Fast personalized electrophysiological models from computed tomography images for ventricular tachycardia ablation planning. (23rd November 2018)

• Record Type: Journal Article
• Authors: Cedilnik, Nicolas; Duchateau, Josselin; Dubois, Rémi; Sacher, Frédéric; Jaïs, Pierre; Cochet, Hubert; Sermesant, Maxime
• Is Part Of: Europace. Volume 20(2018)Supplement 3
• Page Start: iii94
• Page End: iii101
• Publication Date: 2018-11-23
• Subjects: Electrophysiology -- Computational modelling -- Myocardial infarction -- Computed tomography -- Catheter ablation -- Sudden cardiac death; Arrhythmia -- Treatment -- Periodicals; Cardiac pacing -- Periodicals; Catheter ablation -- Periodicals; Heart -- Physiology -- Periodicals; Electrophysiology -- Periodicals; 617.4120645
• DOI: 10.1093/europace/euy228
• Languages: English
• ISSNs: 1099-5129

Abstract

Abstract: Aims: Clinical application of patient-specific cardiac computer models requires fast and robust processing pipelines that can be seamlessly integrated into clinical workflows. We aim at building such a pipeline from computed tomography (CT) images to personalized cardiac electrophysiology (EP) model. The simulation output could be useful in the context of post-infarct ventricular tachycardia (VT) radiofrequency ablation (RFA) planning for pre-operative targets prediction. Methods and results: The support for model personalization is a patient-specific virtual three-dimensional heart obtained from CT images. Here, the scar is identified as thinning of the myocardial wall on automatically computed thickness maps. We then use an Eikonal model of wave front propagation with reduced velocity in the damaged areas. An image-based vessel enhancement algorithm can automatically identify VT isthmuses. The personalized model is used for virtual pacing. We obtained a very fast pipeline that enables simulations in only a few minutes. It is fully automated starting from the semi-automated image segmentation phase. The computational time frame is compatible with the construction of a virtual pacing tool. In this tool, onset points and an optional directional block could be interactively selected. The directional block is a simple way to model tissue refractoriness. Output activation maps are compared with EP data acquired pre-operatively. We show that this framework allows the reproduction of recorded re-entrant VT activation patterns. Conclusion: Our simulation framework has an application in VT RFA intervention planning. It could be used to guide EP explorations and even predict ablation targets pre-operatively. This could reduce intervention duration and improve success rate.