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氟卡尼、索他洛尔和维拉帕米治疗无明显心脏异常患者室性心动过速的疗效。

Efficacy of flecainide, sotalol, and verapamil in the treatment of right ventricular tachycardia in patients without overt cardiac abnormality.

作者信息

Gill J S, Mehta D, Ward D E, Camm A J

机构信息

Department of Cardiological Sciences, St George's Hospital Medical School, London.

出版信息

Br Heart J. 1992 Oct;68(4):392-7. doi: 10.1136/hrt.68.10.392.

Abstract

OBJECTIVE

A comparison of the efficacy of verapamil, sotalol, and flecainide to suppress right ventricular tachycardia (VT) in patients with a clinically normal heart.

DESIGN

Patients underwent treatment serially with verapamil (360 mg daily), sotalol (240 or 320 mg daily), and flecainide (200 or 300 mg daily), (the larger dose was for patients heavier than 80 kg) to suppress tachycardia. Each drug was given orally for five half lives before testing.

PATIENTS

23 patients with right VT associated with a clinically normal heart were studied.

OUTCOME MEASURES

The effects of drug treatment were examined by the number of ventricular events on 24 hour Holter monitoring, and the ability of tachycardia to be induced by treadmill exercise testing (Bruce protocol) and programmed ventricular stimulation (Wellens protocol), compared with drug free baseline tests.

SETTING

Patients were studied in a tertiary referral centre.

RESULTS

All three drugs suppressed ventricular salvos (> 3, < 5 consecutive ventricular premature contractions) (p < 0.01) and VT (p < 0.05) on Holter monitoring and did not differ statistically in effect. Exercise induced VT was also suppressed by all three drugs (p < 0.01), and of these sotalol was the most effective although this was not statistically significant (14/23 inducible when drug free, 4/23 on flecainide, 2/23 on sotalol, 5/23 on verapamil). Sustained and non-sustained VT induced by programmed stimulation was also suppressed by the three drugs (p < 0.01) and again sotalol was the best of these though the differences did not achieve statistical significance (17/23 inducible when drug free, 4/17 on flecainide, 2/17 on sotalol, and 6/17 on verapamil). Proarrhythmic effects of drugs were found in a few patients. There was no difference in the efficacy of the drugs in patients with histological abnormalities of the myocardium when compared with those of normal histology.

CONCLUSIONS

Ventricular tachycardia associated with a clinically normal heart can be suppressed by flecainide, sotalol, or verapamil. In individual patients sotalol was the most frequently effective drug (effective in > 89% of patients) and is a suitable choice for first line treatment.

摘要

目的

比较维拉帕米、索他洛尔和氟卡尼对临床心脏正常患者室性心动过速(VT)的抑制效果。

设计

患者依次接受维拉帕米(每日360毫克)、索他洛尔(每日240或320毫克)和氟卡尼(每日200或300毫克,体重超过80公斤的患者用较大剂量)治疗以抑制心动过速。每种药物在测试前口服五个半衰期。

患者

研究了23例临床心脏正常但伴有右室性心动过速的患者。

观察指标

通过24小时动态心电图监测的室性事件数量,以及与无药基线测试相比,平板运动试验(布鲁斯方案)和程控心室刺激(韦伦斯方案)诱发心动过速的能力,来检查药物治疗的效果。

地点

在一家三级转诊中心对患者进行研究。

结果

所有三种药物在动态心电图监测中均能抑制室性早搏(>3次、<5次连续室性早搏)(p<0.01)和室性心动过速(p<0.05),且效果在统计学上无差异。所有三种药物也都能抑制运动诱发的室性心动过速(p<0.01),其中索他洛尔最有效,尽管这在统计学上不显著(无药时23例中有14例可诱发,氟卡尼治疗时4例,索他洛尔治疗时2例,维拉帕米治疗时5例)。程控刺激诱发的持续性和非持续性室性心动过速也被这三种药物抑制(p<0.01),同样索他洛尔效果最佳,尽管差异未达到统计学显著性(无药时23例中有17例可诱发,氟卡尼治疗时4例,索他洛尔治疗时2例,维拉帕米治疗时6例)。在少数患者中发现了药物的促心律失常作用。与心肌组织学正常的患者相比,药物对心肌组织学异常患者的疗效无差异。

结论

氟卡尼、索他洛尔或维拉帕米可抑制临床心脏正常患者的室性心动过速。在个体患者中,索他洛尔是最常有效的药物(在>89%的患者中有效),是一线治疗的合适选择。

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