What is the recommended dose of tranexamic acid (TXA) for stroke?

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Last updated: October 21, 2025View editorial policy

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Recommended Dose of Tranexamic Acid for Stroke

Tranexamic acid (TXA) for stroke should be administered at a loading dose of 1 g intravenously over 10 minutes, followed by an intravenous infusion of 1 g over 8 hours, and should be given as soon as possible and within 3 hours of symptom onset. 1, 2, 3

Dosing Recommendations by Stroke Type

Hemorrhagic Stroke

  • For intracerebral hemorrhage (ICH), the recommended dose is 1 g IV bolus over 10 minutes followed by 1 g IV infusion over 8 hours 4, 5
  • Administration should occur within 8 hours of symptom onset, though earlier treatment (within 3 hours) is associated with better outcomes 4, 5
  • The TICH-2 trial showed modest reductions in early death and hematoma expansion with this dosing regimen, though no significant difference in functional status at 90 days 5

Ischemic Stroke

  • Current guidelines do not specifically recommend TXA for ischemic stroke 1
  • For ischemic stroke, recombinant tissue plasminogen activator (rtPA) remains the standard treatment at 0.9 mg/kg (maximum 90 mg) within 3-4.5 hours of symptom onset 1
  • TXA is not indicated as a primary treatment for ischemic stroke as it has antifibrinolytic properties that could theoretically counteract thrombolytic therapy 1

Timing Considerations

  • Effectiveness of TXA decreases by approximately 10% for every 15-minute delay in administration 2, 3
  • Administration should occur as soon as possible after onset of bleeding 1, 3
  • Administration after 3 hours post-injury may increase risk of death due to bleeding 3
  • Pre-hospital administration should be considered to ensure early treatment 3

Route of Administration

  • Intravenous administration is the recommended and evidence-based route 1, 2
  • Current guidelines do not include specific recommendations for intramuscular dosing of TXA 2
  • The European guidelines explicitly state their recommendations apply to intravenous administration only 2

Safety Considerations

  • TXA is generally well-tolerated with no increase in thromboembolic events reported in major trials 4, 5
  • Fewer serious adverse events were observed with TXA compared to placebo in the TICH-2 trial 5
  • Higher doses of TXA are associated with increased risk of seizures, particularly in cardiac surgery patients 3
  • Blood pressure should be monitored and controlled during administration 1

Special Populations

  • For traumatic brain injury, TXA has shown benefit in reducing head injury-related death when administered within 3 hours, particularly in mild to moderate TBI 3
  • Early treatment with TXA showed reduction in mortality in mild and moderate head injury but not in severe head injury 1

Common Pitfalls

  • Delaying administration beyond 3 hours significantly reduces effectiveness 3
  • Using TXA in ischemic stroke patients who are candidates for thrombolytic therapy could theoretically counteract the beneficial effects of thrombolytics 1
  • Limiting TXA use only to patients with diagnosed hyperfibrinolysis could result in missed opportunities to prevent mortality 6
  • Older studies using different dosing regimens (such as 6g daily) may not reflect current evidence-based recommendations 7

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Intramuscular Administration of Tranexamic Acid (TXA)

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Tranexamic Acid in Trauma-Related Hemorrhage and Other Clinical Indications

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Tranexamic acid in trauma: how should we use it?

Journal of thrombosis and haemostasis : JTH, 2015

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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