Stopping Apixaban Before Colonoscopy
For colonoscopy with polypectomy (high bleeding risk), stop apixaban 48 hours (2 days) before the procedure in patients with normal or mildly impaired renal function (CrCl ≥50 mL/min), which allows 4 half-lives to elapse and reduces residual anticoagulant effect to approximately 6%. 1, 2
Preoperative Discontinuation Strategy
Standard Renal Function (CrCl ≥50 mL/min)
- Colonoscopy with biopsy only (low-moderate risk): Stop apixaban 24 hours (1 day) before the procedure, skipping 2 doses if taking twice daily 1, 2
- Colonoscopy with polypectomy (high bleeding risk): Stop apixaban 48 hours (2 days) before the procedure, skipping 4 doses 1, 2, 3
- The FDA label specifically states apixaban should be discontinued at least 48 hours prior to elective surgery or invasive procedures with moderate or high risk of bleeding 3
Moderate Renal Impairment (CrCl 30-50 mL/min)
- High bleeding risk procedures: Extend discontinuation to 72 hours (3 days) before colonoscopy with polypectomy 4, 1
- Apixaban has 25% renal clearance, and moderate renal dysfunction prolongs the half-life to approximately 10-12 hours, necessitating longer interruption 1, 2
Severe Renal Impairment (CrCl <30 mL/min)
- Minimum 72 hours discontinuation is required, though evidence in this population is limited 1
- Consider drug-specific anti-Xa level measurement to confirm adequate clearance before proceeding 1
Critical Considerations
Bleeding Risk Classification
- High bleeding risk includes polypectomy, sphincterotomy, laser therapy, mucosal ablation, and variceal treatment 4, 5
- Low-moderate bleeding risk includes diagnostic colonoscopy with biopsy only 4, 1
- Research demonstrates that polypectomy carries a 2.2% bleeding risk overall, with warfarin increasing this risk 13-fold 6
Bridging Anticoagulation
- Do not use heparin or LMWH bridging during the apixaban interruption period 1, 2, 3
- The FDA label explicitly states "bridging anticoagulation during the 24 to 48 hours after stopping apixaban and prior to the intervention is not generally required" 3
- High-quality evidence from the PAUSE trial showed bridging increases major bleeding risk (2-5%) without reducing thrombotic events 2
- The only exception would be extremely high thrombotic risk situations (mechanical mitral valve, stroke within past month) requiring multidisciplinary review 2
Postoperative Resumption
Timing Based on Procedure Risk
- Diagnostic colonoscopy or simple biopsy: Resume apixaban 24 hours after the procedure at the usual dose (5 mg twice daily), ensuring at least 6 hours have elapsed and adequate hemostasis is established 1, 2, 3
- Colonoscopy with polypectomy: Resume apixaban 48-72 hours after the procedure once hemostasis is confirmed 1, 2
- For high thrombotic risk patients, consider reduced dose (2.5 mg twice daily) for the first 2-3 days, then return to full dose 1, 2
Safety Considerations
- Apixaban reaches peak effect within 1-3 hours of administration, so premature resumption can precipitate bleeding 1
- Research shows that resuming anticoagulation 1 day post-polypectomy did not significantly increase bleeding rates in retrospective series 7
- If therapeutic apixaban must be delayed beyond 48 hours in high thrombotic risk patients, use prophylactic-dose LMWH for the first 2-3 days 2
Common Pitfalls and Caveats
Laboratory Monitoring
- Do not use INR or aPTT to guide timing—these tests are insensitive to apixaban effect 1, 2
- Anti-factor Xa assays correlate with apixaban exposure but are not needed when standardized interruption protocols are followed 1, 2
Renal Function Assessment
- Mandatory calculation of creatinine clearance before determining interruption length, as moderate-to-severe impairment significantly prolongs apixaban elimination 1, 2
- Patients with declining renal function require extended preoperative interruption even if baseline function was acceptable 1
Timing Errors
- Excessively long interruption (>3-4 days in normal renal function) raises thromboembolic risk without additional bleeding protection 1
- Premature resumption before adequate hemostasis markedly increases major bleeding risk without lowering thrombotic events 2
- The British Society of Gastroenterology notes that polypectomy bleeding rates in anticoagulated patients (14-23%) far exceed rates in non-anticoagulated patients (0.07-1.7%) 4