Inverse localization of earliest cardiac activation sites from activation maps based on the viscous Eikonal equation.

In this study we propose a novel method for identifying the locations of earliest activation in the human left ventricle from activation maps measured at the epicardial surface. Electrical activation is modeled based on the viscous Eikonal equation. The sites of earliest activation are identified by solving a minimization problem. Arbitrary initial locations are assumed, which are then modified based on a shape derivative based perturbation field until a minimal mismatch between the computed and the given activation maps on the epicardial surface is achieved. The proposed method is tested in two numerical benchmarks, a generic 2D unit-square benchmark, and an anatomically accurate MRI-derived 3D human left ventricle benchmark to demonstrate potential utility in a clinical context. For unperturbed input data, our localization method is able to accurately reconstruct the earliest activation sites in both benchmarks with deviations of only a fraction of the used spatial discretization size. Further, with the quality of the input data reduced by spatial undersampling and addition of noise, we demonstrate that an accurate identification of the sites of earliest activation is still feasible.

An Inverse Problem Involving a Viscous Eikonal Equation with Applications in Electrophysiology.

In this work we discuss the reconstruction of cardiac activation instants based on a viscous Eikonal equation from boundary observations. The problem is formulated as a least squares problem and solved by a projected version of the Levenberg-Marquardt method. Moreover, we analyze the well-posedness of the state equation and derive the gradient of the least squares functional with respect to the activation instants. In the numerical examples we also conduct an experiment in which the location of the activation sites and the activation instants are reconstructed jointly based on an adapted version of the shape gradient method from (J. Math. Biol. 79, 2033-2068, 2019). We are able to reconstruct the activation instants as well as the locations of the activations with high accuracy relative to the noise level.