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在持续性室性心动过速患者中使用喷替索胺(CM 7857)进行电药理学测试。

Electropharmacological test with pentisomide (CM 7857) in patients with sustained ventricular tachycardia.

作者信息

Vergara G, Inama G, Guarnerio M, Rando F, Oldani V, Furlanello F

机构信息

Divisione di Cardiologia e Centro Aritmologico, Ospedale S. Chiara, Trento.

出版信息

G Ital Cardiol. 1990 Jun;20(6):543-8.

PMID:2227224
Abstract

Pentisomide (CM 7857) is a new class I antiarrhythmic drug whose effect on sustained ventricular tachycardia has only been slightly investigated to date. The aim of this paper is to examine the pentisomide action on selected patients with ventricular tachycardia inducible during intracavitary electrophysiological study. Thus, 12 patients (9 M, 3 F, mean age: 45.2 years, range: 24-78), all but two with detectable heart disease, underwent electropharmacological tests with pentisomide after they had resulted "non responders" (8 patients) or had had a proarrhythmic worsening effect (3 patients) to electropharmacological tests with amiodarone or flecainide or propafenone or mexiletine. After the inducibility and the reproducibility of ventricular tachycardia has been assessed in the basal state, all patients underwent several attempts to reinduce ventricular tachycardia, during the i.v. infusion of pentisomide 1.5 mg/kg/5 min followed by continuous infusion of 1 mg/kg/h, at the same time drug plasma level was assessed. Ventricular tachycardia inducibility was still inducible after pentisomide, but with a longer cycle length (446 +/- 88 versus 337 +/- 82 msec) than in the basal state (p less than 0.0025). No patients had proarrhythmic worsening effects. The pentisomide plasma level (available in 5 patients) ranged from 3.4 to 22.3 (mean 8.9 micrograms/ml). Four patients underwent chronic oral treatment (in 1 pt in association with amiodarone) with a good clinical outcome (mean follow-up 6.25 months, range 1-12). We stress the absence of proarrhythmic worsening effects and the powerful effect of the drug on ventricular tachycardia cycle length.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

喷替索胺(CM 7857)是一种新型I类抗心律失常药物,迄今为止,其对持续性室性心动过速的作用仅得到了少量研究。本文旨在研究喷替索胺对在腔内电生理研究中可诱发室性心动过速的特定患者的作用。因此,12例患者(9例男性,3例女性,平均年龄:45.2岁,范围:24 - 78岁),除2例外均患有可检测出的心脏病,在对胺碘酮、氟卡尼、普罗帕酮或美西律进行电药理学测试后,若结果为“无反应者”(8例患者)或出现促心律失常恶化效应(3例患者),则接受喷替索胺的电药理学测试。在基础状态下评估室性心动过速的可诱发性和可重复性后,所有患者在静脉输注喷替索胺1.5 mg/kg/5分钟,随后以1 mg/kg/小时持续输注期间,多次尝试再次诱发室性心动过速,同时评估药物血浆水平。喷替索胺给药后仍可诱发室性心动过速,但与基础状态相比,心动周期更长(446±88对337±82毫秒)(p<0.0025)。无患者出现促心律失常恶化效应。喷替索胺血浆水平(5例患者可获得)范围为3.4至22.3(平均8.9微克/毫升)。4例患者接受了长期口服治疗(1例患者与胺碘酮联合使用),临床效果良好(平均随访6.25个月,范围1 - 12个月)。我们强调该药物不存在促心律失常恶化效应,且对室性心动过速的心动周期有显著作用。(摘要截断于250字)

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