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三磷酸腺苷与维拉帕米对阵发性折返性交界性心动过速的临床及电生理效应比较

Comparative clinical and electrophysiologic effects of adenosine triphosphate and verapamil on paroxysmal reciprocating junctional tachycardia.

作者信息

Belhassen B, Glick A, Laniado S

机构信息

Department of Cardiology, Tel-Aviv Medical Center, Ichilov Hospital, Israel.

出版信息

Circulation. 1988 Apr;77(4):795-805. doi: 10.1161/01.cir.77.4.795.

Abstract

The efficacy, electrophysiologic effects, and side effects of adenosine triphosphate (ATP) and verapamil in the short-term management of paroxysmal reciprocating junctional tachycardia (PRJT) were compared in 20 patients. All patients had inducible sustained PRJT during control electrophysiologic study. Fourteen patients had PRJT involving a retrograde accessory pathway, and six patients had atrioventricular (AV) nodal reentrant tachycardia ("slow-fast" type). ATP, which has a very short half-life, was first administered (10 mg iv over 1 sec) during sustained PRJT. If PRJT did not terminate within 2 min, a bolus of 20 mg ATP was given. Verapamil (5 mg iv over 15 sec) was subsequently administered during sustained PRJT, and if the latter did not terminate within 3 min another bolus of 5 mg verapamil was given. The cycle lengths of PRJT before administration of 10 or 20 mg ATP and 5 mg verapamil were similar. The 10 mg dose of ATP terminated PRJT in 17 of the 20 patients, and 20 mg ATP was required to terminate PRJT in the three remaining patients. The 5 mg dose of verapamil terminated PRJT in 15 patients, whereas an additional bolus of 5 mg terminated PRJT in one of the remaining five patients. The overall efficacy of ATP (20/20, 100%) was significantly greater than that of verapamil (16/20, 80%) (p less than .05); however, there was no significant difference between the conversion rate of PRJT after administration of 10 mg ATP (17/20) and 5 mg verapamil (15/20). ATP terminated PRJT more quickly than verapamil (mean 24 sec vs mean 51 sec; p less than .01). Termination of PRJT by either ATP or verapamil was mainly related to a block in the AV node in patients with accessory pathways and to a block in the antegrade slow pathway in patients with AV nodal reentry. Cycle length alternans before termination of tachycardia was observed more frequently after verapamil than after ATP (7/16 vs 1/20; p less than .01). The total incidence of transient second-degree AV nodal block and various cardiac supraventricular and ventricular arrhythmias was higher after termination of PRJT by ATP than after verapamil (17/20 vs 5/16; p less than .001). A higher incidence of transient but frequently uncomfortable noncardiac side effects was observed after ATP. We conclude that ATP (10 to 20 mg) is more effective and more rapid than verapamil (5 or 5 + 5 mg) in terminating PRJT but results in a higher incidence of cardiac and noncardiac side effects.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

对20例阵发性折返性交界性心动过速(PRJT)患者比较了三磷酸腺苷(ATP)和维拉帕米在短期治疗中的疗效、电生理效应及副作用。所有患者在对照电生理研究期间均可诱发持续性PRJT。14例患者的PRJT涉及逆向附加通路,6例患者为房室(AV)结折返性心动过速(“慢-快”型)。ATP半衰期极短,在持续性PRJT期间首先静脉注射(10mg,1秒内推注)。若PRJT在2分钟内未终止,则给予20mg ATP推注。随后在持续性PRJT期间静脉注射维拉帕米(5mg,15秒内推注),若后者在3分钟内未终止,则再给予5mg维拉帕米推注。给予10或20mg ATP及5mg维拉帕米前PRJT的周期长度相似。10mg剂量的ATP使20例患者中的17例PRJT终止,其余3例患者需20mg ATP才能终止PRJT。5mg剂量的维拉帕米使15例患者的PRJT终止,其余5例患者中有1例需再给予5mg推注才能终止PRJT。ATP的总体疗效(20/20,100%)显著高于维拉帕米(16/20,80%)(p<0.05);然而,给予10mg ATP后PRJT的转复率(17/20)与给予5mg维拉帕米后(15/20)之间无显著差异。ATP比维拉帕米更快地终止PRJT(平均24秒对平均51秒;p<0.01)。ATP或维拉帕米终止PRJT主要与附加通路患者的AV结阻滞及AV结折返患者的前向慢径路阻滞有关。维拉帕米终止心动过速前观察到的周期长度交替比ATP更频繁(7/16对1/20;p<0.01)。ATP终止PRJT后短暂二度AV结阻滞及各种心脏室上性和室性心律失常的总发生率高于维拉帕米(17/20对5/16;p<0.001)。ATP后观察到短暂但常令人不适的非心脏副作用发生率更高。我们得出结论,ATP(10至20mg)在终止PRJT方面比维拉帕米(5或5+5mg)更有效、更迅速,但导致心脏和非心脏副作用的发生率更高。(摘要截短至400字)

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