Maintenance of long-term clinical benefit with sirolimus-eluting coronary stents - Three-year results of the RAVEL trial

Article

关键词: ULTRASOUND FOLLOW-UP;    INTRAVASCULAR ULTRASOUND;    NEOINTIMAL FORMATION;    CELL-CYCLE;    RAPAMYCIN;    ARTERIES;    IMPLANTATION;    RESTENOSIS;    PROLIFERATION;    INHIBITION;   

DOI  :  10.1161/01.CIR.0000156334.24955.B2

来源: SCIE

【 摘 要 】

Background - The use of sirolimus- eluting coronary stents has been associated with a nearly complete elimination of restenosis at 6 months and with a very low 1-year incidence of major adverse cardiac events (MACE). This analysis examined whether these beneficial effects persist over the longer term. Methods and Results - This multicenter trial randomly assigned 238 patients to revascularization of single, de novo, native coronary artery lesions with sirolimus- eluting versus conventional bare-metal stents. Survival free from target lesion revascularization (TLR), target vessel failure (TVF), and MACE up to 3 years of follow-up was compared between the 2 treatment groups. Complete data sets were available in 94.2% of patients treated with sirolimus- eluting stents and in 94.1% of patients randomized to the control group. The cumulative 1-, 2-, and 3-year event-free survival rates were 99.2%, 96.5%, and 93.7% for TLR and 95.8%, 92.3%, and 87.9% for TVF, respectively, in the sirolimus- eluting stent group, versus 75.9%, 75.9%, and 75.0% for TLR and 71.2%, 69.4%, and 67.3% for TVF in the control group (P < 0.001 for both comparisons at 3 years). Rates of MACE at 3 years were 15.8% in patients randomly assigned to sirolimus- eluting stents versus 33.1% in patients assigned to bare-metal stents (P = 0.002). One patient treated with a sirolimus- eluting stent died of a cardiac cause between 12 and 36 months. Conclusions - Treatment of de novo coronary stenosis with sirolimus- eluting stents was associated with a sustained clinical benefit and very low rates of TLR and of other MACE up to 3 years after device implantation.

【 授权许可】

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