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口服氟卡尼、索他洛尔和维拉帕米用于终止阵发性室上性心动过速。

Oral flecainide, sotalol, and verapamil for the termination of paroxysmal supraventricular tachycardia.

作者信息

Hamer A W, Strathmore N, Vohra J K, Hunt V D

机构信息

Department of Cardiology, Royal Melbourne Hospital, Parkville, Australia.

出版信息

Pacing Clin Electrophysiol. 1993 Jul;16(7 Pt 1):1394-400. doi: 10.1111/j.1540-8159.1993.tb01734.x.

Abstract

The ability to terminate supraventricular tachycardia (SVT) acutely with an oral dose of flecainide (2.5-3.3 mg/kg), sotalol (2.0-2.9 mg/kg), and verapamil (3.3-3.7 mg/kg) was investigated in an observational study of six patients with SVT normally controlled by an antitachycardia pacemaker. The pacemaker was programmed to induce SVT and the stability of SVT was observed for 90 minutes as a baseline. Subsequent studies involved testing of the three antiarrhythmic drugs on separate occasions, given in random order as crushed tablets in orange juice during pacemaker induced SVT, with plasma drug levels collected every 15 minutes for 90 minutes post drug ingestion. Sotalol produced drug induced slowing of SVT in all six patients, with termination of SVT in three patients by 60-65 minutes, with maximum plasma levels of 0.76-2.09 micrograms/mL achieved by 90 minutes. Flecainide produced maximum plasma levels of 83-745 ng/mL, 60-90 minutes post ingestion, and slowed SVT in three patients. SVT was terminated in three patients after 45-85 minutes, but no effect on SVT was seen in two patients who had inadequate plasma levels (< or = 166 ng/mL) from doses < 3 mg/kg. Verapamil produced maximum plasma levels of 0 (undetectable) to 388 ng/mL, 45-90 minutes post ingestion, and slowed SVT in three patients, but only one of these patients reverted to sinus rhythm (at 40 min). No effect on SVT was seen in three patients due to undetectable plasma levels. We concluded that sotalol (> or = 2 mg/kg) and flecainide (> or = 3 mg/kg) appeared to be suitable oral drugs for termination of SVT.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在一项观察性研究中,对6例通常由抗心动过速起搏器控制的室上性心动过速(SVT)患者,研究了口服氟卡尼(2.5 - 3.3毫克/千克)、索他洛尔(2.0 - 2.9毫克/千克)和维拉帕米(3.3 - 3.7毫克/千克)急性终止SVT的能力。将起搏器编程以诱发SVT,并观察SVT 90分钟的稳定性作为基线。随后的研究包括在不同时间分别测试这三种抗心律失常药物,在起搏器诱发SVT期间,将其作为压碎的片剂随机顺序加入橙汁中服用,服药后90分钟内每15分钟采集血浆药物水平。索他洛尔使所有6例患者的SVT药物性减慢,3例患者在60 - 65分钟时SVT终止,90分钟时血浆最高水平达到0.76 - 2.09微克/毫升。氟卡尼服药后60 - 90分钟血浆最高水平为83 - 745纳克/毫升,3例患者的SVT减慢。3例患者在45 - 85分钟后SVT终止,但2例服用剂量<3毫克/千克导致血浆水平不足(≤166纳克/毫升)的患者,SVT未受影响。维拉帕米服药后45 - 90分钟血浆最高水平为0(不可检测)至388纳克/毫升,3例患者的SVT减慢,但其中只有1例患者恢复窦性心律(40分钟时)。3例患者因血浆水平不可检测,SVT未受影响。我们得出结论,索他洛尔(≥2毫克/千克)和氟卡尼(≥3毫克/千克)似乎是用于终止SVT的合适口服药物。(摘要截短至250字)

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