Novel Oral Anticoagulants (NOACs) for Anticoagulation in Atrial Fibrillation, DVT, and PE
NOACs are recommended as first-line therapy over vitamin K antagonists for most patients with non-valvular atrial fibrillation, deep vein thrombosis, or pulmonary embolism due to their superior net clinical benefit, including comparable efficacy and improved safety profiles. 1
Recommendations for Atrial Fibrillation
Patient Assessment and Risk Stratification
- Use the CHA₂DS₂-VASc score to assess stroke risk in non-valvular AF 1
- For patients with CHA₂DS₂-VASc score ≥2 (men) or ≥3 (women), oral anticoagulation is strongly recommended 1
- For patients with CHA₂DS₂-VASc score of 1 (men) or 2 (women), oral anticoagulation should be considered based on bleeding risk and patient preferences 1
- Assess bleeding risk using the HAS-BLED score to identify modifiable risk factors 1
NOAC Selection
- Apixaban (5 mg twice daily) should be considered the preferred NOAC for most patients due to:
- Dabigatran 150 mg twice daily may be preferred for patients at high risk of ischemic stroke as it's the only agent with superior efficacy compared to warfarin 1
- For patients with high bleeding risk or prior gastrointestinal bleeding, apixaban or dabigatran 110 mg twice daily may be preferred 1
Dosing Considerations
- Apixaban: Reduce to 2.5 mg twice daily if patient has at least two of: age ≥80 years, weight ≤60 kg, or serum creatinine ≥1.5 mg/dL 1
- Rivaroxaban: Reduce to 15 mg once daily if CrCl 30-49 mL/min 1
- Dabigatran: Consider 110 mg twice daily for patients ≥80 years, concomitant verapamil use, high bleeding risk, or moderate renal impairment 1
- Edoxaban: Reduce to 30 mg once daily if weight ≤60 kg, CrCl ≤50 mL/min, or concomitant P-gp inhibitor therapy 1
Renal Function Monitoring
- Baseline and regular assessment of renal function is recommended for all patients on NOACs 1
- For patients with moderate renal impairment, check renal function 2-3 times per year 1
- NOACs are not recommended in patients with severe renal impairment (CrCl <30 mL/min for dabigatran, edoxaban, and rivaroxaban; <25 mL/min for apixaban) 1
Recommendations for DVT/PE Treatment
For acute DVT/PE treatment:
- Apixaban: 10 mg twice daily for 7 days, followed by 5 mg twice daily 1
- Rivaroxaban: 15 mg twice daily for 21 days, followed by 20 mg once daily 1
- Dabigatran: Initial parenteral anticoagulation (LMWH), followed by 150 mg twice daily 1
- Edoxaban: Initial parenteral anticoagulation, followed by 60 mg once daily (30 mg if CrCl ≤50 mL/min, weight ≤60 kg, or with P-gp inhibitors) 1
For extended treatment/secondary prevention:
- Consider reduced-dose apixaban (2.5 mg twice daily) or rivaroxaban (10 mg once daily) after 6 months of treatment 1
Special Clinical Scenarios
Cardioversion
- For AF >48 hours or unknown duration:
Perioperative Management
- For elective procedures with low bleeding risk:
- Discontinue NOACs 24 hours before procedure 1
- For procedures with high bleeding risk:
- Discontinue NOACs based on renal function: 2-4 days for most patients, longer for those with renal impairment 1
- Resume NOACs 24-72 hours post-procedure when surgical hemostasis is achieved 1
Bleeding Management
- For minor bleeding: Delay next dose or temporarily discontinue NOAC 1
- For moderate-severe bleeding: Consider activated charcoal if recent ingestion, supportive care, and specific reversal agents if available 1
- Reinitiation of anticoagulation after bleeding should be considered by a multidisciplinary team 1
Advantages of NOACs over Warfarin
- More predictable pharmacokinetics with fixed dosing 3
- No routine coagulation monitoring required 3, 4
- Fewer drug-food interactions 3
- Lower risk of intracranial hemorrhage 4, 2
- Rapid onset and offset of action 3, 5
Common Pitfalls and Caveats
- Patient adherence is crucial for NOACs due to their shorter half-lives compared to warfarin 6
- Once-daily regimens (rivaroxaban, edoxaban) may improve adherence but missing a dose has greater impact on anticoagulation 6
- NOACs are contraindicated in patients with mechanical heart valves or moderate-to-severe mitral stenosis 1
- Avoid combination of NOACs with antiplatelet therapy unless specifically indicated, as this significantly increases bleeding risk 1
- Regular assessment of renal function is essential as all NOACs have some degree of renal elimination 1