Atrial arrhythmias are frequently treated using catheter ablation during electrophysiological (EP) studies. However, success rates are only moderate and could be improved with the help of personalized simulation models of the atria. In this work, we present a workflow to generate and validate personalized EP simulation models based on routine clinical computed tomography (CT) scans and intracardiac electrograms. From four patient data sets, we created anatomical models from angiographic CT data with an automatic segmentation algorithm. From clinical intracardiac catheter recordings, individual conduction velocities were calculated. In these subject-specific EP models, we simulated different pacing maneuvers and measurements with circular mapping catheters that were applied in the respective patients. This way, normal sinus rhythm and pacing from a coronary sinus catheter were simulated. Wave directions and conduction velocities were quantitatively analyzed in both clinical measurements and simulated data and were compared. On average, the overall difference of wave directions was 15° (8%), and the difference of conduction velocities was 16 cm/s (17%). The method is based on routine clinical measurements and is thus easy to integrate into clinical practice. In the long run, such personalized simulations could therefore assist treatment planning and increase success rates for atrial arrhythmias.
Whole organ scale patient specific biophysical simulations contribute to the understanding, diagnosis and treatment of complex diseases such as cardiac arrhythmia. However, many individual steps are required to bridge the gap from an anatomical scan to a personal- ized biophysical model. In biophysical modeling, differential equations are solved on spatial domains represented by volumetric meshes of high resolution and in model-based segmentation, surface or volume meshes represent the patients geometry. We simplify the personalization pro- cess by representing the simulation mesh and additional relevant struc- tures relative to the segmentation mesh. Using a surface correspondence preserving model-based segmentation algorithm, we facilitate the inte- gration of anatomical information into biophysical models avoiding a complex processing pipeline. In a simulation study, we observe surface correspondence of up to 1.6mm accuracy for the four heart chambers. We compare isotropic and anisotropic atrial excitation propagation in a personalized simulation.
The delineation of anatomical structures in medical images can be achieved in an efficient and robust manner using statistical anatomical organ models, which has been demonstrated for an already considerable set of organs, including the heart. While it is possible to provide models with sufficient shape variability to cope, to a large extent, with inter-patient variability, as long as object topology is conserved, it is a fundamental problem to cope with topological organ variability. We address this by creating a set of model variants and selecting the most appropriate model variant for the patient at hand. We propose a hybrid method combining model-based image analysis with a guided region growing approach for automated anatomical variant selection and apply it to the left atrium in cardiac CT images. Concerning the human heart, the left atrium is the most variable sub-structure with a variable number of pulmonary veins draining into it. It is of large clinical interest in the context of atrial fibrillation and related interventions.
Atrial myofiber orientation is complex and has multiple discrete layers and bundles. A novel robust semi-automatic method to incorporate atrial anisotropy and heterogeneities into patient-specific models is introduced. The user needs to provide 22 distinct seed-points from which a network of auxiliary lines is constructed. These are used to define fiber orientation and myocardial bundles. The method was applied to 14 patient-specific volumetric models derived from CT, MRI and photographic data. Initial electrophysiological simulations show a significant influence of anisotropy and heterogeneity on the excitation pattern and P-wave duration (20.7% shortening). Fiber modeling results show good overall correspondence with anatomical data. Minor modeling errors are observed if more than four pulmonary veins exist in the model. The method is an important step towards creating realistic patient-specific atrial models for clinical applications.
Electrophysiological simulations of the atria could improve diagnosis and treatment of cardiac arrhythmia, like atrial fibrillation or flutter. For this purpose, a precise segmentation of both atria is needed. However, the atrial epicardium and the electrophysiological structures needed for electrophysiological simulations are barely or not at all detectable in CT-images. Therefore, a model based segmentation of only the atrial endocardium was developed as a landmark generator to facilitate the registration of a finite wall thickness model of the right and left atrial myocardium. It further incorporates atlas information about tissue structures relevant for simulation purposes like Bachmanns bundle, terminal crest, sinus node and the pectinate muscles. The correct model based segmentation of the atrial endocardium was achieved with a mean vertex to surface error of 0.53 mm for the left and 0.18 mm for the right atrium respectively. The atlas based myocardium segmentation yields physiologically correct results well suited for electrophysiological simulations.
Catheter ablation of complex atrial arrhythmias is a frequently applied procedure, but its success rates are only moderate and highly dependent on the experience of the physician. Personalized atrial simulation models could assist the physician in treatment planning and thus increase success rates. In this work we created a personalized anatomical model for a specific patient from CT image data. Left atrial conduction velocity and local wave directions were determined from intracardiac electrogram (EGM) recordings. We simulated normal sinus rhythm and the clinical pacing protocol using a Cellular Automaton. The incidence direction and conduction velocity were extracted from the simulated data and compared to the results of the clinical EGMs of the same patient. We then showed that the incidence angles differed by less than 15% and that the conduction velocity error was below 12 cm/s. This implies that the model has similar electric properties compared to the real atria. In conclusion, we have presented a workflow for model personalization and validation.
A framework for the automatic extraction and generation of patient-specific organ models from different image modalities is presented. These models can be used to extract and represent diagnostic information about the heart and its function. Furthermore, the models can be used for treatment planning and an overlay of the models onto X-ray fluoroscopy images can support navigation when performing an intervention in the CathLab.