三维有限元分析预测骨重塑对种植体疲劳极限的影响。

Megha Satpathy, Yuanyuan Duan, Logan Betts, Matthew Priddy, Jason A Griggs
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引用次数: 3

摘要

背景:应用有限元分析方法评价小直径种植体周围骨重塑对其疲劳极限的影响。方法:使用微型计算机断层扫描(Skyscan 1172)对种植体组件进行扫描,该组件包括缩小直径的种植体(Biomet-3i外六角)、基台(GingiHue®)和连接螺钉(Gold-Tite Square螺钉)。使用Mimics (Materialise)和光学显微镜(Keyence)测量其尺寸。使用SOLIDWORKS(达索系统)构建物理标本的数字复制品。在SOLIDWORKS中设计了两层(皮质骨和松质骨)柱状骨标本架。创建了两个组件:(a)模型1:具有非重塑骨;(b)模型2:种植体螺纹附近区域的松质骨重塑。在ABAQUS (SIMULIA)软件中进行有限元分析。在模型1中,皮质骨和松质骨的杨氏模量分别为20 GPa和14 GPa。对于模型2,植入体螺钉附近的松质骨区域的杨氏模量为20gpa。采用fe-safe (SIMULIA)软件估算疲劳极限。结果:模型1和模型2在100 N载荷下的最大von Mises应力均为439.9 MPa,且位于连接器螺钉处。模型1和模型2的疲劳极限均为116.4 N。结论:结果表明,根据ISO 14801测试的种植体疲劳抗力可以准确预测,而无需费心模拟临床病例中骨-种植体界面处发生的非均匀刚度。
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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Effect of Bone Remodeling on Dental Implant Fatigue Limit Predicted Using 3D Finite Element Analysis.

Background: To evaluate the effect of bone remodelling around a reduced-diameter dental implant on its fatigue limit using finite element analysis (FEA).

Methods: A dental implant assembly, which included a reduced-diameter dental implant (Biomet-3i external hex), an abutment (GingiHue®) and a connector screw (Gold-Tite Square screw), was scanned using micro-computed tomography (Skyscan 1172). Its dimensions were measured using Mimics (Materialise) and an optical microscope (Keyence). The digital replicas of the physical specimens were constructed using SOLIDWORKS (Dassault Systems). A cylindrical bone specimen holder with two layers (cortical and cancellous bone) was designed in SOLIDWORKS. Two assemblies were created: (a) Model 1: Having non-remodelled bone; (b) Model 2: Cancellous bone remodelled at the regions adjacent to the implant screw threads. FEA was performed in ABAQUS (SIMULIA). In Model 1, the Young's modulus of cortical and cancellous bone were 20 GPa and 14 GPa, respectively. For Model 2, the region of the cancellous bone adjacent to the implant screw threads was assigned a Young's modulus of 20 GPa. fe-safe (SIMULIA) was used to estimate the fatigue limit.

Results: The maximum von Mises stress under 100 N load was 439.9 MPa for both models 1 and 2 and was located at the connector screw. The fatigue limit was 116.4 N for both models 1 and 2.

Conclusions: The results suggest that implant fatigue resistance tested according to ISO 14801 may be accurately predicted without bothering to simulate the non-homogeneous stiffness that occurs at the bone-implant interface in the clinical case.

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