textabstractBACKGROUND: Early results of sirolimus-eluting stent implantation showed a nearly complete abolition of neointimal hyperplasia. The question remains, however, whether the early promising results will still be evident at long-term follow-up. The objective of our study was to evaluate the efficiency of sirolimus-eluting stent implantation for up to 2 years of follow-up. METHODS AND RESULTS: Fifteen patients with de novo coronary artery disease were treated with 18-mm sirolimus-eluting Bx-Velocity stents (Cordis) loaded with 140 microg sirolimus/cm2 metal surface area in a slow release formulation. Quantitative angiography (QCA) and intravascular ultrasound (IVUS) were performed according to standard protocol. Sirolimus-eluting ste...
OBJECTIVES: The goal of this work was to verify whether the superiority of the sirolimus-eluting...
ObjectivesOur purpose was to evaluate the long-term use of sirolimus-eluting stents (SES) and bare-m...
ObjectivesThe aim of this study was to examine the 5-year clinical safety and efficacy outcomes in p...
textabstractBACKGROUND: The safety and efficacy of sirolimus-eluting stenting have been demonstrated...
This editorial refers to ‘Angioscopic differences in neointimal coverage and in persistence of throm...
ObjectivesThis study sought to assess the temporal course of neointimal hyperplasia (NIH) formation ...
textabstractBACKGROUND: We have previously reported the safety and effectiveness of sirolimus-elutin...
AIMS: The DESSOLVE III OCT substudy aimed to compare serially neointimal hyperplasia volume obstruct...
Aims: The DESSOLVE III OCT substudy aimed to compare serially neointimal hyperplasia volume obstruct...
ObjectivesFive-year clinical follow-up has been scheduled per protocol by the 4 Cypher (Cordis/Johns...
BACKGROUND: Studies focusing on short- and mid-term follow up support the beneficial role of sirolim...
Many studies have demonstrated that late or very late thrombosis after drug-eluting stent (DES) impl...
ObjectivesThe purpose of this study was to examine the two-year clinical outcomes in patients enroll...
ObjectivesThe goal of this work was to verify whether the superiority of the sirolimus-eluting stent...
textabstractBACKGROUND: Restenosis after conventional stenting is almost exclusively caused by neoin...
OBJECTIVES: The goal of this work was to verify whether the superiority of the sirolimus-eluting...
ObjectivesOur purpose was to evaluate the long-term use of sirolimus-eluting stents (SES) and bare-m...
ObjectivesThe aim of this study was to examine the 5-year clinical safety and efficacy outcomes in p...
textabstractBACKGROUND: The safety and efficacy of sirolimus-eluting stenting have been demonstrated...
This editorial refers to ‘Angioscopic differences in neointimal coverage and in persistence of throm...
ObjectivesThis study sought to assess the temporal course of neointimal hyperplasia (NIH) formation ...
textabstractBACKGROUND: We have previously reported the safety and effectiveness of sirolimus-elutin...
AIMS: The DESSOLVE III OCT substudy aimed to compare serially neointimal hyperplasia volume obstruct...
Aims: The DESSOLVE III OCT substudy aimed to compare serially neointimal hyperplasia volume obstruct...
ObjectivesFive-year clinical follow-up has been scheduled per protocol by the 4 Cypher (Cordis/Johns...
BACKGROUND: Studies focusing on short- and mid-term follow up support the beneficial role of sirolim...
Many studies have demonstrated that late or very late thrombosis after drug-eluting stent (DES) impl...
ObjectivesThe purpose of this study was to examine the two-year clinical outcomes in patients enroll...
ObjectivesThe goal of this work was to verify whether the superiority of the sirolimus-eluting stent...
textabstractBACKGROUND: Restenosis after conventional stenting is almost exclusively caused by neoin...
OBJECTIVES: The goal of this work was to verify whether the superiority of the sirolimus-eluting...
ObjectivesOur purpose was to evaluate the long-term use of sirolimus-eluting stents (SES) and bare-m...
ObjectivesThe aim of this study was to examine the 5-year clinical safety and efficacy outcomes in p...