Three-Year Outcome of Sirolimus -Eluting Versus Bare-Metal Stents for the Treatment of ST-Segment Elevation Myocardial Infarction (from the MISSION! Intervention Study)

To compare the long-term efficacy and safety of sirolimus-eluting stents (SES) to those of bare-metal stents (BMS) for ST-segment elevation myocardial infarction, outcomes were assessed in 310 patients (mean age age 59 ± 11 years, 78% men) included in the randomized MISSION! Intervention Study: A Pr...

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Published inThe American journal of cardiology Vol. 106; no. 1; pp. 4 - 12
Main Authors Atary, Jael Z., MD, van der Hoeven, Bas L., MD, PhD, Liem, Su San, MD, PhD, Jukema, J. Wouter, MD, PhD, van der Bom, Johanna G., MD, PhD, Atsma, Douwe E., MD, PhD, Bootsma, Marianne, MD, PhD, Zeppenfeld, Katja, MD, PhD, van der Wall, Ernst E., MD, PhD, Schalij, Martin J., MD, PhD
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.07.2010
Elsevier
Elsevier Limited
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Summary:To compare the long-term efficacy and safety of sirolimus-eluting stents (SES) to those of bare-metal stents (BMS) for ST-segment elevation myocardial infarction, outcomes were assessed in 310 patients (mean age age 59 ± 11 years, 78% men) included in the randomized MISSION! Intervention Study: A Prospective Randomised Controlled Trial to Evaluate the Efficacy of Drug-Eluting Stents Versus Bare-Metal Stents for the Treatment of Acute Myocardial Infarction after a median follow-up period of 38 months. All patients were treated with aspirin (lifelong) and clopidogrel for 1 year after stent implantation. Except for a significant difference between reference vessel diameters (SES 2.76 mm vs BMS 2.92 mm, p = 0.02), there were no significant differences in baseline and angiographic characteristics between the treatment groups (158 SES, 152 BMS). A significant difference between SES and BMS patients for all revascularization end points was found after the first year of follow-up. However, at 3 years of follow-up, although there was still a trend toward better clinical outcomes in SES-treated patients, differences were no longer significant (death 4.4% vs 6.6%, p = 0.41; target vessel–related myocardial infarction 2.5% vs 4.6%, p = 0.32; target vessel revascularization 8.9% vs 15.8%, p = 0.06), target lesion revascularization 6.3% vs 12.5%, p = 0.06; and target vessel failure 12.0% vs 19.7%, p = 0.06). Three cases of very late (definite) stent thrombosis were observed in the SES group (1.9%) versus none in the BMS group (p = 0.14). In conclusion, the significant SES benefit (compared to BMS) in patients with ST-segment elevation myocardial infarctions at 1-year follow-up in terms of target vessel revascularizations decreased to some extent because of more similar target vessel revascularization rates during the 2 subsequent years. Rates of death and nonfatal recurrent MI remained comparable.
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ISSN:0002-9149
1879-1913
DOI:10.1016/j.amjcard.2010.02.005