Effect of tranexamic acid on platelet ADP during extracorporeal circulation

Abstract

Seventeen adults received the antifibrinolytic drug tranexamic acid during cardiac surgery utilizing extracorporeal circulation (ECC). In 8 patients, drug administration began prior to skin incision (pre‐ECC); infusions commenced after ECC and protamine administration in another 9 patients (post‐ECC). Compared with the post‐ECC group, the pre‐ECC group exhibited less bleeding via mediastinal drains (420 vs. 655 mL/12 h median, P = 0.024), decreased frequency of the presence (≥10 γg/mL) of fibrin split products (P < 0.05), and greater platelet dense granule content of adenosine diphosphate after surgery (15.47 vs. 4.05 nmoles/mg protein median, P = 0.021). Follow‐up in vitro study of tranexamic acid inhibition of plasmin‐induced platelet activation utilizing normal human platelet rich plasma and porcine plasmin revealed a 13‐fold lower concentration of tranexamic acid for 50% inhibition when plasmin was preincubated with the drug (1.2 γg/mL, 95% CI = 1.13 – 1.60 γg/mL) compared to when platelet rich plasma was preincubated with the drug (16 γg/mL, 95% CI = 7.3 – 99. γg/mL). Plasmin inactivated with tranexamic acid retained its ability to inhibit thrombininduced platelet activation, thus suggesting that tranexamic acid inhibits plasmin's catalytic activity and not its binding to platelets. Both clot lysis and platelet dysfunction may contribute to bleeding after ECC. Tranexamic acid blocks plasmin‐induced partial platelet activation during ECC, thus preserving platelet function and promoting hemostasis after ECC.