Key result
Thin-strut sirolimus-eluting stents linked to ~22% lower 1-year target lesion failure versus thicker biolimus-eluting stents.
Why the study?
Recent improvements in coronary stent design have focused on thinner struts, different alloys, and biocompatible polymers, prompting evaluation of a newer generation thin-strut cobalt chromium SES versus a second-generation thicker strut stainless steel BES in PCI practice.
Does a thin-strut cobalt chromium sirolimus-eluting stent reduce adverse clinical events compared to a thicker strut stainless steel biolimus-eluting stent in patients undergoing PCI?
Cohort (n=10,875)
Yes
Does a thin-strut cobalt chromium sirolimus-eluting stent reduce adverse clinical events compared to a thicker strut stainless steel biolimus-eluting stent in patients undergoing PCI?
Absolute Event Rate: 3.2% vs 4.1%
p-value: p=0.03
A newer generation thin-strut sirolimus-eluting stent is associated with lower rates of myocardial infarction and composite failure endpoints at 1 year compared to a thicker strut biolimus-eluting stent in real-world PCI practice.
Should not yet change stent selection in PCI; leaves open confirmation of thin-strut benefit in randomized trials.
OBJECTIVES: Recent improvements in coronary stent design have focussed on thinner struts, different alloys and architecture, more biocompatible polymers, and shorter drug absorption times. This study evaluates safety and efficacy of a newer generation thin-strut cobalt chromium sirolimus-eluting coronary stent (SES, Ultimaster) in comparison with a second-generation thicker strut stainless steel biolimus-eluting stent (BES, Nobori) in percutaneous coronary intervention (PCI) practice. METHODS: A propensity score analysis was performed to adjust for differences in baseline characteristics of 8137 SES patients and 2738 BES patients of two PCI registries (e-Ultimaster and NOBORI 2). An independent clinical event committee adjudicated all endpoint-related adverse events. RESULTS: The use of SES, as compared with BES was associated with a significantly lower rate of myocardial infarction (MI) (1.2% vs 2.2%; P = 0.0006) and target vessel-related MI (1.1% vs 1.8%; P = 0.002) at 1 year. One-year composite endpoints of all predefined endpoints were lower in patients undergoing SES implantation (target lesion failure: 3.2% vs 4.1%; P = 0.03, target vessel failure: 3.7% vs 5.0%; P = 0.003, patient-oriented composite endpoint 5.7% vs 6.8%; P = 0.03). No significant differences between SES and BES were observed in all-cause death (2.0% vs 1.6%; P = 0.19), cardiac death (1.2% vs 1.2%; P = 0.76) or stent thrombosis (0.6% vs 0.8%; P = 0.43). CONCLUSIONS: These findings suggest an improved clinical safety and efficacy of a newer generation thin-strut SES as compared with a second-generation thicker strut BES.
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Vlieger et al. (2020) conducted a cohort in Coronary artery disease requiring percutaneous coronary intervention (n=10,875). Thin-strut cobalt chromium sirolimus-eluting stent (Ultimaster) vs. Thicker strut stainless steel biolimus-eluting stent (Nobori) was evaluated on Target lesion failure (composite of cardiac death, target vessel-MI and clinically driven target lesion revascularization) (p=0.03). The thin-strut cobalt chromium sirolimus-eluting stent significantly reduced 1-year target lesion failure to 3.2% compared to 4.1% with the thicker strut stainless steel biolimus-eluting stent.
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