Why the study?
Does cangrelor and transition to an oral P2Y12 inhibitor increase bleeding compared to an oral P2Y12 inhibitor alone in patients with out-of-hospital cardiac arrest undergoing PCI?
Does cangrelor and transition to an oral P2Y12 inhibitor increase bleeding compared to an oral P2Y12 inhibitor alone in patients with out-of-hospital cardiac arrest undergoing PCI?
In patients with out-of-hospital cardiac arrest undergoing PCI, bridging with cangrelor before transitioning to an oral P2Y12 inhibitor does not significantly increase the risk of major bleeding compared to using an oral P2Y12 inhibitor alone.
Cangrelor bridging was not associated with excess major bleeding in OHCA PCI; leaves open need for randomized confirmation.
AIMS: Cangrelor is used to bridge the gap of insufficient platelet inhibition in patients with out-of-hospital cardiac arrest (OHCA) undergoing percutaneous coronary intervention (PCI). METHODS AND RESULTS: In a retrospective chart review study, we investigated the incidence of bleeding and stent thrombosis in patients with OHCA undergoing PCI who received either cangrelor and transition to an oral P2Y12 inhibitor or an oral P2Y12 inhibitor alone. Subgroups consisted of patients treated with conventional cardiopulmonary resuscitation (CPR) and extracorporeal CPR. The primary endpoint was Bleeding Academic Research Consortium (BARC) 3-5 bleeding at 30 days. Between January 2016 and March 2025, 414 patients were included of which 267 received cangrelor and an oral P2Y12 inhibitor and 147 received an oral P2Y12 inhibitor alone. BARC 3-5 bleeding at 30 days occurred at a similar rate in the cangrelor group and the oral P2Y12 inhibitor group (18.4% vs. 19.0%, respectively; adjusted OR, 0.79; 95% CI, 0.45-1.39). BARC 3-5 bleeding at 6, 24 and 48 h was similar between the cangrelor group and the oral P2Y12 inhibitor group in patients treated with conventional and extracorporeal CPR. In patients treated with extracorporeal CPR, stent thrombosis occurred less frequently in the cangrelor group compared with the oral P2Y12 inhibitor group (2.1% vs. 4.5%, respectively; adjusted OR, 0.32, 95% CI, 0.03-3.14), but without reaching statistical significance. CONCLUSION: In patients with OHCA undergoing PCI, BARC 3-5 bleeding occurred at a similar rate in patients receiving either cangrelor and transition to an oral P2Y12 inhibitor or an oral P2Y12 inhibitor alone.
No takes yet. Share an insight, caveat, or question.
Gelbenegger et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: