Epicardial and Endocardial Activation During Sustained Ventricular Tachycardia in Man

Ventricular activation during ventricular tachycardia was studied by intraoperative epicardial and endocardial mapping in 21 patients with coronary artery disease and previous myocardial infarction who underwent operation for recurrent ventricular tachycardia. Twenty-nine morphologically distinct tachycardias were mapped; 18 tachycardias had a right bundle branch block morphology and 11 had a left bundle branch block morphology. After cannulation for bypass, the tachycardias were induced and electrograms were recorded at 55-75 epicardial sites. After starting cardiopulmonary bypass, the infarction was incised and electrograms were recorded at 28-55 left ventricular endocardial sites during ventricular tachycardia. All mapping data were analyzed with three simultaneously recorded ECG leads and two reference electrograms. Earliest activation in all tachycardias occurred on the endocardial surface of the infarction. In each tachycardia, endocardial electrical activity was recorded before the onset of the QRS complex. Earliest epicardial activation in the 29 tachycardias occurred 10 msec after the onset of the QRS complex. Epicardial breakthrough occurred on the right (19 tachycardias) as well as the left ventricle (10 tachycardias). We conclude that ventricular tachycardia associated with ischemic heart disease originates near the endocardial surface of the left ventricle along the border of the infarction and that epicardial mapping alone is insufficient to identify the site of origin of these tachycardias.

[1]  L. Horowitz,et al.  Ventricular resection guided by epicardial and endocardial mapping for treatment of recurrent ventricular tachycardia. , 1980, The New England journal of medicine.

[2]  L. Horowitz,et al.  Cellular electrophysiology of human myocardial infarction. 1. Abnormalities of cellular activation. , 1979, Circulation.

[3]  L. Horowitz,et al.  Sustained ventricular tachycardia: evidence for protected localized reentry. , 1978, The American journal of cardiology.

[4]  L. Horowitz,et al.  The Limitations of Epicardial Mapping as a Guide to the Surgical Therapy of Ventricular Tachycardia , 1978, Circulation.

[5]  L. Horowitz,et al.  Continuous Local Electrical Activity: A Mechanism of Recurrent Ventricular Tachycardia , 1978, Circulation.

[6]  L. Horowitz,et al.  Recurrent Sustained Ventricular Tachycardia: 1. Mechanisms , 1978, Circulation.

[7]  Allessie,et al.  Circus movement in rabbit atrial muscle as a mechanism of tachycardia. III. The "leading circle" concept: a new model of circus movement in cardiac tissue without the involvement of an anatomical obstacle. , 1977, Circulation research.

[8]  J. Spear,et al.  The Origin of Ventricular Arrhythmias 24 Hours Following Experimental Anterior Septal Coronary Artery Occlusion , 1977, Circulation.

[9]  H. Wellens,et al.  Observations on Mechanisms of Ventricular Tachycardia in Man , 1976, Circulation.

[10]  A. L. Wit,et al.  Triggered Activity in Cardiac Muscle Fibers of the Simian Mitral Valve , 1976, Circulation research.

[11]  L. Horowitz,et al.  Subendocardial Origin of Ventricular Arrhythmias in 24‐Hour‐Old Experimental Myocardial Infarction , 1976, Circulation.

[12]  J. Boineau,et al.  Surgical treatment of ventricular arrhythmias using epicardial, transmural, and endocardial mapping. , 1975, The Annals of thoracic surgery.

[13]  J. Gallagher,et al.  Ventricular aneurysm with ventricular tachycardia. Report of a case with epicardial mapping and successful resection. , 1975, The American journal of cardiology.

[14]  H. Wellens Pathophysiology of ventricular tachycardia in man. , 1975, Archives of internal medicine.

[15]  C. Thorburn,et al.  Surgical treatment of ventricular tachycardia after epicardial mapping studies. , 1975, British heart journal.

[16]  D. Harrison,et al.  Surgical treatment of refractory life-threatening ventricular tachycardia. , 1973, The American journal of cardiology.

[17]  J. Boineau,et al.  Comparison of Human Ventricular Activation with a Canine Model in Chronic Myocardial Infarction , 1971, Circulation.