PMID- 32528566 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20240328 IS - 1880-4276 (Print) IS - 1883-2148 (Electronic) IS - 1880-4276 (Linking) VI - 36 IP - 3 DP - 2020 Jun TI - Comparison of effectiveness and safety between uninterrupted direct oral anticoagulants with and without switching to dabigatran in atrial fibrillation ablation. PG - 417-424 LID - 10.1002/joa3.12333 [doi] AB - 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. CI - (c) 2020 The Authors. Journal of Arrhythmia published by John Wiley & Sons Australia, Ltd on behalf of the Japanese Heart Rhythm Society. FAU - Harada, Masahide AU - Harada M AUID- ORCID: 0000-0002-2345-9557 AD - Department of Cardiology Fujita Health University Toyoake Japan. FAU - Motoike, Yuji AU - Motoike Y AD - Department of Cardiology Fujita Health University Toyoake Japan. FAU - Nomura, Yoshihiro AU - Nomura Y AD - Department of Cardiology Fujita Health University Toyoake Japan. FAU - Nishimura, Asuka AU - Nishimura A AD - Department of Cardiology Fujita Health University Toyoake Japan. FAU - Koshikawa, Masayuki AU - Koshikawa M AD - Department of Cardiology Fujita Health University Toyoake Japan. FAU - Murayama, Kazuhiro AU - Murayama K AD - Joint Research Laboratory of Advanced Medical Imaging Fujita Health University Toyoake Japan. FAU - Ohno, Yoshiharu AU - Ohno Y AD - Joint Research Laboratory of Advanced Medical Imaging Fujita Health University Toyoake Japan. FAU - Watanabe, Eiichi AU - Watanabe E AD - Department of Cardiology Fujita Health University Toyoake Japan. FAU - Izawa, Hideo AU - Izawa H AD - Department of Cardiology Fujita Health University Toyoake Japan. FAU - Ozaki, Yukio AU - Ozaki Y AD - Department of Cardiology Fujita Health University Toyoake Japan. LA - eng PT - Journal Article DEP - 20200318 PL - Japan TA - J Arrhythm JT - Journal of arrhythmia JID - 101263026 PMC - PMC7280006 OTO - NOTNLM OT - anticoagulant OT - atrial fibrillation OT - catheter ablation OT - silent brain infarction OT - thromboembolism COIS- MH received speaker fees from Nippon Boehringer Ingelheim and Bristol-Myers Squibb. EW received research funds from Daiichi-Sankyo and received speaker fee from Bristol-Myers Squibb and Biotronik Japan. YM, YN, AN, MK, KM, YO, and YO have nothing to disclose. EDAT- 2020/06/13 06:00 MHDA- 2020/06/13 06:01 PMCR- 2020/03/18 CRDT- 2020/06/13 06:00 PHST- 2020/01/02 00:00 [received] PHST- 2020/02/15 00:00 [revised] PHST- 2020/03/01 00:00 [accepted] PHST- 2020/06/13 06:00 [entrez] PHST- 2020/06/13 06:00 [pubmed] PHST- 2020/06/13 06:01 [medline] PHST- 2020/03/18 00:00 [pmc-release] AID - JOA312333 [pii] AID - 10.1002/joa3.12333 [doi] PST - epublish SO - J Arrhythm. 2020 Mar 18;36(3):417-424. doi: 10.1002/joa3.12333. eCollection 2020 Jun.