首页> 外文期刊>Journal of cardiovascular electrophysiology >Effect of sodium channel blockers on ST segment, QRS duration, and corrected QT interval in patients with Brugada syndrome.
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Effect of sodium channel blockers on ST segment, QRS duration, and corrected QT interval in patients with Brugada syndrome.

机译:钠通道阻滞剂对Brugada综合征患者ST段,QRS持续时间和校正QT间隔的影响。

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INTRODUCTION: Brugada syndrome is characterized by an ST segment elevation in leads V1-V3 and a high incidence of ventricular fibrillation (VF). A mutation in a cardiac Na+ channel gene, SCN5A, has been linked to Brugada syndrome, and sodium channel blockers have been shown to be effective in unmasking the syndrome when concealed. The aim of this study was to examine the effects of Na+ channel blockers on ST segment elevation, QRS, corrected QT (QTc) interval, and ventricular arrhythmias in patients with Brugada syndrome. METHODS AND RESULTS: We examined the effects of three different Na+ channel blockers (flecainide, disopyramide, and mexiletine) on the amplitude of the ST segment 20 msec after the end of QRS (ST20), QRS duration, QTc interval measured from 12-lead ECG, and ventricular arrhythmias in 12 Brugada and 10 control patients. Maximum ST20 observed in the V2 or V3 leads under baseline conditions was greater in the Brugada patients than in control patients, whereas QRS duration and maximum QTc interval were no different between the two groups. Flecainide and disopyramide, but not mexiletine, significantly increased maximum ST20 and QRS duration in both groups, although these effects were much more pronounced in the Brugada patients. The increases in ST20 and QRS duration with flecainide were significantly larger than those with disopyramide. An increase of 0.15 mV in ST20 with flecainide separated the two groups without overlap. Ventricular premature complexes developed only with flecainide in Brugada patients (3/12) displaying a marked ST elevation but not widening of QRS. CONCLUSION: Our findings suggest that Na+ channel blockers amplify existing I(Na) and possibly other ion channel defects, with a potency inversely proportional to the rate of dissociation of the drug from the Na+ channel, thus causing a prominent elevation of the ST segment and, in some cases, prolongation of QRS duration in patients with Brugada syndrome.
机译:简介:Brugada综合征的特征是V1-V3导联ST段抬高,心室颤动(VF)发生率很高。心脏Na +通道基因SCN5A的突变已与Brugada综合征相关,并且钠通道阻滞剂已被证明可有效隐藏隐蔽症状。这项研究的目的是检查Na +通道阻滞剂对Brugada综合征患者ST段抬高,QRS,校正QT(QTc)间隔和室性心律不齐的影响。方法和结果:我们检查了三种不同的Na +通道阻滞剂(氟卡尼类,二吡酰胺和美西律)对QRS(ST20)结束后20毫秒ST段幅度的影响,QRS持续时间,从12导联测量的QTc间隔12例Brugada和10例对照患者的心电图和室性心律不齐。在Brugada患者中,在基线条件下V2或V3导联中观察到的最大ST20大于对照组患者,而两组之间的QRS持续时间和最大QTc间隔无差异。氟卡尼和二吡酰胺,但美西律没有显着增加两组的最大ST20和QRS持续时间,尽管这些作用在Brugada患者中更为明显。氟卡尼使ST20和QRS持续时间的增加显着大于二吡乙酰胺。氟卡尼使ST20中的0.15 mV升高将两组分开,没有重叠。 Brugada患者(3/12)仅用氟卡尼开发的室性早搏复合物显示出显着的ST升高,但QRS并未展宽。结论:我们的发现表明,Na +通道阻滞剂会放大现有的I(Na)以及可能存在的其他离子通道缺陷,其效力与药物从Na +通道的解离速率成反比,从而导致ST段和,在某些情况下,可延长Brugada综合征患者的QRS持续时间。

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