Epicardial sock mapping following monophasic and biphasic shocks of equal voltage with an endocardial lead system. 1996

M Usui, and R L Callihan, and R G Walker, and G P Walcott, and D L Rollins, and P D Wolf, and W M Smith, and R E Ideker
Department of Medicine, University of Alabama at Birmingham 35294-0019, USA.

BACKGROUND The reason for the increased defibrillation efficacy of biphasic shocks over monophasic shock is not definitely known. RESULTS In six anesthetized pigs, we mapped the epicardium after transvenous defibrillation shocks to compare the activation patterns following successful biphasic shocks with unsuccessful monophasic shocks of the same voltage. The heart was exposed and a 510-electrode sock with approximately 4-mm interelectrode spacing was pulled over the entire ventricular epicardium and sutured to the pericardium. Defibrillation catheters were placed in the right ventricular apex and in the superior vena cava. Paired monophasic 12 msec and biphasic 6/6 msec defibrillation shocks were given using an up-down protocol to keep shock strength between the defibrillation thresholds for the two waveforms so that the biphasic shock was successful while the monophasic shock was not. Activation fronts immediately following 60 paired shocks were recorded and analyzed by animated maps of the first derivative of the electrograms. The ventricles were divided into apical (I), middle (II), and basal (III) thirds, and early sites, i.e., the sites from which activation fronts first appeared on the epicardium following the shock, were grouped according to their location. Postshock intervals, i.e., the time from the shock until earliest epicardial activation occurred, were also determined. No ectopic activation fronts followed the shock in 20 biphasic episodes. In the other 40 paired episodes, the number of early sites was smaller after biphasic shocks than after monophasic shocks [monophasic: 198 (total), 3.3 +/- 0.9 (mean +/- SD) per shock episode; biphasic: 67, 1.1 +/- 1.0, P < 0.05]. For biphasic but not monophasic shocks, early sites were less likely to arise from the middle (II) and basal (III) thirds than from the apical third (I) [monophasic: I: 84 (42%), II: 68 (34%), III: 46 (23%); biphasic: I: 49 (73%), II: 10 (15%), III: 8 (12%), P < 0.05]. Postshock intervals were significantly shorter for monophasic shocks (54 +/- 14 msec) than for biphasic shocks (75 +/- 23 msec, P < 0.05). CONCLUSIONS The decreased number of activation fronts and the longer delay following the shock for the earliest epicardial appearance of those activation fronts that do occur may be responsible for the increased defibrillation efficacy for biphasic shocks.

UI MeSH Term Description Entries
D004554 Electric Countershock An electrical current applied to the HEART to terminate a CARDIAC ARRHYTHMIA. Cardiac Electroversion,Cardioversion,Defibrillation, Electric,Electroversion, Cardiac,Electrical Cardioversion,Electroversion Therapy,Therapy, Electroversion,Cardiac Electroversions,Cardioversion, Electrical,Cardioversions,Cardioversions, Electrical,Countershock, Electric,Countershocks, Electric,Defibrillations, Electric,Electric Countershocks,Electric Defibrillation,Electric Defibrillations,Electrical Cardioversions,Electroversion Therapies,Electroversions, Cardiac,Therapies, Electroversion
D004566 Electrodes Electric conductors through which electric currents enter or leave a medium, whether it be an electrolytic solution, solid, molten mass, gas, or vacuum. Anode,Anode Materials,Cathode,Cathode Materials,Anode Material,Anodes,Cathode Material,Cathodes,Electrode,Material, Anode,Material, Cathode
D004597 Electroshock Induction of a stress reaction in experimental subjects by means of an electrical shock; applies to either convulsive or non-convulsive states. Electroconvulsive Shock,Electroconvulsive Shocks,Electroshocks,Shock, Electroconvulsive,Shocks, Electroconvulsive
D004699 Endocardium The innermost layer of the heart, comprised of endothelial cells. Endocardiums
D006321 Heart The hollow, muscular organ that maintains the circulation of the blood. Hearts
D006328 Cardiac Catheterization Procedures in which placement of CARDIAC CATHETERS is performed for therapeutic or diagnostic procedures. Catheterization, Cardiac,Catheterization, Heart,Heart Catheterization,Cardiac Catheterizations,Catheterizations, Cardiac,Catheterizations, Heart,Heart Catheterizations
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D013552 Swine Any of various animals that constitute the family Suidae and comprise stout-bodied, short-legged omnivorous mammals with thick skin, usually covered with coarse bristles, a rather long mobile snout, and small tail. Included are the genera Babyrousa, Phacochoerus (wart hogs), and Sus, the latter containing the domestic pig (see SUS SCROFA). Phacochoerus,Pigs,Suidae,Warthogs,Wart Hogs,Hog, Wart,Hogs, Wart,Wart Hog
D014693 Ventricular Fibrillation A potentially lethal cardiac arrhythmia that is characterized by uncoordinated extremely rapid firing of electrical impulses (400-600/min) in HEART VENTRICLES. Such asynchronous ventricular quivering or fibrillation prevents any effective cardiac output and results in unconsciousness (SYNCOPE). It is one of the major electrocardiographic patterns seen with CARDIAC ARREST. Fibrillation, Ventricular,Fibrillations, Ventricular,Ventricular Fibrillations
D016276 Ventricular Function The hemodynamic and electrophysiological action of the HEART VENTRICLES. Function, Ventricular,Functions, Ventricular,Ventricular Functions

Related Publications

M Usui, and R L Callihan, and R G Walker, and G P Walcott, and D L Rollins, and P D Wolf, and W M Smith, and R E Ideker
January 1993, Circulation research,
M Usui, and R L Callihan, and R G Walker, and G P Walcott, and D L Rollins, and P D Wolf, and W M Smith, and R E Ideker
March 1996, American heart journal,
M Usui, and R L Callihan, and R G Walker, and G P Walcott, and D L Rollins, and P D Wolf, and W M Smith, and R E Ideker
December 1990, American heart journal,
M Usui, and R L Callihan, and R G Walker, and G P Walcott, and D L Rollins, and P D Wolf, and W M Smith, and R E Ideker
January 1996, Pacing and clinical electrophysiology : PACE,
M Usui, and R L Callihan, and R G Walker, and G P Walcott, and D L Rollins, and P D Wolf, and W M Smith, and R E Ideker
March 2003, Pacing and clinical electrophysiology : PACE,
M Usui, and R L Callihan, and R G Walker, and G P Walcott, and D L Rollins, and P D Wolf, and W M Smith, and R E Ideker
February 1997, Journal of cardiovascular electrophysiology,
M Usui, and R L Callihan, and R G Walker, and G P Walcott, and D L Rollins, and P D Wolf, and W M Smith, and R E Ideker
January 1995, Pacing and clinical electrophysiology : PACE,
M Usui, and R L Callihan, and R G Walker, and G P Walcott, and D L Rollins, and P D Wolf, and W M Smith, and R E Ideker
August 1992, The American journal of cardiology,
M Usui, and R L Callihan, and R G Walker, and G P Walcott, and D L Rollins, and P D Wolf, and W M Smith, and R E Ideker
January 1993, The American journal of cardiology,
M Usui, and R L Callihan, and R G Walker, and G P Walcott, and D L Rollins, and P D Wolf, and W M Smith, and R E Ideker
January 2002, Journal of electrocardiology,
Copied contents to your clipboard!