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Arrhythmogenesis of surgical atrial incisions and lesions in Maze procedure: insights from high-resolution mapping of atrial tachycardias.

Authors :
Hu, Wei
Zhou, Dongchen
Ding, Xiangwei
Yang, Gang
Liu, Hailei
Wang, Zidun
Chen, Hongwu
Ju, Weizu
Li, Mingfang
Zhang, Fengxiang
Yang, Jian
Han, Jie
Wu, Xianhao
Qiu, Zhaohui
Zheng, Liangrong
Chen, Minglong
Source :
EP: Europace; Jan2023, Vol. 25 Issue 1, p137-145, 9p
Publication Year :
2023

Abstract

Background Atrial tachycardias (ATs) frequently develop after a surgical Maze procedure. We aimed to elucidate the electrophysiologic mechanisms and their arrhythmogenic substrates of these ATs. Methods and results We retrospectively reviewed 20 patients (14 females, mean age of 55.5 ± 8.6 years) with post-Maze ATs who underwent high-resolution mapping at three institutions. The slow conduction areas, reentry circuits, voltage signals, complex electrograms, and their correlation with the surgical incisions and lesions placed in the surgical Maze procedures were analyzed. Thirty-six ATs with a mean cycle length of 260.0 ± 67.6 ms were mapped in these patients. Among them, 22 (61.1%) were anatomical macro-reentrant ATs (AMAT), 12 (33.3%) non-AMATs (localized ATs), and 2 (5.6%) focal ATs, respectively. Epicardial conduction bridges were observed in 6/20 (30.0%) patients and 7/36 (19.4%) ATs. Different arrhythmogenic substrates were identified in these ATs, including slow conduction regions within the previous lesion areas or between the incisions and anatomical structures, the prolonged activation pathways caused by the short lesions connecting the tricuspid annulus, and the circuits around the long incisions and/or lesions. Conclusions Reentry is the main mechanism of the post-Maze ATs. The pro-arrhythmic substrates are most likely caused by surgical incisions and lesions. The slow conduction regions and the protected channels yielded from these areas are the major arrhythmogenic factors. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10995129
Volume :
25
Issue :
1
Database :
Complementary Index
Journal :
EP: Europace
Publication Type :
Academic Journal
Accession number :
161902410
Full Text :
https://doi.org/10.1093/europace/euac102