Coronary disease & ACS

De-escalation from ticagrelor to clopidogrel in patients with acute myocardial infarction: the TALOS-AMI high bleeding risk (HBR) substudy

EuroInterventionPublished Secondary analysis of the TALOS-AMI randomised trial

Authors' conclusion

In stabilised acute myocardial infarction patients, unguided de-escalation from ticagrelor to clopidogrel was associated with a lower rate of net adverse clinical outcomes irrespective of HBR status. The effect of de-escalation of P2Y12 inhibition on reducing haemorrhagic events was greater in patients with HBR.

Study context

Population
Stabilised acute MI patients after percutaneous coronary intervention (PCI), by HBR status (modified Academic Research Consortium (ARC) criteria)589 (22.4%) HBR
Participants
2,625 patients
Comparison
De-escalation vs ticagrelor plus aspirin, by HBR status
Methodological detailsnon-prespecified post hoc analysis
  • Non-prespecified post hoc analysis

Primary result

As reported in the abstract

Net adverse clinical events, by HBR status (subgroup) · 1 year post-PCI
De-escalation vs Active controlHazard ratio (95% CI)
HBR
0.47(0.26–0.84)
non-HBR
0.59(0.41–0.84)

Safety

OutcomeHR (95% CI)
BARC bleeding type 3 or 5, HBR patientsLess common among HBR patients only0.24 (0.07–0.84)

Parts of this Brief are withheld: the automatic checks could not confirm them against the abstract.

Original publication

De-escalation from ticagrelor to clopidogrel in patients with acute myocardial infarction: the TALOS-AMI HBR substudy. EuroIntervention. Published 4 December 2023. doi:10.4244/eij-d-23-00427

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