Sippensgroenewegen A, Spekhorst H, van Hemel N M, Kingma J H, Hauer R N, de Bakker J M, Grimbergen C A, Janse M J, Dunning A J
Department of Cardiology, Heart Lung Institute, University Hospital, Utrecht, The Netherlands.
J Am Coll Cardiol. 1994 Dec;24(7):1708-24. doi: 10.1016/0735-1097(94)90178-3.
This study examined the performance of the 62-lead body surface electrocardiogram (ECG) in identifying the site of origin of ventricular tachycardia in patients with a previous myocardial infarction.
Because the accuracy of ECG localization of ventricular tachycardia using standard 12-lead recordings is restricted to the identification of rather large ventricular areas, application of multiple torso lead recordings may augment the resolving power of the surface ECG and result in more discrete localization of arrhythmogenic foci.
Thirty-two patients were selected for electrophysiologically guided ablative therapy for drug-resistant postinfarction ventricular tachycardia. In these patients, QRS integral maps of distinct monomorphic ventricular tachycardia configurations were correlated with a previously generated infarct-specific reference data base of paced QRS integral maps. Each paced pattern in the data base corresponded with ectopic endocardial impulse formation at 1 of 18 or 22 discrete segments of the left ventricle with a previous anterior or inferior myocardial infarction, respectively. Electrocardiographic localization was compared with the results obtained during intraoperative or catheter endocardial activation sequence mapping.
Body surface mapping was performed during 101 distinct ventricular tachycardia configurations. Compared with the activation mapping data that were acquired in 64 of 101 ventricular tachycardias, body surface mapping identified the correct segment of origin in 40 (62%) of 64 tachycardias, a segment adjacent to the segment where the arrhythmia actually originated in 19 (30%) of 64 tachycardias and a segment disparate from the actual segment of origin in 5 (8%) of 64 tachycardias. With respect to infarct location, the segment of origin was correctly identified in 28 (60%) of 47 ventricular tachycardias in patients with anterior, 7 (70%) of 10 tachycardias in patients with inferior and 5 (71%) of 7 tachycardias in patients with combined anterior and inferior myocardial infarction.
This study shows that body surface mapping enables precise localization of the origin of postinfarction ventricular tachycardia in 62% and regional approximation in 30% of tachycardias. The multiple-lead ECG may be used to guide and shorten catheter-based mapping procedures during ventricular tachycardia and to provide relevant information on the origin of tachycardias that cannot be mapped with conventional single-site mapping techniques because of unfavorable characteristics.
本研究检测了62导联体表心电图(ECG)在识别既往心肌梗死患者室性心动过速起源部位方面的性能。
由于使用标准12导联记录进行室性心动过速的心电图定位准确性仅限于识别较大的心室区域,因此应用多个躯干导联记录可能会增强体表心电图的分辨能力,并导致心律失常起源灶的定位更加精确。
选择32例患者进行电生理指导下的药物难治性心肌梗死后室性心动过速消融治疗。在这些患者中,将不同单形性室性心动过速形态的QRS积分图与先前生成的梗死特异性起搏QRS积分图参考数据库进行关联。数据库中的每个起搏模式分别对应于左心室18或22个离散节段中1个节段的异位心内膜冲动形成,这些患者分别有先前的前壁或下壁心肌梗死。将心电图定位结果与术中或导管心内膜激动顺序标测结果进行比较。
在101种不同的室性心动过速形态期间进行了体表标测。与101例室性心动过速中64例获得的激动标测数据相比,体表标测在64例心动过速中的40例(62%)中识别出了正确的起源节段,在64例心动过速中的19例(30%)中识别出了与心律失常实际起源节段相邻的节段,在64例心动过速中的5例(8%)中识别出了与实际起源节段不同的节段。就梗死部位而言,在前壁心肌梗死患者的47例室性心动过速中有28例(60%)、下壁心肌梗死患者的10例心动过速中有7例(70%)以及前壁和下壁心肌梗死合并患者的7例心动过速中有5例(71%)正确识别出了起源节段。
本研究表明,体表标测能够在62%的室性心动过速中精确定位心肌梗死后室性心动过速的起源,在30%的心动过速中进行区域近似定位。多导联心电图可用于指导和缩短室性心动过速期间基于导管的标测程序,并提供因特征不佳而无法用传统单部位标测技术进行标测的心动过速起源的相关信息。