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1.
Circulation ; 114(9): 921-8, 2006 Aug 29.
Article in English | MEDLINE | ID: mdl-16908768

ABSTRACT

BACKGROUND: Sirolimus-eluting stents markedly reduce the risk of restenosis compared with bare metal stents. However, it is not known whether there are differences in effectiveness between bare metal and sirolimus-eluting stents in patients with total coronary occlusions. METHODS AND RESULTS: In a prospective, randomized, single-blind, 2-center trial, we enrolled 200 patients with total coronary occlusions: Half (n = 100) were randomly assigned to receive bare metal BxVelocity stents and half (n = 100) to receive sirolimus-eluting Cypher stents. The primary end point was angiographic binary in-segment restenosis rate at 6-month follow-up. Secondary end points were a composite of major adverse cardiac events, target vessel failure, binary in-stent restenosis rate, in-stent and in-segment minimal lumen diameter, percent diameter stenosis, and late luminal loss at 6-month follow-up. The sirolimus stent group showed a significantly lower in-stent binary restenosis rate of 7% compared with 36% in the bare metal stent group (P < 0.001). The in-segment binary restenosis rate was 11% in the group receiving a sirolimus stent versus 41% in the bare metal stent group (P < 0.0001), resulting in a target lesion revascularization rate of 4% in the sirolimus group versus 19% in the bare metal group (P < 0.001). Patients who received the drug-eluting stent also had significantly lower rates of target vessel revascularization, target vessel failure, and all major adverse cardiac events. CONCLUSIONS: In patients with total coronary occlusions, use of the sirolimus-eluting stents are superior to the bare metal stents with significant reduction in angiographic binary restenosis, resulting in significantly less need for target lesion and target vessel revascularization.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Coronary Stenosis/surgery , Sirolimus/therapeutic use , Stents , Aged , Coronary Angiography , Coronary Stenosis/diagnostic imaging , Coronary Stenosis/drug therapy , Equipment Design , Female , Follow-Up Studies , Humans , Male , Middle Aged , Myocardial Ischemia/etiology , Risk Factors , Single-Blind Method
2.
Am Heart J ; 149(3): e1-3, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15864219

ABSTRACT

Primary intracoronary stent placement after successfully crossing chronic total occlusions (CTO) decreases the high restenosis rate at long-term follow-up compared with conventional balloon angioplasty. Several studies have shown the efficacy of sirolimus-eluting stents in selected groups of patients. Whether sirolimus-eluting stents are superior to bare metal stents in CTO is unknown. In this prospective randomized trial, bare metal stent implantation will be compared with sirolimus-eluting stent implantation for the treatment of CTO. A total of 200 patients will be followed up for 12 months with angiographic follow-up at 6 months. Quantitative coronary analysis will be performed by an independent core laboratory. The primary end point is the binary angiographic restenosis and reocclusion rate.


Subject(s)
Coronary Restenosis/diagnostic imaging , Coronary Stenosis/therapy , Multicenter Studies as Topic/methods , Randomized Controlled Trials as Topic/methods , Sirolimus/administration & dosage , Stents/classification , Angioplasty, Balloon/methods , Chronic Disease , Coronary Angiography , Coronary Stenosis/diagnostic imaging , Delayed-Action Preparations , Follow-Up Studies , Humans , Patient Selection , Research Design
3.
Am Heart J ; 147(5): e22, 2004 May.
Article in English | MEDLINE | ID: mdl-15131557

ABSTRACT

BACKGROUND: Primary intracoronary stent placement after successfully crossing chronic total coronary occlusions may decrease the high restenosis rate at long-term follow-up compared with conventional balloon angioplasty. METHODS: In a prospective, randomized trial, balloon angioplasty was compared with stent implantation for the treatment of chronic total occlusions. Patients were followed for 12 months with angiographic follow-up at 6 months. Quantitative coronary analysis was performed by an independent core lab. RESULTS: A total of 200 patients were enrolled. Baseline characteristics were evenly distributed. After the procedure the mean minimal luminal diameter in the conventional group was 2.34 +/- 0.46 mm versus 2.90 +/- 0.41 mm in the stented group (P <.0001). The 6-month angiographic follow-up showed a mean minimal luminal diameter of 1.57 +/- 0.74 mm in the conventional group versus 1.93 +/- 0.85 mm in the stented group (P =.009) and a mean diameter stenosis of 44.7% +/- 25.0% versus 35.5% +/- 26.5% (P =.036). Binary angiographic restenosis (>50% diameter stenosis) was seen in 33% in the conventional group versus 22% in the stented group (P =.137). The reocclusion rates were 7.3% and 8.2%, respectively (P = 1.00). At 12 month follow-up, the rate of target lesion revascularization was significantly higher in the conventional group (29% versus 13%, P <.0001). CONCLUSION: These data demonstrate that stenting of chronic total occlusions is superior to balloon angioplasty alone with a statistically significant reduction in the need for target lesion revascularization and a lower, but not significant, restenosis rate.


Subject(s)
Angioplasty, Balloon, Coronary/methods , Coronary Disease/therapy , Stents , Chronic Disease , Coronary Angiography , Coronary Disease/drug therapy , Coronary Disease/surgery , Female , Follow-Up Studies , Humans , Male , Middle Aged , Prospective Studies , Recurrence , Statistics as Topic
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