Association between CK-MB Area Under the Curve and Tranexamic Acid Utilization in Patients Undergoing Coronary Artery Bypass Surgery.
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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https://hdl.handle.net/10161/13719Published Version (Please cite this version)
10.1007/s11239-017-1480-6Publication Info
van Diepen, Sean; Merrill, Peter D; Carrier, Michel; Tardif, Jean-Claude; Podgoreanu,
Mihai; Alexander, John H; & Lopes, Renato D (2017). Association between CK-MB Area Under the Curve and Tranexamic Acid Utilization in
Patients Undergoing Coronary Artery Bypass Surgery. J Thromb Thrombolysis. 10.1007/s11239-017-1480-6. Retrieved from https://hdl.handle.net/10161/13719.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
John Hunter Peel Alexander
Professor of Medicine
John H. Alexander, MD, MHS is a cardiologist and Professor of Medicine in the Department
of Medicine, Division of Cardiology at Duke University School of Medicine, as well
as the Vice Chief, Clinical Research in the Division of Cardiology. He is the Director
of Cardiovascular Research at the Duke Clinical Research Institute where he oversees
a large group of clinical research faculty and a broad portfolio of cardiovascular
clinical trials and observational clinical research programs. He is a
Renato Delascio Lopes
Professor of Medicine
Atrial Fibrillation Antithrombotic Therapy in patients with Acute Coronary Syndromes
Elderly patients with Heart Disease Biomarkers in Acute Coronary Syndromes and Atrial
Fibrillation Thrombosis and Anticoagulation and novel antithrombotic agents Metabolomics
in Cardiovascular Medicine
Mihai V. Podgoreanu
Associate Professor of Anesthesiology
Basic-Translational: 1. Systems biology approaches to modeling perioperative cardiovascular
injury and adaptation. 2. Mechanisms of perioperative myocardial injury; functional
genomics applied to perioperative myocardial injury. 3. Metabolic consequences of
perioperative myocardial ischemia-reperfusion injury. 4. Animal models and comparative
genomic approaches to study perioperative myocardial ischemia-reperfusion injury.
5. Functional genomics of vein graft diseas
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