Key result
Periprocedural dabigatran switch linked to ~39% fewer silent cerebral events after AF ablation.
Why the study?
Recent studies showed the feasibility of uninterrupted DOACs with a temporary switch to dabigatran for AF ablation, but direct comparison of effectiveness and safety against uninterrupted factor Xa inhibitors was needed.
Does a temporary switch to dabigatran on the day of atrial fibrillation ablation reduce silent cerebral events and bleeding complications in patients on factor Xa inhibitors?
Observational (n=348)
Open-label
No
Does a temporary switch to dabigatran on the day of atrial fibrillation ablation reduce silent cerebral events and bleeding complications in patients on factor Xa inhibitors?
A temporary switch to dabigatran on the day of atrial fibrillation ablation in patients taking factor Xa inhibitors reduces preclinical silent cerebral events without increasing bleeding risk.
Answers are grounded in this paper and cite their sources.
May support dabigatran bridge to lower silent cerebral events; hypothesis-generating and requires randomized confirmation before practice change.
Introduction Recent studies have demonstrated the feasibility of uninterrupted direct oral anticoagulants (DOACs) with a temporary switch to dabigatran (“dabigatran bridge”) for atrial fibrillation (AF) ablation. We compared the effectiveness and safety between uninterrupted DOACs with and without the “dabigatran bridge” in patients taking factor Xa inhibitors. Methods AF patients on factor Xa inhibitors (rivaroxaban/apixaban/edoxaban) undergoing catheter ablation were eligible (n = 348). Brain MRI was performed within 2 days after the procedure to detect silent cerebral events (SCEs). Rivaroxaban/apixaban/edoxaban were uninterruptedly used in 153 patients (Group 1); these DOACs were switched to dabigatran on the day of AF ablation in 195 patients (Group 2). After propensity score matching, the unfractionated heparin (UFH) amount and the activated clotting time (ACT) kinetics during the procedure, the SCE incidence, and the follow‐up complications (30 days, thromboembolism and major/minor bleeding) in the two groups were compared. Results Group 2 had higher initial ACT value and shorter time to optimal ACT (>300 seconds) than Group 1 (184 ± 36 s vs 145 ± 22 s, and 34 ± 29 s vs 43 ± 34 s, P < .05, respectively). Group 2 tended to require less amount of UFH to achieve optimal ACT than Group 1, but the total amount of UFH for the procedure was comparable. Group 2 had lower SCE incidence than Group 1 (16.2% vs 26.4%, P < .05). The prevalence of follow‐up complications was unchanged between the two groups. Conclusions Switching to dabigatran on the day of AF ablation decreases preclinical thromboembolic events with similar bleeding risk to uninterrupted factor Xa inhibitors.
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Harada et al. (2020) conducted an observational in Atrial fibrillation (n=348). Temporary switch to dabigatran (dabigatran bridge) vs. Uninterrupted factor Xa inhibitors was evaluated on Incidence of silent cerebral events (SCEs) detected by brain MRI within 2 days after the procedure (p=<0.05). Switching to dabigatran on the day of atrial fibrillation ablation reduced the incidence of silent cerebral events compared to uninterrupted factor Xa inhibitors (16.2% vs 26.4%, p<0.05).
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