Effect of Biolimus-Eluting Stents With Biodegradable Polymer vs Bare-Metal Stents on Cardiovascular Events Among Patients With Acute Myocardial Infarction

Peter Jüni, Marco Roffi, Andreas Baumbach, Stephan Windecker, Ran Kornowski, Lorenz Räber, Dik Heg, Henning Kelbæk, Miodrag Ostojić, David Tüller, Clemens von Birgelen, Aris Moschovitis, Ahmed A. Khattab, Peter Wenaweser, Robert F. Bonvini, Giovanni Pedrazzini, Klaus Weber, Sven Trelle, Thomas F. Lüscher, Masanori Taniwaki, Christian M. Matter, Bernhard Meier, for the COMFORTABLE AMI Trial Investigators
2012-08-22

SCID:  54.1/zqngpwtp
CONTEXT: The efficacy and safety of drug-eluting stents compared with bare-metal stents remains controversial in patients with ST-segment elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PCI). OBJECTIVE: To compare stents eluting biolimus from a biodegradable polymer with bare-metal stents in primary PCI. DESIGN, SETTING, AND PATIENTS: A prospective, randomized, single-blinded, controlled trial of 1161 patients presenting with STEMI at 11 sites in Europe and Israel between September 19, 2009, and January 25, 2011. Clinical follow-up was performed at 1 and 12 months. INTERVENTION: Patients were randomized 1:1 to receive the biolimus-eluting stent (n = 575) or the bare-metal stent (n = 582). MAIN OUTCOME MEASURES: Primary end point was the rate of major adverse cardiac events, a composite of cardiac death, target vessel-related reinfarction, and ischemia-driven target-lesion revascularization at 1 year. RESULTS: Major adverse cardiac events at 1 year occurred in 24 patients (4.3%) receiving biolimus-eluting stents with biodegradable polymer and 49 patients (8.7%) receiving bare-metal stents (hazard ratio [HR], 0.49; 95% CI, 0.30-0.80; P = .004). The difference was driven by a lower risk of target vessel-related reinfarction (3 [0.5%] vs 15 [2.7%]; HR, 0.20; 95% CI, 0.06-0.69; P = .01) and ischemia-driven target-lesion revascularization (9 [1.6%] vs 32 [5.7%]; HR, 0.28; 95% CI, 0.13-0.59; P < .001) in patients receiving biolimus-eluting stents compared with those receiving bare-metal stents. Rates of cardiac death were not significantly different (16 [2.9%] vs 20 [3.5%], P = .53). Definite stent thrombosis occurred in 5 patients (0.9%) treated with biolimus-eluting stents and 12 patients (2.1%; HR, 0.42; 95% CI, 0.15-1.19; P = .10) treated with bare-metal stents. CONCLUSION: Compared with a bare-metal stent, the use of biolimus-eluting stents with a biodegradable polymer resulted in a lower rate of the composite of major adverse cardiac events at 1 year among patients with STEMI undergoing primary PCI. TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT00962416.
Publication Details
Publication Date
2012-08-22
Journal
Publisher
ISSN
Access Type
Author Information
Authors
Peter Jüni
Marco Roffi
Andreas Baumbach
Stephan Windecker
Ran Kornowski
Lorenz Räber
Dik Heg
Henning Kelbæk
Miodrag Ostojić
David Tüller
Clemens von Birgelen
Aris Moschovitis
Ahmed A. Khattab
Peter Wenaweser
Robert F. Bonvini
Giovanni Pedrazzini
Klaus Weber
Sven Trelle
Thomas F. Lüscher
Masanori Taniwaki
Christian M. Matter
Bernhard Meier
for the COMFORTABLE AMI Trial Investigators
Explore More Research
Use the citation graph to discover related papers and expand your research horizons.
Click any node to explore
Download PDF
100%