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High-resolution noncontact charge-density mapping of endocardial activation
Andrew Grace, Stephan Willems, Christian Meyer, Atul Verma, Patrick Heck, Min Zhu, Xinwei Shi, Derrick Chou, Lam Dang, Christoph Scharf, Günter Scharf, Graydon Beatty
Andrew Grace, Stephan Willems, Christian Meyer, Atul Verma, Patrick Heck, Min Zhu, Xinwei Shi, Derrick Chou, Lam Dang, Christoph Scharf, Günter Scharf, Graydon Beatty
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Clinical Research and Public Health Cardiology

High-resolution noncontact charge-density mapping of endocardial activation

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Abstract

BACKGROUND. Spatial resolution in cardiac activation maps based on voltage measurement is limited by far-field interference. Precise characterization of electrical sources would resolve this limitation; however, practical charge-based cardiac mapping has not been achieved. METHODS. A prototype algorithm, developed from first principles of electrostatic field theory, derives charge density (CD) as a spatial representation of the true sources of the cardiac field. The algorithm processes multiple, simultaneous, noncontact voltage measurements within the cardiac chamber to inversely derive the global distribution of CD sources across the endocardial surface. RESULTS. Comparison of CD to an established computer-simulated model of atrial conduction demonstrated feasibility in terms of spatial, temporal, and morphologic metrics. Inverse reconstruction matched simulation with median spatial errors of 1.73 mm and 2.41 mm for CD and voltage, respectively. Median temporal error was less than 0.96 ms and morphologic correlation was greater than 0.90 for both CD and voltage. Activation patterns observed in human atrial flutter reproduced those established through contact maps, with a 4-fold improvement in resolution noted for CD over voltage. Global activation maps (charge density–based) are reported in atrial fibrillation with confirmed reduction of far-field interference. Arrhythmia cycle-length slowing and termination achieved through ablation of critical points demonstrated in the maps indicates both mechanistic and pathophysiological relevance. CONCLUSION. Global maps of cardiac activation based on CD enable classification of conduction patterns and localized nonpulmonary vein therapeutic targets in atrial fibrillation. The measurement capabilities of the approach have roles spanning deep phenotyping to therapeutic application. TRIAL REGISTRATION. ClinicalTrials.gov NCT01875614. FUNDING. The National Institute for Health Research (NIHR) Translational Research Program at Royal Papworth Hospital and Acutus Medical.

Authors

Andrew Grace, Stephan Willems, Christian Meyer, Atul Verma, Patrick Heck, Min Zhu, Xinwei Shi, Derrick Chou, Lam Dang, Christoph Scharf, Günter Scharf, Graydon Beatty

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Figure 5

Initial clinical validation in typical cavotricuspid-isthmus–dependent atrial flutter.

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Initial clinical validation in typical cavotricuspid-isthmus–dependent a...
Example of typical, counter-clockwise flutter in the right atrium. In the upper panel, the propagation-history color bands are set to display a fixed propagation-history map of the entire cycle length, shown in anterior-posterior (AP) and left-anterior-oblique (LAO) views. Signals can be visualized from any position on the map (labeled on the anatomical mesh) and at any instant of time due to the global, simultaneous calculation of the inverse solution. The duration of propagation history can be adjusted by the operator and is demarcated by the translucent-gray region in the lower panel. The yellow time cursor at the right edge of the history window corresponds to the leading edge of the red color band on the map, shown reaching the roof from the septum. The other color bands, located progressively clockwise, represent the location of the wavefront at earlier instants of time. The span of the color bands, across space, and the associated duration of the translucent-gray region, across time, were set equal to the flutter-cycle length (CL, 255 ms). Accordingly, waveforms sampled from 8 evenly spaced locations around the entire right atrium reproduce the expected morphology and timing of propagation, while the map reveals the activation sequence progressing inferiorly from the roof on the lateral wall (LAT), medially on the isthmus (CTI), and superiorly on the septum (SEP). IVC, inferior vena cava; RAA, right atrial appendage; SVC, superior vena cava; TV, tricuspid valve.

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