Table 1.
Drug | Composition | Mechanism of Action | Elimination | Pharmaco-dynamics | Suggested Dosing in Adults | Approval |
---|---|---|---|---|---|---|
Aprotinin | Protein, isolated from bovine lung tissue | protease inhibitor Reversibly complexes with the active sites of plasmin, kallikrein, and trypsin Inhibition of: fibrinolysis, factor XIIa induced contact activation, thrombin induced platelet activation inflammatory response |
predominantly proteolysis, ~60% % renal |
initial plasmaT½ 150 min, terminal T½ life 10 h |
“Full Dose”: 2× 106 KIU bolus patient, 2× 106 KIU bolus CPB, continuous infusion of 5×105 KIU “Half Dose”: 1×106 KIU bolus patient, 1×106 KIU bolus CPB, continuous infusion of 2.5×105 KIU |
suspended since 2008; suspension lifted in Canada in 2011 and Europe in 2012 In the US still suspended |
Tranexamic Acid | synthetic lysine analogue | antifibrinolytic; competitive inhibition of the activation of plasminogen to plasmin | renal | plasma ½ life 3 h | “High Dose”: 30 mg/kg bolus patient, 2 mg/kg CPB, continuous infusion of 16mg/kg “Low Dose”: 10 mg/kg bolus patient, 1-2 mg CPB, continuous infusion of 1 mg/kg |
US, Canada, Europe |
Epsilon Aminocaproic Acid | synthetic lysine analogue | antifibrinolytic: competitive inhibition of the activation of plasminogen to plasmin | renal | plasma T½ life 2 h | 100 mg/kg bolus patient, 5 mg/kg CPB, continuous infusion of 30 mg/kg |
US, Canada |
From reference 5 (Anesthesiology. 2015;123(1):214-21).