Echo-Based FSI Models to Simulate Ventricular Electrical Signal Conduction in Pig Pacemaker Models

Q4 Biochemistry, Genetics and Molecular Biology
Longling Fan, Jing Yao, Chun Yang, Di Xu, D. Tang
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引用次数: 1

Abstract

Cardiac pacing has been an effective treatment in the management of patients with arrhythmia. Different pacemaker location may have different impact on pacemaker effectiveness. A novel image-based ventricle animal modeling approach was proposed to integrate echocardiography images, propagating dynamic electric potential on ventricle surface to perform myocardial function assessment. The models will be used to simulate ventricular electrical signal conduction and optimize pacemaker location for better cardiac outcome.  One health female adult pig weight 42.5kg was used to make pacing animal model with different ventricle pacing locations. Pig health status was assessed before undergoing experimental procedures. Ventricle surface electric signal, blood pressure and echo image were acquired 15 minutes after the pacemaker was implanted.  Echo-based left ventricle (LV) fluid-structure interaction (FSI) models were constructed to perform ventricle function analysis and investigate impact of pacemaker location on cardiac outcome.  The nonlinear Mooney-Rivlin model was used for ventricle tissue material model. With the measured electric signal map from the pig associated with the actual pacemaker site, electric potential conduction of myocardium was modeled by material stiffening and softening in our model, with stiffening simulating contraction and softening simulating relaxation. Material stiffness parameters were adjusted in a cardiac cycle to match Echo-measured LV deformation and volume variations. Mapping between material stiffness and ventricle electric signal was quantified using data measured from the animal with different pacemaker locations. Ventricle model without pacemaker and three ventricle models with the following pacemaker locations were simulated: right ventricular apex (RVA), posterior interventricular septum (PIVS) and right ventricular outflow tract (RVOT). Data for ventricle volume change, ejection fraction, stress and strain, flow velocity and shear stress data were collected for comparisons. Our results demonstrating that PIVS pacing model had higher peak flow velocity and stress/strain.  It indicated that PIVS pacemaker site may be the best location.  This modeling approach could be used as “virtual surgery” to try various pacemaker locations and avoid risky and dangerous surgical experiments on real patients.
基于回波的FSI模型模拟猪起搏器模型的心室电信号传导
心脏起搏是治疗心律失常的一种有效方法。不同的起搏器位置可能对起搏器的效果有不同的影响。提出了一种新的基于图像的心室动物建模方法,整合超声心动图图像,在心室表面传播动态电位,进行心肌功能评估。这些模型将用于模拟心室电信号传导和优化起搏器位置,以获得更好的心脏预后。选取一只体重42.5kg的健康雌性成年猪,制作不同心室起搏位置的起搏动物模型。在进行实验程序之前评估猪的健康状况。起搏器植入15分钟后,采集心室表面电信号、血压和回声图像。建立基于回声的左心室(LV)流固相互作用(FSI)模型进行心室功能分析,探讨起搏器位置对心脏转归的影响。脑室组织材料模型采用非线性Mooney-Rivlin模型。利用实测的猪与实际起搏器部位相关联的电信号图,我们的模型采用材料的硬化和软化来模拟心肌的电位传导,硬化模拟收缩,软化模拟松弛。在心脏周期中调整材料刚度参数,以匹配echo测量的左室变形和体积变化。材料刚度与心室电信号之间的映射关系通过测量不同起搏器位置的动物的数据进行量化。模拟无起搏器的心室模型和有起搏器位置的3个心室模型:右心室尖部(RVA)、后室间隔(PIVS)和右心室流出道(RVOT)。收集心室容积变化、射血分数、应力应变、流速和剪应力数据进行比较。结果表明,PIVS起搏模型具有更高的峰值流速和应力/应变。提示PIVS起搏器部位可能是最佳位置。这种建模方法可以作为“虚拟手术”,尝试不同的起搏器位置,避免在真实患者身上进行风险和危险的手术实验。
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来源期刊
Molecular & Cellular Biomechanics
Molecular & Cellular Biomechanics CELL BIOLOGYENGINEERING, BIOMEDICAL&-ENGINEERING, BIOMEDICAL
CiteScore
1.70
自引率
0.00%
发文量
21
期刊介绍: The field of biomechanics concerns with motion, deformation, and forces in biological systems. With the explosive progress in molecular biology, genomic engineering, bioimaging, and nanotechnology, there will be an ever-increasing generation of knowledge and information concerning the mechanobiology of genes, proteins, cells, tissues, and organs. Such information will bring new diagnostic tools, new therapeutic approaches, and new knowledge on ourselves and our interactions with our environment. It becomes apparent that biomechanics focusing on molecules, cells as well as tissues and organs is an important aspect of modern biomedical sciences. The aims of this journal are to facilitate the studies of the mechanics of biomolecules (including proteins, genes, cytoskeletons, etc.), cells (and their interactions with extracellular matrix), tissues and organs, the development of relevant advanced mathematical methods, and the discovery of biological secrets. As science concerns only with relative truth, we seek ideas that are state-of-the-art, which may be controversial, but stimulate and promote new ideas, new techniques, and new applications.
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