Abstract

Among drug-eluting stents (DESs), the durable polymer everolimus-eluting stent (EES) and resolute zotarolimus-eluting stent (R-ZES) are widely used in clinical practice and have contributed to improve the outcomes of patients undergoing percutaneous coronary intervention (PCI). Few studies addressed their long-term comparative performance in patients with acute coronary syndrome (ACS). We aimed to investigate the 5 year comparative efficacy of EES and R-ZES in ACS. We queried ACTION-ACS, a large-scale database of ACS patients undergoing PCI. The treatment groups were analyzed using propensity score matching. The primary endpoint was a composite of mortality, myocardial infarction (MI), stroke, repeat PCI, and definite or probable stent thrombosis, which was addressed at the five-year follow-up. A total of 3497 matched patients were analyzed. Compared with R-ZES, a significant reduction in the primary endpoint at 5 years was observed in patients treated with EES (hazard ratio (HR) [95%CI] = 0.62 [0.54–0.71], p < 0.001). By landmark analysis, differences between the two devices emerged after the first year and were maintained thereafter. The individual endpoints of mortality (HR [95%CI] = 0.70 [0.58–0.84], p < 0.01), MI (HR [95%CI] = 0.55 [0.42–0.74], p < 0.001), and repeat PCI (HR [95%CI] = 0.65 [0.53–0.73], p < 0.001) were all significantly lower in the EES-treated patients. Stroke risk did not differ between EES and R-ZES. In ACS, a greater long-term clinical efficacy with EES vs. R-ZES was observed. This difference became significant after the first year of the ACS episode and persisted thereafter.

Highlights

  • The advent of modern, second-generation coronary drug-eluting stents (DESs) has contributed to improve the outcomes of patients with coronary artery disease (CAD)undergoing percutaneous coronary intervention (PCI) by refining metallic design, polymer coatings, and the introduction of newer antiproliferative drugs [1]

  • Segment elevation myocardial infarction (STEMI) had acute myocardial injury with clinical evidence of acute myocardial ischemia according to the fourth universal definition of myocardial infarction

  • Patients treated with everolimus-eluting stent (EES) stent had a significantly lower risk of major adverse cardiovascular and cerebrovascular events (MACCEs) at 5 years: 36.8% vs. 46.3% (HR [95% confidence interval (CI)] = 0.62 [0.54–0.71], p < 0.001, Figure 2A)

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Summary

Introduction

The advent of modern, second-generation coronary drug-eluting stents (DESs) has contributed to improve the outcomes of patients with coronary artery disease (CAD)undergoing percutaneous coronary intervention (PCI) by refining metallic design, polymer coatings, and the introduction of newer antiproliferative drugs [1]. The advent of modern, second-generation coronary drug-eluting stents (DESs) has contributed to improve the outcomes of patients with coronary artery disease (CAD). Among CAD patients, those with acute coronary syndrome (ACS) constitute a high-risk cohort experiencing more frequent adverse clinical events [2]. There is a paucity of data concerning the long-term comparison of second-generation DES in the ACS context. Zotarolimus-eluting resolute stents (R-ZESs) (Medtronic) and everolimus-eluting stents (EESs), such as Xience (Abbott Vascular) and Promus Element (Boston Scientific), are second-generation DES widely used in clinical practice. Two studies have reported comparable outcomes in the long-term between these devices [4,5]. They were all-comers trials with many stable CAD patients included

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