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Preliminary Validation of Electroporation-Electrolysis (E2) for Cardiac Ablation Using a Parameterisable In-Vivo Model

机译:使用参数化In-Vivo模型对电穿孔电解(E2)的初步验证

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Atrial fibrillation is the most common arrhythmia, increasing the risk of stroke, heart failure and death, and a growing epidemic. Electroporation ablation is emerging in cardiac ablation for atrial fibrillation as a fast, tissue-specific and non-thermal alternative to existing technologies tied by their thermal action to shortcomings in efficacy, speed and risk. Studies so far have aimed to translate the success of irreversible electroporation from tumour treatment, with its kilovolt pulses, to cardiac ablation. However, these high voltages may be less appealing for cardiac ablation from clinical, technical and regulatory standpoints. A novel ablation technique combining electroporation and electrolysis in a single pulse E2 uses lower voltages. A custom E2 ablation system was developed and tested on an in vivo tissue model. Histopathological analysis showed lesions of clinically relevant depth, achieved without any acute complications or severe muscle contractions. Lesions were mapped onto a numerical model developed to refine further prototyping. This study provides preliminary prototype validation and the methodological foundation for dose optimisation towards endocardial application.
机译:心房颤动是最常见的心律失常,增加中风,心力衰竭和死亡的风险以及不断增长的流行病。电穿孔消融在心脏消融中出现心脏消融,作为心房颤动的快速,组织特异性和非热替代方法,其对效力,速度和风险的缺点所束的现有技术。到目前为止的研究旨在通过沿河豚治疗,与千伏脉冲一起转化不可逆电穿孔的成功,以便心脏消融。然而,这些高电压可能对来自临床,技术和监管观点来说的心脏消融可能不那么吸引。一种新的烧蚀技术,在单个脉冲E2中结合电穿孔和电解使用较低电压。在体内组织模型中开发并测试了自定义E2消融系统。组织病理学分析显示出临床相关深度的病变,达到无任何急性并发症或严重的肌肉收缩。病变被映射到开发的数值模型上,以改进进一步的原型。本研究提供了初步原型验证和对心内膜应用剂量优化的方法基础。

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