Impact of Bisoprolol on Ventricular Arrhythmias in Experimental Myocardial Infarction.

Chonnam Medical Journal Pub Date : 2021-05-01 Epub Date: 2021-05-24 DOI:10.4068/cmj.2021.57.2.132
Hyun Kuk Kim, Kyung Seob Lim, Sung Soo Kim, Joo-Young Na
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引用次数: 1

Abstract

Following acute myocardial infarction (AMI), early use of beta-blockers (BBs) reduced the incidences of ventricular arrhythmia (VA) and death in the pre reperfusion era. However, some studies have reported a worsening of clinical outcomes and therefore, this study used a porcine model of AMI to evaluate the efficacy of bisoprolol on VAs and mortality. Twenty pigs were divided into two groups with one group using oral bisoprolol which was given for 3 hours before the experiment and then maintained for 7 days. A loop recorder was implanted, AMI was induced by balloon occlusion for 60 min, and then, reperfusion. One week later, the echocardiography and loop recorder data were analyzed in the surviving animals. Bisoprolol did not increase the heart rate (62.9±14.5 vs 79.0±20.3; p=0.048), lower the rate of premature ventricular contractions (PVC) (0.8±0.8 vs 11.0±12.8; p=0.021) or tend to lower recurrent VA (0.6±0.5 vs 1.1±1.1; p=0.131) during coronary artery occlusion. After reperfusion, bisoprolol did reduce VA in the early AMI period (0.1±0.3 vs 4.2±4.6; p=0.001) and it was not associated with the extent of myocardial recovery. In this porcine model, early oral bisoprolol might help reduce the incidences of PVC and recurrent VA and determine whether effects are more pronounced during the early AMI period. Our results suggest that bisoprolol might help reduce lethal VA and cardiac death following AMI in this reperfusion era.

比索洛尔对实验性心肌梗死室性心律失常的影响。
急性心肌梗死(AMI)后,早期使用β受体阻滞剂(BBs)可降低再灌注前室性心律失常(VA)和死亡的发生率。然而,一些研究报告了临床结果的恶化,因此,本研究使用猪AMI模型来评估比索洛尔对VAs和死亡率的疗效。将20头猪分为两组,一组在试验前口服比索洛尔3 h,维持7 d。植入循环记录仪,球囊闭塞诱导心肌梗死60 min,再灌注。一周后,对存活动物的超声心动图和循环记录仪数据进行分析。比索洛尔没有增加心率(62.9±14.5 vs 79.0±20.3);p=0.048),较低的室性早搏(PVC)率(0.8±0.8 vs 11.0±12.8;p=0.021)或倾向于降低复发性VA(0.6±0.5 vs 1.1±1.1;P =0.131)。再灌注后,比索洛尔降低AMI早期VA(0.1±0.3 vs 4.2±4.6);P =0.001),与心肌恢复程度无关。在这个猪模型中,早期口服比索洛尔可能有助于减少PVC和复发性VA的发生率,并确定在AMI早期是否效果更明显。我们的研究结果表明,在这个再灌注时代,比索洛尔可能有助于减少AMI后的致死性VA和心脏死亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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