Abstract

The optimal antithrombotic strategy following left atrial appendage occlusion (LAAO) is not yet clearly established. Low-dose non-vitamin K antagonist oral anticoagulants (NOAC) might represent a valid alternative, but data regarding their usage is scarce. The aim of this study was to examine the efficacy and safety of low-dose NOAC compared to single (SAPT) or dual antiplatelet therapies (DAPT) after LAAO. We included consecutive patients with non-valvular atrial fibrillation who underwent LAAO and received low-dose apixaban, SAPT, or DAPT at discharge. The primary objective of this study included an efficacy endpoint (thromboembolic events and device related thrombosis (DRT)) and a safety endpoint (incidence of major bleeding) within the first three months after LAAO. A total of 139 patients were included. This group involved SAPT in 26 (18%), DAPT in 73 (53%), and apixaban in 40 (29%) patients. Follow-up at three-months showed no significant differences in the primary efficacy endpoint (2 (8%) SAPT, 3 (4%) DAPT and 0 (0%) apixaban; p value = 0.25). In contrast, the primary safety endpoint occurred more frequently in DAPT patients (7 (10%) DAPT, 0 (0%), SAPT and 0 with apixaban; p value = 0.03). Combining both efficacy and safety outcomes, low dose apixaban had a lower rate of events (2 (8%) with SAPT, 9 (12%) with DAPT and 0 (0%) with apixaban; p = 0.046). Low-dose apixaban after LAAO may be a valid alternative to DAPT and SAPT as depicted by the reduction in the occurrence of major bleedings and combined DRT/major bleedings respectively. Randomized data will be necessary to validate this strategy.

Highlights

  • It has been estimated that 6–12 million people worldwide will suffer non valvular atrial fibrillation (NVAF) in the US by 2050, and 17.9 million people will experience this condition in Europe by 2060 [1]

  • Among non-vitamin K antagonist oral anticoagulants (NOAC), apixaban has shown a remarkable safety and efficacy profile with low rates of ischemic and hemorrhagic events compared to vitamin K antagonist (VKA) or single antiplatelet therapy (SAPT) [8]

  • The aim of our study was to examine the efficacy and safety of low-dose NOAC compared to single antiplatelet therapy (SAPT)

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Summary

Introduction

It has been estimated that 6–12 million people worldwide will suffer non valvular atrial fibrillation (NVAF) in the US by 2050, and 17.9 million people will experience this condition in Europe by 2060 [1]. Oral anticoagulation (OAC) therapy is the standard of care to prevent thrombus formation and cardioembolic events in patients with NVAF [3]. 10 to 20% of patients with NVAF have an absolute or relative contraindication to oral anticoagulation therapy due to increased risk of bleeding [4]. Percutaneous left atrial appendage occlusion (LAAO) has demonstrated to be an alternative for the prevention of cardioembolic events in these patients [5,6] while avoiding long-term risks of OAC. LAAO devices require short-term (one to three months) postprocedural oral antithrombotic therapy to prevent device-related thrombosis (DRT). Among non-vitamin K antagonist oral anticoagulants (NOAC), apixaban has shown a remarkable safety and efficacy profile with low rates of ischemic and hemorrhagic events compared to vitamin K antagonist (VKA) or single antiplatelet therapy (SAPT) [8]. The aim of our study was to examine the efficacy and safety of low-dose NOAC compared to single antiplatelet therapy (SAPT)

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