What is the role of tranexamic acid (TXA) in the management of upper gastrointestinal bleeding (UGIB)?

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Last updated: November 23, 2025View editorial policy

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Tranexamic Acid Should NOT Be Used for Upper Gastrointestinal Bleeding

Tranexamic acid is not recommended for the management of upper gastrointestinal bleeding and should be confined to clinical trials only. The British Society of Gastroenterology explicitly states that despite earlier promising data, tranexamic acid lacks evidence supporting its efficacy in modern GI bleeding management and is associated with increased thromboembolic risk 1, 2.

Why Tranexamic Acid Is Not Recommended

Evidence Quality Issues

  • Historical studies are not applicable to current practice because they were conducted before the routine use of high-dose proton pump inhibitors and modern endoscopic therapy, making their extrapolation to contemporary care uncertain 1.

  • Earlier meta-analyses showing 40% mortality reduction disappeared when limited to high-quality trials with low risk of bias, as noted by the British Society of Gastroenterology 1.

  • Recent high-quality evidence demonstrates no significant benefit: tranexamic acid shows no reduction in mortality (RR 0.98,95% CI 0.88-1.09) or rebleeding rates (RR 0.92,95% CI 0.82-1.04) 2.

Safety Concerns

  • Tranexamic acid significantly increases thromboembolic risk, including deep venous thrombosis (RR 2.01,95% CI 1.08-3.72) and pulmonary embolism (RR 1.78,95% CI 1.06-3.0) 2.

  • The European Association for the Study of the Liver strongly recommends against using tranexamic acid in patients with cirrhosis and active variceal bleeding due to unfavorable risk-benefit profile 2.

What Should Be Used Instead

Pharmacologic Management

  • High-dose intravenous PPI therapy is the cornerstone: patients with bleeding ulcers and high-risk stigmata who have successful endoscopic therapy should receive IV loading dose followed by continuous infusion for 3 days 3.

  • Continue oral PPI therapy twice daily through 14 days, then once daily for total duration depending on the bleeding lesion nature 3.

Endoscopic Management

  • Perform endoscopy within 24 hours of presentation for diagnosis and treatment 3, 2.

  • Use thermocoagulation, sclerosant injection, or clips for high-risk stigmata - these are the recommended endoscopic hemostasis methods 3.

  • Epinephrine injection alone is not recommended - it must be combined with another modality 3.

Risk Stratification

  • Use Glasgow Blatchford score of 1 or less to identify very low-risk patients who may not require hospitalization 3.

  • High-risk patients should be hospitalized for at least 72 hours after endoscopic hemostasis 3.

Common Pitfalls to Avoid

  • Do not use tranexamic acid based on older meta-analyses - these included methodologically flawed studies from the pre-PPI and pre-modern endoscopy era 1.

  • Do not extrapolate trauma bleeding data to GI bleeding - despite proven efficacy in trauma-related bleeding, the evidence does not support tranexamic acid use in GI bleeding 1.

  • Hospital pathways for acute GI bleeding management should not routinely include tranexamic acid, as recommended by the British Society of Gastroenterology 1, 2.

References

Guideline

Tranexamic Acid in 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

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 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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