Indications
Bleeding in Presence of Hyperfibrinolysis (see Hyperfibrinolytic States, [[Hyperfibrinolytic States]])
Plasminogen Activator Inhibitor-1 (PAI-1) Deficiency (see Plasminogen Activator Inhibitor-1 Deficiency, [[Plasminogen Activator Inhibitor-1 Deficiency]])
Von Willebrand Disease (see Von Willebrand Disease, [[Von Willebrand Disease]])
Trauma (see Trauma-General, [[Trauma-General]])
- Clinical Efficacy
- Systematic Review of Anti-Fibrinolytics in Acute Trauma (Cochrane Database Syst Rev, 2015) [MEDLINE]
- Tranexamic Acid Decreased Mortality Rate in Trauma with Hemorrhage without Increasing the Risk of Adverse Effects
- Tranexamic Acid Should Be GIven within 3 hrs of Injury: treatment later than 3 hrs is likely to be ineffective or harmful (data from CRASH-2 Trial)
- Unclear if Tranexamic Acid Has Efficacy in Traumatic Brain Injury (TIB) (see Traumatic Brain Injury, [[Traumatic Brain Injury]])
Pharmacology
- Anti-Fibrinolytic (see Anti-Fibrinolytics, [[Anti-Fibrinolytics]]): lysine analogue which binds to kringle domains of plasminogen, disrupting interaction between plasminogen (and plasmin) and lysine residues within fibrin
- Epsilon Aminocaproic Acid (see Epsilon Aminocaproic Acid, [[Epsilon Aminocaproic Acid]]): binds plasminogen (and plasmin) 1/8 as avidly as tranexamic acid -> may exert a less potent anti-hemorrhagic effect
Metabolism
Administration
Dose Adjustment
Adverse Effects
Other Adverse Effects
References
- Effects of tranexamic acid on death, vascular occlusive events, and blood transfusion in trauma patients with significant haemorrhage (CRASH-2): a randomised, placebo-controlled trial. Lancet. 2010;376:23–32 [MEDLINE]
- Antifibrinolytic drugs for acute traumatic injury. Cochrane Database Syst Rev. 2015 May 9;(5):CD004896. doi: 10.1002/14651858.CD004896.pub4. [MEDLINE]