Once versus twice daily aspirin after coronary bypass surgery: a randomized trial

J S Paikin1,2, J Hirsh2,3, J S Ginsberg2,4

  • 1Hamilton General Hospital, McMaster University, Hamilton, ON, Canada.

Insights

Twice-daily aspirin (acetyl-salicylic acid) dosing improves response after coronary artery bypass graft surgery. Further trials are needed to confirm if this dosing regimen reduces clinical events like graft failure.

Area of Science:

  • Cardiovascular medicine
  • Pharmacology
  • Surgical outcomes

Background:

  • Coronary artery bypass graft (CABG) failure is linked to myocardial infarction and mortality.
  • Transient aspirin (acetyl-salicylic acid, ASA) hyporesponsiveness post-CABG can impair its effectiveness in preventing thrombotic graft failure.
  • Previous studies indicate that higher ASA dosing frequency can overcome reduced ASA response after CABG.

Purpose of the Study:

  • To evaluate if ASA 325 mg once-daily or 162 mg twice-daily improves ASA response compared to 81 mg once-daily post-CABG surgery.
  • To determine the optimal ASA dosing strategy for patients following CABG.

Main Methods:

  • A randomized trial involving adult patients undergoing CABG surgery.
  • Patients were assigned to receive ASA 81 mg once-daily, 325 mg once-daily, or 162 mg twice-daily.
  • The primary outcome was the median serum thromboxane B2 (TXB2) level on postoperative day 4.

Main Results:

  • Patients receiving ASA 162 mg twice-daily showed significantly lower median TXB2 levels on postoperative day 4 compared to those on ASA 81 mg once-daily.
  • ASA 325 mg once-daily showed similar TXB2 levels to the 81 mg once-daily group.
  • Pooled analysis confirmed that multiple daily dosing (twice or four times daily) of ASA was more effective in suppressing TXB2 formation than once-daily regimens.

Conclusions:

  • Multiple daily dosing of aspirin is superior to once-daily dosing (81 mg or 325 mg) in suppressing serum TXB2 levels after CABG surgery.
  • A twice-daily aspirin regimen warrants further investigation in a clinical outcome study to assess its impact on graft patency and patient survival.

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