Acute cardiac care & resuscitation

Pre-treatment with P2Y12 inhibitors in acute myocardial infarction with cardiogenic shock

Eur Heart J Cardiovasc PharmacotherPublished cohort

Main finding · MACE (composite of all-cause death, ischaemic stroke, myocardial infarction, or stent thrombosis)Result — go to the resultWeighted hazard ratio 1.11 95% CI 0.82–1.50

Authors' conclusion

In patients with AMI-CS, pretreatment with a P2Y12 inhibitor oral load was associated with an increased risk of major bleeding without benefit on MACE.

Study context

Population
Patients hospitalized between 2012 and 2023 with AMI-CS admitted for coronary angiography within 24 h of admission (ACTION-SHOCK cohort)patients with AMI-CS admitted to the catheterization laboratory within 24 h of admission
Participants
421 patients
Exposure
Pre-treatment with P2Y12 inhibitor vs no pre-treatment
  • Pre-treatmentn = 224
Outcome
MACE:
  • All-cause death
  • Ischaemic stroke
  • Myocardial infarction
  • Stent thrombosis
Follow-up
30 days
Methodological detailsinverse probability weighting (IPW) approach, consecutive patients
  • Inverse probability weighting (IPW) approach
  • Consecutive patients

Main finding

As reported in the abstract

Weighted hazard ratio

1.11

95% CI 0.82–1.50

By group

Pre-treatmentvs No pre-treatment
wHR 1.11 (95% CI 0.82–1.50)

Observational data: associations, not effects.

Further findings

Major adverse cardiovascular events (MACE) or major bleeding at 30 days, STEMI/NSTEMI subgroups

Effect consistent across STEMI/NSTEMI patients

Safety

OutcomePre-treatmentNo pre-treatmentwHR (95% CI)
Major bleeding (BARC grade 3, 4, or 5) · 30 daysIPW42.2%32.3%1.48 (1.05–2.08)

Original publication

Pre-treatment with P2Y12 inhibitors in acute myocardial infarction with cardiogenic shock. Eur Heart J Cardiovasc Pharmacother. Published 1 April 2025. doi:10.1093/ehjcvp/pvaf019

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