Physicians' Academy for Cardiovascular Education

Effect of NOAC vs. VKA on clinical outcomes in AF patients independent of burden of comorbidities

Efficacy and Safety of Edoxaban Compared to Warfarin According to the Burden of Diseases in Patients with Atrial Fibrillation: Insights from the ENGAGE AF-TIMI 48

Literature - Nicolau AM, Corbalan R, Nicolau JC et al. - Eur Heart J Cardiovasc Pharmacother 2019,

Introduction and methods

Patients with AF often have many comorbidities [1]. Comorbidities can increase bleeding risk in patients on anticoagulants [2,3]. Also, risk of stroke increases with many comorbidities and increasing age.

Treatment with warfarin or other VKAs can effectively reduce the risk of stroke and systemic embolic events (SEE) in AF patients [4]. However, anticoagulant therapy is often withheld in patients with a high bleeding risk or other perceived contraindications [5,6]. The decision to prescribe antithrombotic agents can be influenced by the presence of multiple comorbidities [7]. This study investigated the relationship between the burden of comorbidities and relative efficacy and safety of edoxaban vs. warfarin.

The current study was a post-hoc analysis of the ENGAGE AF-TIMI 48 trial. The ENGAGE AF-TIMI 48 trial was a three-group, randomized, double-blind, double-dummy, multinational trial in 21105 AF patients with moderate-to-high-risk (CHADS2 score ≥2). Patients with severe comorbidities such as active malignancies, advanced liver disease, class IV or V chronic kidney disease, and hepatitis B or C were excluded. Patients were randomized to receive warfarin (n=7036), higher dose edoxaban regimen (HDER) (60 mg, n=7035), or lower dose edoxaban regimen (LDER) (30 mg, n=7034). The median follow-up was 2.8 years. The updated Charlson Comorbidity index (CCI) was used to classify the burden of comorbidities [8]. Data were analyzed by prespecified CCI categories: 0 (32.0% of patients), 1 (7.3%), 2 (42.1%), 3 (12.7%) or ≥4 (6.0%).

The primary efficacy outcome was stroke or SEE. Key secondary efficacy endpoint was major adverse cardiac events (MACE), defined as MI, stroke, SEE or CV death. Primary safety outcome was major bleeding. The net clinical outcome was a composite of stroke/systemic embolism, major bleeding or death.

Main results


Elevated CCI scores were associated with higher event rates for stroke, SEE, MACE and major bleedings. No significant interactions were found between the burden of concomitant diseases and the efficacy and safety outcomes of HDER relative to warfarin. This suggests that edoxaban can be considered as an option for anticoagulation treatment of AF patients regardless of the degree of concomitant diseases.


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