a Department of Cardiology , Jiangmen Central Hospital , Jiangmen , China.
b Department of Cardiology , the Sixth People's Hospital of Chengdu , Chengdu , China.
Postgrad Med. 2019 Jan;131(1):43-51. doi: 10.1080/00325481.2019.1546531. Epub 2018 Dec 3.
Chronic kidney disease (CKD) patients are associated with very high rate of adverse cardiovascular outcomes after drug-eluting stents (DES) implantation. The clinical outcomes of second-generation DES versus first-generation DES in CKD patients remain controversial.
The aim of the current study was to perform a systematic review and meta-analysis to assess the safety and efficacy of second-generation DES versus first-generation DES in CKD patients.
A systematical search of databases of PubMed, EMBASE, and Cochrane Library was conducted for eligible studies comparing the clinical outcomes of first-generation DES versus second-generation DES. Sirolimus-eluting and paclitaxel-eluting stents were classified as first-generation DES, and everolimus-eluting, zotarolimus-eluting, and biolimus-eluting stent (BES) were classified as second-generation DES. A pooled odds ratio (OR) and 95% confidence interval (CI) were used to summary the estimates. Heterogeneity, subgroup analysis, sensitivity analysis and publication bias were also performed.
We identified 14 trials involving 9,542 patients with CKD undergoing percutaneous coronary intervention. First-generation DES implantation was associated with higher risk of long-term all-cause mortality (OR, 1.31; 95% CI, 1.02-1.69; P = 0.04; I = 0%), in stent restenosis (OR, 1.69; 95% CI, 1.14-2.49; P = 0.008; I = 49%) and stent thrombosis (OR, 1.64; 95% CI, 1.00-2.69; P = 0.05; I = 49%) compared with second-generation DES implantation. First-generation DES and second-generation DES showed similar efficacy in decreasing risk of repeat revascularization, myocardial infarction (MI), or major adverse cardiac events (MACE) between first-generation and second-generation DES implantation.
In CKD patients, the use of second-generation DES was associated with lower risk of long-term all-cause mortality, in stent restenosis and stent thrombosis as compared with first-generation DES. No differences were found regarding repeat revascularization, MI, and MACE.
在药物洗脱支架(DES)植入后,慢性肾脏病(CKD)患者的不良心血管结局发生率非常高。第二代 DES 与第一代 DES 在 CKD 患者中的临床结局仍存在争议。
本研究旨在进行系统评价和荟萃分析,以评估 CKD 患者中第二代 DES 与第一代 DES 的安全性和疗效。
对 PubMed、EMBASE 和 Cochrane 图书馆的数据库进行系统检索,以纳入比较第一代 DES 与第二代 DES 临床结局的研究。西罗莫司洗脱和紫杉醇洗脱支架被归类为第一代 DES,依维莫司洗脱、佐他莫司洗脱和生物可吸收支架(BES)被归类为第二代 DES。使用合并优势比(OR)和 95%置信区间(CI)来总结估计值。还进行了异质性、亚组分析、敏感性分析和发表偏倚。
我们确定了 14 项涉及 9542 例接受经皮冠状动脉介入治疗的 CKD 患者的试验。第一代 DES 植入与长期全因死亡率(OR,1.31;95%CI,1.02-1.69;P=0.04;I=0%)、支架内再狭窄(OR,1.69;95%CI,1.14-2.49;P=0.008;I=49%)和支架血栓形成(OR,1.64;95%CI,1.00-2.69;P=0.05;I=49%)的风险增加相关,与第二代 DES 植入相比。第一代 DES 和第二代 DES 在降低第一代和第二代 DES 植入后重复血运重建、心肌梗死(MI)或主要不良心脏事件(MACE)的风险方面显示出相似的疗效。
在 CKD 患者中,与第一代 DES 相比,使用第二代 DES 与长期全因死亡率、支架内再狭窄和支架血栓形成风险降低相关。在重复血运重建、MI 和 MACE 方面没有差异。