Elizabeth Cherry

Department of Physics and Department of Computer Science
Duke University

now at
Department of Physics
Hofstra University


Among the most challenging issues in physiology is understanding the dynamics of and developing the ability to control cardiac tissue. Despite decades of research, about a quarter of a million adults die every year in the USA from sudden cardiac death, generally due to ventricular fibrillation. Many properties of the heart are at least partially understood, but the mechanisms responsible for initiation and maintenance of potentially life-threatening arrhythmias remain unclear. Experiments are difficult to perform due to limitations associated with measuring information in three-dimensional structures. For instance, experimental techniques typically allow voltage data to be recorded on an array of electrodes on the exterior and/or interior surfaces of the heart. More recently, optical mapping using voltage-sensitive dyes have been used to obtain voltage information at a higher spatial resolution, but still only surface data is available. Because understanding the full three-dimensional dynamics from such limited data is so difficult, computational physiology plays an extremely important role in investigating the complex dynamics of cardiac tissue.

My research involves trying to understand better the dynamics of arrthymias by simulating mathematical models of cardiac tissue electrophysiological processes. While much of this work is focused on physiology, some effort also must be spent researching simulation methods, due to the heavy computational demands of many simulations. Currently my collaborators and I are conducting research in several areas.

Three level adaptive mesh refinement calculation of the 2D Luo-Rudy 1 model for a large square domain, 8 cm x 8 cm. On the left, electric potential V is plotted and color coded with dark blue for V > -5 mV, red for -5 > V > -65 mV, and yellow for V < -80 mV. The fronts appear as thin dark blue lines. On the right is the hierarchical Cartesian mesh structure. The yellow and green regions correspond to the fine (level 2) and finest (level 3) grids and track closely the fronts.

Recent and upcoming conference presentations:

SIAM Conference on Life Sciences. Contributions of Tissue Structures to Cardiac Arrhythmias. March 2002.

Biomedical Engineering Society Conference. The Role of Long-range and Interatrial Connections in Atrial Arrhythmias: A Simulation Study. October 2001.

Additional information:


Learn more about the heart and cardiovascular diseases:


Some Researchers Doing Related Work:

Cardiac Electrophysiology:

Adaptive Mesh Refinement: