Tang C W, Scheinman M M, Van Hare G F, Epstein L M, Fitzpatrick A P, Lee R J, Lesh M D
Department of Medicine, University of California San Francisco 94143-1354, USA.
J Am Coll Cardiol. 1995 Nov 1;26(5):1315-24. doi: 10.1016/0735-1097(95)00307-X.
This study sought to construct an algorithm to differentiate left atrial from right atrial tachycardia foci on the basis of surface electrocardiograms (ECGs).
Atrial tachycardia is an uncommon form of supraventricular tachycardia, often resistant to drug therapy.
A total of 31 consecutive patients with atrial tachycardia due to either abnormal automaticity or triggered rhythm underwent detailed atrial endocardial mapping and successful radiofrequency catheter ablation of a single atrial focus. P wave configuration was analyzed from 12-lead ECGs during tachycardia during either spontaneous or pharmacologically induced atrioventricular block. P waves inscribed above the isoelectric line (TP interval) were classified as positive, below as negative, above and below (or conversely, below and above) as biphasic and flat P waves as isoelectric (0). In 17 patients the tachycardia was located in the right atrium: crista terminalis (n = 4); right atrial appendage (n = 4); lateral wall (n = 4); posteroinferior right atrium (n = 3); tricuspid annulus (n = 1); and near the coronary sinus (n = 1). In 14 patients, atrial tachycardia was located in the left atrium: at the entrance of the right (n = 6) or left (n = 4) superior pulmonary veins; left inferior pulmonary vein (n = 1); inferior left atrium (n = 1); base of left atrial appendage (n = 1); and high lateral left atrium (n = 1).
There were no differences in P wave vectors between sites at the right atrial lateral wall versus the right atrial appendage or between sites at the entrance of right versus left superior pulmonary veins. However, analysis of P wave configuration showed that leads aVL and V1 were most helpful in distinguishing right atrial from left atrial foci. The sensitivity and specificity of using a positive or biphasic P wave in lead aVL to predict a right atrial focus was 88% and 79%, respectively. The sensitivity and specificity of a positive P wave in lead V1 in predicting a left atrial focus was 93% and 88%, respectively.
本研究旨在构建一种基于体表心电图(ECG)鉴别左房与右房心动过速起源灶的算法。
房性心动过速是室上性心动过速的一种不常见形式,常对药物治疗耐药。
共有31例因异常自律性或触发节律导致房性心动过速的连续患者接受了详细的心房内膜标测,并成功对单个心房起源灶进行了射频导管消融。在心动过速期间,于自发或药物诱导的房室传导阻滞时,从12导联ECG分析P波形态。等电位线(TP间期)以上记录的P波分类为正向,以下为负向,上下(或相反,下上)为双相,平P波为等电位(0)。17例患者的心动过速位于右房:界嵴(n = 4);右心耳(n = 4);侧壁(n = 4);右房后下壁(n = 3);三尖瓣环(n = 1);冠状窦附近(n = 1)。14例患者的房性心动过速位于左房:右(n = 6)或左(n = 4)上肺静脉入口处;左下肺静脉(n = 1);左房下部(n = 1);左心耳基部(n = 1);左房高侧壁(n = 1)。
右房侧壁与右心耳部位之间或右上肺静脉与左上肺静脉入口处之间的P波向量无差异。然而,P波形态分析显示,aVL导联和V1导联在鉴别右房与左房起源灶方面最有帮助。aVL导联出现正向或双相P波预测右房起源灶的敏感性和特异性分别为88%和79%。V1导联出现正向P波预测左房起源灶的敏感性和特异性分别为93%和88%。
1)体表P波形态分析在鉴别右房与左房心动过速起源灶方面表现相当不错。2)II、III和aVF导联有助于为鉴别上部与下部起源灶提供线索。