Temporal Trends in the Outcomes of Percutaneous Coronary Intervention With Zotarolimus Eluting Stents Versus Everolimus Eluting Stents: A Meta-Analysis of Randomized Controlled Trials

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-06-18 DOI:10.1002/clc.24306
Jawad Basit, Mushood Ahmed, Aimen Shafiq, Zaofashan Zaheer, Abdulqadir J. Nashwan, Aleena Ahmed, Mohammad Hamza, Usman Naseer, Shafaqat Ali, Neelesh Gupta, Yasar Sattar, Akram Kawsara, Ramesh Daggubati, M. Chadi Alraies
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Abstract

Introduction

Long-term follow-up results of various trials comparing Zotarolimus eluting stents (ZES) with Everolimus eluting stents (EES) have been published recently. Additionally, over the last decade, there have been new trials comparing the ZES with various commercially available EES. We aim to conduct an updated meta-analysis in light of new evidence from randomized controlled trials (RCTs) to provide comprehensive evidence regarding the temporal trends in the clinical outcomes.

Methods

A comprehensive literature search was conducted across PubMed, Cochrane, and Embase. RCTs comparing ZES with EES for short (<2 years), intermediate (2–3 years), and long-term follow-ups (3–5 years) were included. Relative risk was used to pool the dichotomous outcomes using the random effects model employing the inverse variance method. All statistical analysis was conducted using Revman 5.4.

Results

A total of 18 studies reporting data at different follow-ups for nine trials (n = 14319) were included. At short-term follow-up (<2 years), there were no significant differences between the two types of stents (all-cause death, cardiac death, Major adverse cardiovascular events (MACE), target vessel myocardial infarction, definite or probable stent thrombosis or safety outcomes (target vessel revascularization, target lesion revascularization, target vessel failure, target lesion failure). At intermediate follow-up (2–3 years), EES was superior to ZES for reducing target lesion revascularization (RR = 1.28, 95% CI = 1.05–1.58, p < 0.05). At long-term follow-up (3–5 years), there were no significant differences between the two groups for any of the pooled outcomes (p > 0.05).

Conclusion

ZES and EES have similar safety and efficacy at short, intermediate, and long-term follow-ups.

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使用佐他莫司洗脱支架与埃维罗莫司洗脱支架进行经皮冠状动脉介入治疗结果的时间趋势:随机对照试验的 Meta 分析。
导言:最近发表了多项比较佐他洛利木洗脱支架(ZES)和依维莫司洗脱支架(EES)的长期随访结果。此外,在过去十年中,又有一些新的试验将 ZES 与各种市售 EES 进行了比较。我们旨在根据随机对照试验(RCTs)的新证据进行最新的荟萃分析,为临床结果的时间趋势提供全面的证据:在 PubMed、Cochrane 和 Embase 中进行了全面的文献检索。方法:在 PubMed、Cochrane 和 Embase 中进行了全面的文献检索:共纳入了 18 项研究,报告了 9 项试验(n = 14319)的不同随访数据。结论:ZES和EES的安全性相似:在短期、中期和长期随访中,ZES 和 EES 具有相似的安全性和有效性。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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