Single-Beat Noninvasive Imaging of Ventricular Endocardial and Epicardial Activation in Patients Undergoing CRT

BACKGROUND: Little is known about the effect of cardiac resynchronization therapy (CRT) on endo- and epicardial ventricular activation. Noninvasive imaging of cardiac electrophysiology (NICE) is a novel imaging tool for visualization of both epi- and endocardial ventricular electrical activation. METHODOLOGY/PRINCIPAL FINDINGS: NICE was performed in ten patients with congestive heart failure (CHF) undergoing CRT and in ten patients without structural heart disease (control group). NICE is a fusion of data from high-resolution ECG mapping with a model of the patient's individual cardiothoracic anatomy created from magnetic resonance imaging. Beat-to-beat endocardial and epicardial ventricular activation sequences were computed during native rhythm as well as during ventricular pacing using a bidomain theory-based heart model to solve the related inverse problem. During right ventricular (RV) pacing control patients showed a deterioration of the ventricular activation sequence similar to the intrinsic activation pattern of CHF patients. Left ventricular propagation velocities were significantly decreased in CHF patients as compared to the control group (1.6±0.4 versus 2.1±0.5 m/sec; p<0.05). CHF patients showed right-to-left septal activation with the latest activation epicardially in the lateral wall of the left ventricle. Biventricular pacing resulted in a resynchronization of the ventricular activation sequence and in a marked decrease of total LV activation duration as compared to intrinsic conduction and RV pacing (129±16 versus 157±28 and 173±25 ms; both p<0.05). CONCLUSIONS/SIGNIFICANCE: Endocardial and epicardial ventricular activation can be visualized noninvasively by NICE. Identification of individual ventricular activation properties may help identify responders to CRT and to further improve response to CRT by facilitating a patient-specific lead placement and device programming

Kalbin Elektriksel Aktivitesinin 3 Boyutlu Transmembran Potansiyel Dağılımları Cinsinden Girişimsiz Olarak Görüntülenmesi

TÜBİTAK EEEAG Proje01.04.2015Vücut yüzeyi potansiyel (VYP) ölçümlerinden kalpteki elektriksel kaynakların kestirilmesine ters elektrokardiografi (EKG) problemi denir. Bu yöntem, ölümcül de olabilecek kalp hastalıklarının teşhisinde ve tedavi planlamasında hekimlere yol gösterme potansiyeline sahiptir. Ancak, bu problem kötü konumlanmış bir problemdir ve ölçümlerdeki az miktarda gürültü bile sınırsız çözümler bulunmasına yol açmaktadır. Bunun üstesinden gelebilmek için literatürde, başta Tikhonov düzenlileştirmesi olmak üzere çeşitli düzenlileştirme yöntemleri uygulanmıştır. Ancak uygulanan her yöntem farklı durumlarda test edilmiştir; henüz hangi yöntemin en iyi yöntem olduğu konusunda fikir birliği sağlanamamıştır. Son zamanlarda, üç boyutlu miyokart dokusunda da detaylı bilgi verebildiği için, transmembran potansiyelleri (TMP) cinsinden ters EKG çözümleri popülerleşmiştir. Ancak henüz bu alanda az sayıda çalışma vardır ve özellikle farklı kalp aritmilerinde farklı yöntemlerin nasıl performans sergileyeceği bilinmemektedir. Bu projede temel amaç, bu açığı kapatmak, farklı elektriksel dağılımlar için literatürdeki belli başlı yöntemlerle ters EKG problemini çözmektir. Bu projede, kapsamlı bir çalışmayla, önerilen yöntemlerin performansları aynı test verisiyle ve aynı kriterler kullanılarak objektif bir şekilde karşılaştırılabilmiştir. Ayrıca farklı aritmiler için TMP benzetimleri ve buna bağlı VYPler elde edildiği için, yöntemlerin bu farklı aritmiler karşısında nasıl bir performans sergilediği de araştırılmıştır. Öncelikle Aliev-Panfilov yöntemiyle farklı kalp aktiviteleri için TMP benzetimleri yapılmış, ardından ileri EKG problemi çözülerek bu dağılımlardan VYP dağılımları bulunmuştur. Bu dağılımlar ters EKG çözümlerinde kullanılmıştır. Uygulanan beş değişik ters EKG çözüm yönteminden her durumda en başarılı yöntemin Bayesian MAP olduğu gözlenmiştir. TTLS, LTTLS ve LSQR yöntemlerinin de uyarım noktalarını ve dalga önünü bulmakta çok kötü performans sergilemediği görülmüştür. Bu proje kapsamında iki ayrı dalda daha literatüre katkı sağlanmıştır. Bunlardan ilki, fiber yönelimlerinin TMP dağılımlarına etkilerinin incelenmesidir. Başka bir kalpten aktarılan fiber yönelimini kullanmanın izotropik varsayım kullanmaktan daha doğru sonuçlar verdiği gözlenmiştir. İkinci katkı da, TMP dağılımları cinsinden FEM yöntemi ile ileri problem çözümünün doğrulamasıdır. Uygun ağ sıklığına ulaşıldığında sayısal çözümün analitik çözüme yakınsadığı gösterilmiştir.Inverse electrocardiography is the estimation of cardiac electrical sources from body surface potential (BSP) measurements. Inverse solutions can guide the physicians for diagnosis and treatment planning of lethal heart diseases. However, inverse problem is ill-posed and even small perturbations in the measurements yield unbounded errors in the solutions. To overcome this difficulty, many regularization approaches have been proposed in literature. However, these methods have been applied and tested under varying conditions in different studies; there is no consensus among researchers on the method with the best performance. Lately, solutions in terms of transmembrane potentials (TMP) have become popular, since they provide information about the electrical activity of the three dimensional myocardium. There are few studies in this area and it is still an open question how different methods will perform under different arrythmia conditions. The main goal in this project is to solve the inverse problem in terms of TMPs, using different approaches but under the same (and diverse) cardiac conditions. First, we obtained TMP distributions for various cardiac electrical activity assumptions using Aliev-Panfilov model. Then we solved the forward ECG problem to obtain the corresponding BSPs, which were later used in the inverse problem solutions. Among the five inverse approaches, Bayesian MAP estimation had the best performance under all conditions. TTLS, LTTLS and LSQR were also successful in finding the initial stimulation points and recovering the wavefront. We made contributions in two more areas in this project. The first one is our study of fiber orientation effects on TMP distributions. We found that even using fiber orientations from a different heart is much better than using the isotropic assumption. The second one is the analytical verification of the FEM based forward problem; with an appropriate mesh size, we showed that the numerical solution converges to the analytical solution

Contributions To The Methodology Of Electrocardiographic Imaging (ECGI) And Application Of ECGI To Study Mechanisms Of Atrial Arrhythmia, Post Myocardial Infarction Electrophysiological Substrate, And Ventricular Tachycardia In Patients

ABSTRACT OF THE DISSERTATION Contributions to the Methodology of Electrocardiographic Imaging: ECGI) and Application of ECGI to Study Mechanisms of Atrial Arrhythmia, Post Myocardial Infarction Electrophysiological Substrate, and Ventricular Tachycardia in Patients by Yong Wang Doctor of Philosophy in Biomedical Engineering Washington University in St. Louis, 2009 Professor Yoram Rudy, Chair Electrocardiographic Imaging: ECGI) is a noninvasive imaging modality for cardiac electrophysiology and arrhythmia. ECGI reconstructs epicardial potentials, electrograms and isochrones from body-surface electrocardiograms combined with heart-torso geometry from computed tomography: CT). The application of a new meshless method, the Method of Fundamental Solutions: MFS) is introduced to ECGI with the following major advantages: 1. Elimination of meshing and manual mesh optimization processes, thereby enhancing automation and speeding the ECGI procedure. 2. Elimination of mesh-induced artifacts. 3. Simpler implementation. These properties of MFS enhance the practical application of ECGI as a clinical diagnostic tool. The current ECGI mode of operation is offline with generation of epicardial potential maps delayed to data acquisition. A real time ECGI procedure is proposed, by which the epicardial potentials can be reconstructed while the body surface potential data are acquired: \u3c 1msec/frame) during a clinical procedure. This development enables real-time monitoring, diagnosis, and interactive guidance of intervention for arrhythmia therapy. ECGI is applied to map noninvasively the electrophysiological substrate in eight post-MI patients during sinus rhythm: SR). Contrast-enhanced MRI: ceMRI) is conducted to determine anatomical scar. ECGI imaged regions of electrical scar corresponded closely in location, extent, and morphology to the anatomical scars. In three patients, late diastolic potentials are imaged in the scar epicardial border zone during SR. Scar-related ventricular tachycardia: VT) in two patients are imaged, showing the VT activation sequence in relation to the abnormal electrophysiological substrate. ECGI imaging the substrate in a beat-by-beat fashion could potentially help in noninvasive risk stratification for post-MI arrhythmias and facilitate substrate-based catheter ablation of these arrhythmias. ECGI is applied to eleven consecutive patients referred for VT catheter ablation procedure. ECGI is performed either before: 8 patients) or during: 3 patients) the ablation procedure. Blinded ECGI and invasive electrophysiology: EP) study results are compared. Over a wide range of VT types and locations, ECGI results are consistent with EP data regarding localization of the arrhythmia origin: including myocardial depth) and mechanism: focal, reentrant, fascicular). ECGI also provides mechanistic electrophysiological insights, relating arrhythmia patterns to the myocardial substrate. The study shows ECGI has unique potential clinical advantages, especially for hemodynamically intolerant VT or VT that is difficult to induce. Because it provides local cardiac information, ECGI may aid in better understanding of mechanisms of ventricular arrhythmia. Further prospective trials of ECGI with clinical endpoints are warranted. Many mechanisms for the initiation and perpetuation of atrial fibrillation: AF) have been demonstrated over the last several decades. The tools to study these mechanisms in humans have limitations, the most common being invasiveness of a mapping procedure. In this paper, we present simultaneous noninvasive biatrial epicardial activation sequences of AF in humans, obtained using the Electrocardiographic Imaging: ECGI) system, and analyzed in terms of mechanisms and complexity of activation patterns. We performed ECGI in 36 patients with a diagnosis of AF. To determine ECGI atrial accuracy, atrial pacing from different sites was performed in six patients: 37 pacing events), and ECGI was compared to registered CARTO images. Then, ECGI was performed on all 36 patients during AF and ECGI epicardial maps were analyzed for mechanisms and complexity. ECGI noninvasively imaged the low-amplitude signals of AF in a wide range of patients: 97% procedural success). The spatial accuracy in determining initiation sites as simulated by atrial pacing was ~ 6mm. ECGI imaged many activation patterns of AF, most commonly multiple wavelets: 92%), with pulmonary vein: 69%) and non-pulmonary vein: 62%) trigger sites. Rotor activity was seen rarely: 15%). AF complexity increased with longer clinical history of AF, though the degree of complexity of nonparoxysmal AF varied and overlapped. ECGI offers a way to identify unique epicardial activation patterns of AF in a patient-specific manner. The results are consistent with contemporary animal models of AF mechanisms and highlight the coexistence of a variety of mechanisms among patients

Functional Mapping of Three-Dimensional Electrical Activation in Ventricles

University of Minnesota Ph.D. dissertation. 2010. Major: Biomedical Engineering. Advisor: Bin He. 1 computer file (PDF); 139 pages.Ventricular arrhythmias account for nearly 400,000 deaths per year in the United States alone. Electrical mapping of the ventricular activation could facilitate the diagnosis and treatment of arrhythmias, e.g. guiding catheter ablation. To date, both direct mapping and non-contact mapping techniques have been routinely used in electrophysiology labs for obtaining the electrical activity on the endocardial surface. Non-invasive functional mapping methods are also developed to estimate the electrical activity on the epicardium or on both epicardium and endocardium from the body surface measurements. Though successful, the results using above methods are all limited on the surface of the heart and thus cannot directly characterize the cardiac events originating within the myocardial wall. Our group's goal is to develop a functional mapping method to estimate the three-dimensional cardiac electrical activity from either non-invasive body surface potential maps or minimally-invasive intracavitary potential maps, by solving the so-called "inverse problem". Hence the information under the surface of the heart could be revealed to better characterize the cardiac activation. In the present thesis study, the previously developed three-dimensional cardiac electrical imaging (3DCEI) approach has been further investigated. Its function is expanded for not only estimating the global activation sequence but also reconstructing the potential at any myocardial site throughout the ventricle. New algorithms under the 3DCEI scheme are also explored for more powerful mapping capability. The performance of the enhanced 3DCEI approach is rigorously evaluated in both control and diseased swine models when the clinical settings are mimicked. The promising results validate the feasibility of estimating detailed three-dimensional cardiac activation by using the 3DCEI approach, and suggest that 3DCEI has great potential of guiding the clinical management of cardiac arrhythmias in a more efficient way

Solving the inverse problem of electrocardiography in a realistic environment

Heart disease is a leading cause of death worldwide. Straightforward information about the cardiac electrophysiology can help to improve the quality of diagnosis of heart diseases. The inverse problem of electrocardiography and the intracardiac catheter measurement are two ways to get access to the electrophysiology in the heart. In this thesis six research topics related to these two techniques are included

Personalized Multi-Scale Modeling of the Atria: Heterogeneities, Fiber Architecture, Hemodialysis and Ablation Therapy

This book targets three fields of computational multi-scale cardiac modeling. First, advanced models of the cellular atrial electrophysiology and fiber orientation are introduced. Second, novel methods to create patient-specific models of the atria are described. Third, applications of personalized models in basic research and clinical practice are presented. The results mark an important step towards the patient-specific model-based atrial fibrillation diagnosis, understanding and treatment

Non-Invasive Electrocardiographic Imaging of Ventricular Activities: Data-Driven and Model-Based Approaches

Die vorliegende Arbeit beleuchtet ausgewählte Aspekte der Vorwärtsmodellierung, so zum Beispiel die Simulation von Elektro- und Magnetokardiogrammen im Falle einer elektrisch stillen Ischämie sowie die Anpassung der elektrischen Potentiale unter Variation der Leitfähigkeiten. Besonderer Fokus liegt auf der Entwicklung neuer Regularisierungsalgorithmen sowie der Anwendung und Bewertung aktuell verwendeter Methoden in realistischen in silico bzw. klinischen Studien

ECG Imaging of Ventricular Activity in Clinical Applications

ECG imaging was performed in humans to reconstruct ventricular activation patterns and localize their excitation origins. The precision of the non-invasive reconstructions was evaluated against invasive measurements and found to be in line with the state-of-the-art literature. Statistics were produced for various excitation origins and reveal the beat-to-beat robustness of the imaging method