犬模型室性心动过速周期长度的自发变化及其与心外膜最早激活部位的关系。

M J Gómez, F Hélie, G Sierra, P Rocque, A Vinet, R Cardinal, R Nadeau
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引用次数: 0

摘要

背景:本研究的目的是研究持续单形态性室性心动过速(MVT)和多形态性室性心动过速(PVT)发作时周期长度的自发变化,并将这些变化与心跳的最早心外膜激活位点联系起来。方法:采用袜子电极阵列对24只开胸麻醉犬双心室表面记录的127张单极电图进行等时激活图绘制。房室传导阻滞后,左冠状动脉前降支在心室起搏(140/min)下闭塞60 min,然后再灌注。7只犬在再灌注后5min刺激左星状神经节。结果:7例mvt(再灌注)和4例pvt(交感神经刺激)的周期长度变化表现为初始加速,达到最小周期长度,然后减速,最后终止。等时图显示从最早激活开始呈放射状扩散,无传导阻滞。MVT的周期长度(481 +/- 80 msec)有15 +/- 17 msec的搏动变化,对应于最早激活位点的小位移,聚集在缺血心肌的边界上。在pts中,周期长度(352 +/- 90 msec, p < 0.01)的变异性为62 +/- 23 msec,与左右心室最早激活部位的广泛变化相对应。线性回归分析显示,周期长度变异性与最早激活的电极数之间存在强而显著的相关性(r = 0.77, p < 0.0001)。结论:在单态型和多态型室性心动过速模型中,周期长度变异性与最早激活的电极数量有显著相关性。mvt为集中起源,周期长度规则;pvt为分散起源,周期长度不规则。这些结果表明,心跳最早的心外膜激活部位可能是决定周期长度动态的一个因素。
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Spontaneous changes in ventricular tachycardia cycle length and their relation to earliest sites of epicardial activation in a canine model.

Background: The purpose of this study was to examine the spontaneous changes in cycle length during episodes of sustained monomorphic (MVT) and polymorphic (PVT) ventricular tachycardias and to relate these changes with the earliest epicardial activation site of the beat.

Methods: Isochronal activation maps were obtained from 127 unipolar electrograms recorded from the surface of both ventricles with a sock electrode array in 24 open chest anesthetized dogs. After atrioventricular block, the left anterior descending coronary artery was occluded for 60 min under ventricular pacing (140/min), followed by reperfusion. In 7 dogs the left stellate ganglion was stimulated 5 min after reperfusion.

Results: In 7 MVTs (reperfusion) and 4 PVTs (sympathetic stimulation), cycle length changes showed an initial acceleration, reaching a minimum cycle length and then decelerating before termination. Isochronal maps showed radial spread from earliest activation, without conduction block. Cycle length (481 +/- 80 msec) in MVT had beat to beat variations of 15 +/- 17 msec corresponding to small shifts in sites of the earliest activation, clustered along the border of the ischemic myocardium. In PVTs the cycle length (352 +/- 90 msec, p < 0.01) had a variability of 62 +/- 23 msec, corresponding to wide changes in the sites of earliest activation in right and left ventricles. Linear regression analysis showed a strong and significant correlation between cycle length variability and the number of electrodes with the earliest activation (r = 0.77, p < 0.0001).

Conclusion: In these models of monomorphic and polymorphic ventricular tachycardias, cycle length variability showed a significant correlation with the number of electrodes with the earliest activation. MVTs showed concentrated origins with regular cycle length, whereas PVTs showed dispersed origins with irregular cycle length. These results suggest that the earliest epicardial activation site of the beat could be a factor in determining the dynamics in the cycle length.

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