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Author Spotlight: Enhancing Coronary Artery Revascularization
Published on: September 15, 2023
Association between CK-MB Area Under the Curve and Tranexamic Acid Utilization in Patients Undergoing Coronary Artery
Sean van Diepen1, Peter D Merrill2, Michel Carrier3
1Department of Critical Care and Division of Cardiology, 2C2 Cardiology Walter MacKenzie Center, University of Alberta Hospital, 8440 112th St., Edmonton, AB, T6G 2B7, Canada. sv9@ualberta.ca.
Insights
Tranexamic acid (TA) use after coronary artery bypass graft (CABG) surgery was linked to increased myonecrosis, a marker of heart muscle damage. However, TA did not increase the risk of death or myocardial infarction within 30 days post-CABG.
Area of Science:
- Cardiology
- Cardiac Surgery
- Pharmacology
Background:
- Myonecrosis post-coronary artery bypass graft (CABG) surgery is a significant predictor of mortality.
- Tranexamic acid (TA), an anti-fibrinolytic, is used to reduce blood loss but its effect on post-CABG myonecrosis is not well-established.
- Previous studies suggest TA does not increase myocardial infarction (MI) risk.
Purpose of the Study:
- To investigate the association between tranexamic acid (TA) treatment and myonecrosis following CABG surgery.
- To evaluate the impact of TA on 30-day cardiovascular death or MI in CABG patients.
Main Methods:
- A trial involving 656 patients receiving TA and 770 not receiving TA.
- Inverse probability weighting of propensity scores was used to adjust for confounding factors.
- Primary outcome: creatine kinase MB (CK-MB) area under the curve (AUC) at 24 hours.
- Secondary outcome: 30-day incidence of cardiovascular death or MI.
Main Results:
- Patients receiving TA had a higher median 24-hour CK-MB AUC (301.9 vs 253.5 ng·h/mL, p < 0.001), indicating increased myonecrosis.
- No significant difference was observed in the 30-day incidence of cardiovascular death or MI between the TA and no-TA groups (8.7% vs 8.3%, adjusted OR 0.99; 95% CI 0.67-1.45).
- TA-treated patients were more likely to be female and have pre-existing conditions like heart failure or previous MI.
Conclusions:
- Tranexamic acid (TA) administration in CABG patients is associated with a higher risk of myonecrosis.
- TA treatment did not increase the risk of 30-day cardiovascular death or myocardial infarction.
- Further research is needed to understand the pathophysiology of TA-induced myonecrosis and its clinical implications.
Abstract:
Myonecrosis after coronary artery bypass graft (CABG) surgery is associated with excess mortality. Tranexamic acid (TA), an anti-fibrinolytic agent, has been shown to reduce peri-operative blood loss without increasing the risk of myocardial infarction (MI); however, no large study has examined the association between TA treatment and post-CABG myonecrosis. In the MC-1 to Eliminate Necrosis and Damage in Coronary Artery Bypass Graft Surgery II trial, inverse probability weighting of the propensity to receive TA was used to test for differences among the 656 patients receiving and 770 patients not receiving TA. The primary outcome was creatine kinase MB (CK-MB) area under the curve (AUC) through 24 h. The secondary outcome was 30-day cardiovascular death or MI. Patients who received TA were more frequently female, had a previous MI, heart failure, low molecular weight heparin therapy, on-pump CABG, valvular surgery, and saphenous vein or radial grafts. The median 24-h CK-MB AUC was higher in TA-treated patients [301.9 (IQR 196.7-495.6) vs 253.5 (153.4-432.5) ng h/mL, p < 0.001]. No differences in the 30-day incidence of cardiovascular death or MI were observed (8.7 vs 8.3%, adjusted OR 0.99; 95% CI 0.67-1.45, p = 0.948). In patients undergoing CABG, TA use was associated with a higher risk of myonecrosis; however, no differences were observed in death or MI. Future larger studies should be directed at examining the pathophysiology of TA myonecrosis, and its association with subsequent clinical outcomes.
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