Electromechanical endocardial mapping distinguished infarcted from healthy myocardium, with unipolar voltages significantly lower in MI regions than in control patients (7.2 vs 19.7 mV; P<0.001).
Observational (n=24)
Prior myocardial infarction (n=24)
Electromechanical endocardial mapping vs Control patients without prior MI
Left ventricular endocardial unipolar voltage, p=<0.001
Absolute Event Rate: 7.2% vs 19.7%
p-value: p=<0.001
BACKGROUND: A catheter-based left ventricular (LV) endocardial mapping procedure using electromagnetic field energy for positioning of the catheter tip was designed to acquire simultaneous measurements of endocardial voltage potentials and myocardial contractility. We investigated such a mapping system to distinguish between infarcted and normal myocardium in an animal infarction model and in patients with coronary artery disease. METHODS AND RESULTS: Measurements of LV endocardial unipolar (UP) and bipolar (BP) voltages and local endocardial shortening were derived from dogs at baseline (n=12), at 24 hours (n=6), and at 3 weeks (n=6) after occlusion of the left anterior descending coronary artery. Also, 12 patients with prior myocardial infarction (MI) and 12 control patients underwent the LV endocardial mapping study for assessment of electromechanical function in infarcted versus healthy myocardial regions. In the canine model, a significant decrease in voltage potentials was noted in the MI zone at 24 hours (UP, 42. 8+/-9.6 to 29.1+/-12.2 mV, P=0.007; BP, 11.6+/-2.3 to 4.9+/-1.2 mV, P<0.0001) and at 3 weeks (UP, 41.0+/-8.9 to 13.9+/-3.9 mV, P<0.0001; BP, 11.2+/-2.8 to 2.4+/-0.4 mV, P<0.0001). No change in voltage was noted in zones remote from MI. In patients with prior MI, the average voltage was 7.2+/-2.7 mV (UP)/1.4+/-0.7 mV (BP) in MI regions, 17.8+/-4.6 mV (UP)/4.5+/-1.1 mV (BP) in healthy zones remote from MI, and 19.7+/-4.4 mV (UP)/5.8+/-1.0 mV (BP) in control patients without prior MI (P<0.001 for MI values versus remote zones or control patients). In the canine model and patients, local endocardial shortening was significantly impaired in MI zones compared with controls. CONCLUSIONS: These preliminary data suggest that infarcted myocardium could be accurately diagnosed and distinguished from healthy myocardium by a reduction in both electrical voltage and mechanical activity. Such a diagnostic electromechanical mapping study might be clinically useful for accurate assessment of myocardial function and viability.
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Ran Kornowski
Interventional Cardiology
Mun K. Hong
Bassett Medical Center
Lior Gepstein
Electrophysiology
Circulation
Rappaport Family Institute for Research in the Medical Sciences
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Kornowski et al. (Tue,) conducted a observational in Prior myocardial infarction (n=24). Electromechanical endocardial mapping vs. Control patients without prior MI was evaluated on Left ventricular endocardial unipolar voltage (p=<0.001). Electromechanical endocardial mapping distinguished infarcted from healthy myocardium, with unipolar voltages significantly lower in MI regions than in control patients (7.2 vs 19.7 mV; P<0.001).
synapsesocial.com/papers/6a153bfccb0379474a8209a1 — DOI: https://doi.org/10.1161/01.cir.98.11.1116