Regional differences in ventricular fibrillation in the open-chest porcine left ventricle

被引:46
作者
Nanthakumar, K [1 ]
Huang, J [1 ]
Rogers, JM [1 ]
Johnson, PL [1 ]
Newton, JC [1 ]
Walcott, GP [1 ]
Justice, RK [1 ]
Rollins, DL [1 ]
Smith, WM [1 ]
Ideker, RE [1 ]
机构
[1] Univ Alabama Birmingham, Birmingham, AL 35294 USA
关键词
ventricular fibrillation; electrical mapping; mechanisms of arrhythmias;
D O I
10.1161/01.RES.0000038945.66661.21
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It has been hypothesized that during ventricular fibrillation (VF), the fastest activating region, the dominant domain, contains a stable reentrant circuit called a mother rotor. This hypothesis postulates that the mother rotor spawns wavefronts that propagate to maintain VF elsewhere and implies that the ratio of wavefronts propagating off a region to those propagating onto it (propoff/propon) should be >1 for the dominant domain but <1 elsewhere. To test this prediction in the left ventricular (LV) epicardium of a large animal, most of the LV free wall was mapped with 1008 electrodes in 7 pigs. VF activation rate was faster in the posterior than in the anterior LV (10.0+/-1.3Hz versus 9.3+/-1.3Hz; P<0.001). The anterior LV had a higher fraction of wavefronts that blocked than did the posterior LV and had a propoff/propon ratio <1 (P<0.001). The mean conduction velocity vectors of the VF wavefronts pointed in the direction from the posterior to the anterior LV. Although these findings favor a dominant domain in the posterior LV, the facts that the anterior LV had a higher incidence of reentry than did the posterior LV and that the posterior LV did not have propoff/propon significantly different from 1 do not. Thus, quantitative regional differences are present over the porcine LV epicardium during VF. Although these differences are not totally consistent with the presence of a dominant domain within the LV free wall, the mean conduction velocity vector is consistent with one in the septum.
引用
收藏
页码:733 / 740
页数:8
相关论文
共 28 条
[1]   EFFICIENT ELECTRODE SPACING FOR EXAMINING SPATIAL-ORGANIZATION DURING VENTRICULAR-FIBRILLATION [J].
BAYLY, PV ;
JOHNSON, EE ;
IDRISS, SF ;
IDEKER, RE ;
SMITH, WM .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 1993, 40 (10) :1060-1066
[2]   High-frequency periodic sources underlie ventricular fibrillation in the isolated rabbit heart [J].
Chen, J ;
Mandapati, R ;
Berenfeld, O ;
Skanes, AC ;
Jalife, J .
CIRCULATION RESEARCH, 2000, 86 (01) :86-93
[3]  
Choi BR, 2001, CIRC RES, V88, pE49
[4]  
CHOI BR, 2001, CIRC RES, V16, P88
[5]   Preventing ventricular fibrillation by flattening cardiac restitution [J].
Garfinkel, A ;
Kim, YH ;
Voroshilovsky, O ;
Qu, ZL ;
Kil, JR ;
Lee, MH ;
Karagueuzian, HS ;
Weiss, JN ;
Chen, PS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (11) :6061-6066
[6]   Spatial and temporal organization during cardiac fibrillation [J].
Gray, RA ;
Pertsov, AM ;
Jalife, J .
NATURE, 1998, 392 (6671) :75-78
[7]  
Gurvich NL, 1957, FIBRILLATION DEFIBRI
[8]   CORRELATION BETWEEN INVIVO TRANSMEMBRANE ACTION-POTENTIAL DURATIONS AND ACTIVATION-RECOVERY INTERVALS FROM ELECTROGRAMS - EFFECTS OF INTERVENTIONS THAT ALTER REPOLARIZATION TIME [J].
HAWS, CW ;
LUX, RL .
CIRCULATION, 1990, 81 (01) :281-288
[9]   Evolution of the organization of epicardial activation patterns during ventricular fibrillation [J].
Huang, JA ;
Rogers, JM ;
Kenknight, BH ;
Rollins, DL ;
Smith, WM ;
Ideker, RE .
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 1998, 9 (12) :1291-1304
[10]   Role of structural complexities of septal tissue in maintaining ventricular fibrillation in isolated, perfused canine ventricle [J].
Ikeda, T ;
Kawase, A ;
Nakazawa, K ;
Ashihara, T ;
Namba, T ;
Takahashi, K ;
Sugi, K ;
Yamaguchi, T .
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 2001, 12 (01) :66-75