首页> 外文期刊>Cardiology >Differential effects of adenosine on antegrade fast pathway, antegrade slow pathway, and retrograde fast pathway in atrioventricular nodal reentry.
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Differential effects of adenosine on antegrade fast pathway, antegrade slow pathway, and retrograde fast pathway in atrioventricular nodal reentry.

机译:腺苷对房室结折返中顺行快速途径,顺行缓慢途径和逆行快速途径的不同作用。

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摘要

Adenosine has a potent negative dromotropic effect. However, comparative effects of adenosine on the three pathways of atrioventricular (AV) nodal reentry remain unclear. In this study, we sought to determine the effects of adenosine on the antegrade fast, antegrade slow, and retrograde fast pathway conduction in patients with AV nodal reentrant tachycardia (AVNRT). Twenty patients with common slow-fast AVNRT (mean cycle length 360 +/- 49 ms) were studied. The effects of adenosine on the antegrade slow pathway and on the retrograde fast pathway conduction were determined during sustained AVNRT and constant right ventricular pacing at identical cycle lengths (mean 360 +/- 49 ms), respectively. Incremental doses of adenosine were rapidly administered: initial dose of 0.5 mg, followed by stepwise increases of 0.5 or 1.0 mg given at 5-min intervals until termination of AVNRT or second-degree ventriculoatrial block occurred. After the antegrade slow pathway conduction was selectively and completely ablated by radiofrequency catheter ablation, the effect of adenosine on the antegrade fast pathway conduction was evaluated. The dose-response curve of adenosine and the dose of adenosine required to produce AV or ventriculoatrial block among the representative three conduction pathways were compared. The dose-response curve for the effect of adenosine on the antegrade fast pathway lies to the left and upward to that of the effect of adenosine on the antegrade slow pathway which in turn lies to the left and upward to that of the retrograde fast pathway. The mean dose of adenosine required to produce conduction block at antegrade fast, antegrade slow, and retrograde fast pathways were 1.4 +/- 0.5, 4.2 +/- 1.6, and 8.5 +/- 2.6 mg, respectively (p < 0.01). Adenosine has a differential potency to depress antegrade fast, antegrade slow, and retrograde fast pathway conduction in patients with AVNRT. The depressant effect of adenosine on the antegrade fast pathway is more potent than that on the antegrade slow pathway which in turn is more potent than that on the retrograde fast pathway conduction.
机译:腺苷具有强的负变色作用。但是,腺苷对房室结折返的三种途径的比较效果仍不清楚。在这项研究中,我们试图确定腺苷对房室结折返性心动过速(AVNRT)患者的顺行快,顺行慢和逆行快通路传导的影响。研究了20例常见的慢速AVNRT(平均周期长度360 +/- 49 ms)。在持续的AVNRT和恒定的右心室起搏期间,分别以相同的周期长度(平均360 +/- 49 ms)确定腺苷对顺行慢路径和逆行快速路径传导的影响。迅速增加剂量的腺苷:初始剂量为0.5 mg,然后以5分钟为间隔逐步增加0.5或1.0 mg,直到终止AVNRT或二级脑室阻塞。射频导管消融选择性地完全消融顺行性慢通路传导后,评估腺苷对顺行性快速通路传导的影响。比较了代表性的三种传导途径中腺苷的剂量反应曲线和产生AV或心室阻塞的腺苷剂量。腺苷对顺行快速途径的剂量-反应曲线在左边和上方,而腺苷对顺行慢路径的作用的剂量-反应曲线在左边,而在逆行快速途径的剂量反应曲线向左和向上。在顺行快,顺行慢和逆行快通路上产生传导阻滞所需的腺苷平均剂量分别为1.4 +/- 0.5、4.2 +/- 1.6和8.5 +/- 2.6 mg(p <0.01)。腺苷具有压低AVNRT患者快速顺行,缓慢顺行和逆行快速途径传导的能力。腺苷对顺行快速途径的抑制作用比对顺行缓慢途径的抑制作用强,后者对逆行快速途径的传导作用反而更有效。

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