TY - JOUR
T1 - Maintenance therapy with a P2Y12 receptor inhibitor after cangrelor in patients with acute coronary syndrome. The ELECTRA-SIRIO 2 investigators’ viewpoint
AU - Kubica, Jacek
AU - Adamski, Piotr
AU - Gajda, Robert
AU - Kubica, Aldona
AU - Ostrowska, Małgorzata
AU - Casu, Gavino
AU - Gorog, Diana
AU - Gurbel, Paul
AU - Hajdukiewicz, Tomasz
AU - Jaguszewski, Miłosz
AU - Jeong, Young-Hoon
AU - Kosobucka-Ozdoba, Agata
AU - Motovska, Zuzana
AU - Niezgoda, Piotr
AU - Piasecki, Maciej
AU - Podhajski, Przemysław
AU - Raggi, Paolo
AU - Rahimov, Uzeyir
AU - Siller-Matula, Jolanta
AU - Skonieczny, Grzegorz
AU - Szarpak, Łukasz
AU - Szymański, Paweł
AU - Tantry, Udaya
AU - Navarese, Eliano
N1 - © 2025 Via Medica. This is an open access article under the Creative Commons Attribution Non-Commercial No-Derivatives CC BY-NC-ND licence, https://creativecommons.org/licenses/by-nc-nd/4.0/
PY - 2025/1/8
Y1 - 2025/1/8
N2 - 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.
AB - 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.
KW - antiplatelet therapy, cangrelor, ticagrelor, P2Y12 receptor inhibition
KW - P2Y12 receptor inhibition
KW - cangrelor
KW - ticagrelor
KW - antiplatelet therapy
KW - Platelet Aggregation Inhibitors/administration & dosage
KW - Humans
KW - Treatment Outcome
KW - Adenosine Monophosphate/analogs & derivatives
KW - Drug Interactions
KW - Acute Coronary Syndrome/drug therapy
KW - Purinergic P2Y Receptor Antagonists/administration & dosage
KW - Percutaneous Coronary Intervention
UR - https://www.scopus.com/pages/publications/86000557965
U2 - 10.5603/cj.98323
DO - 10.5603/cj.98323
M3 - Article
C2 - 39776051
SN - 1898-018X
VL - 32
SP - 83
EP - 89
JO - Cardiology Journal (CJ)
JF - Cardiology Journal (CJ)
IS - 1
ER -