Unipolar atrial electrogram morphology from an epicardial and endocardial perspective

医学 心脏病学 内科学 分馏 窦性心律 心房颤动 心内膜 化学 有机化学
作者
Lisette J.M.E. van der Does,Paul Knops,Christophe P. Teuwen,Maria-Corina Șerban,Roeliene Starreveld,Eva A.H. Lanters,Elisabeth M.J.P. Mouws,Charles Kik,Ad J.J.C. Bogers,Natasja M.S. de Groot
出处
期刊:Heart Rhythm [Elsevier BV]
卷期号:15 (6): 879-887 被引量:36
标识
DOI:10.1016/j.hrthm.2018.02.020
摘要

Background Endo–epicardial asynchrony (EEA) and the interplay between the endocardial and epicardial layers could be important in the pathophysiology of atrial arrhythmias. The morphologic differences between epicardial and endocardial atrial electrograms have not yet been described, and electrogram morphology may hold information about the presence of EEA. Objective The purpose of this study was to directly compare epicardial to endocardial unipolar electrogram morphology during sinus rhythm (SR) and to evaluate whether EEA contributes to electrogram fractionation by correlating fractionation to spatial activation patterns. Methods In 26 patients undergoing cardiac surgery, unipolar electrograms were simultaneously recorded from the epicardium and endocardium at the inferior, middle, and superior right atrial (RA) free wall during SR. Potentials were analyzed for epi–endocardial differences in local activation time, voltage, RS ratio, and fractionation. The surrounding and opposite electrograms of fractionated deflections were evaluated for corresponding local activation times in order to determine whether fractionation originated from EEA. Results The superior RA was predisposed to delayed activation, EEA, and fractionation. Both epicardial and endocardial electrograms demonstrated an S-predominance. Fractionation was mostly similar between the 2 sides; however, incidentally deflections up to 4 mV on 1 side could be absent on the other side. Remote activation was responsible for most fractionated deflections (95%) in SR, of which 4% could be attributed to EEA. Conclusion Local epi–endocardial differences in electrogram fractionation occur occasionally during SR but will likely increase during arrhythmias due to increasing EEA and (functional) conduction disorders. Electrogram fractionation can originate from EEA, and this study demonstrated that unipolar electrogram fractionation can potentially identify EEA.
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