K. Gillette, A. Prassl, J. Bayer, E. Vigmond, A. Neic, G. Plank
{"title":"Automatic Generation of Bi-Ventricular Models of Cardiac Electrophysiology for Patient Specific Personalization Using Non-Invasive Recordings","authors":"K. Gillette, A. Prassl, J. Bayer, E. Vigmond, A. Neic, G. Plank","doi":"10.22489/CinC.2018.265","DOIUrl":null,"url":null,"abstract":"Introduction: Personalized in silico models of cardiac electrophysiology based on non-invasive recordings, such as body surface potential maps, are considered of pivotal importance in clinical modeling applications. Efficient, automated workflows are desired to construct patientspecific models for clinical use. Objective: We aimed to develop an automated workflow for the generation of a parameterizable cardiac EP model capable of simulating body surface potential maps independent of user interaction. Methods: A cardiac bi-ventricular model with torso was segmented and meshed from clinical MRI scans. Universal ventricular coordinates were computed for userindependent definition of fibers, a fast conducting endocardial layer, and earliest activation on the endocardium. The extracellular epicardial potential distribution was simulated and projected to the torso surface to acquire a body surface potential map. Results: Total model generation from segmentation required approximately 2 hours. Automatized simulation of a single depolarization sequence required approximately 30 minutes using a forward element method implementation. Discussion: The proposed workflow integrated recentlydeveloped technologies to generate a parameterizable cardiac EP model within clinical time scales.","PeriodicalId":215521,"journal":{"name":"2018 Computing in Cardiology Conference (CinC)","volume":"9 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2018 Computing in Cardiology Conference (CinC)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22489/CinC.2018.265","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 7
Abstract
Introduction: Personalized in silico models of cardiac electrophysiology based on non-invasive recordings, such as body surface potential maps, are considered of pivotal importance in clinical modeling applications. Efficient, automated workflows are desired to construct patientspecific models for clinical use. Objective: We aimed to develop an automated workflow for the generation of a parameterizable cardiac EP model capable of simulating body surface potential maps independent of user interaction. Methods: A cardiac bi-ventricular model with torso was segmented and meshed from clinical MRI scans. Universal ventricular coordinates were computed for userindependent definition of fibers, a fast conducting endocardial layer, and earliest activation on the endocardium. The extracellular epicardial potential distribution was simulated and projected to the torso surface to acquire a body surface potential map. Results: Total model generation from segmentation required approximately 2 hours. Automatized simulation of a single depolarization sequence required approximately 30 minutes using a forward element method implementation. Discussion: The proposed workflow integrated recentlydeveloped technologies to generate a parameterizable cardiac EP model within clinical time scales.