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腺苷与室上性心动过速的治疗

Adenosine and the treatment of supraventricular tachycardia.

作者信息

Rankin A C, Brooks R, Ruskin J N, McGovern B A

机构信息

Cardiac Arrhythmia Service, Massachusetts General Hospital, Boston 02114.

出版信息

Am J Med. 1992 Jun;92(6):655-64. doi: 10.1016/0002-9343(92)90784-9.

Abstract

Adenosine has recently become widely available for the treatment of paroxysmal supraventricular tachycardia. In order to evaluate its role in the management of arrhythmias, we have reviewed the literature on the cellular mechanisms, metabolism, potential for adverse effects, and clinical experience of the efficacy and safety of intravenous adenosine. Adenosine produces transient atrioventricular nodal block when injected as an intravenous bolus. This is of therapeutic value in the conversion to sinus rhythm of the majority of paroxysmal supraventricular tachycardias, which involve the atrioventricular node in a re-entrant circuit. The mean success rate was 93% from over 600 reported episodes. Compared with other antiarrhythmic agents, adenosine is remarkable for its rapid metabolism and brevity of action, with a half-life of a few seconds. It commonly produces subjective symptoms, particularly chest discomfort, dyspnea, and flushing, which are of short duration only. No serious adverse effect has been reported. Arrhythmias may recur within minutes in a minority of patients. Comparative studies have shown that adenosine is as effective as verapamil in the treatment of supraventricular tachycardia, and has less potential for adverse effects. Patients with supraventricular tachycardia should initially be treated using vagotonic physical maneuvers. Immediate electrical cardioversion is indicated if the arrhythmia is associated with hemodynamic collapse. Adenosine is the preferred drug in those patients in whom verapamil has failed or may cause adverse effects, such as those with heart failure or wide-complex tachycardia. The safety profile of adenosine suggests that it should be the drug of first choice for the treatment of supraventricular tachycardia, but only limited comparative data to support this view are available at present.

摘要

腺苷最近已广泛用于治疗阵发性室上性心动过速。为了评估其在心律失常管理中的作用,我们回顾了有关细胞机制、代谢、不良反应可能性以及静脉注射腺苷疗效和安全性的临床经验的文献。静脉推注腺苷时会产生短暂的房室结阻滞。这对于大多数阵发性室上性心动过速转为窦性心律具有治疗价值,这些心动过速在折返环路中涉及房室结。据报道,超过600例发作的平均成功率为93%。与其他抗心律失常药物相比,腺苷的显著特点是代谢迅速、作用短暂,半衰期仅为几秒。它通常会产生主观症状,尤其是胸部不适、呼吸困难和面部潮红,且持续时间较短。尚未报告有严重不良反应。少数患者可能在数分钟内心律失常复发。比较研究表明,腺苷在治疗室上性心动过速方面与维拉帕米同样有效,且不良反应可能性较小。室上性心动过速患者最初应采用增强迷走神经功能的物理手法进行治疗。如果心律失常伴有血流动力学崩溃,则应立即进行电复律。对于维拉帕米治疗失败或可能引起不良反应的患者,如心力衰竭或宽QRS波心动过速患者,腺苷是首选药物。腺苷的安全性表明它应是治疗室上性心动过速的首选药物,但目前仅有有限的比较数据支持这一观点。

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