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IC类抗心律失常药物与美西律联合药物治疗对室性心动过速的作用

Role of combination drug therapy with a class IC antiarrhythmic agent and mexiletine for ventricular tachycardia.

作者信息

Mendes L, Podrid P J, Fuchs T, Franklin S

机构信息

Medical Service, Boston University School of Medicine, Massachusetts.

出版信息

J Am Coll Cardiol. 1991 May;17(6):1396-402. doi: 10.1016/s0735-1097(10)80153-6.

DOI:10.1016/s0735-1097(10)80153-6
PMID:2016457
Abstract

The combination of mexiletine and a class IC antiarrhythmic agent (encainide, propafenone or flecainide) was evaluated by electrophysiologic testing in 14 patients with a history of sustained ventricular tachycardia whose tachycardia remained inducible during therapy with the class IC drug alone. During the control drug-free state, all patients had inducible ventricular tachycardia, with a mean cycle length of 260 ms (range 190 to 400). During monotherapy with the IC agent the tachycardia remained inducible in each patient, but there was a significant increase in the cycle length to 340 ms (240 to 500) (p less than 0.001). The effective refractory period of the ventricle was not altered. Treatment with mexiletine (oral in 13 and intravenous in 1) was begun and electrophysiologic testing was repeated. Ventricular tachycardia in one patient was rendered noninducible and one patient had arrhythmia aggravation. The tachycardia in the remaining 12 patients remained inducible but its average cycle length increased further to 392 ms (340 to 460) (p = NS). Nine patients had rate slowing and the average cycle length of the ventricular tachycardia in this group was significantly increased (302 to 388 ms, p less than 0.05). The average effective refractory period was significantly increased during combination therapy (267 ms) compared with no drug therapy (235 ms) and therapy with the class IC drug alone (247 ms) (p less than 0.05). After a mean follow-up interval of 22 months, seven patients continue on the combined treatment and have no ventricular tachycardia.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对14例有持续性室性心动过速病史且在单独使用IC类药物治疗期间心动过速仍可诱发的患者,通过电生理检查评估了美西律与IC类抗心律失常药物(恩卡尼、普罗帕酮或氟卡尼)联合使用的效果。在无药物对照状态下,所有患者均可诱发出室性心动过速,平均周期长度为260毫秒(范围190至400毫秒)。在使用IC类药物单药治疗期间,每位患者的心动过速仍可诱发,但周期长度显著增加至340毫秒(240至500毫秒)(p<0.001)。心室有效不应期未改变。开始使用美西律治疗(13例口服,1例静脉注射)并重复电生理检查。1例患者的室性心动过速变为不可诱发,1例患者心律失常加重。其余12例患者的心动过速仍可诱发,但其平均周期长度进一步增加至392毫秒(340至460毫秒)(p=无显著差异)。9例患者心率减慢,该组室性心动过速的平均周期长度显著增加(302至388毫秒,p<0.05)。与无药物治疗(235毫秒)和单独使用IC类药物治疗(247毫秒)相比,联合治疗期间平均有效不应期显著延长(267毫秒)(p<0.05)。平均随访22个月后,7例患者继续联合治疗,未发生室性心动过速。(摘要截短至250字)

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