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Updated: Aug 26, 2025

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Published on: May 26, 2015
Asymptomatic left circumflex artery stenosis is associated with higher arrhythmia recurrence after persistent atrial
Rodrigue Garcia1,2, Mathilde Clouard1, Fabian Plank3
1Cardiology Department, University Hospital of Poitiers, Poitiers, France.
Insights
Coronary artery disease obstruction, specifically in the circumflex artery, increases the risk of atrial fibrillation recurrence after ablation. This finding highlights the importance of assessing coronary artery disease in patients undergoing atrial fibrillation ablation.
Area of Science:
- Cardiology
- Electrophysiology
- Medical Imaging
Background:
- The role of stable coronary artery disease (CAD) in persistent atrial fibrillation (AF) pathophysiology is not well understood.
- Previous studies have linked myocardial infarction to AF, but the impact of obstructive CAD requires further investigation.
Purpose of the Study:
- To investigate the association between obstructive coronary artery disease (CAD) and the recurrence of atrial fibrillation (AF) after ablation in patients without a prior history of CAD.
- To determine if specific locations of CAD obstruction influence AF recurrence rates post-ablation.
Main Methods:
- Retrospective observational study of 496 patients undergoing persistent AF ablation with preprocedural cardiac computed tomography (CCT).
- Obstructive CAD defined as ≥ 50% luminal stenosis; patients with known CAD or revascularization were excluded.
- Follow-up averaged 24 months to assess AF recurrence.
Main Results:
- Obstructive CAD was present in 17.4% of patients; overall AF recurrence was 41.7%.
- No significant difference in AF recurrence was observed between patients with and without obstructive CAD (43.0% vs. 41.5%, P=0.79).
- Left circumflex artery obstruction was associated with a higher recurrence rate (56% vs. 32% at 2 years, P≤0.01) and independently predicted recurrence (HR 2.32, P<0.01).
Conclusions:
- Obstruction in the circumflex artery, identified by CCT, independently doubles the risk of AF recurrence post-ablation.
- This finding suggests a potential pathophysiological link between circumflex artery stenosis and AF recurrence.
- Further research is warranted to elucidate the relationship between circumflex artery obstruction and AF recurrence.
Background:
The pathophysiology of persistent atrial fibrillation (AF) remains unclear. While several studies have demonstrated an association between myocardial infarction and atrial fibrillation, the role of stable coronary artery disease (CAD) is still unknown. As a result, we aimed to assess the association between CAD obstruction and AF recurrence after persistent AF ablation in patients with no history of CAD.
Materials And Methods:
This observational retrospective study included consecutive patients who underwent routine preprocedural cardiac computed tomography (CCT) before persistent AF ablation between September 2015 and June 2018 in 5 European University Hospitals. Exclusion criteria were CAD or coronary revascularization previously known or during follow-up. Obstructive CAD was defined as luminal stenosis ≥ 50%.
Results:
All in all, 496 patients (mean age 61.8 ± 10.0 years, 76.2% males) were included. CHA2DS2-VASc score was 0 or 1 in 225 (36.3%) patients. Obstructive CAD was present in 86 (17.4%) patients. During the follow-up (24 ± 19 months), 207 (41.7%) patients had AF recurrence. The recurrence rate was not different between patients with and without obstructive CAD (43.0% vs. 41.5%, respectively; P = 0.79). When considering the location of the stenosis, the recurrence rate was higher in the case of left circumflex obstruction: 56% vs. 32% at 2 years (log-rank P ≤ 0.01). After Cox multivariate analysis, circumflex artery obstruction (HR 2.32; 95% CI 1.36-3.98; P < 0.01) was independently associated with AF recurrence.
Conclusion:
Circumflex artery obstruction detected with CCT was independently associated with 2-fold increase in the risk of AF recurrence after persistent AF ablation. Further research is necessary to evaluate this pathophysiological relationship.
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