Can tranexamic acid (TXA) stop a gastrointestinal (GI) bleed?

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Last updated: October 14, 2025View editorial policy

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Tranexamic Acid for Gastrointestinal Bleeding

Tranexamic acid (TXA) should not be used for the treatment of gastrointestinal bleeding due to lack of benefit and increased risk of thromboembolic events. 1, 2

Evidence Against TXA Use in GI Bleeding

  • High-dose intravenous tranexamic acid shows no benefit in reducing mortality or rebleeding in gastrointestinal bleeding, based on high-certainty evidence from the HALT-IT trial 1, 2
  • The HALT-IT trial, a large international randomized controlled trial with 12,009 patients, found no reduction in death due to bleeding within 5 days (RR 0.99,95% CI 0.82-1.18) 2
  • TXA significantly increased the risk of venous thromboembolic events (deep vein thrombosis or pulmonary embolism) compared to placebo (RR 1.85,95% CI 1.15-2.98) 2
  • The British Society of Gastroenterology suggests that use of TXA in acute lower GI bleeding should be confined to clinical trials only 3
  • The European Association for the Study of the Liver strongly recommends against using TXA in patients with cirrhosis and active variceal bleeding 1

Management Recommendations for GI Bleeding

  • Standard management with resuscitation, endoscopic therapy, and pharmacological treatments should be prioritized for all GI bleeding 1
  • For upper GI bleeding, proton pump inhibitors and prompt endoscopic intervention remain the cornerstone of treatment 3
  • For variceal bleeding, standard therapy with vasoactive drugs, antibiotics, and endoscopic band ligation should be used instead of TXA 1
  • All hospitals should have a GI bleeding lead and agreed pathways for the management of acute lower GI bleeding 3
  • Hospitals that routinely admit patients with lower GI bleeding should have access to 7-day on-site colonoscopy and facilities to provide endoscopic therapy 3

Special Considerations

  • While TXA has proven benefits in trauma and surgical bleeding (with a loading dose of 1g over 10 minutes followed by 1g over 8 hours when given within 3 hours of injury), this benefit does not translate to GI bleeding 3, 1
  • Some older, smaller studies suggested potential benefits of TXA in GI bleeding 4, 5, but these have been superseded by the high-quality HALT-IT trial 2
  • Low-dose or enteral TXA administration has been studied with some promising results 1, 6, but current evidence is insufficient to recommend this approach outside of clinical trials

Potential Pitfalls

  • Do not extrapolate the benefits of TXA seen in trauma and surgical bleeding to GI bleeding scenarios, as the pathophysiology differs significantly 1
  • Avoid using TXA in patients with liver cirrhosis and variceal bleeding due to increased risk of thrombotic complications 1
  • For patients on direct oral anticoagulants (DOACs) with GI bleeding, focus on withholding the anticoagulant and considering reversal agents rather than adding TXA 3
  • Be aware that TXA administration more than 3 hours after injury in trauma settings is associated with increased mortality, suggesting timing is critical when TXA is indicated 3

In conclusion, current high-quality evidence does not support the use of tranexamic acid for GI bleeding management, and its use may increase thromboembolic risk.

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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