Anterolateral Myocardial Infarction
Related entities
Findings (27)
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90
None
adverseMI patients with aortic stenosis receiving both DAPT and oral anticoagulant therapy had substantially increased bleeding risk compared to MI patients without AS on DAPT alone, suggesting additive effe
Effect: adverse; HR 2.47; CI: 95% CI 1.56-3.90