Department of Cardiology, Geneva University Hospitals, Geneva, Switzerland.
Department of Cardiology, Geneva University Hospitals, Geneva, Switzerland.
JACC Cardiovasc Interv. 2021 Nov 22;14(22):2461-2473. doi: 10.1016/j.jcin.2021.09.028.
The authors sought to compare the differential effects of ultrathin-strut and thicker-strut drug-eluting stents (DES) in patients with chronic (CCS) versus acute (ACS) coronary syndromes.
Newest-generation ultrathin-strut DES reduce target lesion failure (TLF) compared with thicker-strut second-generation DES in patients undergoing percutaneous coronary intervention.
PubMed, Embase, and Cochrane Central Register of Controlled Trials were searched for randomized controlled trials comparing newer-generation ultrathin-strut (<70 μm) versus thicker-strut (≥70 μm) DES. Patients were divided based on baseline clinical presentation (CCS versus ACS). The primary endpoint was TLF, a composite of cardiac death, target vessel myocardial infarction, or clinically indicated target lesion revascularization (TLR).
A total of 22,766 patients from 16 randomized controlled trials were included, of which 9 trials reported TLF rates in ACS patients. At a mean follow-up of 12.2 months, the risk of TLF was lower among patients treated with ultrathin-strut compared with thicker-strut DES (risk ratio [RR]: 0.85; 95% CI: 0.75-0.95; P = 0.006). The difference was driven by a lower risk of clinically-indicated TLR (RR: 0.75; 95% CI: 0.63-0.89; P < 0.001) among patients treated with ultrathin-strut DES. The treatment effect was consistent between patients presenting with CCS and ACS (relative RR: 0.97; 95% CI: 0.73-1.31; P for interaction = 0.854). In patients with ST-segment elevation myocardial infarction, TLF risk was lower among those treated with ultrathin- compared with thicker-strut DES (RR: 0.74; 95% CI: 0.54-0.99; P = 0.049).
Ultrathin-strut DES reduce the risk of TLF compared with thicker-strut second-generation DES in patients undergoing percutaneous coronary intervention, a difference caused by a lower risk of ischemia-driven TLR. The treatment effect was consistent among patients with CCS and ACS.
作者旨在比较慢性(CCS)和急性(ACS)冠状动脉综合征患者中使用超薄支架和较厚支架药物洗脱支架(DES)的差异影响。
在接受经皮冠状动脉介入治疗的患者中,最新一代超薄支架DES 降低了靶病变失败(TLF)的风险,与较厚支架第二代 DES 相比。
在 PubMed、Embase 和 Cochrane 对照试验中心注册数据库中检索了比较新一代超薄支架(<70μm)与较厚支架(≥70μm)DES 的随机对照试验。根据基线临床表现(CCS 与 ACS)将患者分为两组。主要终点是 TLF,包括心脏死亡、靶血管心肌梗死或临床指示的靶病变血运重建(TLR)的复合终点。
共有来自 16 项随机对照试验的 22766 名患者纳入研究,其中 9 项试验报告了 ACS 患者的 TLF 发生率。在平均 12.2 个月的随访中,与较厚支架 DES 相比,超薄支架 DES 治疗患者的 TLF 风险较低(风险比 [RR]:0.85;95%CI:0.75-0.95;P=0.006)。这一差异的原因是超薄支架 DES 治疗患者的临床指示性 TLR 风险较低(RR:0.75;95%CI:0.63-0.89;P<0.001)。在 CCS 和 ACS 患者中,治疗效果一致(相对 RR:0.97;95%CI:0.73-1.31;P 交互=0.854)。在 ST 段抬高型心肌梗死患者中,与较厚支架 DES 相比,超薄支架治疗患者的 TLF 风险较低(RR:0.74;95%CI:0.54-0.99;P=0.049)。
在接受经皮冠状动脉介入治疗的患者中,与较厚支架第二代 DES 相比,超薄支架 DES 降低了 TLF 的风险,这是由缺血驱动的 TLR 风险降低引起的。在 CCS 和 ACS 患者中,治疗效果一致。