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Mortality benefit with prasugrel in the TRITON-TIMI 38 coronary artery bypass grafting cohort: risk-adjusted
Peter K Smith1, Lawrence T Goodnough, Jerrold H Levy
1Duke University Medical Center, Durham, NC 27710, USA. smith058@mc.duke.edu
Insights
Prasugrel use before coronary artery bypass grafting (CABG) increased bleeding but significantly lowered mortality compared to clopidogrel. This suggests a potential benefit despite increased bleeding risks in CABG patients.
Area of Science:
- Cardiology
- Cardiovascular Surgery
- Pharmacology
Background:
- Limited evidence exists for prasugrel use in patients requiring urgent or emergency coronary artery bypass grafting (CABG).
- Previous experience with clopidogrel in CABG patients has raised concerns about perioperative bleeding complications.
Purpose of the Study:
- To characterize bleeding, transfusion, and other outcomes in patients undergoing CABG.
- To compare outcomes related to the timing of prasugrel or clopidogrel withdrawal before CABG.
Main Methods:
- Analysis of a subset of the TRITON-TIMI 38 study involving patients randomized to aspirin with either clopidogrel or prasugrel who underwent isolated CABG (N = 346).
- Data collection via a supplemental case report form, combined with the existing TRITON-TIMI 38 database.
- Statistical correction for baseline imbalances using elements of the European System for Cardiac Operative Risk Evaluation and The Society of Thoracic Surgeons predictive algorithm.
Main Results:
- Patients receiving prasugrel showed significantly higher mean 12-hour chest tube blood loss (655 ± 580 ml) compared to clopidogrel (503 ± 378 ml; p = 0.050).
- No significant differences were observed in red blood cell transfusion or total donor exposure between the prasugrel and clopidogrel groups.
- All-cause mortality was significantly reduced with prasugrel (2.31%) compared to clopidogrel (8.67%; adjusted odds ratio: 0.26; p = 0.025).
Conclusions:
- Although prasugrel was associated with increased bleeding and re-exploration for bleeding, it demonstrated a lower rate of death post-CABG compared to clopidogrel.
- These findings suggest that the survival benefit of prasugrel may outweigh the increased bleeding risk in select CABG patients.
Objectives:
The objective of this study was to characterize the bleeding, transfusion, and other outcomes of patients related to the timing of prasugrel or clopidogrel withdrawal before coronary artery bypass grafting (CABG).
Background:
There is little evidence to guide clinical decision making regarding the use of prasugrel in patients who may need urgent or emergency CABG. Experience with performing CABG in the presence of clopidogrel has raised concern about perioperative bleeding complications that are unresolved.
Methods:
A subset of the TRITON-TIMI 38 study (Trial to Assess Improvement in Therapeutic Outcomes by Optimizing Platelet Inhibition with Prasugrel-Thrombolysis In Myocardial Infarction 38), in which patients with acute coronary syndrome were randomized to treatment with aspirin and either clopidogrel or prasugrel, underwent isolated CABG (N = 346). A supplemental case report form was designed and administered, and the data combined with the existing TRITON-TIMI 38 database. Baseline imbalances were corrected for using elements of the European System for Cardiac Operative Risk Evaluation and The Society of Thoracic Surgeons predictive algorithm.
Results:
A significantly higher mean 12-h chest tube blood loss (655 ± 580 ml vs. 503 ± 378 ml; p = 0.050) was observed with prasugrel compared with clopidogrel, without significant differences in red blood cell transfusion (2.1 U vs. 1.7 U; p = 0.442) or the total donor exposure (4.4 U vs. 3.0 U; p = 0.463). All-cause mortality was significantly reduced with prasugrel (2.31%) compared with 8.67% with clopidogrel (adjusted odds ratio: 0.26; p = 0.025).
Conclusions:
Despite an increase in observed bleeding, platelet transfusion, and surgical re-exploration for bleeding, prasugrel was associated with a lower rate of death after CABG compared with clopidogrel.
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