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Pipeline to Build and Test Robust 3D T1 Mapping-Based Heart Models for EP Interventions: Preliminary Results

机译:用于EP干预的构建和测试基于3D T1鲁棒性的心脏模型的管道:初步结果

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Computational models are powerful tools in electrophysiology (EP), helping us understand and predict arrhythmia associated with heart attack (i.e., myocardial infarction), a major cause of sudden cardiac death. Our broad aim is to combine novel scar imaging methods with fast computational models to enable accurate predictions of electrical wave propagation, and then to test these models in preclinical frameworks prior to clinical translation. In this work we used n = 3 swine with chronic infarct, which underwent MR followed by conventional x-ray guided electro-anatomical EP mapping. For scar imaging, we employed our T1-mapping MR method based on multi-contrast late enhancement (MCLE) at 1 × 1 mm in-plane resolution and 5 mm slice thickness. Next, we used the MCLE images as input to a fuzzy-logic algorithm and segmented the infarcted area into two zones: infarct core IC (dense fibrosis) and grey-zone, GZ (i.e., arrhythmia substrate). We further built 3D heart models from the stack of segmented 2D MCLE images, integrating tissue zones (healthy, IC and GZ) into detailed tetrahedral heart meshes (~1.5 mm element size). Finally, we investigated the accuracy of model predictions by comparing measured maps of activation times (i.e., depolarization times) with simulated maps obtained by employing a macroscopic formalism and reaction-diffusion equations. We obtained an acceptable small mean absolute error between the simulated and measured depolarization times (~ 12 ms, in average). Future work will focus on refining MR imaging resolution and use the models to guide ablation procedures.
机译:计算模型是电生理学(EP)的强大工具,可帮助我们了解和预测与心脏病发作(即心肌梗塞)相关的心律失常,后者是心脏猝死的主要原因。我们的广泛目标是将新颖的疤痕成像方法与快速计算模型相结合,以实现电波传播的准确预测,然后在临床翻译之前在临床前框架中测试这些模型。在这项工作中,我们使用了n = 3的慢性梗死猪,对它进行了MR,然后进行常规X射线引导的电解剖EP映射。对于疤痕成像,我们采用了基于多对比度后期增强(MCLE)的T1映射MR方法,其面内分辨率为1×1 mm,切片厚度为5 mm。接下来,我们将MCLE图像用作模糊逻辑算法的输入,并将梗塞区域分为两个区域:梗塞核心IC(密集纤维化)和灰色区GZ(即心律失常基质)。我们从分割的2D MCLE图像堆栈中进一步构建了3D心脏模型,将组织区域(健康的,IC和GZ)整合到详细的四面体心脏网格中(元素尺寸约为1.5毫米)。最后,我们通过比较测得的激活时间(即去极化时间)图与采用宏观形式主义和反应扩散方程式获得的模拟图来研究模型预测的准确性。我们在模拟和测量的去极化时间(平均〜12毫秒)之间获得了可接受的小平均绝对误差。未来的工作将集中在完善MR成像分辨率上,并使用这些模型来指导消融程序。

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