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三尖瓣埃布斯坦畸形患者症状性复发性心动过速的电生理基础与管理

The electrophysiologic basis and management of symptomatic recurrent tachycardia in patients with Ebstein's anomaly of the tricuspid valve.

作者信息

Smith W M, Gallagher J J, Kerr C R, Sealy W C, Kasell J H, Benson D W, Reiter M J, Sterba R, Grant A O

出版信息

Am J Cardiol. 1982 Apr 1;49(5):1223-34. doi: 10.1016/0002-9149(82)90048-0.

Abstract

Twenty-two patients with Ebstein's anomaly were evaluated because of recurrent tachycardia. A total of 30 accessory pathways were present in 21 of the 22 patients. Twenty-six accessory pathways were of the atrioventricular (A-V) type while four were Mahaim fibers. Multiple accessory pathways were present in eight patients. Twenty-five of the 26 accessory A-V pathways were right-sided, either in the posterior septum (12 pathways) or the posterolateral free wall (13 pathways); one patient with corrected transposition of the great arteries had a left-sided accessory A-V pathway in a lateral free wall location. Patients with accessory A-V pathways had a long minimal ventriculoatrial (V-A) conduction time during reciprocating tachycardia (192 +/- 47 ms) and usually showed a persistent complete or incomplete right bundle branch block morphology. At surgery, preexcitation was invariably localized to the atrialized ventricle. The long V-A conduction time during reciprocating tachycardia appeared to consist of late activation of the local ventricle in the region of the accessory pathway with a further delay occurring before excitation of adjacent atrium presumably due to conduction over the accessory pathway. Accessory A-V pathways were successfully sectioned with no deaths in 13 of 15 patients. On the basis of these data, certain electrocardiographic findings encountered in the study of patients with recurrent tachycardia should point to the possibility of associated Ebstein's anomaly: morphology of the surface electrocardiogram suggesting preexcitation of the right posterior septum or right posterolateral free wall as well as the combination during reciprocating tachycardia of a long V-A interval and right bundle branch block.

摘要

22例埃布斯坦畸形患者因反复出现心动过速接受评估。22例患者中的21例共存在30条旁路。26条旁路为房室(A-V)型,4条为Mahaim纤维。8例患者存在多条旁路。26条房室旁路中的25条位于右侧,要么在后部间隔(12条旁路),要么在右后外侧游离壁(13条旁路);1例大动脉转位矫正患者在外侧游离壁位置有1条左侧房室旁路。房室旁路患者在折返性心动过速期间有较长的最小心室心房(V-A)传导时间(192±47毫秒),通常表现为持续的完全或不完全右束支传导阻滞形态。手术时,预激总是局限于房化心室。折返性心动过速期间较长的V-A传导时间似乎是由旁路区域局部心室的延迟激活组成,在相邻心房兴奋之前进一步延迟,可能是由于通过旁路的传导。15例患者中有13例成功切断房室旁路,无死亡病例。基于这些数据,在反复心动过速患者研究中遇到的某些心电图表现应提示存在相关埃布斯坦畸形的可能性:体表心电图形态提示右后间隔或右后外侧游离壁预激,以及折返性心动过速期间长V-A间期和右束支传导阻滞的组合。

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