Management of Apixaban (Eliquis) Before Colonoscopy
For patients on apixaban (Eliquis), the medication should be discontinued at least 48 hours prior to colonoscopy if polypectomy or other high-risk endoscopic procedures may be performed. 1
Risk Stratification for Endoscopic Procedures
Low-Risk Procedures
- Diagnostic colonoscopy with biopsies
- Biliary or pancreatic stenting
- Device-assisted enteroscopy without polypectomy
For low-risk procedures, the British Society of Gastroenterology (BSG) and European Society of Gastrointestinal Endoscopy (ESGE) guidelines suggest:
- Simply omit the morning dose of apixaban on the day of the procedure 1
- No bridging anticoagulation is required
High-Risk Procedures
- Polypectomy
- Endoscopic mucosal resection (EMR)
- Endoscopic submucosal dissection (ESD)
- Dilation of strictures
- Endoscopic ultrasound with fine needle aspiration
For high-risk procedures such as colonoscopy with potential polypectomy:
- Last dose of apixaban should be taken at least 48 hours before the procedure 1
- For patients with impaired renal function (CrCl 30-50 mL/min), extend this to 72 hours 1
- For patients with severely impaired renal function, hematology consultation is recommended
Special Considerations
Renal Function
Renal function significantly affects the clearance of apixaban:
- Normal renal function (CrCl ≥50 mL/min): Discontinue 48 hours before high-risk procedures
- Moderate renal impairment (CrCl 30-50 mL/min): Discontinue 72 hours before high-risk procedures
- Severe renal impairment (CrCl <30 mL/min): Consult hematology 2
Thrombotic Risk Assessment
The management strategy should consider the patient's thrombotic risk:
- Low thrombotic risk: Follow standard discontinuation protocol
- High thrombotic risk (e.g., recent venous thromboembolism, mechanical heart valve): Consider hematology consultation for potential bridging therapy
Post-Procedure Management
- Resume apixaban up to 48 hours after the procedure depending on the bleeding and thrombotic risks 1
- For most cases, apixaban can be restarted as soon as adequate hemostasis has been established 3
- The FDA label specifically states: "Apixaban tablets should be restarted after surgical or other procedures as soon as adequate hemostasis has been established" 3
Bleeding Risk Considerations
The risk of post-polypectomy bleeding is increased in patients on anticoagulants:
- Overall risk of post-polypectomy bleeding is <0.5% in general population 4
- Risk increases with anticoagulant use, especially with direct oral anticoagulants
- Patients should be advised of this increased bleeding risk 1
Common Pitfalls to Avoid
- Inadequate discontinuation time: Failing to stop apixaban early enough before high-risk procedures
- Unnecessary bridging: Unlike warfarin, apixaban generally does not require bridging with heparin due to its shorter half-life 1
- Delayed resumption: Unnecessarily delaying anticoagulant resumption increases thrombotic risk
- Failure to adjust timing based on renal function: Patients with impaired renal function need longer discontinuation periods
- Not communicating with cardiologists: For patients at high thrombotic risk, consultation with cardiology may be necessary
By following these evidence-based guidelines, the risk of both bleeding complications and thromboembolic events can be minimized for patients on apixaban undergoing colonoscopy.