Should Eliquis (apixaban) be discontinued before a colonoscopy?

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Last updated: September 23, 2025View editorial policy

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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

  1. Inadequate discontinuation time: Failing to stop apixaban early enough before high-risk procedures
  2. Unnecessary bridging: Unlike warfarin, apixaban generally does not require bridging with heparin due to its shorter half-life 1
  3. Delayed resumption: Unnecessarily delaying anticoagulant resumption increases thrombotic risk
  4. Failure to adjust timing based on renal function: Patients with impaired renal function need longer discontinuation periods
  5. 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.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Regional Anesthesia and Anticoagulation Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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