Mitral isthmus ablation with and without temporary spot occlusion of the coronary sinus: a randomized clinical comparison of acute outcomes.

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Version: Final published version
Serval ID
serval:BIB_301DB2EA945E
Type
Article: article from journal or magazin.
Collection
Publications
Title
Mitral isthmus ablation with and without temporary spot occlusion of the coronary sinus: a randomized clinical comparison of acute outcomes.
Journal
Journal of Cardiovascular Electrophysiology
Author(s)
Hocini M., Shah A.J., Nault I., Rivard L., Linton N., Narayan S., Myiazaki S., Jadidi A.S., Knecht S., Scherr D., Wilton S.B., Roten L., Pascale P., Pedersen M., Derval N., Sacher F., Jaïs P., Clémenty J., Haïssaguerre M.
ISSN
1540-8167 (Electronic)
ISSN-L
1045-3873
Publication state
Published
Issued date
2012
Volume
23
Number
5
Pages
489-496
Language
english
Notes
Publication types: Journal Article ; Randomized Controlled Trial Publication Status: ppublish
Abstract
OBJECTIVE: To evaluate the safety and outcomes of mitral isthmus (MI) linear ablation with temporary spot occlusion of the coronary sinus (CS). Background: CS blood flow cools local tissue precluding transmurality and bidirectional block across MI lesion.
METHODS: In a randomized, controlled trial (CS-occlusion = 20, Control = 22), MI ablation was performed during continuous CS pacing to monitor the moment of block. CS was occluded at the ablation site using 1 cm spherical balloon, Swan-Ganz catheter with angiographic confirmation. Ablation was started at posterior mitral annulus and continued up to left inferior pulmonary vein (LIPV) ostium using an irrigated-tip catheter. If block was achieved, balloon was deflated and linear block confirmed. If not, additional ablation was performed epicardially (power ≤25 W). Ablation was abandoned after ∼30 minutes, if block was not achieved.
RESULTS: CS occlusion (mean duration -27 ± 9 minutes) was achieved in all cases. Complete MI block was achieved in 13/20 (65%) and 15/22 (68%) patients in the CS-occlusion and control arms, respectively, P = 0.76. Block was achieved with significantly small number (0.5 ± 0.8 vs 1.9 ± 1.1, P = 0.0008) and duration (1.2 ± 1.7 vs 4.2 ± 3.5 minutes, P = 0.009) of epicardial radiofrequency (RF) applications and significantly lower amount of epicardial energy (1.3 ± 2.4 vs 6.3 ± 5.7 kJ, P = 0.006) in the CS-occlusion versus control arm, respectively. There was no difference in total RF (22 ± 9 vs 23 ± 11 minutes, P = 0.76), procedural (36 ± 16 vs 39 ± 20 minutes, P = 0.57), and fluoroscopic (13 ± 7 vs 15 ± 10 minutes, P = 0.46) durations for MI ablation between the 2 arms. Clinically uneventful CS dissection occurred in 1 patient
CONCLUSIONS: Temporary spot occlusion of CS is safe and significantly reduces the requirement of epicardial ablation to achieve MI block. It does not improve overall procedural success rate and procedural duration. Tissue cooling by CS blood flow is just one of the several challenges in MI ablation.
Keywords
Aged, Atrial Fibrillation/diagnosis, Atrial Fibrillation/physiopathology, Balloon Occlusion/adverse effects, Catheter Ablation/adverse effects, Chi-Square Distribution, Coronary Angiography, Coronary Sinus/radiography, Electrophysiologic Techniques, Cardiac, Feasibility Studies, Female, France, Humans, Male, Middle Aged, Mitral Valve/physiopathology, Mitral Valve/surgery, Time Factors, Treatment Outcome
Pubmed
Web of science
Create date
12/06/2014 16:22
Last modification date
20/08/2019 14:14
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