Related Experiment Video
Updated: Sep 13, 2025

Microfluidics in Assessing Platelet Function
Published on: November 8, 2024
Tranexamic Acid Timing and Mortality Impact After Trauma.
Adnan Ali1, Russell L Gruen2, Stephen A Bernard3
1Clinical Hub for Interventional Research, John Curtin School of Medical Research, The Australian National University, Canberra, Australian Capital Territory, Australia.
Early administration of tranexamic acid (TXA) within 90 minutes of injury significantly reduces trauma mortality. Beyond this window, TXA shows no significant benefit in preventing 28-day deaths in trauma patients.
Area of Science:
- Trauma resuscitation
- Emergency medicine
- Pharmacology
Background:
- Current trauma resuscitation guidelines recommend tranexamic acid (TXA) within 3 hours of injury, based on CRASH-2 trial data.
- This 3-hour window has not been independently replicated, prompting further investigation into optimal timing.
Purpose of the Study:
- To determine if 28-day mortality after trauma varies with the time to the first TXA dose.
- To precisely define the therapeutic window for TXA administration in major trauma patients.
Main Methods:
- Exploratory analysis of the PATCH-Trauma trial involving adults with major trauma and suspected coagulopathy.
- Patients received either TXA or placebo; time from injury to first TXA dose was analyzed using continuous functions.
- Log-binomial regression was used to assess mortality risk within 28 days based on treatment timing.
Main Results:
- The study included 1,287 patients; median time to first TXA dose was 79 minutes.
- Mortality risk increased with delayed TXA administration, with benefits most pronounced up to 90 minutes post-injury.
- TXA administration within 90 minutes significantly reduced 28-day mortality (aRR 0.64), while administration after 90 minutes showed no significant benefit (aRR 1.04).
Conclusions:
- The optimal therapeutic window for administering TXA in trauma patients appears to be within 90 minutes of injury.
- This finding suggests a narrower, more critical window for TXA efficacy than previously established.
Related Concept Videos
Venous Thrombosis III: Interprofessional Care
Extrinsic and Intrinsic Pathways of Hemostasis
The Extrinsic Pathway
The extrinsic pathway of coagulation is typically initiated by tissue damage that exposes blood to tissue factor (TF), a protein released by the damaged tissue cells outside the blood vessels—this interaction with TF triggers biochemical reactions involving specific clotting factors. The key player here is Factor VII, which...
Anticoagulant Drugs: Low-Molecular-Weight Heparins
Venous Thrombosis IV: Nursing Management
Cardiopulmonary Resuscitation IV: Pharmacological Management
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...

