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[维拉帕米在室上性心动过速研究与治疗中的应用,特别提及预激综合征]

[Verapamil in the study and treatment of supraventricular tachycardias, with special reference to pre-excitation].

作者信息

Krikler D M

出版信息

Minerva Med. 1975 May 26;66(39):1914-22.

PMID:236526
Abstract

Verapamil is a novel antiarrhythmic agent which appears to act as a calcium-ion antagonist, blocking calcium transport across the myocardial cell membrane. It was given intravenously, in a dose of 10 mg, to thirty-two patients suffering from paroxysmal supraventricular tachycardia, and sinus rhythm was achieved promptly in all. Identical results were obtained in a further ten patients with supraventricular tachycardias associated with the Wolff-Parkinson-White or other pre-excitation syndromes. In a separate group of eighteen patients in whom A-V junctional tachycardias were induced during intracardiac electrography, conversion to sinus rhythm was achieved in fifteen patients, with prolongation of the cycle length in the others. Circus-movement tachycardias were induced in eight patients with the Wolff-Parkinson-White syndrome, and conversion to sinus rhythm was achieved in seven. The results were less consistent in patients with other supraventricular arrhythmias including ectopic atrial tachycardia and atrial flutter, and, in the single patient with supraventricular and ventricular tachycardias, only the former was controlled. In the single patient with atrial fibrillation complicating the wolff-Parkinson-White syndrome who received Verapamil, sinus rhythm was restored. Side effects were few and mild, with rare exceptions of profound hypotension, bradycardia and asystole; their management is discussed, and reasons are advanced why their occurrence is likely to be related either to the concomitant administration of beta-adrenergic blockers or to the presence of sinoatrial disease. It appears that Verapamil is particularly suitable for the treatment of supraventricular tachycardias due to a circus movement as calcium antagonism is likely to be most effective in the N region of the atrioventricular node.

摘要

维拉帕米是一种新型抗心律失常药物,似乎作为钙离子拮抗剂发挥作用,阻断钙离子跨心肌细胞膜的转运。对32例阵发性室上性心动过速患者静脉注射10mg剂量的维拉帕米,所有患者均迅速恢复窦性心律。另外10例伴有预激综合征或其他预激综合征的室上性心动过速患者也获得了相同的结果。在另一组18例患者中,心内电描记时诱发房室交界性心动过速,15例患者转为窦性心律,其他患者的心动周期延长。对8例预激综合征患者诱发折返性心动过速,7例转为窦性心律。对于包括异位房性心动过速和心房扑动在内的其他室上性心律失常患者,结果不太一致,在1例同时患有室上性和室性心动过速的患者中,仅控制了前者。在1例患有预激综合征并发心房颤动并接受维拉帕米治疗的患者中,恢复了窦性心律。副作用很少且轻微,极少数情况下会出现严重低血压、心动过缓和心脏停搏;讨论了其处理方法,并提出了其发生可能与同时使用β-肾上腺素能阻滞剂或存在窦房结疾病有关的原因。由于钙拮抗作用在房室结的N区域可能最有效,维拉帕米似乎特别适合治疗由折返运动引起的室上性心动过速。

相似文献

1
[Verapamil in the study and treatment of supraventricular tachycardias, with special reference to pre-excitation].[维拉帕米在室上性心动过速研究与治疗中的应用,特别提及预激综合征]
Minerva Med. 1975 May 26;66(39):1914-22.
2
Verapamil in cardiac arrhythmias: an overview.维拉帕米治疗心律失常:综述
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3
Clinical experience with verapamil.维拉帕米的临床经验。
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4
Adenosine: a clinical experience and comparison with verapamil for the termination of supraventricular tachycardias.腺苷:终止室上性心动过速的临床经验及与维拉帕米的比较
Prog Clin Biol Res. 1987;230:283-99.
5
[Medical management of tachycardias (author's transl)].[心动过速的医学管理(作者译)]
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6
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Minerva Med. 1975 May 26;66(39):1904-13.
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Verapamil and the heart: Pharmacological and Therapeutic Considerations.维拉帕米与心脏:药理学及治疗学考量
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8
[Electrophysiologic effect of sotalol in supraventricular tachycardias].[索他洛尔对室上性心动过速的电生理作用]
Z Kardiol. 1985 Sep;74(9):506-11.
9
Effects of intravenous verapamil on cardiac arrhythmias and on the electrocardiogram.静脉注射维拉帕米对心律失常及心电图的影响。
Am Heart J. 1975 Oct;90(4):487-98. doi: 10.1016/0002-8703(75)90431-7.
10
[Antiarrhythmic effects of verapamil].[维拉帕米的抗心律失常作用]
Arch Inst Cardiol Mex. 1976 May-Jun;46(3):305-16.