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室性心动过速的基质标测:假设与误解

Substrate Mapping for Ventricular Tachycardia: Assumptions and Misconceptions.

作者信息

Josephson Mark E, Anter Elad

机构信息

Harvard-Thorndike Electrophysiology Institute, Cardiovascular Division, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.

Harvard-Thorndike Electrophysiology Institute, Cardiovascular Division, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.

出版信息

JACC Clin Electrophysiol. 2015 Oct;1(5):341-352. doi: 10.1016/j.jacep.2015.09.001. Epub 2015 Sep 10.

Abstract

Substrate mapping was developed to treat poorly tolerated infarct-related ventricular tachycardias (VTs). This concept was based on 30-year-old data derived from surgical and percutaneous mapping during sinus rhythm and VT that demonstrated specific electrograms (EGMs) that characterized the "arrhythmogenic substrate" of VT. Electrogram characteristics of the arrhythmogenic VT substrate during sinus rhythm included low-voltage, fractionation, long duration, split signals, and isolated late potentials as well as EGMs demonstrating adjacent early and late activation. Introduction of electroanatomical mapping (EAM) systems during the mid-1990s has allowed investigators to record electrograms in 3 dimensions and to identify sites assumed to represent the central common pathway ("isthmus") during re-entrant VTs. However, several important assumptions and misconceptions make currently used "substrate mapping" techniques inaccurate. These include: 1) re-entrant circuits are produced by fixed barriers of immutable "inexcitable" scar; 2) low voltage amplitude (≤0.5 mV) implies dense "inexcitable" scar; 3) isthmuses identified in patients with tolerated VTs using entrainment mapping are both valid and provide an accurate depiction of isthmuses in less hemodynamically tolerated VTs; and 4) current mapping tools and methods can delineate specific electrophysiologic features that will determine the barriers forming channels during re-entrant VTs. None of these assumptions has been validated and recent experimental and human data using higher resolution mapping with very small electrodes cast doubt on their validity. These data call for re-evaluation of substrate-mapping techniques to characterize the arrhythmogenic substrate of post-infarction VT. Standardization of recording techniques including electrode size, interelectrode spacing, tissue contact, catheter orientation, and wavefront activation must be taken into consideration.

摘要

基质标测技术是为治疗耐受性差的梗死相关室性心动过速(VT)而研发的。这一概念基于30年前在窦性心律和室性心动过速期间进行手术和经皮标测所获得的数据,这些数据显示了特定的心电图(EGM),其表征了室性心动过速的“致心律失常基质”。窦性心律期间致心律失常性室性心动过速基质的心电图特征包括低电压、碎裂、持续时间长、信号分裂、孤立的晚期电位以及显示相邻早期和晚期激活的心电图。20世纪90年代中期引入的电解剖标测(EAM)系统使研究人员能够在三维空间记录心电图,并识别折返性室性心动过速期间假定代表中央共同通路(“峡部”)的部位。然而,目前使用的“基质标测”技术存在一些重要的假设和误解,导致其不准确。这些包括:1)折返环路是由不可变的“不兴奋”瘢痕的固定屏障产生的;2)低电压幅度(≤0.5mV)意味着致密的“不兴奋”瘢痕;3)使用拖带标测在耐受性室性心动过速患者中识别出的峡部是有效的,并且能准确描绘血流动力学耐受性较差的室性心动过速中的峡部;4)当前的标测工具和方法可以描绘出特定的电生理特征,这些特征将决定折返性室性心动过速期间形成通道的屏障。这些假设均未得到验证,最近使用非常小的电极进行高分辨率标测的实验和人体数据对其有效性提出了质疑。这些数据呼吁重新评估基质标测技术,以表征梗死后室性心动过速的致心律失常基质。必须考虑记录技术的标准化,包括电极大小、电极间距、组织接触、导管方向和波前激活。

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