TXA Central
TXA Central is a resource for health professionals caring for patients with acute severe bleeding
TXA Central is a resource for health professionals caring for patients with acute severe bleeding
Intravenous (IV) Tranexamic Acid (TXA) reduces death from bleeding in patients with postpartum haemorrhage (PPH) and traumatic injuries.
However, patients must be treated urgently – most haemorrhage deaths occur within hours of bleeding onset, and treatment delay reduces the survival benefit from TXA. With every 15 minute delay, 10% of the survival benefit is lost.
One of the main obstacles to reducing treatment delay is the need for an IV injection.
In trauma patients, securing IV access at the injury scene can be difficult, particularly in trapped patients.
In countries with limited pre-hospital care, most trauma patients arrive at hospital too late to benefit from TXA.
The WOMAN trial showed that IV administration of TXA reduces PPH deaths by one-third, TXA was incorporated into the World Health Organisation guidelines.
To ensure equitable access to this life-saving treatment, finding other routes to give TXA became a WHO priority.
Because many women die soon after PPH onset and the life-saving effect of TXA decreases by 10% with every 15-minute delay, finding alternatives to IV administration offers women effective emergency care wherever they give birth.
Click HERE to watch a PPH stakeholder webinar discussing alternative routes for the administration of tranexamic acid (TXA) in post-partum haemorrhage (PPH).
What concentration of tranexamic acid is needed to inhibit fibrinolysis?
A systematic review to determine the minimal concentration of TXA in the blood that is required to inhibit fibrinolysis
No information currently
No information currently
PBPK Trial
Physiologically based modeling of tranexamic acid pharmacokinetics following intravenous, intramuscular, subcutaneous, and oral administration in healthy volunteers
No information currently
No information currently
PharmacoTXA Trial Protocol
This is a Phase 1 trial in healthy volunteers to determine the bioavailability and pharmacokinetics of TXA following administration of TXA by different routes and relevant doses
PharmacoTXA results (BJA)
A clinical study looking at alternative routes for tranexamic acid administration in woman with postpartum haemorrhage
No information currently
WOMANPharmaco-TXA Trial Protocol
This is a Phase 2 trial assessing the pharmacokinetics and pharmacodynamics of tranexamic acid administered by intravenous, intramuscular and oral liquid routes in women giving birth by caesarean section with at least one risk factor for PPH
WOMANPharmaco-TXA Trial
The main aim of this study is to ascertain whether IM and oral solution of TXA will be well absorbed at levels sufficient to inhibit fibrinolysis in pregnant women.
No information currently
Intramuscular injection of TXA in Bleeding Trauma Patients
Trauma-INTACT Trial Results
The Trauma-INTACT trial is an open-label, multi-centre pharmacokinetics study of IM TXA. The results show that TXA is well tolerated and rapidly absorbed via the IM route in bleeding trauma patients
IM TXA means huge implications for trauma care
1g intramuscular TXA shown to be well tolerated & reach a therapeutic level of 5mg/L-1 in 4 mins, remaining > this conc for 10hrs
TXA in military
For soldiers, assault victims, war & terrorism casualties, etc, early admin of TXA could be the difference between life or death. First responders could administer worldwide in all settings with IM being a simple alternative administration route to IV TXA
Trauma-INTACT Trial Protocol
Pharmacokinetics of intramuscular tranexamic acid in trauma patients: a clinical trial
Stakeholder webinar: Alternative routes for the administration of tranexamic acid (TXA) in post-partum haemorrhage (PPH)
Post-partume haemorrhage stakeholders Webinar: Alternative routes for the administration of tranexamic acid (TXA) in post-partum haemorrhage (PPH)