Drach Andrew, Khalighi Amir H, Sacks Michael S
Center for Cardiovascular Simulation, Institute for Computational Engineering and Sciences, Department of Biomedical Engineering, The University of Texas at Austin, Austin, TX, USA.
Int J Numer Method Biomed Eng. 2018 Feb;34(2). doi: 10.1002/cnm.2921. Epub 2017 Sep 5.
Multiple studies have demonstrated that the pathological geometries unique to each patient can affect the durability of mitral valve (MV) repairs. While computational modeling of the MV is a promising approach to improve the surgical outcomes, the complex MV geometry precludes use of simplified models. Moreover, the lack of complete in vivo geometric information presents significant challenges in the development of patient-specific computational models. There is thus a need to determine the level of detail necessary for predictive MV models. To address this issue, we have developed a novel pipeline for building attribute-rich computational models of MV with varying fidelity directly from the in vitro imaging data. The approach combines high-resolution geometric information from loaded and unloaded states to achieve a high level of anatomic detail, followed by mapping and parametric embedding of tissue attributes to build a high-resolution, attribute-rich computational models. Subsequent lower resolution models were then developed and evaluated by comparing the displacements and surface strains to those extracted from the imaging data. We then identified the critical levels of fidelity for building predictive MV models in the dilated and repaired states. We demonstrated that a model with a feature size of about 5 mm and mesh size of about 1 mm was sufficient to predict the overall MV shape, stress, and strain distributions with high accuracy. However, we also noted that more detailed models were found to be needed to simulate microstructural events. We conclude that the developed pipeline enables sufficiently complex models for biomechanical simulations of MV in normal, dilated, repaired states.
多项研究表明,每位患者独特的病理几何结构会影响二尖瓣(MV)修复的耐久性。虽然MV的计算建模是改善手术结果的一种有前景的方法,但复杂的MV几何结构排除了使用简化模型的可能性。此外,缺乏完整的体内几何信息给患者特异性计算模型的开发带来了重大挑战。因此,需要确定预测性MV模型所需的详细程度。为了解决这个问题,我们开发了一种新颖的流程,可直接从体外成像数据构建具有不同保真度的、富含属性的MV计算模型。该方法结合了加载和卸载状态下的高分辨率几何信息,以实现高水平的解剖细节,随后对组织属性进行映射和参数嵌入,以构建高分辨率、富含属性的计算模型。随后通过将位移和表面应变与从成像数据中提取的位移和应变进行比较,开发并评估了分辨率较低的模型。然后,我们确定了在扩张和修复状态下构建预测性MV模型的关键保真度水平。我们证明,特征尺寸约为5毫米、网格尺寸约为1毫米的模型足以高精度地预测MV的整体形状、应力和应变分布。然而,我们也注意到,需要更详细的模型来模拟微观结构事件。我们得出结论,所开发的流程能够为正常、扩张和修复状态下的MV生物力学模拟构建足够复杂的模型。