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Effect of two doses of aspirin on thromboxane biosynthesis and platelet function in patients undergoing coronary
Marta Brambilla1, Alessandro Parolari, Marina Camera
1Centro Cardiologico Monzino, IRCCS, Via Parea, 4, 20138 Milano, Italy.
Insights
Higher aspirin doses (325 mg) reduce residual platelet activity after coronary artery bypass graft (CABG) surgery compared to lower doses (100 mg). This improved platelet inhibition is crucial for preventing thrombotic events in post-CABG patients.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Hematology
Background:
- Aspirin post-coronary artery bypass graft (CABG) surgery improves survival.
- Many patients remain at risk for thrombotic events due to insufficient platelet inhibition via the thromboxane (TX) pathway.
Purpose of the Study:
- To evaluate the effect of two aspirin doses (100 mg vs. 325 mg) on platelet function and TX biosynthesis in post-CABG patients.
- To determine if a higher aspirin dose reduces residual platelet reactivity.
Main Methods:
- Prospective single-center study of 56 CABG patients randomly assigned to 100 mg or 325 mg enteric-coated aspirin daily for five days.
- Assessed platelet function using light-transmission aggregometry and PFA-100(R).
- Measured TX biosynthesis in stimulated platelets, serum, urine, and lipopolysaccharide-cultured whole blood.
Main Results:
- Insufficient TX inhibition was observed with 100 mg aspirin but not with 325 mg.
- The higher aspirin dose (325 mg) resulted in lower incidence of residual platelet activity.
- Different assays yielded varying results for aspirin resistance, indicating they are not interchangeable.
Conclusions:
- Early post-CABG, 325 mg aspirin reduces residual platelet activity more effectively than 100 mg.
- Assay methodology impacts the detection of aspirin resistance in post-CABG patients.
Abstract:
Early post-operative aspirin improves survival in patients undergoing coronary artery bypass graft (CABG). However, most patients do not benefit of aspirin after CABG, still remaining at risk of thrombotic events due to insufficient platelet inhibition, specifically via the thromboxane (TX) pathway. We evaluated the effect of two aspirin doses (100 or 325 mg daily, enteric coated formulations) on platelet function and TX biosynthesis in patients after CABG and assessed whether the incidence of residual platelet reactivity could be reduced by the higher dose. Fifty-six patients undergoing CABG were randomly assigned to 100 or 325 mg aspirin daily for five days in a prospective single-centre study. Treatment effect was assessed by measuring either platelet function (light-transmission aggregometry and point-of-care PFA-100(R)) or TX biosynthesis in collagen-stimulated platelets, serum, urine, and in lipopolysaccharide (LPS)-cultured whole blood (WB). An insufficient TX inhibition was observed with 100 mg aspirin but not with the higher dose. The different effect of the two doses was, however, highlighted by either TX (platelet- or serum-derived) or by PFA-100(R) but not by the other assays. In conclusion, early after CABG, the incidence of residual platelet activity was lower in patients who received 325 mg aspirin. Moreover, evidence was provided that different methods yield different results in the detection of aspirin resistance, rendering them not interchangeable.
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