Thoraxcenter, Department of Cardiology, Erasmus Medical Center Rotterdam, The Netherlands.
Int J Cardiol. 2013 Dec 5;170(1):36-42. doi: 10.1016/j.ijcard.2013.10.006. Epub 2013 Oct 12.
Newer generation everolimus-eluting stents (EES) improve clinical outcome compared to early generation sirolimus-eluting stents (SES) and paclitaxel-eluting stents (PES). We investigated whether the advantage in safety and efficacy also holds among the high-risk population of diabetic patients during long-term follow-up.
Between 2002 and 2009, a total of 1963 consecutive diabetic patients treated with the unrestricted use of EES (n=804), SES (n=612) and PES (n=547) were followed throughout three years for the occurrence of cardiac events at two academic institutions. The primary end point was the occurrence of definite stent thrombosis.
The primary outcome occurred in 1.0% of EES, 3.7% of SES and 3.8% of PES treated patients ([EES vs. SES] adjusted HR=0.58, 95% CI 0.39-0.88; [EES vs. PES] adjusted HR=0.29, 95% CI 0.13-0.67). Similarly, patients treated with EES had a lower risk of target-lesion revascularization (TLR) compared to patients treated with SES and PES ([EES vs. SES], 5.6% vs. 11.5%, adjusted HR=0.68, 95% CI: 0.55-0.83; [EES vs. PES], 5.6% vs. 11.3%, adjusted HR=0.51, 95% CI: 0.33-0.77). There were no differences in other safety end points, such as all-cause mortality, cardiac mortality, myocardial infarction (MI) and MACE.
In diabetic patients, the unrestricted use of EES appears to be associated with improved outcomes, specifically a significant decrease in the need for TLR and ST compared to early generation SES and PES throughout 3-year follow-up.
与早期的依维莫司洗脱支架(SES)和紫杉醇洗脱支架(PES)相比,新一代依维莫司洗脱支架(EES)改善了临床结果。我们研究了在长期随访中,高危糖尿病患者人群的安全性和疗效优势是否仍然存在。
在 2002 年至 2009 年间,共有 1963 例连续的糖尿病患者在两个学术机构中接受了不受限制的 EES(n=804)、SES(n=612)和 PES(n=547)治疗,随访 3 年以观察心脏事件的发生。主要终点是确定的支架血栓形成的发生。
EES、SES 和 PES 治疗患者的主要结局发生率分别为 1.0%、3.7%和 3.8%([EES 与 SES]调整后的 HR=0.58,95%CI 0.39-0.88;[EES 与 PES]调整后的 HR=0.29,95%CI 0.13-0.67)。同样,与 SES 和 PES 治疗的患者相比,EES 治疗的患者发生靶病变血运重建(TLR)的风险较低([EES 与 SES],5.6%与 11.5%,调整后的 HR=0.68,95%CI:0.55-0.83;[EES 与 PES],5.6%与 11.3%,调整后的 HR=0.51,95%CI:0.33-0.77)。其他安全性终点,如全因死亡率、心脏死亡率、心肌梗死(MI)和 MACE,没有差异。
在糖尿病患者中,无限制地使用 EES 似乎与改善结果相关,特别是与早期 SES 和 PES 相比,在 3 年随访期间,TLR 和 ST 的需求显著减少。