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Ticagrelor vs Clopidogrel in ACS patients undergoing PCI in routine clinical practice

Main Takeaway

  • Risk for net adverse clinical events (NACE) was not significantly different between ticagrelor at 12 months compared with clopidogrel
    • Study population: 62,580 patients with acute coronary syndrome (ACS) who underwent percutaneous coronary intervention (PCI) in routine clinical practice
  • Ticagrelor was associated with higher risks for haemorrhagic events and dyspnoea vs clopidogrel

Why This Matters

  • Recent observational studies question whether ticagrelor vs clopidogrel is associated with better outcomes in routine clinical practice
    • Current guidelines: recommend ticagrelor with aspirin in preference to clopidogrel in patients with ACS

Study Design

Retrospective cohort study: 183,579 patients (age range, 30-89 years) with ACS who underwent PCI and received ticagrelor or clopidogrel

 

Patients were matched using propensity score:

  • Ticagrelor (n=31,290)
  • Clopidogrel (n=31,290)

Primary endpoint: NACE at 12 months

  • Ischaemic events
    [recurrent acute myocardial infarction, revascularisation or ischaemic stroke]
  • Haemorrhagic events
    [haemorrhagic stroke or gastrointestinal bleeding]

Secondary outcomes: NACE or mortality, all-cause mortality, composite ischaemic events, composite haemorrhagic events, individual components of the primary outcome, dyspnoea at 12 months

Key Results

95.5% of matched patients used aspirin with ticagrelor or clopidogrel among the 31,290 propensity-matched pairs

The risk for NACE was not significantly different between ticagrelor and clopidogrel groups (HR, 1.05; 95% CI, 1.00-1.10; P=0.06)

  • No significant difference was found between the 2 groups for:
    • NACE or mortality (HR, 1.03; 95% CI, 0.98-1.08; P=0.21)
    • Ischaemic events (HR, 1.03; 95% CI, 0.98-1.08; P=0.32)
    • All-cause mortality (HR, 0.97; 95% CI, 0.81-1.16; P=0.74)
  • Ticagrelor vs clopidogrel group showed a significantly higher risk for:
    • Haemorrhagic events (HR, 1.35; 95% CI, 1.13-1.61; P=0.001)
    • Dyspnoea (HR, 1.21; 95% CI, 1.17-1.26; P<0.001)

Limitations

  • The study did not include information on aspirin dosage, angiographic findings, or PCI procedure
  • The burden of overall bleeding events could have been underestimated or overestimated
  • Neither the proportion of patients who switched antiplatelet drugs nor its effects were quantified
  • The effect of pre-treatment with an antiplatelet agent was not assessed
  • The mortality rate might have been underestimated
  • Patients who used prasugrel for dual antiplatelet therapy were not included

MAT-BH-2200184/v2/Jun 2023