An efficient finite element approach for modeling fibrotic clefts in the heart.
An efficient finite element approach for modeling fibrotic clefts in the heart.
复制标题
用于模拟心脏纤维化裂隙的有效有限元方法。
DOI:
10.1109/tbme.2013.2292320
复制
发表时间:
2014-03
期刊:
影响因子:
--
通讯作者:
Plank G
中科院分区:
文献类型:
--
作者:
Costa CM;Campos FO;Prassl AJ;dos Santos RW;Sánchez-Quintana D;Ahammer H;Hofer E;Plank G
Advanced medical imaging technologies provide a wealth of information on cardiac anatomy and structure at a paracellular resolution, allowing to identify micro-structural discontinuities which disrupt the intracellular matrix. Current state-of-the-art computer models built upon such datasets account for increasingly finer anatomical details, however, structural discontinuities at the paracellular level are typically discarded in the model generation process, owing to the significant costs which incur when using high resolutions for explicit representation. In this study, a novel discontinuous finite element (dFE) approach for discretizing the bidomain equations is presented, which accounts for fine-scale structures in a computer model without the need to increase spatial resolution. In the dFE method this is achieved by imposing infinitely thin lines of electrical insulation along edges of finite elements which approximate the geometry of discontinuities in the intracellular matrix. Simulation results demonstrate that the dFE approach accounts for effects induced by microscopic size scale discontinuities, such as the formation of microscopic virtual electrodes, with vast computational savings as compared to high resolution continuous finite element models. Moreover, the method can be implemented in any standard continuous finite element code with minor effort.