block may be suitable for use in orthopaedics.

THE TRANSLATIONAL POTENTIAL OF THIS ARTICLE

This study assessed the failure mechanism of retrieved bone plates and used this data to develop a novel plate incorporating a 1.5 mm block of pure Mg block at the position corresponding to the fracture line. The novel plate exhibited excellent compression resistance, bending resistance and rotational resistance due to the alleviation of stress concentrations. The Mg block has the potential to degrade over time to promote fracture healing and prevents fatigue fracture of plates.

摘要

背景

接骨板断裂会给患者带来极大痛苦,并增加公共财政负担。本研究旨在探究49块取自翻修手术的接骨板的失效机制,并引入纯镁(Mg)块以通过降低刚度来改善接骨板的生物力学性能,并可能通过Mg块的降解来刺激接骨板的生物学反应。

方法

结合临床数据对接骨板进行形态学分析和成分分析,以确定接骨板的断裂原因。根据结构特征,将49块回收的接骨板分为:传统接骨板(TP)、不对称接骨板(AP)、重建接骨板(RP)和中央增强接骨板(CEP),并分别在一种商用接骨板中对它们的结构特征进行归一化处理。使用经过验证的股骨有限元模型对接骨板的生物力学性能进行评估。还将厚度为1毫米、1.5毫米和2毫米的纯镁块纳入CEP中进行评估。

结果

结果表明,回收的接骨板主要因延迟愈合或不愈合导致的疲劳骨折而失效(44/49),当发生延迟愈合或不愈合时,在负重区域使用纯钛接骨板比钛合金接骨板增加了骨折风险。TP表现出最高的抗压强度和抗弯强度,而CEP具有最高的抗旋转强度。随着Mg块厚度的增加,接骨板在压缩时的应力降低,但旋转时的应力增加。带有1.5毫米Mg块的接骨板表现出优异的抗压强度、抗弯强度和抗旋转强度。

结论

延迟愈合或不愈合导致的疲劳骨折是临床上接骨板的主要失效原因。在接骨板中加入Mg块可改善生物力学性能,并具有促进骨愈合的潜力。带有1.5毫米Mg块的接骨板可能适用于骨科。

本文的转化潜力

本研究评估了回收接骨板的失效机制,并利用这些数据开发了一种新型接骨板,在对应骨折线的位置包含一个1.5毫米的纯镁块。由于应力集中的缓解,新型接骨板表现出优异的抗压强度、抗弯强度和抗旋转强度。Mg块有可能随着时间推移而降解,以促进骨折愈合并防止接骨板疲劳骨折。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3103/11470186/23af5b00f816/ga1.jpg

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