What is the recommended dose of Eliquis (apixaban) for patients with atrial fibrillation?

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Apixaban Dosing for Atrial Fibrillation

The standard dose of apixaban for atrial fibrillation is 5 mg orally twice daily, with dose reduction to 2.5 mg twice daily ONLY when patients meet at least TWO of the following criteria: age ≥80 years, body weight ≤60 kg, or serum creatinine ≥1.5 mg/dL. 1, 2, 3

Standard Dosing Algorithm

  • Start with 5 mg twice daily for the vast majority of patients with nonvalvular atrial fibrillation, as this regimen demonstrated a 21% reduction in stroke or systemic embolism (HR 0.79,95% CI 0.66-0.95) and a 31% reduction in major bleeding compared to warfarin in the ARISTOTLE trial 4, 2

  • No loading dose or bridging anticoagulation is required when initiating apixaban 4

Dose Reduction Criteria: The "Two Out of Three" Rule

Reduce to 2.5 mg twice daily ONLY when ≥2 of these are present: 1, 2, 3

  • Age ≥80 years
  • Body weight ≤60 kg
  • Serum creatinine ≥1.5 mg/dL

Critical pitfall: In real-world practice, approximately 60% of patients receiving reduced-dose apixaban do not actually meet the criteria for dose reduction 5. Clinicians frequently underdose based on a single criterion (particularly age alone), which is incorrect and may expose patients to inadequate stroke protection 5. You must have TWO criteria present, not just one.

Renal Function Considerations

  • CrCl >30 mL/min: Apply the standard dosing algorithm above (5 mg twice daily unless ≥2 dose-reduction criteria met) 1, 2

  • CrCl 15-30 mL/min: Use 5 mg twice daily unless ≥2 dose-reduction criteria are met, then use 2.5 mg twice daily 1, 2

  • End-stage renal disease on hemodialysis: Start with 5 mg twice daily, reducing to 2.5 mg twice daily ONLY if age ≥80 years OR body weight ≤60 kg (note: only ONE criterion needed in dialysis patients, not two) 4, 2

  • CrCl <15 mL/min NOT on dialysis: Apixaban is contraindicated 4, 3

  • CrCl >95 mL/min: Edoxaban is contraindicated in this range, but apixaban 5 mg twice daily remains appropriate 1

Special Clinical Scenarios

Prior Stroke or TIA

  • Use the same dosing algorithm as for patients without prior stroke—the benefit of apixaban is independent of stroke history 4, 2
  • Recent data suggest patients with subclinical atrial fibrillation and prior stroke/TIA derive greater absolute benefit from apixaban (7% absolute risk reduction over 3.5 years) compared to those without prior stroke (1% absolute risk reduction) 6

Concurrent Antiplatelet Therapy

  • After coronary intervention, use apixaban with clopidogrel (NOT aspirin) after a brief periprocedural period to reduce bleeding risk while maintaining efficacy 4, 2
  • The AUGUSTUS trial demonstrated that appropriately reduced-dose apixaban (when dose-reduction criteria met) had similar safety and efficacy to standard-dose apixaban in patients with recent ACS or PCI 7

Monitoring Requirements

  • Assess renal function before starting and at least annually thereafter, with more frequent monitoring (every 3-6 months) if CrCl 30-50 mL/min or other risk factors for deterioration present 4, 2

  • No routine coagulation monitoring (INR, aPTT) is required 1, 4

  • Evaluate body weight periodically, particularly in patients near the 60 kg threshold, as weight changes may affect dose-reduction criteria 2

  • Assess clinically for signs of bleeding or thromboembolism at follow-up visits 1, 2

Switching Between Anticoagulants

From Warfarin to Apixaban

  • Discontinue warfarin and start apixaban when INR falls below 2.0—no bridging therapy needed 4, 3

From Apixaban to Warfarin

  • Discontinue apixaban and begin BOTH parenteral anticoagulant AND warfarin at the time of the next scheduled apixaban dose, continuing parenteral anticoagulant until INR reaches therapeutic range 4, 3

From Other DOACs to Apixaban

  • Simply discontinue the other DOAC and start apixaban at the time the next dose of the previous DOAC would have been due 4

Perioperative Management

  • Discontinue at least 48 hours prior to elective surgery with moderate or high bleeding risk 3

  • Discontinue at least 24 hours prior to procedures with low bleeding risk or where bleeding would be easily controlled 3

  • Restart as soon as adequate hemostasis is established after the procedure 3

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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