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维拉帕米治疗阵发性室上性心动过速

Verapamil in the treatment of paroxysmal supraventricular tachycardia.

作者信息

Krikler D M, Spurrell R A

出版信息

Postgrad Med J. 1974 Jul;50(585):447-53. doi: 10.1136/pgmj.50.585.447.

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 tachycardia, 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起作用,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(如 Wolff-Parkinson-White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,在心内电图检查时诱发房室交界性心动过速,其中15例恢复为窦性心律,其他患者的心动周期延长。对8例Wolff-Parkinson-White综合征患者诱发了折返性心动过速,其中7例恢复为窦性心律。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例伴有Wolff-Parkinson-White综合征并发心房颤动的患者接受维拉帕米治疗后,恢复了窦性心律。副作用很少且轻微,仅有罕见的严重低血压、心动过缓和心脏停搏的例外情况;文中讨论了对这些副作用的处理,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。

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