SummaryQuestions about the long-term safety over the beneficial effects of drug-eluting stents (DES) have grown. We compared the long-term safety and efficacy of DES and bare-metal stents (BMS) in patients with acute myocardial infarction (AMI). A total of 1,017 AMI patients treated with stent implantation were followed for 3 years; 660 (64.9%) patients were treated with at least one DES and 357 (35.1%) patients were treated with at least one BMS. The primary endpoints were total mortality and the composite of major adverse cardiac events (MACE) including total mortality, re-MI, target lesion revascularization (TLR), and coronary artery bypass graft. At 3-years, the overall risks of cardiac and all-cause mortality were not different between the groups. However, the use of DES significantly decreased TLR (17.4% versus 7.1%, adjusted hazard ratio [HR] 0.44, 95% confidence interval [CI] 0.30 to 0.65) and the composite of MACEs (27.2% versus 19.5%, adjusted HR 0.65, 95% CI 0.48 to 0.87) with no differences in MI. The risk of MACE up to 1 year (HR 0.56, 95% CI 0.39 to 0.80) was higher in BMS patients, whereas from 1 year to 2 years (HR 0.55, 95% CI 0.27 to 1.10) and from 2 years to 3 years (HR 1.13, 95% CI 0.56 to 2.28), it was similar between the groups. The use of DES does not have a significant effect on overall long-term clinical survival compared with that of BMS in AMI patients. However, the use of DES reduced the need for re-intervention and the risk of MACE, mostly within 1 year. (Int Heart J 2011; 52: 78-83)Key words: Acute myocardial infarction, Drug-eluting stent, Bare-metal stent D rug-eluting stents (DES) have caused drastic changes in interventional cardiology. Their use is associated with a reduction of neointimal hyperplasia, decreased risk of restenosis, and less frequent revascularization compared with bare-metal stents (BMS).1-4) However, questions about the long-term safety over the beneficial effects of DES have grown regarding the actual usefulness of DES because of the possible increased incidence of thrombosis and deaths compared with BMS during clinical follow-up. [5][6][7][8] Two recent randomized trials demonstrated that there was no significant difference between DES and BMS in terms of long-term survival, survival free of myocardial infarction (MI), and stent thrombosis. 9,10) One study even observed increased late mortality with DES versus BMS.
11)We compared all-cause death and the composite of major adverse cardiac events (MACE) including all-cause death, re-MI, target lesion revascularization (TLR), and coronary artery bypass graft (CABG) after implantation of DES and BMS.
MethodsStudy population: The study population consisted of a total of 2,705 patients enrolled in the acute coronary syndrome registry who underwent percutaneous coronary intervention (PCI) at the Heart Center of Chonnam National University Hospital, South Korea between January 2004 and July 2006. A total of 1,237 patients had a final diagnosis of acute MI (AMI) and underwent primary PCI (PCI performed within 24 hour...