Division of Cardiology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia.
Leon H. Charney Division of Cardiology, New York University School of Medicine, New York, New York.
JACC Cardiovasc Interv. 2017 Mar 13;10(5):462-473. doi: 10.1016/j.jcin.2016.12.002.
The authors sought to perform a meta-analysis of randomized clinical trials (RCTs) comparing the safety and efficacy of biodegradable polymer drug-eluting stents (BP-DES) to second-generation durable polymer drug-eluting stents (DP-DES).
Prior meta-analyses have established the superiority of BP-DES over bare-metal stents and first-generation DP-DES; however, their advantage compared with second-generation DP-DES remains controversial.
The authors searched PubMed and Scopus databases for RCTs comparing BP-DES to the second-generation DP-DES. Outcomes included target vessel revascularization (TVR) as efficacy outcome and cardiac death, myocardial infarction (MI), and definite or probable stent thrombosis (ST) as safety outcomes. In addition, we performed landmark analysis for endpoints beyond 1 year of follow-up and a subgroup analysis based on the stent characteristics.
The authors included 16 RCTs comprising 19,886 patients in the meta-analysis. At the longest available follow-up (mean duration 26 months), we observed no significant differences in TVR (p = 0.62), cardiac death (p = 0.46), MI (p = 0.98), or ST (risk ratio: 0.83, 95% confidence interval: 0.64 to 1.09; p = 0.19). Our landmark analysis showed that BP-DES were not associated with a reduction in the risk of very late ST (risk ratio: 0.87, 95% confidence interval: 0.49 to 1.53; p = 0.62). Similar outcomes were seen regardless of the eluting drug (biolimus vs. sirolimus), the stent platform (stainless steel vs. alloy), the kinetics of polymer degradation or drug release (<6 months vs. >6 months), the strut thickness of the BP-DES (thin <100 μm vs. thick >100 μm), or the DAPT duration (≥6 months vs. ≥12 months).
BP-DES have similar safety and efficacy profiles to second-generation DP-DES.
作者旨在对比较生物可降解聚合物药物洗脱支架(BP-DES)与第二代持久聚合物药物洗脱支架(DP-DES)安全性和疗效的随机临床试验(RCT)进行荟萃分析。
先前的荟萃分析已经证实 BP-DES 优于裸金属支架和第一代 DP-DES;然而,与第二代 DP-DES 相比,其优势仍存在争议。
作者在 PubMed 和 Scopus 数据库中搜索比较 BP-DES 与第二代 DP-DES 的 RCT。结果包括作为疗效结果的靶血管血运重建(TVR)和作为安全性结果的心脏死亡、心肌梗死(MI)和确定或可能的支架血栓形成(ST)。此外,我们还对随访时间超过 1 年的终点进行了里程碑分析,并根据支架特征进行了亚组分析。
作者将 16 项 RCT 纳入荟萃分析,共计 19886 例患者。在最长的可获得随访(平均随访时间 26 个月)中,我们未观察到 TVR(p=0.62)、心脏死亡(p=0.46)、MI(p=0.98)或 ST(风险比:0.83,95%置信区间:0.64 至 1.09;p=0.19)方面的显著差异。我们的里程碑分析表明,BP-DES 与降低极晚期 ST 的风险无关(风险比:0.87,95%置信区间:0.49 至 1.53;p=0.62)。无论洗脱药物(比马前列素与西罗莫司)、支架平台(不锈钢与合金)、聚合物降解或药物释放的动力学(<6 个月与>6 个月)、BP-DES 的支架厚度(<100μm 与>100μm 厚)或 DAPT 持续时间(≥6 个月与≥12 个月)如何,都有相似的结果。
BP-DES 与第二代 DP-DES 具有相似的安全性和疗效特征。