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索他洛尔与ⅠA类药物联合使用可预防持续性室性心动过速复发。

Sotalol and type IA drugs in combination prevent recurrence of sustained ventricular tachycardia.

作者信息

Dorian P, Newman D, Berman N, Hardy J, Mitchell J

机构信息

Department of Medicine, University of Toronto, Ontario, Canada.

出版信息

J Am Coll Cardiol. 1993 Jul;22(1):106-13. doi: 10.1016/0735-1097(93)90823-j.

Abstract

OBJECTIVES

This study assessed the efficacy of the combination of sotalol and either quinidine or procainamide in preventing sustained ventricular tachycardia inducibility and recurrence and prospectively evaluated the ability of the drug combination to prevent ventricular tachycardia recurrence when the arrhythmia remained inducible but was modified.

BACKGROUND

Individual antiarrhythmic drugs are often ineffective in preventing the induction and recurrence of sustained ventricular tachycardia. Beta-adrenergic blockade and prolongation of refractoriness may be important components of successful antiarrhythmic therapy in patients with ventricular tachycardia. We reasoned that the combination of sotalol, which has beta-adrenergic blocking properties and prolonged ventricular refractoriness, and quinidine or procainamide, two agents that slow conduction and prolong refractory periods, would be effective therapy in such patients.

METHODS

We administered low dose sotalol (205 +/- 84 mg/day) plus quinidine sulfate (1,278 +/- 479 mg/day) or procainamide (2,393 +/- 1,423 mg/day) to 50 patients with spontaneous sustained ventricular tachycardia or fibrillation and inducible ventricular tachycardia.

RESULTS

In 21 (46%) of 46 patients, ventricular tachycardia was rendered noninducible at electrophysiologic study (group I), and in 17 patients (37%), inducible tachycardia was modified according to prospectively identified criteria (group II), for a combined 83% response rate. Ventricular refractory periods increased from 252 +/- 24 to 316 +/- 28 ms and from 265 +/- 33 to 316 +/- 24 ms in groups I and II, respectively (p < 0.001), but from 234 +/- 19 to only 286 +/- 13 ms in the group of patients with unmodified ventricular tachycardia inducibility (n = 8, group III, p < 0.001). Cycle length of induced ventricular tachycardia slowed from 324 +/- 62 to 432 +/- 70 ms in group II patients (p < 0.001), whereas it slowed less in group III patients (279 +/- 73 to 314 +/- 63 ms, p = NS). Forty-two of the 50 patients (including all patients in groups I and II) were discharged on treatment with the drug combination. After 25 +/- 19 months of follow-up, the actuarial recurrence rate of ventricular tachycardia was 6%, 6% and 11% at 1, 2 and 3 years, respectively. Among patients in whom this drug combination was unsuccessful at electrophysiologic study (group III) and in those who received alternative therapy after combination therapy was discontinued because of side effects, actuarial recurrence rates were 9%, 14% and 32% at 1, 2 and 3 years, respectively.

CONCLUSIONS

The combination of sotalol plus quinidine or procainamide markedly prolongs ventricular refractoriness and slows induced ventricular tachycardia in a high proportion of patients. Patients with modified or noninducible tachycardia have a low rate of arrhythmia recurrence in follow-up. This drug combination deserves further evaluation.

摘要

目的

本研究评估索他洛尔与奎尼丁或普鲁卡因胺联合使用在预防持续性室性心动过速诱发和复发方面的疗效,并前瞻性评估当心律失常仍可诱发但已改变时该药物联合方案预防室性心动过速复发的能力。

背景

单一抗心律失常药物在预防持续性室性心动过速的诱发和复发方面往往无效。β-肾上腺素能阻滞和不应期延长可能是室性心动过速患者抗心律失常治疗成功的重要组成部分。我们推测,具有β-肾上腺素能阻滞特性且能延长心室不应期的索他洛尔,与两种能减慢传导并延长不应期的药物奎尼丁或普鲁卡因胺联合使用,对这类患者会是有效的治疗方法。

方法

我们对50例有自发性持续性室性心动过速或颤动且可诱发室性心动过速的患者给予低剂量索他洛尔(205±84毫克/天)加硫酸奎尼丁(1278±479毫克/天)或普鲁卡因胺(2393±1423毫克/天)。

结果

在46例患者中的21例(46%),在电生理研究中室性心动过速变为不可诱发(I组),17例患者(37%),根据前瞻性确定的标准可诱发的心动过速得到改变(II组),综合有效率为83%。I组和II组的心室不应期分别从252±24毫秒增加到316±28毫秒和从265±33毫秒增加到316±24毫秒(p<0.001),但在室性心动过速诱发未改变的患者组(n = 8,III组,p<0.001)中从234±19毫秒仅增加到286±13毫秒。II组患者诱发的室性心动过速的周长从324±62毫秒减慢到432±70毫秒(p<0.001),而III组患者减慢较少(279±73毫秒到314±63毫秒,p = 无显著差异)。50例患者中的42例(包括I组和II组的所有患者)出院时接受该药物联合治疗。经过25±19个月的随访,室性心动过速的精算复发率在1年、2年和3年分别为6%、6%和11%。在电生理研究中该药物联合方案无效的患者(III组)以及因副作用停用联合治疗后接受替代治疗的患者中,精算复发率在1年、2年和3年分别为9%、14%和32%。

结论

索他洛尔加奎尼丁或普鲁卡因胺联合使用能显著延长心室不应期,并使很大比例的患者诱发的室性心动过速减慢。心动过速改变或不可诱发的患者在随访中心律失常复发率较低。这种药物联合方案值得进一步评估。

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