Department of Cardiology, West China Hospital, Sichuan University, Chengdu, China.
J Interv Cardiol. 2013 Jun;26(3):228-38. doi: 10.1111/j.1540-8183.2013.12017.x. Epub 2013 Feb 6.
Damage to the vascular endothelium may be one of the pathophysiological causes of in-stent thrombosis and restenosis. Endothelial progenitor cell (EPC) capture stents (ECS) have the ability to accelerate the damage repair process. However, the clinical outcomes of ECS remain unknown thus far.
To evaluate the impact of ECS use on the clinical outcomes of patients with coronary artery disease by comparing ECS to drug-eluting stent (DES) and/or bare metal stent (BMS).
Studies and abstracts were retrieved from the PubMed, Cochrane Library, and EMBASE online databases and from the conference compilations of the American Heart Association (AHA), the American College of Cardiology (ACC), and Transcatheter Cardiovascular Therapeutics (TCT). These studies were analyzed to investigate whether there was a difference in the clinical therapeutic effects between the ECS group and the DES/BMS group. The primary clinical end-point events were in-stent thrombosis and target lesion revascularization (TLR). The secondary clinical end-point events were target lesion failure (TLF), total mortality, cardiac death, and myocardial infarction (MI).
A total of 2,024 patients were enrolled in the analysis of in-stent thrombosis. There was no significant difference in the incidence of in-stent thrombosis between the ECS group and the DES/BMS group. A total of 1,745 patients were enrolled in the analysis of TLR, and there was no significant difference in the TLR incidence between the ECS group and the DES/BMS group. However, compared with DES, the TLR incidence for ECS increased 1.73-fold (relative risk [RR]: 1.73, 95% confidence interval [95% CI]: 1.01-2.94, P = 0.04). Moreover, the incidence of cardiac death and TLF also increased 3.54-fold (RR: 3.54, 95% CI: 1.13-11.08, P = 0.03) and 1.90-fold (RR: 1.90, 95% CI: 1.05-3.45, P = 0.03), respectively. But compared with BMS, there is no significance of the clinical events.
Compared with DES/BMS use, ECS use may not reduce the incidence of in-stent thrombosis and TLR. In addition, the incidence of TLR and cardiac death with ECS is possibly relatively higher compared with DES and no difference compared with BMS, but this also needs more large RCTs to guarantee.
血管内皮损伤可能是支架内血栓形成和再狭窄的病理生理原因之一。内皮祖细胞(EPC)捕获支架(ECS)具有加速损伤修复过程的能力。然而,到目前为止,ECS 的临床结果仍不清楚。
通过比较 ECS 与药物洗脱支架(DES)和/或金属裸支架(BMS),评估 ECS 使用对冠心病患者临床结局的影响。
从 PubMed、Cochrane 图书馆和 EMBASE 在线数据库以及美国心脏协会(AHA)、美国心脏病学会(ACC)和经导管心血管治疗(TCT)会议汇编中检索研究和摘要,以调查 ECS 组与 DES/BMS 组之间临床治疗效果是否存在差异。主要临床终点事件为支架内血栓形成和靶病变血运重建(TLR)。次要临床终点事件为靶病变失败(TLF)、总死亡率、心脏性死亡和心肌梗死(MI)。
共纳入 2024 例患者进行支架内血栓形成分析。ECS 组与 DES/BMS 组支架内血栓形成发生率无显著差异。共纳入 1745 例患者进行 TLR 分析,ECS 组与 DES/BMS 组 TLR 发生率无显著差异。然而,与 DES 相比,ECS 的 TLR 发生率增加了 1.73 倍(相对风险 [RR]:1.73,95%置信区间 [95%CI]:1.01-2.94,P = 0.04)。此外,心脏性死亡和 TLF 的发生率也分别增加了 3.54 倍(RR:3.54,95%CI:1.13-11.08,P = 0.03)和 1.90 倍(RR:1.90,95%CI:1.05-3.45,P = 0.03)。但是与 BMS 相比,临床事件没有统计学意义。
与 DES/BMS 相比,ECS 可能不会降低支架内血栓形成和 TLR 的发生率。此外,与 DES 相比,ECS 的 TLR 和心脏性死亡发生率可能相对较高,与 BMS 相比则无差异,但这也需要更多大型 RCT 来保证。