Background: Transcatheter left atrial appendage occlusion (LAAO) has emerged as an alternative treatment for stroke prevention in patients with atrial fibrillation (AF) at high risk of thromboembolism, who cannot tolerate long-term oral anticoagulation (OAC). Questions persist regarding effectiveness and safety of this treatment and the optimal post-interventional antithrombotic regimen after LAAO., Methods: We retrospectively gathered data from 428 patients who underwent percutaneous LAAO in 6 Italian high-volume centres, aimed at describing the real-world utilization, safety, and effectiveness of LAAO procedures, also assessing the clinical outcomes associated with different antithrombotic strategies., Results: Among the entire population, 20 (4.7 %) patients experienced a combination of pericardial effusion and periprocedural major bleeding: 8 (1.9 %) pericardial effusion, 1 (0.3 %) fatal bleeding, and 3 (0.7 %) non-fatal procedural major bleeding. Patients were discharged with different antithrombotic regimens: dual (DAPT) (27 %) or single (SAPT) (26 %) antiplatelet therapy, OAC (27 %), other antithrombotic regimens (14 %). Very few patients were not prescribed with antithrombotic drugs (6 %). At a medium 523 ± 58 days follow-up, 14 patients (3.3 %) experienced all-cause death, 6 patients (1.4 %) cardiovascular death, 3 patients (0.7 %) major bleeding, 10 patients (2.6 %) clinically relevant non-major bleeding, and 3 patients (0.7 %) ischemic stroke. At survival analysis, with DAPT as the reference group, OAC therapy was associated with better outcomes., Conclusions: Our findings confirm that LAAO is a safe procedure. Different individualized post-discharge antithrombotic regimens are now adopted, likely driven by the perceived thrombotic and hemorrhagic risk. The incidence of both ischemic and bleeding events tends to be low., Competing Interests: The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Daniele Sacchetta: payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing or educational events from Medtronic. Fabrizio Ricci: support for attending meetings and/or travel from Bayer. Antonio Dello Russo: consultant for Abbott and Medtronic. Giuseppe Patti: grant or contract from Abbott, Chiesi, Biotronic, Boston; consulting fees from Amgen, Sanofi, Novartis, Daichi Sankyo, Amarin, Aurora BioPharma, Malesci, PIAM, Boheringer Ingheleim, Bayer, Pfizer/BMS, Astra Zeneca, Biotronik, Terumo, Medtronic, Abbott, Edwards, Amicus, Novo Nordisk, Chiesi; payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing or educational events from Amgen, Sanofi, Novartis, Daichi Sankyo, Amarin, Aurora BioPharma, Malesci, PIAM, Boheringer Ingheleim, Bayer, Pfizer/BMS, Astra Zeneca, Biotronik, Terumo, Medtronic, Abbott, Edwards, Amicus, Novo Nordisk, Chiesi; participation on a Data Safety Monitoring Board or Advisory Board for Amgen, Daichi Sankyo, Amarin, Aurora Bayer, Pfizer/BMS, MSD. Giulia Renda: grant or contract to my Institution from Bayer and Janssen/Bristol-Myers Squibb (not related to the manuscript); speaker/consultant/advisory board fees from Bayer, Boehringer Ingelheim, Menarini; support for attending meetings from Bayer and Daiichi Sankyo., (© 2024 The Author(s).)