About this trial
Tranexamic axid is routinely used as an antifibrinolytic agent in cardiac surgery to reduce the risk of blood loss and transfusion. However, there is no consensus regarding the dosage regimen of tranexamic acid that should be administered. The purpose of this study is to compare different dosages of tranexamic acid in cardiac surgery using cardiopulmonary bypass regarding the duration of inhibition of fibrinolysis as measured by the ClotPro test.
Blood samples will be taken from the arterial line placed in the patient at specified time points in order to perform viscoelastic tests (ClotPro, TPA test), to detect successful inhibition of fibrinolysis and to measure tranexamic acid levels in the patient's blood. In case the action of tranexamic acid stops early postoperatively an additional dose of the medication will be administered to the patient.
Eligibility criteria
Qualifiers
Patients undergoing elective cardiac surgery using cardiopulmonary bypass
Patients to have discontinued anticoagulant and antiplatelet therapy preoperatively according to guidelines.
Disqualifiers
Age below 18 years
Patient refusal
Pregnancy
End-stage renal disease
Trial design
Treatments tested in this trial
- Tranexamic acid at a dose of 10 mg/kg followed by 1 mg/kg/h
- Tranexamic acid at a dose of 20 mg/kg
- Tranexamic acid at a dose of 30 mg/kg