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Published on: March 15, 2022
Evaluation of aspirin's effect on platelet function early after coronary artery bypass grafting
Frantisek Bednar1, Tomas Tencer, Petr Plasil
1Cardiocentre, 3rd Department of Internal Medicine and Cardiology, 3rd Medical School, Charles University and Kralovske Vinohrady University Hospital, Prague, Czech Republic. fandabednar@email.cz
Insights
Aspirin therapy shows insufficient platelet inhibition in the early days after coronary artery bypass grafting (CABG). Optimal platelet inhibition was not achieved until day 5, suggesting a need for improved antiplatelet strategies post-CABG.
Area of Science:
- Cardiology
- Pharmacology
- Vascular Surgery
Background:
- Aspirin therapy is standard for reducing mortality and ischemic complications after coronary artery bypass grafting (CABG).
- However, the efficacy of oral aspirin in achieving adequate platelet inhibition during the early postoperative period after CABG remains incompletely understood.
Purpose of the Study:
- To assess the pharmacologic effect and efficacy of aspirin on platelet function in the initial postoperative days following CABG.
- To utilize specific laboratory tests to evaluate aspirin's effectiveness in this critical early phase.
Main Methods:
- A prospective study involving 30 patients undergoing CABG at a single cardiac surgery center.
- Postoperative aspirin efficacy (200 mg/d) was evaluated using serum thromboxane B2 (TxB2) suppression and arachidonic acid-induced platelet aggregometry (MULTIPLATE analyzer).
- Laboratory samples were collected preoperatively and on postoperative days 1 through 5.
Main Results:
- Serum TxB2 inhibition greater than 90% was not achieved until postoperative day 5 in 55% of patients.
- Effective platelet inhibition, defined by MULTIPLATE analyzer values below 300 AU*min, was only reached by 34% of patients on day 5.
- Both key laboratory markers indicated impaired aspirin efficacy in the early postoperative period after CABG.
Conclusions:
- Aspirin's ability to inhibit thromboxane B2 production and platelet aggregation is significantly impaired in the first few days after CABG.
- These findings suggest that current aspirin dosing may be insufficient for optimal early antiplatelet effect in this patient population.
- A more effective antiplatelet strategy could potentially enhance early graft patency and improve clinical outcomes following CABG.
Objective:
Aspirin therapy decreases mortality and ischemic complication rates after coronary artery bypass grafting (CABG). However, platelet inhibition after oral aspirin seems to be insufficient in the early postoperative period. There are incomplete data reporting aspirin efficacy early after CABG. The aim of this study was to assess the pharmacologic effect of aspirin on platelets in the first postoperative days using the most specific laboratory tests for the evaluation of aspirin efficacy.
Design:
A prospective study.
Setting:
A clinical study in one cardiac surgery center and measurements in two pharmacologic institutions.
Participants:
Thirty patients.
Interventions:
Postoperative aspirin efficacy (200 mg/d) was assessed by the suppression of serum thromboxane B(2) (TxB(2)) and by arachidonic acid-induced aggregometry using the MULTIPLATE analyzer. Samples were collected before surgery and on postoperative days 1-5.
Methods And Main Results:
The median baseline value (range) of serum TxB(2) was 1.6 ng/mL (1.4-1.9). The median TxB(2) inhibition >90% (the value required for full platelet inhibition) was not achieved until day 5 (-91%, 0.13 ng/mL [0.08-0.22], p < 0.001) and in only 55% of patients. The median baseline ASPI value was 805 (640-975) aggregation units (AU)*min. A significant decrease in aspirin insufficiency was not seen before postoperative day 5 (390 [243-621], p < 0.003) and only 34% of patients reached an effective platelet inhibition on day 5 (cutoff < 300 AU*min).
Conclusions:
The effect of aspirin on inhibition of TxB(2) production and arachidonic acid-induced platelet aggregation is impaired during the first postoperative days after CABG. A more effective antiplatelet strategy presumably could increase early graft patency and improve clinical outcomes after CABG.
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