Abstract

Biodegradable polymers (BDPs) and ultrathin struts were recently introduced to drug-eluting stents (DES) to further improve outcomes. In this study, we analyzed and compared the effect of the ultrathin strut BDP-DES (UBDP-DES) with the conventional durable polymer-DES (DP-DES) in patients with ST-segment elevation myocardial infarction (STEMI) who underwent primary percutaneous coronary intervention (PPCI). A total of 356 STEMI patients (n = 160 in the UBDP-DES group and n = 196 in the DP-DES group) were enrolled. The primary endpoint was target lesion failure (TLF), including cardiac death, target vessel myocardial infarction, and ischemic-driven, target lesion revascularization (ID-TLR). The mean age was 60.3 ± 12.7 years (male 81.7%), and the median follow-up duration was 63.8 months. TLF was numerically more frequent in the UBDP-DES group (8.1% vs. 4.1%; HR 2.14; 95% CI 0.89–5.18; p = 0.091). Propensity score matching (PSM) was performed to balance discrepancies in the baseline characteristics due to patients in the UBDP-DES group initially having more unstable vital signs. However, after PSM (n = 116 in each group), there was no significant difference in TLF (5.3% vs. 5.3%; HR 1.04, 95% CI 0.34-3.22; p = 0.947) or other secondary endpoints including ID-TLR. In the subgroup analysis, subjects with initial acute heart failure (AHF), defined as Killip class ≥ 3, were associated with 13.6% chance of 30-day mortality (9-fold of those without AHF), although chances of repeat revascularization were low (3.0%). Among patients with AHF, the UBDP-DES group was associated with a numerically higher chance of TLF compared with the DP-DES group. There was no difference in TLF between groups in patients without AHF. This study showed that UBDP-DES has long-term clinical outcomes similar to those of conventional DP-DES in real-world Korean STEMI patients receiving PPCI, especially in those without initial AHF.

Highlights

  • Drug-eluting stents (DESs) have changed the landscape of percutaneous coronary intervention (PCI) by markedly reducing the rate of in-stent restenosis [1]

  • Peak levels of troponin-I was higher in the durable polymer DESs (DP-DES) group, while there was no difference in peak creatinine kinase myocardial band (CK-MB) or NT-proBNP

  • The BIOSTEMI (BDP sirolimus-eluting stents versus durable polymer everolimuseluting stents in patients with segment elevation myocardial infarction (STEMI)) trial showed that the UBDP-DES had superior results in terms of composite endpoint driven by lower rates of ID-TLR [23]

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Summary

Introduction

Drug-eluting stents (DESs) have changed the landscape of percutaneous coronary intervention (PCI) by markedly reducing the rate of in-stent restenosis [1]. The OrsiroTM (Biotronik AG, Bülach, Switzerland) stent adopts both the BDP and ultrathin struts, which have shown promising results [22,23]. We sought to retrospectively compare the real-world long-term outcomes of the ultrathin strut BDP-DES (UBDP-DES), the OrsiroTM (Biotronik AG, Bülach, Switzerland) stent, and the durable polymer DESs (DP-DES), the Xience VTM (Abbott Vascular, Santa Clara, CA, USA) and Endeavor ResoluteTM (Medtronic Vascular, Santa Rosa, CA, USA), in patients with or without AHF who underwent primary percutaneous coronary intervention (PPCI) due to ST-segment elevation myocardial infarction (STEMI)

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