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Clopidogrel increases blood transfusion and hemorrhagic complications in patients undergoing cardiac surgery
Christine R Herman1, Karen J Buth, Blaine A Kent
1Division of Cardiac Surgery, Queen Elizabeth II Health Sciences Center, Halifax, Nova Scotia, Canada.
Insights
Recent clopidogrel use before cardiac surgery increases transfusion and bleeding risks. Surgeons should consider the time since the last dose to mitigate complications in acute coronary syndrome patients.
Area of Science:
- Cardiology
- Cardiovascular Surgery
- Pharmacology
Background:
- Increasing use of clopidogrel for acute coronary syndrome.
- Patients undergoing urgent cardiac surgery may have impaired platelet function due to clopidogrel.
- Need to assess the impact of recent clopidogrel administration on surgical outcomes.
Purpose of the Study:
- To determine if recent clopidogrel administration predicts transfusion and hemorrhagic complications in cardiac surgery patients.
- To evaluate the association between clopidogrel cessation interval and adverse outcomes.
- To identify risk factors for complications in patients on clopidogrel.
Main Methods:
- Retrospective study of isolated coronary artery bypass graft (CABG), isolated valve, or combined CABG/valve surgery patients (2004-2008).
- Outcomes assessed: transfusion and hemorrhagic complication.
- Clopidogrel stop interval analyzed in daily increments (0-5 days, >5 days, none) using logistic regression.
Main Results:
- 26.4% of 3,779 patients received clopidogrel preoperatively.
- Overall transfusion rate: 34.1%; hemorrhagic complication rate: 4.1%.
- Clopidogrel use within 24 hours independently predicted transfusion (OR 2.4) and hemorrhagic complication (OR 2.1).
Conclusions:
- Patients receiving clopidogrel within 24 hours of cardiac surgery face higher risks of transfusion and bleeding.
- The interval since the last clopidogrel dose is a critical factor in surgical planning.
- Timing of surgery should be adjusted based on clopidogrel cessation to minimize patient risk.
Background:
Utilization of the irreversible antiplatelet agent clopidogrel is increasing in the treatment acute coronary syndrome patients. Consequently, more patients are presenting for urgent cardiac surgery with an irreversible defect in platelet function. The objective of this study was to determine whether recent clopidogrel administration predicts transfusion and hemorrhagic complication in cardiac surgery patients.
Methods:
This retrospective study included all patients undergoing isolated coronary artery bypass graft surgery (CABG), isolated valve, or CABG plus valve at a single center between 2004 and 2008. The outcomes of interest were transfusion and hemorrhagic complication. Clopidogrel stop interval was defined as the time between last dose and presentation to the operating room, and was examined in daily increments from 0 to 5 days, more than 5 days, and not receiving clopidogrel preoperatively. By logistic regression, the association of clopidogrel stop interval with transfusion and with hemorrhagic complication was examined after adjusting for other risk factors.
Results:
Of 3,779 patients included in this study, 26.4% (999) received clopidogrel preoperatively. The overall rates of transfusion and hemorrhagic complication were 34.1% and 4.1%, respectively. Clopidogrel use within 24 hours was an independent predictor of transfusion (odds ratio 2.4; 95% confidence interval: 1.8 to 3.3) and of hemorrhagic complication (odds ratio 2.1; 95% confidence interval: 1.3 to 3.6).
Conclusions:
Patients receiving clopidogrel within 24 hours of surgery are at increased risk for transfusion and hemorrhagic complication. Timing of surgery for patients receiving clopidogrel should take into account the interval from the last dose.
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