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再灌注后室性心律失常:与梗死面积有关联吗?

Ventricular arrhythmias after reperfusion: is there a correlation with infarct size?

作者信息

Krejcy K, Krumpl G, Todt H, Windisch A, Mousavi M, Raberger G

机构信息

Institute of Pharmacology, University of Vienna, Austria.

出版信息

Can J Physiol Pharmacol. 1991 Jul;69(7):958-63. doi: 10.1139/y91-145.

Abstract

The aim of this investigation was to examine whether any correlation exists between enzymatically estimated infarct size and arrhythmias arising in response to coronary reperfusion. Four hour occlusion of the left anterior coronary artery followed by reperfusion was carried out in conscious dogs. Serum creatine phosphokinase (CPK) analysis and planimetric determination of infarct size were performed. The Holter monitoring technique was used to analyze the arrhythmias. A good correlation was observed between the number of premature ventricular complexes (PVC) occurring during 4-h coronary artery occlusion and peak serum CPK values (CPKmax; r = 0.74). While PVC in the early 2-h reperfusion phase and on days 1 and 2 of the late reperfusion phase did not show a correlation with CPKmax nor with occlusion arrhythmias, arrhythmic activity on day 3 of the late reperfusion phase correlated well with CPKmax (r = 0.71) and occlusion arrhythmias (r = 0.75). Whereas it cannot be ruled out that arrhythmias on days 1 and 2 are related to coronary reperfusion as well as to the established infarction, we speculated that arrhythmias on day 3 are delayed arrhythmias in response to the occlusion procedure and not a consequence of reperfusion. Providing that arrhythmias occurring in the early reperfusion phase are almost exclusively induced by the arrhythmogenic phenomenon of reperfusion, we conclude that in contrast to occlusion arrhythmias, reperfusion arrhythmias are not markers of infarct size. Thus, a higher number of arrhythmias after reperfusion is not necessarily associated with a larger infarct size.

摘要

本研究的目的是检验酶法估算的梗死面积与冠状动脉再灌注后出现的心律失常之间是否存在任何相关性。对清醒犬进行左冠状动脉前降支闭塞4小时后再灌注。进行了血清肌酸磷酸激酶(CPK)分析和梗死面积的平面测量。采用动态心电图监测技术分析心律失常。观察到在冠状动脉闭塞4小时期间出现的室性早搏(PVC)数量与血清CPK峰值(CPKmax;r = 0.74)之间存在良好的相关性。虽然再灌注早期2小时以及再灌注后期第1天和第2天的PVC与CPKmax以及闭塞性心律失常均无相关性,但再灌注后期第3天的心律失常活动与CPKmax(r = 0.71)和闭塞性心律失常(r = 0.75)密切相关。虽然不能排除第1天和第2天的心律失常与冠状动脉再灌注以及已形成的梗死有关,但我们推测第3天的心律失常是对闭塞操作的延迟性心律失常,而非再灌注的结果。假设再灌注早期出现的心律失常几乎完全是由再灌注的致心律失常现象诱发的,我们得出结论,与闭塞性心律失常不同,再灌注心律失常不是梗死面积的标志物。因此,再灌注后心律失常数量较多不一定与较大的梗死面积相关。

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