Sinus Rhythm Parameters in the Infarct Border Zone Are Useful to Assess Reentrant Ventricular Tachycardia
Edward J Ciaccio1,2, James Coromilas3, Henry H Hsia4
1Department of Medicine-Division of Cardiology, Columbia University College of Physicians and Surgeons, New York, New York, USA.
Introduction:
Reentrant ventricular tachycardia (VT) is an important clinical problem, with underlying biophysical mechanisms that remain incompletely understood. Substrate compilation maps were used to detect subtle spatial gradients and for assessing inducibility of sustained VT.
Method/Results:
A subepicardial infarct was created via left anterior descending coronary artery (LAD) ligation in canine hearts. After 3-5 days, electrical activity was marked and mapped using a 312-electrode array in 60 postinfarction hearts (30 noninducible for VT, 30 with sustained VT). Compilation maps were constructed by summing the N = 30 individual experiment maps of parameters from representative sinus rhythm (SR) and VT cycles. Gradients were determined by averaging multiarray data row-by-row, and by dividing 312-grid sites into LAD-proximate vs. apical-lateral-proximate halves. Prediction of VT induction was done using SR activation statistics. Compilation maps revealed that SR activation times were prolonged in inducible vs. non-inducible experiments (means 21.64 vs. 13.58 msec, p < 0.001). SR activation means and standard deviations per experiment (N = 312 sites) were predictive of reentrant VT inducibility (sensitivity = 28/30 or 93.3%, specificity = 26/30 or 86.7%). SR electrogram duration lengthened in inducible vs. non-inducible VT experiments (36.54 vs. 32.40 msec, p < 0.001). VT electrogram duration averaged 34.70 msec, differing from both SR measurements (p ≤ 0.003). Isthmus electrogram duration averaged 33.6 msec in SR vs. 40.6 msec in VT. The SR electrogram duration in VT inducible experiments exhibited a gradient with values increasing away from the LAD (r2 = 0.79, p < 0.001), perhaps resulting from decreasing blood perfusion.
Conclusions:
Compilation maps provide insights into profiles of SR spatiotemporal activation, to predict arrhythmia inducibility in reentrant VT substrates.
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