Recommended Anticoagulation Regimens for Atrial Fibrillation, DVT, and PE
Direct oral anticoagulants (DOACs) such as apixaban, dabigatran, edoxaban, or rivaroxaban are the first-line therapy for atrial fibrillation, DVT, and PE due to their efficacy, safety profile, and convenience compared to traditional vitamin K antagonists. 1
Atrial Fibrillation Anticoagulation
Patient Selection and Risk Assessment
- Anticoagulation is indicated for patients with nonvalvular atrial fibrillation at intermediate or high risk of stroke (CHADS₂ score ≥1) 2
- For valvular atrial fibrillation (particularly with mechanical heart valves), vitamin K antagonists (warfarin) remain the only recommended option 3
First-line Therapy for Nonvalvular AF
- DOACs are preferred over warfarin for stroke prevention in nonvalvular AF 1, 3
- Recommended DOAC options:
- Apixaban: 5 mg twice daily (2.5 mg twice daily if ≥2 of: age ≥80 years, weight ≤60 kg, serum creatinine ≥1.5 mg/dL) 4
- Dabigatran: 150 mg twice daily (110 mg twice daily for high bleeding risk)
- Rivaroxaban: 20 mg daily with food (15 mg daily if CrCl 15-50 mL/min)
- Edoxaban: 60 mg daily (30 mg daily if CrCl 15-50 mL/min or weight ≤60 kg)
Second-line Therapy
- Warfarin with target INR 2.0-3.0 (if DOACs contraindicated or not tolerated) 5
- Regular INR monitoring required
Deep Vein Thrombosis (DVT) and Pulmonary Embolism (PE)
Initial Treatment
For most patients with DVT or PE, DOACs that don't require initial parenteral therapy are preferred:
Alternative approach (requires overlap):
Special Considerations for PE
- For PE with hypotension (systolic BP <90 mmHg) and low bleeding risk: systemic thrombolytic therapy 5
- For high-risk PE without hypotension but at risk of deterioration: consider thrombolysis 5
- For PE with contraindications to anticoagulation: IVC filter placement 5
- For PE with hypotension and contraindications to thrombolysis: consider catheter-assisted thrombus removal or surgical pulmonary embolectomy if expertise available 5
Cancer-Associated Thrombosis
- LMWH is traditionally preferred over warfarin 5, 1
- Enoxaparin: 1 mg/kg twice daily or 1.5 mg/kg once daily
- Dalteparin: 200 U/kg once daily for first month, then 150 U/kg once daily
- Growing evidence supports DOACs in select cancer patients with low bleeding risk 3
Duration of Anticoagulation
DVT/PE Provoked by Surgery
- 3 months of anticoagulation (not shorter, not longer) 5
DVT/PE Provoked by Nonsurgical Transient Risk Factor
- 3 months of anticoagulation 5
- Extended therapy not recommended, especially with high bleeding risk
Unprovoked DVT/PE
- Minimum 3 months of anticoagulation 5
- First unprovoked event:
- Second unprovoked event:
Cancer-Associated DVT/PE
- Extended anticoagulation recommended while cancer is active 5
- Annual reassessment of risk-benefit ratio 5
Practical Considerations
Monitoring
- DOACs: No routine coagulation monitoring required
- Warfarin: Regular INR monitoring to maintain 2.0-3.0 5
- Baseline testing: CBC, renal/hepatic function, aPTT, PT/INR 1
Bleeding Management
- Major bleeding on warfarin: Vitamin K and 4-factor prothrombin complex concentrate 3
- Dabigatran reversal: Idarucizumab
- Rivaroxaban/apixaban reversal: Andexanet alfa 3
Drug Interactions
- Avoid combining DOACs with strong P-gp inducers like phenytoin 6
- For patients requiring phenytoin who need anticoagulation, warfarin is preferred 6
Perioperative Management
- Warfarin: Stop 5 days before major surgery, restart 12-24 hours after 7
- DOACs: Generally stop 24-48 hours before procedures (timing depends on renal function and bleeding risk)
- Bridging therapy decisions based on thromboembolism vs. bleeding risk 7
Remember that anticoagulation therapy requires regular assessment of bleeding risk, and the continuing use of extended therapy should be reassessed periodically (e.g., annually) 5.