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

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Last updated: May 25, 2025View editorial policy

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From the Guidelines

Tranexamic acid (TXA) should not be used to stop a GI bleed, especially in patients with cirrhosis and active variceal bleeding, due to the lack of beneficial effect and potential increased risk of venous thromboembolic events 1. When considering the use of TXA in GI bleeding, it's essential to weigh the potential benefits against the risks. While TXA has been shown to improve mortality from trauma and has some evidence for its benefit in acute GI bleeding 1, the most recent and highest quality study suggests that it does not have a beneficial effect in stopping GI bleeds, particularly in patients with cirrhosis and variceal bleeding 1. Some key points to consider when evaluating the use of TXA in GI bleeding include:

  • The mechanism of action of TXA, which involves inhibiting fibrinolysis and stabilizing blood clots
  • The potential side effects of TXA, including nausea, vomiting, diarrhea, and a theoretical risk of thromboembolic events
  • The lack of evidence supporting the use of TXA in lower GI bleeds
  • The potential increased risk of venous thromboembolic events associated with TXA use, particularly in patients with cirrhosis and variceal bleeding 1 In clinical practice, the decision to use TXA in GI bleeding should be made on a case-by-case basis, taking into account the individual patient's underlying condition, the severity of the bleeding, and the potential risks and benefits of treatment. However, based on the most recent and highest quality evidence, TXA should not be used as a first-line treatment for GI bleeding, especially in patients with cirrhosis and variceal bleeding 1.

From the Research

Efficacy of Tranexamic Acid in GI Bleeding

  • Tranexamic acid (TXA) has been studied as a potential treatment for gastrointestinal (GI) bleeding, with mixed results 2, 3, 4, 5, 6.
  • A 2021 systematic review and meta-analysis found that TXA significantly reduced the rates of continued bleeding, urgent endoscopic intervention, and mortality in patients with upper GI bleeding 2.
  • Another study published in 2022 found that extended-use high-dose IV TXA did not reduce mortality or bleeding outcomes, but low-dose IV/enteral TXA may be effective in reducing hemorrhage 3.
  • A 2024 meta-analysis found that TXA with acid suppression significantly reduced the risk of rebleeding, units of blood transfused, and the need for salvage therapy in patients with upper GI bleeding 4.
  • However, a 2020 systematic review and meta-analysis found that TXA did not improve outcomes in upper GI bleeding and may increase the risk of venous thromboembolic events 5.
  • A 2025 comprehensive systematic review and meta-analysis found that TXA significantly reduced rebleeding rates, particularly in upper GI bleeding, and was associated with a mortality reduction when administered through both oral and intravenous routes 6.

Safety and Adverse Events

  • The use of TXA in GI bleeding has been associated with an increased risk of thromboembolic events, including deep venous thrombosis and pulmonary embolism 3, 5.
  • However, a 2025 meta-analysis found that there was no definitive evidence that TXA use is associated with thromboembolic events 6.
  • The safety and efficacy of TXA in lower GI bleeding are less clear, with one study finding that TXA was linked to a significant increase in mortality in patients with lower GI bleeding 6.

Clinical Implications

  • The available evidence suggests that TXA may be a useful adjunctive treatment for upper GI bleeding, particularly when combined with acid suppression 2, 4, 6.
  • However, the use of TXA in GI bleeding should be approached with caution, taking into account the potential risks and benefits, as well as individual patient factors 3, 5, 6.

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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