endeavor ii

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ENDEAVOR II •Target vessel failure at 9 months: 7.9% for Endeavor vs. 15.1% for Driver •Target lesion revascularization at 9 months: 4.6% vs. 11.8% (p = 0.0001), respectively •Death: 1.2% vs. 0.5% (p = 0.34), respectively •Stent thrombosis: 0.5% vs. 1.2%, respectively Trial design: Stable patients with native coronary disease were randomized to DES (n = 598) versus BMS (n = 599). Primary outcome was target vessel failure at 9 months. Results Conclusions •Among stable patients undergoing PCI for a single de novo lesion, the use of the Endeavor drug- eluting stent was beneficial. •This stent reduced target vessel failure and target lesion revascularization compared with a Driver bare-metal stent. Fajadet J, et al. Circulation 2006;114:798-806 (p = 0.0001) (p = 0.22) DES BMS % Target vessel failure Stent thrombosis 7.9 15.1 0.5 1.2

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ENDEAVOR II. Target vessel failure at 9 months: 7.9% for Endeavor vs. 15.1% for Driver Target lesion revascularization at 9 months: 4.6% vs. 11.8% (p = 0.0001), respectively Death: 1.2% vs. 0.5% (p = 0.34), respectively Stent thrombosis: 0.5% vs. 1.2%, respectively. - PowerPoint PPT Presentation

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Page 1: ENDEAVOR II

ENDEAVOR II

• Target vessel failure at 9 months: 7.9% for Endeavor vs. 15.1% for Driver

• Target lesion revascularization at 9 months: 4.6% vs. 11.8% (p = 0.0001), respectively

• Death: 1.2% vs. 0.5% (p = 0.34), respectively

• Stent thrombosis: 0.5% vs. 1.2%, respectively

Trial design: Stable patients with native coronary disease were randomized to DES (n = 598) versus BMS (n = 599). Primary outcome was target vessel failure at 9 months.

Results

Conclusions

• Among stable patients undergoing PCI for a single de novo lesion, the use of the Endeavor drug-eluting stent was beneficial.

• This stent reduced target vessel failure and target lesion revascularization compared with a Driver bare-metal stent.

Fajadet J, et al. Circulation 2006;114:798-806

(p = 0.0001)

(p = 0.22)

DES BMS

%

Target vessel failure Stent thrombosis

7.9

15.1

0.5 1.2