Key result
Ticagrelor appears to be the optimal oral agent for continuation of P2Y12 inhibition after cangrelor infusion, as transitioning to thienopyridines is associated with a drug-drug interaction.
Why the study?
Optimal maintenance therapy with an oral P2Y12 receptor inhibitor following cangrelor infusion in ACS patients undergoing PCI remains to be summarized.
Ticagrelor is the preferred oral P2Y12 inhibitor for transitioning from cangrelor in ACS patients due to the lack of drug-drug interactions that are seen with thienopyridines.
Supports prioritizing ticagrelor when transitioning from cangrelor in acute coronary syndromes to avoid drug interactions.
According to the ESC guidelines, cangrelor may be considered in P2Y12-inhibitor-naïve acute coronary syndrome (ACS) patients undergoing percutaneous coronary intervention (PCI). The aim of this review is to summarize available evidence on the optimal maintenance therapy with P2Y12 receptor inhibitor after cangrelor. Transitioning from cangrelor to a thienopyridine, but not ticagrelor, can be associated with a drug-drug interaction (DDI); therefore, a ticagrelor loading dose (LD) can be given any time before, during, or at the end of a cangrelor infusion, while a LD of clopidogrel or prasugrel should be administered at the time the infusion of cangrelor ends or within 30 minutes before the end of infusion in the case of a LD of prasugrel. Administration of any oral antiplatelet agent at the end of a cangrelor infusion will also result in a transient period of increased platelet reactivity. The inter-individual variability of this period is difficult to predict because it depends on many factors related to the patient and the treatment. In addition, experimental studies indicate that cangrelor may exert a cardioprotective effect beyond the blockade of platelet aggregation. Considering the available data, the potential use of cangrelor in ACS patients goes well beyond the current indications. Furthermore, we believe that it might be prudent to avoid use of thienopyridines during and soon after a cangrelor infusion until conclusive data on the effect of the DDI on the clinical outcome are available. On the other hand, ticagrelor seems to be an optimal oral agent for continuation of P2Y12 inhibition in patients receiving cangrelor infusion.
No takes yet. Share an insight, caveat, or question.
Kubica et al. (2025) conducted a review in Acute coronary syndrome. Transition from cangrelor to oral P2Y12 inhibitors was evaluated. Ticagrelor appears to be the optimal oral agent for continuation of P2Y12 inhibition after cangrelor infusion, as transitioning to thienopyridines is associated with a drug-drug interaction.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: