ArticleHeart rhythm O22026
Drug-drug interactions of NOACs with comedication: Prevalence and implications for adverse events in patients with atrial fibrillation.
Article in Heart rhythm O2, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02105844 (Swiss Atrial Fibrillation Cohort Study - SWISS AF), which is not on this map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Swiss Atrial Fibrillation Cohort Study - SWISS AF
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Authors and funding
26 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: The clinical relevance of drug-drug interactions associated with non‒vitamin K-antagonist oral anticoagulants (NOACs) in patients with atrial fibrillation (AF) remains poorly understood. Objective: We evaluated the prevalence of pharmacokinetic and pharmacodynamic drug-drug interactions and their association with adverse clinical outcomes in patients with AF receiving NOACs. Methods: We analyzed patients from the prospective, multicenter Swiss-AF cohort study. We used frailty survival models to investigate the association of the different potential interactions with the respective clinical adverse outcomes (major bleeding, clinically relevant non-major bleeding, any bleeding, ischemic stroke or systemic embolism). Results: Our analysis comprised 1732 patients with AF (mean age 73 ± 8 years, 501 [29%] women) with a median follow-up period of 6 years. For 683 of these patients (39%), we recorded ≥1 potential drug-drug interaction. In the multivariable adjusted model, the hazard ratio of drug-drug interaction was 1.21 (95% confidence interval [CI] 0.84-1.75, Conclusion: In a large real-world cohort of patients with AF, the prevalence of potential interactions of long-term comedication with NOACs was high. We found no strong evidence of an association between these interactions and an increased risk of bleeding or the composite outcome ischemic stroke or systemic embolism. Registration: Clinical Trial Registration: https://clinicaltrials.gov/ct2/show/NCT02105844. ClinicalTrialsgov Identifier: NCT02105844.
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