Simulation of QRST integral maps with a membrane-based computer heart model employing parallel processing

被引:49
作者
Trudel, MC
Dubé, B
Potse, M [1 ]
Gulrajani, RM
Leon, LJ
机构
[1] EBS Inc, Montreal, PQ H2X 3V8, Canada
[2] Univ Montreal, Inst Biomed Engn, Montreal, PQ H3C 3J7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
action-potential duration; cardiac membrane model; computer heart model; parallel processing; QRST integral maps;
D O I
10.1109/TBME.2004.827934
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The simulation of the propagation of electrical activity in a membrane-based realistic-geometry computer model of the ventricles of the human heart, using the governing monodomain reaction-diffusion equation, is described. Each model point is represented by the phase I Luo-Rudy membrane model, modified to represent human action potentials. A separate longer duration action potential was used for the M cells found in the ventricular midwall. Cardiac fiber rotation across the ventricular wall was implemented via an analytic equation, resulting in a spatially varying anisotropic conductivity tensor and, consequently, anisotropic propagation. Since the model comprises approximately 12.5 million points, parallel processing on a multiprocessor computer was used to cut down on simulation time. The simulation of normal activation as well as that of ectopic beats is described. The hypothesis that in situ electrotonic coupling in the myocardium can diminish the gradients of action-potential duration across the ventricular wall was also verified in the model simulations. Finally, the sensitivity of QRST integral maps to local alterations in action-potential duration was investigated.
引用
收藏
页码:1319 / 1329
页数:11
相关论文
共 44 条
[11]   ELECTROPHYSIOLOGIC CHARACTERISTICS OF CELLS SPANNING THE LEFT-VENTRICULAR WALL OF HUMAN HEART - EVIDENCE FOR PRESENCE OF M-CELLS [J].
DROUIN, E ;
CHARPENTIER, F ;
GAUTHIER, C ;
LAURENT, K ;
LEMAREC, H .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1995, 26 (01) :185-192
[12]   TOTAL EXCITATION OF ISOLATED HUMAN HEART [J].
DURRER, D ;
VANDAM, RT ;
FREUD, GE ;
JANSE, MJ ;
MEIJLER, FL ;
ARZBAECHER, RC .
CIRCULATION, 1970, 41 (06) :899-+
[13]   VULNERABILITY TO VENTRICULAR ARRHYTHMIA - ASSESSMENT BY MAPPING OF BODY-SURFACE POTENTIAL [J].
GARDNER, MJ ;
MONTAGUE, TJ ;
ARMSTRONG, CS ;
HORACEK, BM ;
SMITH, ER .
CIRCULATION, 1986, 73 (04) :684-692
[14]  
GULRAJANI RM, 2001, P 3 INT S NON FUNCT, V46, P20
[15]   A flexible method for simulating cardiac conduction in three-dimensional complex geometries [J].
Harrild, DM ;
Penland, RC ;
Henriquez, CS .
JOURNAL OF ELECTROCARDIOLOGY, 2000, 33 (03) :241-251
[16]   A finite volume model of cardiac propagation [J].
Harrild, DM ;
Henriquez, CS .
ANNALS OF BIOMEDICAL ENGINEERING, 1997, 25 (02) :315-334
[17]   Using computer models to understand the roles of tissue structure and membrane dynamics in arrhythmogenesis [J].
Henriquez, CS ;
Papazoglou, AA .
PROCEEDINGS OF THE IEEE, 1996, 84 (03) :334-354
[18]   Simulation of depolarization in a membrane-equations-based model of the anisotropic ventricle [J].
Huiskamp, G .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 1998, 45 (07) :847-855
[19]  
JOYNER RW, 1986, JPN HEART J, V27, P167
[20]  
LEON LJ, 1991, J ELECTROCARDIOL, V24, P1, DOI 10.1016/0022-0736(91)90077-Y