Key result
Diabetes mellitus was associated with a non-significant increase in 1-year MACE compared to non-diabetics in patients with ACS undergoing PCI (12.2% vs 7.2%; HR 1.27; 95% CI 0.89-1.79; P=0.2).
Why the study?
Does diabetes mellitus increase the risk of MACE in moderate-to-high risk ACS patients undergoing PCI on contemporary antiplatelet therapy?
Population
2,047 moderate-risk to high-risk acute coronary syndrome patients undergoing percutaneous coronary…
Comparison
Contemporary antiplatelet therapy in patients… vs Contemporary antiplatelet therapy in patients…
Design
Cohort
Follow-up
1 year
Authors
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Diabetics show nonsignificantly higher MACE post-PCI for ACS with similar bleeding; leaves open whether diabetes independently drives risk in contemporary regimens.
Observational (n=2,047)
Does diabetes mellitus increase the risk of MACE in moderate-to-high risk ACS patients undergoing PCI on contemporary antiplatelet therapy?
Hazard Ratio: 1.27 (95% CI 0.89–1.79)
Absolute Event Rate: 12.2% vs 7.2%
p-value: p=0.2
In ACS patients undergoing PCI, the use of newer antiplatelet agents (ticagrelor or prasugrel) appears to eliminate the excess ischemic risk associated with diabetes that is observed with clopidogrel.
Hamilos et al. (2017) conducted an observational in Acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI) (n=2,047). Diabetes mellitus vs. Nondiabetic patients was evaluated on Major adverse cardiovascular events (MACE), (composite of death, nonfatal myocardial infarction, urgent revascularization, and stroke) (HR 1.27, 95% CI 0.89-1.79, p=0.2). Diabetes mellitus was associated with a non-significant increase in 1-year MACE compared to non-diabetics in patients with ACS undergoing PCI (12.2% vs 7.2%; HR 1.27; 95% CI 0.89-1.79; P=0.2).
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