Heart Center, Segeberger Kliniken GmbH, Academic Teaching Hospital of the Universities of Kiel, Lübeck, and Hamburg, Am Kurpark 1, 23795, Bad Segeberg, Germany.
Cardiology Department, Heart Center Leipzig, University of Leipzig, Leipzig, Germany.
Clin Res Cardiol. 2021 Oct;110(10):1574-1585. doi: 10.1007/s00392-021-01852-9. Epub 2021 Apr 16.
To compare Orsiro biodegradable-polymer sirolimus-eluting stent (Orsiro BP-SES) with durable-polymer everolimus-eluting stent (DP-EES) regarding target lesion failure (TLF) after rotational atherectomy (RA), with a focus on small stents (diameter ≤ 3 mm) where Orsiro BP-SES has 60 µm strut thickness, while DP-EES remains with 81 µm strut thickness.
New-generation drug-eluting stent (DES) is superior to early-generation DES in all percutaneous coronary intervention (PCI) settings including RA. Recently, the Orsiro BP-SES was superior to a DP-EES in an all comer's population.
Among patients who underwent RA at a single center, 121 were treated with Orsiro BP-SES and 164 with DP-EES (Promus and Xience). Those treated with other stent types, presenting with acute myocardial infarction or had a chronic total occlusion were excluded. Incidence of TLF was assessed.
After 2 years, the TLF rate in Orsiro BP-SES and DP-EES groups was 10% and 18%, respectively (adjusted HR 0.55, 95%CI 0.26-1.16, p = 0.115). The rate of TLF was significantly lower in small Orsiro BP-SES with ultra-thin struts as compared to DP-EES with the same diameters (adjusted HR 0.19, 95% CI 0.04-0.87, p = 0.032), driven by lower rates of clinically driven target lesion revascularization (log-rank p = 0.022). Age (p = 0.035), total stent length (p = 0.007) and diabetes mellitus (p = 0.011) emerged as independent predictors of TLF in the whole population.
In the whole cohort, Orsiro BP-SES and DP-EES had comparable rates of long-term TLF after RA. In the small stent subgroup, the Orsiro BP-SES with ultra-thin struts showed significant lower rate of TLF at 2 years.
比较可降解聚合物西罗莫司洗脱支架(Orsiro BP-SES)和永久性聚合物依维莫司洗脱支架(DP-EES)在经皮冠状动脉介入治疗(PCI)中旋磨术后的靶病变失败(TLF),重点关注直径≤3mm 的小支架,Orsiro BP-SES 的支架厚度为 60μm,而 DP-EES 仍为 81μm。
新一代药物洗脱支架(DES)在包括旋磨术在内的所有 PCI 治疗中均优于早期一代 DES。最近,Orsiro BP-SES 在所有患者人群中优于 DP-EES。
在单中心接受旋磨术的患者中,121 例接受 Orsiro BP-SES 治疗,164 例接受 DP-EES(Promus 和 Xience)治疗。排除接受其他支架类型治疗、发生急性心肌梗死或存在慢性完全闭塞的患者。评估 TLF 的发生率。
在 2 年时,Orsiro BP-SES 和 DP-EES 组的 TLF 发生率分别为 10%和 18%(调整后的 HR 0.55,95%CI 0.26-1.16,p=0.115)。与相同直径的 DP-EES 相比,超薄支架的小直径 Orsiro BP-SES 的 TLF 发生率显著降低(调整后的 HR 0.19,95%CI 0.04-0.87,p=0.032),这主要归因于临床驱动的靶病变血运重建率较低(对数秩检验 p=0.022)。年龄(p=0.035)、总支架长度(p=0.007)和糖尿病(p=0.011)是整个队列中 TLF 的独立预测因素。
在整个队列中,旋磨术后 Orsiro BP-SES 和 DP-EES 的长期 TLF 发生率相当。在小支架亚组中,超薄支架的 Orsiro BP-SES 在 2 年时 TLF 发生率显著降低。