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Does preoperative clopidogrel increase bleeding after coronary bypass surgery?
Charumathi Dasarathan1, Karthik Vaidyanathan, Deepthi Chandrasekaran
1Department of Cardiothoracic Surgery, Frontier Lifeline, Dr KM Cherian Heart Foundation, Mogappair, Chennai, India.
Insights
Patients undergoing coronary artery bypass grafting who took clopidogrel within 5 days of surgery did not experience increased bleeding or transfusion needs. Stopping clopidogrel >5 days prior did not significantly alter outcomes.
Area of Science:
- Cardiology
- Cardiovascular Surgery
- Pharmacology
Background:
- Antiplatelet therapy, like clopidogrel, reduces cardiac events in acute coronary syndrome.
- However, these therapies increase bleeding risk, posing challenges for patients needing surgery.
Purpose of the Study:
- To evaluate if clopidogrel use within 5 days of coronary artery bypass grafting (CABG) impacts bleeding outcomes.
- To compare transfusion requirements in patients with different clopidogrel cessation timings before CABG.
Main Methods:
- A study of 342 patients undergoing elective on-pump CABG between 2004 and 2008.
- Patients were divided into two groups: clopidogrel stopped >5 days before surgery (n=191) and ≤5 days before surgery (n=151).
- Bleeding outcomes (drainage at 8h, 12h, and total) and blood product transfusion needs were assessed.
Main Results:
- No significant differences in postoperative drainage were observed between the groups.
- Blood product usage was similar for patients who stopped clopidogrel >5 days earlier versus ≤5 days before surgery.
- No instances of reoperation for hemostasis occurred in either group.
Conclusions:
- Preoperative clopidogrel exposure, even within 5 days of surgery, does not elevate the risk of bleeding complications or transfusion needs during CABG.
- Current guidelines on clopidogrel cessation before CABG may not be necessary to prevent hemostatic complications.
Abstract:
Antiplatelet therapy has been demonstrated to reduce the risk of cardiac events in patients presenting with acute coronary syndrome, yet all effective therapies also increase the risk of bleeding. This study aimed to test the hypothesis that patients undergoing coronary artery bypass grafting, who received clopidogrel within 5 days before surgery, have worse bleeding outcomes and blood transfusion requirements than those who stopped clopidogrel >5 days earlier. We recruited 342 patients who underwent on-pump elective coronary artery bypass grafting between January 2004 and December 2008. Of these, 191 stopped taking clopidogrel >5 days earlier, and 151 stopped ≤5 days before surgery. Postoperative drainage after 8 and 12 h and the total drainage were similar in both groups. There was no significant difference in the amount of blood products used. There was no reexploration in either group. It was concluded that preoperative clopidogrel exposure does not increase the risk of hemostatic reoperation or the requirements for blood and blood product transfusion during and after coronary artery bypass grafting.
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