TY - JOUR
T1 - Percutaneous revascularization and long term clinical outcomes of diabetic patients randomized in the Occluded Artery Trial (OAT)
AU - Overgaard, Christopher B.
AU - Džavík, Vladimír
AU - Buller, Christopher E.
AU - Liu, Li
AU - Banasiak, Waldemar
AU - Devlin, Gerard
AU - Maggioni, Aldo P.
AU - Leor, Jonathan
AU - Burton, Jeffery R.
AU - Reis, Gilmar
AU - Ruzyllo, Witold
AU - Forman, Sandra A.
AU - Lamas, Gervasio A.
AU - Hochman, Judith S.
N1 - Funding Information:
Dr. Overgaard was supported by a Heart and Stroke Foundation of Canada/Astra Zeneca Research Award . Dr. Džavík was supported in part by the Brompton Funds Professorship in Interventional Cardiology .
PY - 2013/10/3
Y1 - 2013/10/3
N2 - Background Percutaneous coronary intervention (PCI) of a persistently totally occluded infarct-related artery (IRA) in stable high-risk patients > 24 h after myocardial infarction (MI) does not reduce the occurrence of death, re-infarction, or heart failure. Diabetic patients are at higher risk for cardiovascular events; we examined their outcomes overall with PCI and optimal medical therapy alone (MED). Methods The long-term (7-year) outcomes of 454 diabetic patients (20.6%) randomized to PCI or MED in the Occluded Artery Trial (OAT) were assessed for the composite primary endpoint of death, re-MI, or New York Heart Association class IV heart failure. Diabetics and non-diabetics were compared and outcomes assessed by treatment strategy. Results The 7-year cumulative primary event rate for diabetic patients was 35.0% vs. 19.4% in the non-diabetic cohort (p < 0.001). Multivariable analyses revealed diabetes to be an independent predictor (p < 0.01) for the primary outcome, fatal or nonfatal recurrent MI, Class IV Heart Failure (HF), and death. The 7-year cumulative primary event rates were 35.3% in the PCI group vs. 34.5% in the medical therapy group in diabetic patients (p = 0.19) and 19.3% in the PCI group vs. 19.5% in the medical therapy group in patients without diabetes (p = 0.60). Conclusions Despite the higher overall risk conferred by the presence of diabetes, PCI did not improve clinical outcomes in this subpopulation, and is not indicated in otherwise stable patients with a totally occluded infarct-related artery in the sub-acute phase after MI.
AB - Background Percutaneous coronary intervention (PCI) of a persistently totally occluded infarct-related artery (IRA) in stable high-risk patients > 24 h after myocardial infarction (MI) does not reduce the occurrence of death, re-infarction, or heart failure. Diabetic patients are at higher risk for cardiovascular events; we examined their outcomes overall with PCI and optimal medical therapy alone (MED). Methods The long-term (7-year) outcomes of 454 diabetic patients (20.6%) randomized to PCI or MED in the Occluded Artery Trial (OAT) were assessed for the composite primary endpoint of death, re-MI, or New York Heart Association class IV heart failure. Diabetics and non-diabetics were compared and outcomes assessed by treatment strategy. Results The 7-year cumulative primary event rate for diabetic patients was 35.0% vs. 19.4% in the non-diabetic cohort (p < 0.001). Multivariable analyses revealed diabetes to be an independent predictor (p < 0.01) for the primary outcome, fatal or nonfatal recurrent MI, Class IV Heart Failure (HF), and death. The 7-year cumulative primary event rates were 35.3% in the PCI group vs. 34.5% in the medical therapy group in diabetic patients (p = 0.19) and 19.3% in the PCI group vs. 19.5% in the medical therapy group in patients without diabetes (p = 0.60). Conclusions Despite the higher overall risk conferred by the presence of diabetes, PCI did not improve clinical outcomes in this subpopulation, and is not indicated in otherwise stable patients with a totally occluded infarct-related artery in the sub-acute phase after MI.
KW - Diabetes
KW - Occluded artery
KW - Open artery hypothesis
KW - Percutaneous coronary intervention
UR - http://www.scopus.com/inward/record.url?scp=84885610854&partnerID=8YFLogxK
U2 - 10.1016/j.ijcard.2013.02.004
DO - 10.1016/j.ijcard.2013.02.004
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AN - SCOPUS:84885610854
SN - 0167-5273
VL - 168
SP - 2416
EP - 2422
JO - International Journal of Cardiology
JF - International Journal of Cardiology
IS - 3
ER -