John H. Stroger Jr. Hospital of Cook County, Chicago, IL, USA.
Wayne State University School of Medicine, Detroit Medical Center, Detroit, MI, USA.
Int J Cardiol. 2024 Oct 1;412:132269. doi: 10.1016/j.ijcard.2024.132269. Epub 2024 Jun 14.
In-stent restenosis (ISR) is seen in up to 20% of cases and is the primary cause of percutaneous coronary intervention (PCI) failure. With the use of re-stenting with a drug-eluting stent (DES), plain old balloon angioplasty (BA) use is decreasing. We aim to compare the efficacy and safety profile of DES over BA in the management of ISR.
Electronic databases were searched to identify all randomized controlled trials (RCTs) comparing DES to BA for coronary ISR. The mantel-Haenszel method with a random effects model was used to calculate pooled risk ratios (RR).
Four trials comprising 912 patients (543 in DES and 369 in the BA group) were included in the final study. The mean follow-up was 45 months. DES was found to be superior with a lower requirement of target vessel revascularization (TVR) (RR: 0.45, 95% CI: 0.31-0.64, p-value <0.0001), and target lesion revascularization (TLR) (RR: 0.59, 95%CI: 0.44-0.78, p-value 0.0002) compared to BA. However, all-cause mortality, cardiovascular mortality, incidence of myocardial infarction (MI), and target lesion thrombosis were not different between the two intervention arms.
DES was found to be superior to BA for the management of coronary ISR with a reduction in the risk of TLR and TVR. No difference in mortality, risk of MI, or target lesion thrombosis was observed between the two interventions.
支架内再狭窄(ISR)的发生率高达 20%,是经皮冠状动脉介入治疗(PCI)失败的主要原因。随着药物洗脱支架(DES)的再置入的应用,普通球囊血管成形术(BA)的应用正在减少。我们旨在比较 DES 和 BA 在 ISR 治疗中的疗效和安全性。
电子数据库检索所有比较 DES 与 BA 治疗冠状动脉 ISR 的随机对照试验(RCT)。采用固定效应模型荟萃分析计算合并风险比(RR)。
最终研究纳入了四项试验,共 912 例患者(DES 组 543 例,BA 组 369 例)。平均随访时间为 45 个月。DES 降低了靶血管血运重建(TVR)(RR:0.45,95%CI:0.31-0.64,p<0.0001)和靶病变血运重建(TLR)(RR:0.59,95%CI:0.44-0.78,p<0.0002)的需求,与 BA 相比具有优势。然而,两组间全因死亡率、心血管死亡率、心肌梗死(MI)发生率和靶病变血栓形成无差异。
DES 与 BA 相比,在治疗冠状动脉 ISR 方面更具优势,可降低 TLR 和 TVR 的风险。两种干预措施之间在死亡率、MI 风险或靶病变血栓形成方面无差异。