Abstract

Background: We aimed to assess the extent to which drug persistence is better with non-vitamin K antagonist oral anticoagulants (NOACs) than vitamin K antagonists (VKAs) in atrial fibrillation (AF) patients and to estimate the difference in therapy persistence depending on NOAC dosing regimen (once daily (QD) vs. twice daily (BID)). Methods: Consecutive patients were followed for 1 year in phase III of the GLORIA-AF registry. Drug persistence was defined as the use of OAC without any discontinuation in >30 days or switching to alternative therapy. Results: Among 21,109 eligible patients in phase III, 17,266 patients who were prescribed OAC at baseline and those who took ≥1 OAC dose were included. The 1-year proportion of patients receiving NOAC and VKA who persisted on treatment was 80% and 75%, respectively. The 1-year persistence with NOACs BID and NOACs QD was 81% and 80%, respectively. Female gender, hypertension, older age, alcohol use, permanent, asymptomatic, and minimally symptomatic AF were associated with better OAC persistence. Region, medication usage predisposing to bleeding, being a current smoker, treatment reimbursement, and proton pump inhibitors were associated with lower OAC persistence. Conclusions: Drug persistence was higher with NOACs (1-year persistence was 80%) than with VKAs (75%). There was little difference in 1-year persistence between NOAC dosing regimens.

Highlights

  • Atrial fibrillation (AF) is the most prevalent cardiac arrhythmia

  • The majority of eligible patients were enrolled in Europe (51% in non-vitamin K antagonist oral anticoagulants (NOACs) group and 57% in vitamin K antagonists (VKAs) group), followed by North America (28% vs. 15%), Asia (14% and 16%), and Latin America (7% and 12%)

  • Baseline characteristics of patients who were on NOACs or VKAs are presented in Supplementary Table S1

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Summary

Introduction

Atrial fibrillation (AF) is the most prevalent cardiac arrhythmia. It is associated with an increased risk of ischaemic stroke, stroke-related morbidity, and mortality [1]. Oral anticoagulant (OAC) therapy is recommended to prevent thromboembolism in patients with AF with ≥1 stroke risk factors [2]. The non-vitamin K antagonist oral anticoagulants (NOACs) have an improved efficacy/safety ratio when compared with vitamin K antagonists (VKAs), and are recommended as first-line therapy for stroke prevention in AF [2]. The 1-year persistence of NOAC and VKA was 84.5% and 89.8%, respectively, in the Randomized Evaluation of Long-Term Anticoagulation Therapy (RE-LY) [5]. We aimed to assess the extent to which drug persistence is better with non-vitamin K antagonist oral anticoagulants (NOACs) than vitamin K antagonists (VKAs) in atrial fibrillation (AF) patients and to estimate the difference in therapy persistence depending on NOAC dosing regimen (once daily (QD) vs twice daily (BID)).

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