Tibial Baseplate Microstructure Governs High Cycle Fatigue Fracture In Vivo

IF 3.2 4区 医学 Q2 ENGINEERING, BIOMEDICAL
Michael A. Kurtz, Jeremy L. Gilbert, Hannah Spece, Gregg R. Klein, Harold E. Cates, Steven M. Kurtz
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Abstract

Previous studies report rare occurrences of tibial baseplate fractures following primary total knee arthroplasty (TKA). However, at a microstructural scale, it remains unclear how fatigue models developed in vitro apply to fractures in vivo. In this study, we asked: (1) do any clinical factors differentiate fracture patients from a broader revision sample; and (2) in vivo, how does microstructure influence fatigue crack propagation? We identified three fractured tibial baseplates from an institutional review board exempt implant retrieval program. Then, for comparison, we collated clinical data from the same database for n = 2120 revision TKA patients with tibial trays. To identify mechanisms, we characterized fracture features using scanning electron and digital optical microscopy. Additionally, we performed cross sectional analysis using focused ion beam milling. The fracture cohort consisted of moderately to very active patients with increased implantation time (15.6 years) compared to the larger revision patient sample (5.1 years, p = 0.009). We did not find a significant difference in patient weight between the two groups (p = 0.98). Macroscopic fracture features aligned well with both previous retrieval analysis and in vitro baseplate fatigue tests. On a micron scale, we identified striations on each baseplate, demonstrating fatigue as the fracture mechanism. In vivo fatigue fracture processes depended on both the alloy (Ti-6Al-4V vs. CoCrMo) and the microstructure of the alloy formed during manufacturing. For Ti-6Al-4V, the presence of equiaxed or acicular microstructure influenced the fatigue crack propagation, the latter arising from large prior β grains and a Widmanstatten microstructure, degrading fatigue strength. CoCrMo alloy fatigue cracks propagated linearly, crystallographically influenced by planar slip. However, we did not document any features of overload or fast fracture, suggesting a high cycle, low stress fatigue regime. Ultimately, the crack profiles we present here may provide insight into fatigue fractures of modern tibial baseplates.

Abstract Image

胫骨底板微结构影响体内高循环疲劳断裂
以往的研究报告显示,初级全膝关节置换术(TKA)后极少发生胫骨底板骨折。然而,在微观结构尺度上,体外开发的疲劳模型如何应用于体内骨折仍不清楚。在这项研究中,我们提出了以下问题:(1)是否有任何临床因素将骨折患者与更广泛的翻修样本区分开来;(2)在体内,微观结构如何影响疲劳裂纹的扩展?我们从机构审查委员会豁免的植入物取回计划中确定了三个骨折的胫骨底板。然后,为了进行比较,我们整理了同一数据库中 2120 名翻修 TKA 患者的临床数据,这些患者都使用了胫骨托盘。为了确定机制,我们使用扫描电子显微镜和数字光学显微镜对骨折特征进行了鉴定。此外,我们还使用聚焦离子束铣进行了截面分析。骨折队列由中度到非常活跃的患者组成,植入时间(15.6 年)比较大的翻修患者样本(5.1 年,P = 0.009)长。我们没有发现两组患者的体重有明显差异(p = 0.98)。宏观骨折特征与之前的回收分析和体外基底板疲劳测试非常吻合。在微米尺度上,我们在每个基板上都发现了条纹,这表明疲劳是断裂机制。体内疲劳断裂过程取决于合金(Ti-6Al-4V 与 CoCrMo)和制造过程中形成的合金微观结构。对于 Ti-6Al-4V 而言,等轴状或针状微观结构的存在影响了疲劳裂纹的扩展,后者产生于较大的先β晶粒和维德曼施塔特微观结构,从而降低了疲劳强度。CoCrMo 合金的疲劳裂纹呈线性扩展,晶体结构受到平面滑移的影响。然而,我们没有记录到任何过载或快速断裂的特征,这表明这是一种高循环、低应力的疲劳机制。最终,我们在此介绍的裂纹剖面可为现代胫骨底板的疲劳断裂提供启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.50
自引率
2.90%
发文量
199
审稿时长
12 months
期刊介绍: Journal of Biomedical Materials Research – Part B: Applied Biomaterials is a highly interdisciplinary peer-reviewed journal serving the needs of biomaterials professionals who design, develop, produce and apply biomaterials and medical devices. It has the common focus of biomaterials applied to the human body and covers all disciplines where medical devices are used. Papers are published on biomaterials related to medical device development and manufacture, degradation in the body, nano- and biomimetic- biomaterials interactions, mechanics of biomaterials, implant retrieval and analysis, tissue-biomaterial surface interactions, wound healing, infection, drug delivery, standards and regulation of devices, animal and pre-clinical studies of biomaterials and medical devices, and tissue-biopolymer-material combination products. Manuscripts are published in one of six formats: • original research reports • short research and development reports • scientific reviews • current concepts articles • special reports • editorials Journal of Biomedical Materials Research – Part B: Applied Biomaterials is an official journal of the Society for Biomaterials, Japanese Society for Biomaterials, the Australasian Society for Biomaterials, and the Korean Society for Biomaterials. Manuscripts from all countries are invited but must be in English. Authors are not required to be members of the affiliated Societies, but members of these societies are encouraged to submit their work to the journal for consideration.
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