Related Experiment Video
Updated: Sep 9, 2025

Catheter Ablation in Combination With Left Atrial Appendage Closure for Atrial Fibrillation
Published on: February 26, 2013
Real-World Polypharmacy and Drug-Drug Interactions in a Large Cohort of Direct Oral Anticoagulant Users With Atrial
Veronica De Angelis1, Ylenia Ingrasciotta2, Maria Carelli3
1Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.
Purpose:
Despite their promising safety profile, use of direct oral anticoagulants (DOACs) presents challenges, particularly concerning polypharmacy and potential drug-drug interactions (DDIs). This study aimed to investigate real-world effects of polypharmacy and DDIs among DOAC users, focusing on patients with atrial fibrillation (AF).
Methods:
A retrospective cohort analysis was conducted using administrative health care data from the Caserta Local Health Unit (2012-2020). Incident DOAC users were categorized by type of anticoagulant (apixaban, dabigatran, rivaroxaban, and edoxaban). Polypharmacy and DDIs were analyzed before and after index date (ID), stratifying results by DOAC and therapeutic indication. The impact of DDIs on safety outcomes, particularly bleeding risk, was assessed. Bleeding outcomes were evaluated within 1 year after ID by multivariate regression models.
Findings:
Among 16,367 incident DOAC users, 68.9% were treated for AF. The number of interacting drugs increased in 55.2% of patients, with a higher prevalence of 3+ interacting drugs in low-dose users (35% vs 29.2% in high-dose users; P < 0.05). Before ID, 35.6% of the overall cohort had 0 interacting drugs compared with 15.2% after ID. Dabigatran users had the highest increase in interacting drugs (61.8%) compared with anti-Xa agents (56%). Patients with 6+ interacting drugs exhibited a 2.5% incidence of major bleeding after ID. Dabigatran use and low-dose DOAC regimens were independently associated with increased bleeding risks.
Implications:
Polypharmacy and DDIs are prevalent among real-world DOAC users, particularly in patients with AF. The observed association between DDIs and bleeding risk underscores the importance of personalized medication management strategies and routine DDI evaluations to optimize DOAC safety.
Related Concept Videos
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
Anticoagulant Drugs: Low-Molecular-Weight Heparins
Venous Thrombosis III: Interprofessional Care
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
Factors Affecting Protein-Drug Binding: Drug Interactions
Displacement interactions can have varying outcomes, ranging from toxicity to virtually...
Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers
Class 1A Antiarrhythmic Drugs: These drugs work by moderately blocking sodium channels,...

