NONINVASIVE ELECTROCARDIOGRAPHIC IMAGING - RECONSTRUCTION OF EPICARDIAL POTENTIALS, ELECTROGRAMS, AND ISOCHRONES AND LOCALIZATION OF SINGLEAND MULTIPLE ELECTROCARDIAC EVENTS
Hs. Oster et al., NONINVASIVE ELECTROCARDIOGRAPHIC IMAGING - RECONSTRUCTION OF EPICARDIAL POTENTIALS, ELECTROGRAMS, AND ISOCHRONES AND LOCALIZATION OF SINGLEAND MULTIPLE ELECTROCARDIAC EVENTS, Circulation, 96(3), 1997, pp. 1012-1024
Background The goal of noninvasive electrocardiographic imaging (ECGI)
is to determine electric activity of the heart by reconstructing maps
of epicardial potentials, excitation times (isochrones), and electrog
rams from data measured on the body surface. Methods and Results Local
electrocardiac events were initiated by pacing a dog heart in a human
torso-shaped tank. Body surface potential measurements (384 electrode
s) were used to compute epicardial potentials noninvasively. The accur
acy of reconstructed epicardial potentials was evaluated by direct com
parison to measured ones (134 electrodes). Protocols included pacing f
rom single sites and simultaneously from two sites with various inters
ite distances. Body surface potentials showed a single minimum for bot
h single- and double-site pacing (intersite distances of 52, 35, and 1
7 mm). Noninvasively reconstructed epicardial electrograms, potentials
, and isochrones closely approximated the measured ones. Single pacing
sites were reconstructed to within less than or equal to 10 mm of the
ir measured positions. Dual sites were located accurately and resolved
for the above intersite distances. Regions of sparse and crowded isoc
hrones, indicating spatial nonuniformities of epicardial activation sp
read, were also reconstructed. Conclusions The study demonstrates that
ECGI can reconstruct epicardial potentials, electrograms, and isochro
nes over the entire epicardial surface during the cardiac cycle. It ca
n provide detailed information on local activation of the heart noninv
asively. Its uses could include localization of cardiac electric event
s (eg, ectopic foci), characterization of nonuniformities of conductio
n, characterization of repolarization properties (eg, dispersion), and
mapping of dynamically changing arrhythmias (eg, polymorphic VT) on a
beat-by-beat basis.