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NORSTENT Trial design: Patients with obstructive coronary artery disease were randomized to a drug-eluting stent (DES) (n = 4,504) versus a bare-metal.

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Presentation on theme: "NORSTENT Trial design: Patients with obstructive coronary artery disease were randomized to a drug-eluting stent (DES) (n = 4,504) versus a bare-metal."— Presentation transcript:

1 NORSTENT Trial design: Patients with obstructive coronary artery disease were randomized to a drug-eluting stent (DES) (n = 4,504) versus a bare-metal stent (BMS) (n = 4,509). Clopidogrel was recommended for 9 months after the procedure. Results (p = 0.66) Death or MI at a median of 5 years: 16.6% of the DES group versus 17.1% of the BMS group (p = 0.66) TLR: 5.3% versus 10.3%, respectively, for DES versus BMS (p < 0.001) Definite stent thrombosis: 0.8% versus 1.2%, respectively, for DES versus BMS (p = ) 17.1 16.6 % Conclusions Similar rates of long-term death or MI were observed with DES versus BMS DES were associated with an approximate 3% absolute reduction in repeat revascularization and a small, but significant reduction in stent thrombosis DES BMS Bønaa KH, et al. N Engl J Med 2016;375:


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