Abstract

ObjectivesThis matched-cohort retrospective study investigated the long-term (9-year) safety and efficacy outcomes of patients with ST-segment elevation myocardial infarction (STEMI) and primary percutaneous coronary intervention (pPCI) with Genous (n = 102) versus TAXUS Liberté (n = 101) stents in 2006–2008.BackgroundIn the era of off-label use of drug-eluting stents for pPCI in patients with STEMI, the use of first-generation Genous stents (endothelial progenitor cell capture stents that have a passive coating and accelerate re-endothelialization) was proposed.MethodsThe primary endpoint was 9-year major adverse cardiac and cerebrovascular events (MACCE), including all-cause death, re-infarction, target vessel revascularization (TVR), and stroke. The secondary endpoints were the separate primary endpoint events at pre-defined time-points (in-hospital, 6 months, and yearly) and stent thrombosis. Time-dependent 9-year composite MACCE, all-cause death, and TVR were compared using Kaplan-Meier estimates and multivariate Cox regression models.ResultsPropensity score analysis confirmed the comparability of the groups. Patients in the Genous and TAXUS groups had 7 and 1 acute definitive stent thrombosis events, respectively (p<0.001). There was a trend towards higher in-hospital MACCE in the Genous group (10.8%) versus the TAXUS group (4.0%). Kaplan-Meier analysis showed that 9-year MACCE was significantly worse in the Genous than in the TAXUS group. The in-hospital, 6-month, 1-year, and 9-year mortality rates were 7.8%, 8.8%, 9.8%, and 23.5% in the Genous group and 2.0%, 3.0%, 4.0%, and 16.8% in the TAXUS group.ConclusionsHigher peri-procedural, in-hospital, and short-term mortality led to worse outcomes for first-generation Genous stents versus TAXUS Liberté stents for pPCI in STEMI. TAXUS Liberté stents had more favorable 9-year clinical outcomes.

Highlights

  • First-generation drug-eluting stents (DESs) reduced the incidence of in-stent restenosis compared to bare metal stents (BMS) in symptomatic coronary arterial disease by inhibiting smooth muscle cell proliferation and preventing intimal hyperplasia

  • There was a trend towards higher in-hospital major adverse cardiac and cerebrovascular events (MACCE) in the Genous group (10.8%) versus the TAXUS group (4.0%)

  • Kaplan-Meier analysis showed that 9-year MACCE was significantly worse in the Genous than in the TAXUS group

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Summary

Introduction

First-generation drug-eluting stents (DESs) reduced the incidence of in-stent restenosis compared to bare metal stents (BMS) in symptomatic coronary arterial disease by inhibiting smooth muscle cell proliferation and preventing intimal hyperplasia. Immunosuppressive, and anti-inflammatory drugs reduced target vessel failure and improved clinical outcomes [1,2,3]. Patients with acute ST-segment elevation myocardial infarction (STEMI) were excluded from the first DES trials due to the uncertainty of the thrombotic effect of DESs on vessel patency [3, 6]. In the early and mid-2000s, it was proposed that BMS and Genous stents be implanted during primary percutaneous coronary intervention (pPCI). In the era of off-label use of drug-eluting stents for pPCI in patients with STEMI, the use of first-generation Genous stents (endothelial progenitor cell capture stents that have a passive coating and accelerate re-endothelialization) was proposed

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