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Clinical context | NOAC | Other anticoagulant | Conclusion (NOACs versus other drugs) |
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VTE0 prophylaxis after orthopedic surgery | | | |
RE-MODEL | Dabigatran etexilate 150 or 220 mg OD | Enoxaparin 40 mg OD SC5 | Same efficacy and safety profile after TKR1 |
RE-NOVATE II | Dabigatran etexilate 220 mg OD | Enoxaparin 40 mg OD SC | Same profile in term of safety and bleeding after THR2 |
RECORD | Rivaroxaban 10 mg OD | Enoxaparin 40 mg OD SC | More effective, without increasing major bleeding after THR/TKR |
ADVANCE II | Apixaban 2.5 mg BID | Enoxaparin 40 mg OD SC | More effective without increased bleeding after TKR |
ADVANCE III | Apixaban 2.5 mg BID | Enoxaparin 40 mg OD SC | Lower rate of VTE without increased bleeding after THR |
Non-valvular atrial fibrillation | | | |
RE-LY3 | Dabigatran etexilate 110 mg or 150 mg BID | Adjusted dose warfarin (INR 2-3) | Efficacy superior for the prevention of stoke with a similar rate of major bleeding |
ROCKET-AF4 | Rivaroxaban daily dose 20 mg | Adjusted dose warfarin | Non-inferiority, no significant difference in term of bleeding |
ARISTOTLE | Apixaban 5 mg BID | Adjusted dose warfarin (INR 2-3) | Superior in preventing stroke or systemic embolism, less bleeding and lower mortality |
VTE Treatment | | | |
RE-COVER II | Dabigatran etexilate 150 mg BID after 5–11 days of LMWH6 or UFH7 | Warfarin | Similar effect on VTE recurrence, lower risk of bleeding for the treatment of acute VTE |
EINSTEIN | Rivaroxaban 15 mg BID for 3 weeks following by 20 mg OD | Enoxaparin SC following by vitamin K antagonist | Simple, single drug approach. Improve benefit-to-risk of anticoagulation |
Acute coronary syndrome | | | |
ATLAS ACS | Rivaroxaban 2.5 BID | Placebo | Reduced the composite endpoint of death from cardiovascular causes, myocardial infarction or stroke. No increase of fatal bleeding. |
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