Is tranexamic acid (TXA) helpful for gastrointestinal (GI) bleeding?

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Last updated: December 23, 2025View editorial policy

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Tranexamic Acid for Gastrointestinal Bleeding

High-dose intravenous tranexamic acid should NOT be used for gastrointestinal bleeding—it provides no mortality or rebleeding benefit and significantly increases thromboembolic complications. 1, 2

Evidence Against High-Dose IV TXA

The most definitive evidence comes from the HALT-IT trial and subsequent meta-analyses showing high-dose IV TXA (1g loading dose followed by 3g over 24 hours) fails to improve outcomes:

  • No mortality reduction (RR 0.98,95% CI 0.88-1.09) 1, 3
  • No reduction in rebleeding (RR 0.92,95% CI 0.82-1.04) 1, 3
  • No reduction in need for surgery (RR 0.91,95% CI 0.76-1.09) 1

Critically, high-dose IV TXA increases serious harms:

  • Deep venous thrombosis increased 2-fold (RR 2.01,95% CI 1.08-3.72) 2, 3
  • Pulmonary embolism increased 78% (RR 1.78,95% CI 1.06-3.0) 2, 3
  • Seizure risk increased 73% (RR 1.73,95% CI 1.03-2.93) 3

Guideline Recommendations

The American College of Gastroenterology explicitly does not recommend high-dose IV TXA for gastrointestinal bleeding due to lack of benefit and increased thrombotic risk. 1

The British Society of Gastroenterology recommends confining TXA use in acute lower GI bleeding to clinical trials only. 1, 2

Special Populations Where TXA Must Be Avoided

Cirrhotic patients with variceal bleeding: The European Association for the Study of the Liver provides a strong recommendation against TXA use in this population due to lack of benefit and increased venous thromboembolism risk. 1, 2 Standard therapy with vasoactive drugs, antibiotics, and endoscopic band ligation should be used instead. 1

Exception—Hereditary Hemorrhagic Telangiectasia (HHT): TXA is recommended only for mild GI bleeding in HHT patients; for moderate-to-severe bleeding requiring transfusion, systemic bevacizumab is preferred. 1

Low-Dose TXA: Insufficient Evidence

While some older, smaller studies suggest low-dose IV or enteral TXA may reduce rebleeding (RR 0.5,95% CI 0.33-0.75) and need for surgery (RR 0.58,95% CI 0.38-0.88), this evidence is of moderate certainty only. 1, 3

Critical caveat: These studies predate modern endoscopic techniques and proton pump inhibitor use, limiting their applicability to current practice. 4 More research is needed before low-dose TXA can be recommended as rescue therapy. 1

What to Do Instead

Prioritize standard evidence-based management:

  • Resuscitation with restrictive transfusion strategy (target hemoglobin 7-9 g/dL in upper GI bleeding) 1
  • Early endoscopic intervention for diagnosis and treatment 2
  • Appropriate pharmacological therapy (proton pump inhibitors for non-variceal bleeding, vasoactive drugs for variceal bleeding) 1
  • For patients on anticoagulants: interrupt DOACs at presentation; consider specific reversal agents (idarucizumab, andexanet) for life-threatening hemorrhage 2

Common Pitfall to Avoid

Do not extrapolate TXA's proven benefits in trauma and surgical bleeding to GI bleeding—disease-specific evidence clearly shows no benefit and significant harm in the GI bleeding context. 1

References

Guideline

Tranexamic Acid for Gastrointestinal Bleeding

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Tranexamic Acid for Gastrointestinal Bleeding

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Systematic review: tranexamic acid for upper gastrointestinal bleeding.

Alimentary pharmacology & therapeutics, 2008

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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