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Published on: February 28, 2012
Warfarin for stroke prevention following anterior ST-elevation myocardial infarction
Nicholas I Buss1, Scott E Friedman, Bruce W Andrus
1Department of Cardiology, The Geisel School of Medicine at Dartmouth/Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA.
Insights
Vitamin K antagonist (VKA) therapy did not significantly reduce ischemic stroke risk after anterior ST-elevation myocardial infarction (STEMI) in patients with reduced ejection fraction. Routine anticoagulation may not be necessary for stroke prevention in this population.
Area of Science:
- Cardiology
- Neurology
- Pharmacology
Background:
- Anterior ST-elevation myocardial infarction (STEMI) survivors with reduced ejection fraction are at risk for ischemic stroke.
- The role of vitamin K antagonist (VKA) therapy in preventing stroke in this specific patient group remains unclear.
- Existing guidelines do not uniformly recommend anticoagulation for stroke prevention post-STEMI in patients with preserved or mildly reduced ejection fraction.
Purpose of the Study:
- To evaluate the efficacy of VKA therapy in preventing ischemic stroke in patients with anterior STEMI and reduced ejection fraction (≤40%).
- To assess the composite outcome of ischemic stroke, death, and clinically relevant bleeding in patients receiving VKA therapy versus those not receiving it.
- To investigate the impact of low-molecular-weight heparin bridging therapy in conjunction with VKA.
Main Methods:
- Prospective registry of anterior STEMI survivors with ejection fraction ≤40% over a 10-year period.
- Comparison of outcomes based on VKA use, including ischemic stroke, death, and bleeding.
- Secondary analysis of low-molecular-weight heparin bridging therapy effects.
Main Results:
- The primary composite outcome occurred in 24.7% of VKA users and 20.5% of non-VKA users (adjusted HR, 1.30; 95% CI, 0.71-2.31).
- Ischemic stroke rates were 2.5% in VKA patients and 0.9% in non-VKA patients (adjusted HR, 2.81; 95% CI, 0.31-25.1).
- Low-molecular-weight heparin bridging therapy was associated with increased bleeding events (adjusted HR, 2.55; 95% CI, 1.04-6.24).
Conclusions:
- Ischemic stroke was infrequent within 6 months post-anterior STEMI, regardless of VKA treatment.
- Routine anticoagulation with VKA therapy may not be beneficial for stroke prevention in this patient cohort.
- Further research is needed to define optimal antithrombotic strategies for anterior STEMI survivors with reduced ejection fraction.
Objectives:
To assess the benefit of vitamin K antagonist (VKA) therapy for prevention of ischemic stroke following anterior ST-elevation myocardial infarction (STEMI) in patients with reduced ejection fraction.
Methods:
A prospective institutional-based registry was used to identify survivors of anterior STEMI with a post-STEMI ejection fraction of 40% or less over a 10-year period. Clinical and procedural characteristics were collected from medical records and vital status from the Social Security Death Index. Outcomes were compared on the basis of VKA use. The primary outcome was a composite of ischemic stroke, death, and clinically relevant bleeding. A secondary analysis examined the effects of low-molecular-weight heparin bridging therapy.
Results:
The primary outcome occurred in 24.7% (40/162) of VKA patients and 20.5% (22/107) of non-VKA patients [adjusted hazard ratio (HR), 1.30; 95% confidence interval (CI), 0.71-2.31]. Ischemic stroke occurred in 2.5 and 0.9% of VKA patients and non-VKA patients, respectively (adjusted HR, 2.81; 95% CI, 0.31-25.1). There was no significant difference in the rate of bleeding or death between groups. The addition of a low-molecular-weight heparin bridge to VKA therapy was associated with increased bleeding events (adjusted HR, 2.55; 95% CI, 1.04-6.24).
Conclusion:
Ischemic stroke was infrequent in the 6 months following anterior STEMI irrespective of VKA treatment status. The routine use of anticoagulation for prevention of stroke following anterior STEMI may not be warranted.
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