How accurate is inverse electrocardiographic mapping? A systematic in vivo evaluation

LR Bear, IJ LeGrice, GB Sands, NA Lever… - Circulation …, 2018 - Am Heart Assoc
LR Bear, IJ LeGrice, GB Sands, NA Lever, DS Loiselle, DJ Paterson, LK Cheng, BH Smaill
Circulation: Arrhythmia and Electrophysiology, 2018Am Heart Assoc
Background: Inverse electrocardiographic mapping reconstructs cardiac electrical activity
from recorded body surface potentials. This noninvasive technique has been used to identify
potential ablation targets. Despite this, there has been little systematic evaluation of its
reliability. Methods: Torso and ventricular epicardial potentials were recorded
simultaneously in anesthetized, closed-chest pigs (n= 5), during sinus rhythm, epicardial,
and endocardial ventricular pacing (70 records in total). Body surface and cardiac electrode …
Background
Inverse electrocardiographic mapping reconstructs cardiac electrical activity from recorded body surface potentials. This noninvasive technique has been used to identify potential ablation targets. Despite this, there has been little systematic evaluation of its reliability.
Methods
Torso and ventricular epicardial potentials were recorded simultaneously in anesthetized, closed-chest pigs (n=5), during sinus rhythm, epicardial, and endocardial ventricular pacing (70 records in total). Body surface and cardiac electrode positions were determined and registered using magnetic resonance imaging. Epicardial potentials were reconstructed during ventricular activation using experiment-specific magnetic resonance imaging–based thorax models, with homogeneous or inhomogeneous (lungs, skeletal muscle, fat) electrical properties. Coupled finite/boundary element methods and a meshless approach based on the method of fundamental solutions were compared. Inverse mapping underestimated epicardial potentials >2-fold (P<0.0001).
RESULTS
Mean correlation coefficients for reconstructed epicardial potential distributions ranged from 0.60±0.08 to 0.64±0.07 across all methods. Epicardial electrograms were recovered with reasonable fidelity at ≈50% of sites (median correlation coefficient, 0.69–0.72), but variation was substantial. General activation spread was reproduced (median correlation coefficient, 0.72–0.78 for activation time maps after spatio-temporal smoothing). Epicardial foci were identified with a median location error ≈16 mm (interquartile range, 9–29 mm). Inverse mapping with meshless method of fundamental solutions was better than with finite/boundary element methods, and the latter were not improved by inclusion of inhomogeneous torso electrical properties.
Conclusions
Inverse potential mapping provides useful information on the origin and spread of epicardial activation. However the spatio-temporal variability of recovered electrograms limit resolution and must constrain the accuracy with which arrhythmia circuits can be identified independently using this approach.
Am Heart Assoc