Key result
Bridging with intravenous cangrelor prior to coronary artery bypass grafting did not significantly increase the risk of excessive CABG-related bleeding compared to placebo (11.8% vs 10.4%, OR 1.15).
Why the study?
Does bridging with intravenous cangrelor increase perioperative complications in patients requiring P2Y12 inhibition who are awaiting CABG?
RCT (n=210)
Double-blind
Randomized
Yes
Does bridging with intravenous cangrelor increase perioperative complications in patients requiring P2Y12 inhibition who are awaiting CABG?
Bridging with intravenous cangrelor prior to CABG maintains platelet inhibition without increasing the risk of perioperative bleeding or complications compared to placebo.
Supports cangrelor bridging before CABG; extends randomized evidence for safe perioperative platelet inhibition.
OBJECTIVE: Oral P2Y₁₂ platelet receptor inhibitors are a cornerstone of reducing complications in patients with acute coronary syndromes or coronary stents. Guidelines advocate discontinuing treatment with P2Y₁₂ platelet receptor inhibitors before surgery. Cangrelor, a short-acting, reversible, intravenously administered P2Y₁₂ platelet inhibitor is effective in achieving appropriate platelet inhibition in patients who are awaiting coronary artery bypass grafting (CABG) and require P2Y₁₂ inhibition. The objective of this study was to assess the effects of preoperative cangrelor on the incidence of perioperative complications, which are currently unknown. METHODS: Patients (n = 210) requiring preoperative clinical administration of thienopyridine therapy were randomized in a multicenter, double-blinded study to receive cangrelor or placebo while awaiting CABG after discontinuation of the thienopyridine. Optimal platelet reactivity, which was defined as <240 P2Y₁₂ platelet reaction units, was measured with serial point-of-care testing (VerifyNow). Pre- and postoperative outcomes, bleeding values, and transfusion rates were compared. To quantify potential risk factors for bleeding, we developed a multivariate logistic model. RESULTS: The differences between the groups in bleeding and perioperative transfusion rates were not significantly different. The rate of CABG-related bleeding was 11.8% (12/102) in cangrelor-treated patients and 10.4% (10/96) in the placebo group (P = .763). Transfusion rates for the groups were similar. Serious postoperative adverse events for the cangrelor and placebo groups were 7.8% (8/102) and 5.2% (5/96), respectively (P = .454). CONCLUSIONS: Compared with placebo, bridging patients with cangrelor prior to CABG effectively maintains platelet inhibition without increasing post-CABG complications, including bleeding and the need for transfusions. These data suggest cangrelor treatment is a potential strategy for bridging patients requiring P2Y₁₂ receptor inhibition while they await surgery.
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Firstenberg et al. (2013) conducted an RCT in Patients requiring coronary artery bypass surgery with indications for thienopyridine therapy (n=210). Cangrelor vs. Placebo was evaluated on Excessive CABG-related bleeding (primary safety end point) (OR 1.15, 95% CI 0.47-2.79, p=.763). Bridging with intravenous cangrelor prior to coronary artery bypass grafting did not significantly increase the risk of excessive CABG-related bleeding compared to placebo (11.8% vs 10.4%, OR 1.15).
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