Success and failure of the defibrillation shock: Insights from a simulation study

被引:47
作者
Skouibine, K
Trayanova, N
Moore, P
机构
[1] Tulane Univ, Dept Biomed Engn, New Orleans, LA 70118 USA
[2] Tulane Univ, Dept Math, New Orleans, LA 70118 USA
[3] Duke Univ, Dept Math, Durham, NC 27706 USA
关键词
spiral wave; defibrillation; virtual electrodes; bidomain model; extension of refractoriness; deexcitation;
D O I
10.1111/j.1540-8167.2000.tb00050.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: This simulation study presents a further inquiry into the mechanisms by which a strong electric shock fails to halt life-threatening cardiac arrhythmias, Methods and Results: The research uses a model of the defibrillation process that represents a. sheet of myocardium as a bidomain, The tissue consists of nonuniformly curved fibers in which spiral wave reentry is initiated. Monophasic defibrillation shocks are delivered via two line electrodes that occupy opposite tissue boundaries. In some simulation experiments, the polarity of the shock is reversed. Electrical activity in the sheet is compared for failed and successful shocks under controlled conditions. The maps of transmembrane potential and activation times calculated during and after the shock demonstrate that weak shocks fail to terminate the reentrant activity via two major mechanisms. As compared with strong shocks, weak shocks result in (1) smaller extension of refractoriness in the areas depolarized by the shock, and (2) slower or incomplete activation of the excitable gap created by deexcitation of the negatively polarized areas, In its turn, mechanism 2 is associated with one or more of the following events: (a) lack of some break excitations, (b) latency in the occurrence of the break excitations, and (c) slower propagation through deexcited areas. Reversal of shock polarity results in a change of the extent of the regions of deexcitation, and thus, in a change in defibrillation threshold. Conclusion: The results of this study indicate the paramount importance of shock-induced deexcitation in both defibrillation and postshock arrhythmogenesis.
引用
收藏
页码:785 / 796
页数:12
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