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(Circulation. 2004;109:920-925.)
© 2004 American Heart Association, Inc.

Basic Science Reports

Mechanisms of Myocardial Capture and Temporal Excitable Gap During Spiral Wave Reentry in a Bidomain Model

Takashi Ashihara, MD, PhD; Tsunetoyo Namba, MD, PhD; Takanori Ikeda, MD, PhD; Makoto Ito, MD, PhD; Kazuo Nakazawa, PhD; Natalia Trayanova, PhD

From the Department of Biomedical Engineering and the Center for Computational Science, Tulane University, New Orleans, La (T.A., N.T.), and the Japanese Working Group on Cardiac Simulation and Mapping, Tokyo, Japan (T.N., T.I., M.I., K.N.).

Correspondence to Takashi Ashihara, MD, PhD, Department of Biomedical Engineering, Boggs Center, Suite 500, Tulane University, New Orleans, LA 70118. E-mail tashihar{at}tulane.edu

Received March 13, 2003; de novo received May 9, 2003; accepted December 2, 2003.

Background— Recent studies have demonstrated that regional capture during cardiac fibrillation is associated with an elevated capture threshold. It is typically assumed that the temporal excitable gap (capture window) during fibrillation reflects the size of the spatial excitable gap (excitable tissue between fibrillation waves). Because capture threshold is high, virtual electrode polarization is expected to be involved in the process. However, little is known about the underlying mechanisms of myocardial capture during fibrillation.

Methods and Results— To clarify these issues, we conducted altogether 3168 simulations of single spiral wave capture in a bidomain sheet. Unipolar stimuli of strengths 4, 8, 16, and 24 mA and 2-ms duration were delivered at 99 locations in the sheet. We found that cathode-break rather than cathode-make excitation was the dominant mechanism of myocardial capture. When the stimulation site was located diagonally with respect to the core (upper left or lower right if the spiral wave rotates counterclockwise), the cathode-break excitation easily invaded the spatial excitable gap and resulted in a successful capture as a result of the formation of virtual anodes in the direction of the myocardial fibers. Thus, the spatial distribution of the temporal excitable gap did not reflect the spatial excitable gap.

Conclusions— The areas exhibiting wide temporal excitable gaps were areas in which the cathode-break excitation wave fronts easily invaded the spatial excitable gap via the virtual anodes. This study provides mechanistic insight into myocardial capture.

Key Words: electrical stimulation • excitation • fibrillation • mapping • reentry

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