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Catheter Ablation in Combination With Left Atrial Appendage Closure for Atrial Fibrillation
Published on: February 26, 2013
Early Discontinuation of Antithrombotic Treatment Following Left Atrial Appendage Closure
Jules Mesnier1, Ignacio Cruz-González2, Dabit Arzamendi3
1Quebec Heart and Lung Institute, Laval University, Quebec City, Quebec, Canada.
Insights
Discontinuing antithrombotic treatment within six months after left atrial appendage closure (LAAC) is safe for many patients. Early discontinuation did not increase risks of death, stroke, or major bleeding in this study.
Area of Science:
- Cardiology
- Interventional Cardiology
- Thrombosis Research
Background:
- Left atrial appendage closure (LAAC) is an alternative to oral anticoagulation for stroke prevention in atrial fibrillation.
- Antithrombotic treatment is standard post-LAAC, but its necessity and duration are debated, especially in high-risk bleeding patients.
- Evidence on the safety of early antithrombotic treatment discontinuation after LAAC is limited.
Purpose of the Study:
- To evaluate the safety and outcomes of early antithrombotic treatment discontinuation following successful LAAC.
- To compare the risks of death, ischemic stroke, and major bleeding in patients with and without early antithrombotic treatment discontinuation.
Main Methods:
- Multicenter study involving 1,082 patients who underwent successful LAAC.
- Early discontinuation defined as stopping all antiplatelet/anticoagulant therapy within 6 months post-procedure.
- Propensity-matched analysis comparing outcomes between patients with and without early discontinuation.
Main Results:
- 13.7% of patients (148/1082) discontinued antithrombotic treatment early.
- Patients discontinuing treatment had lower CHA2DS2-VASc scores and higher rates of prior gastrointestinal bleeding.
- After a median follow-up of 2.1 years, propensity-matched analysis showed no significant difference in death, ischemic stroke, or major bleeding risk between groups.
Conclusions:
- Early antithrombotic treatment discontinuation within 6 months after LAAC was not associated with increased adverse events in selected patients.
- These findings support the safety of shorter antithrombotic therapy durations post-LAAC, guided by clinician judgment, particularly for high bleeding risk individuals.
- Further clinical trials are warranted to confirm these outcomes.
Abstract:
Although antithrombotic treatment is recommended after left atrial appendage closure (LAAC), some patients require discontinuation of antithrombotic treatment after LAAC without evidence on the safety of such a strategy. We sought to evaluate outcomes of patients who had early antithrombotic treatment discontinuation after LAAC. This is a multicenter study including 1,082 patients who underwent successful LAAC. Early discontinuation of antithrombotic treatment was defined as discontinuation of all antiplatelet/anticoagulant treatment within 6 months following the procedure. A propensity-matched analysis was used to compare outcomes of patients with and without early antithrombotic treatment discontinuation. A total of 148 patients (13.7%) had early antithrombotic treatment discontinuation. In the entire population, antithrombotic treatment discontinuation patients exhibited a lower CHA2DS2-VASc score (p <0.001) and a higher rate of previous gastrointestinal bleeding episodes (p = 0.01) compared with patients without discontinuation. After a median follow-up of 2.1 (1,1-3.1) years after antithrombotic treatment discontinuation, the rates of death, ischemic stroke, and major bleeding were 12.1, 0.6, and 3.3 per 100 patient-years. In 119 matched pairs with similar baseline characteristics, antithrombotic treatment discontinuation patients had a similar risk of death (hazard ratio [HR] 1.06, 95% confidence interval [CI] 0.65 to 1.71, p = 0.82), ischemic stroke (HR 0.39, 95% CI 0.04 to 3.79, p = 0.42) and major bleeding (HR 1.48, 95% CI 0.56 to 3.88, p = 0.43) compared with those without discontinuation. In conclusion, antithrombotic treatment was discontinued in 1 of 7 selected patients within 6 months after LAAC, and this was not associated with an increased risk of death or thromboembolic events after a median follow-up of 2 years. These data support the safety of shorter periods of antithrombotic therapy after LAAC in high bleeding risk patients based on clinician judgment. Further trials are warranted.
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