TLR was observed in 10.7% of CYPHERTM treated patients compared to 8.1% of the XIENCE VTM treated patients, but failed to reach statistical significance ( P = 0.11). 20 There was an observed decrease in definite stent thrombosis, 0.7% vs. 1.3% in favor of XIENCE VTM, but again it failed to reach statistical significance ( P = 0.25). 20 The safety and efficacy of the Promus ElementTM stent has been recently demonstrated in a selected clinical trial population. 18 The SCAAR registry is a real world experience of DES implants in Sweden from November 2009 to March 2011.
← all excerpts
Second generation drug-eluting stents: a review of the everolimus-eluting platform.
1
0.1100
0.1100