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Clopidogrel Loading Dose 300 vs. 600 mg in Patients Undergoing One-Stop Hybrid Coronary Revascularization: A
Yulin Guo1, Dongjie Li1, Yingdi Gao1
1Department of Cardiac Surgery, Heart Center and Beijing Key Laboratory of Hypertension, Beijing Chaoyang Hospital, Capital Medical University, Beijing, China.
Insights
The 600 mg clopidogrel loading dose is safe for one-stop hybrid coronary revascularization (HCR), showing no increase in major bleeding events compared to the 300 mg dose. Further research is needed to confirm benefits.
Area of Science:
- Cardiology
- Interventional Cardiology
- Pharmacology
Background:
- Optimal clopidogrel loading dose for one-stop hybrid coronary revascularization (HCR) is not established.
- This study addresses the
- evidence-free
- zone regarding clopidogrel dosing in HCR.
Purpose of the Study:
- To compare major bleeding and ischemic thrombotic events with two clopidogrel loading doses (300 mg vs. 600 mg) in patients undergoing one-stop HCR.
- To evaluate the safety and efficacy of different clopidogrel loading regimens in this specific patient population.
Main Methods:
- Prospective, single-center, randomized pilot study.
- 100 patients undergoing one-stop HCR were randomized to receive either 300 mg or 600 mg of clopidogrel loading dose.
- Evaluation of major bleeding (BARC, PLATO) and composite ischemic thrombotic events post-procedure.
Main Results:
- Postoperative chest drainage volumes were comparable between the 300 mg and 600 mg clopidogrel groups.
- No significant differences in Bleeding Academic Research Consortium (BARC) or PLATelet inhibition and patient Outcomes (PLATO) major bleeding events were observed.
- Composite ischemic thrombotic and adverse events were similar between the two clopidogrel loading dose groups.
Conclusions:
- A 600 mg clopidogrel loading dose does not appear to increase major bleeding events compared to 300 mg in patients undergoing one-stop HCR.
- Further investigation with larger sample sizes is required to fully ascertain the potential benefits of the 600 mg loading dose in one-stop HCR.
Abstract:
Background: The optimal loading dose of clopidogrel in one-stop hybrid coronary revascularization (HCR) remains an "evidence-free" zone. This study aimed to compare the major bleeding and ischemic thrombotic events between different clopidogrel loading doses (300 vs. 600 mg) in one-stop HCR. Methods: In this prospective, single-center, randomized, and parallel pilot study, 100 patients receiving one-stop HCR were randomly assigned to the clopidogrel loading dose 300-mg group or 600-mg group in a 1:1 ratio. Major bleeding events and composite in-hospital ischemic thrombotic and adverse complications were evaluated after the procedure. Results: The results showed that postoperative mean chest drainage of the first 4 days and total drainage were comparable between the two groups. No differences were found in Bleeding Academic Research Consortium (BARC) coronary artery bypass grafting (CABG) related bleeding (4 vs. 2%, P = 1), PLATelet inhibition and patient Outcomes (PLATO) life-threatening bleeding (20 vs. 26%, P = 0.48), and PLATO major bleeding (70 vs. 76%, P = 0.5) in the two groups. The composite ischemic thrombotic and adverse events were also similar. Conclusions: In patients receiving one-stop HCR, clopidogrel 600 mg loading dose did not increase major bleeding events compared with 300 mg. More sufficient data is necessary to evaluate the potential benefits of 600 mg loading dose in one-stop HCR.
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