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Published on: February 28, 2012
Antithrombotic Therapy and First Myocardial Infarction in Patients With Atrial Fibrillation
Christina J-Y Lee1, Jannik L Pallisgaard2, Jonas Bjerring Olesen3
1Department of Health Science and Technology, Aalborg University, and Department of Clinical Epidemiology and Cardiology, Aalborg University Hospital, Aalborg, Denmark; Department of Cardiology, Copenhagen University Hospital Gentofte, Hellerup, Denmark.
Insights
Vitamin K antagonist (VKA) monotherapy is superior to acetylsalicylic acid (ASA) monotherapy for preventing myocardial infarction (MI) and stroke in atrial fibrillation (AF) patients. Dual therapy with VKA and ASA increases bleeding risk without reducing MI risk.
Area of Science:
- Cardiology
- Pharmacology
- Public Health
Background:
- Patients with atrial fibrillation (AF) face elevated risks of thromboembolic events, including stroke and myocardial infarction (MI).
- While anticoagulation is proven superior to antiplatelet agents for stroke prevention in AF, optimal antithrombotic strategies for primary MI protection remain unclear.
Purpose of the Study:
- To investigate the incidence of first-time MI in AF patients based on antithrombotic treatment.
- To estimate the associated risks of stroke and bleeding in relation to different antithrombotic therapies.
Main Methods:
- Utilized Danish nationwide administrative registries to identify patients with first-time AF from 1997-2012, excluding those with prior coronary artery disease.
- Categorized subjects into time-varying exposure groups based on antithrombotic treatment (VKA monotherapy, ASA monotherapy, VKA + ASA dual therapy).
- Employed Poisson regression models to estimate relative risks of MI, stroke, and bleeding.
Main Results:
- Compared to VKA monotherapy, acetylsalicylic acid (ASA) monotherapy showed a significantly higher risk of MI (IRR: 1.54) and stroke (IRR: 2.00).
- Dual therapy (VKA + ASA) also presented a higher risk of MI (IRR: 1.22) and stroke (IRR: 1.30) compared to VKA monotherapy.
- Dual therapy significantly increased bleeding risk (IRR: 1.93) without conferring additional MI protection.
Conclusions:
- Vitamin K antagonist (VKA) monotherapy is associated with lower risks of first-time MI and stroke compared to ASA monotherapy in AF patients.
- Combining VKA with ASA does not reduce MI risk and elevates the risk of bleeding.
Background:
Patients with atrial fibrillation (AF) have increased risk of thromboembolic events such as stroke and myocardial infarction (MI). Although it has been established that the efficacy of anticoagulation is superior to that of antiplatelet agents for stroke prophylaxis in AF, the optimal antithrombotic treatment remains uncertain for primary protection against MI.
Objectives:
The authors investigated the incidence of first-time MI in patients with AF according to antithrombotic treatment and estimated the risk of stroke and bleeding.
Methods:
Subjects with first-time AF diagnosed from 1997 to 2012 without history of coronary artery disease were identified using Danish nationwide administrative registries. Subjects were divided into time varying exposure groups according to antithrombotic treatment. The relative risks of outcomes were estimated by Poisson regression models.
Results:
A total of 71,959 patients (median 75 years of age; females: 47%). At baseline, 37,539 patients (52%) were treated with vitamin K antagonist (VKA) monotherapy, 25,458 (35%) with acetylsalicylic acid (ASA) monotherapy and 8,962 (13%) with dual-therapy (VKA + ASA). The incidence of MI was 3% (n = 2,275). Relative to the VKA-treated group, the associated risk of MI was significantly higher for ASA (incidence rate ratio [IRR]: 1.54; 95% confidence interval [CI]: 1.40 to 1.68) and dual-therapy (IRR: 1.22; 95% CI: 1.06 to 1.40). The bleeding risk was significantly higher for dual-therapy (IRR: 1.93; 95% CI: 1.81 to 2.07). The risk of stroke relative to that of VKA therapy was significantly higher for both ASA (IRR: 2.00; 95% CI: 1.88 to 2.12) and dual-therapy (IRR: 1.30; 95% CI: 1.18 to 1.43).
Conclusions:
VKA monotherapy in patients with AF was associated with a lower risk of first-time MI and stroke than ASA monotherapy. Combination of ASA and VKA therapy was not associated with a lower risk of MI but was associated with increased bleeding risk.
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