阿托伐他汀与瑞舒伐他汀短期治疗对冠状动脉造影/经皮冠状动脉介入治疗患者预防造影剂相关急性肾损伤的比较:一项系统回顾和荟萃分析

IF 2.6 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Mansour Bahardoust, Danyal Yarahmadi, Zahra Aghakhani, Mohammad Mahdi Kakoienejad, Mohammadsadra Shamohammadi, Babak Goodarzy, Ghazaleh Donyadideh, Shabnam Rashidi, Azin Ghaffari
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引用次数: 0

摘要

在不同的研究中,阿托伐他汀与瑞舒伐他汀对经皮冠状动脉介入治疗(PCI)后对比剂相关急性肾损伤(CA-AKI)的预防效果存在差异,这可能是由于初始研究的规模较小。本系统综述和荟萃分析旨在比较阿托伐他汀与瑞舒伐他汀对PCI患者预防CA-AKI的效果。2000年至2024年,两名独立研究人员检索了PubMed、Embase、b谷歌Scholar、Cochrane Library和Web of Science数据库,以寻找评估阿托伐他汀与瑞舒伐他汀对行PCI的心脏患者预防CA-AKI效果的文章。对比剂暴露后48 - 72小时内,血清肌酐(SCr)绝对升高≥0.3 mg/dl或从基线升高≥50%被定义为CA-AKI。本系统评价和荟萃分析是根据PRISMA指南进行的。纳入了8项研究,涉及3,998例接受PCI治疗的患者。8项研究的汇总估计显示,接受他汀类药物治疗的患者PCI后CA-AKI的总发生率为8.5% (95% CI: 7.6, 9.3%)。亚组分析显示,服用阿托伐他汀和瑞舒伐他汀的患者CA-AKI发生率分别为8.5%和8.7%。阿托伐他汀与瑞舒伐他汀对PCI心绞痛患者CA-AKI的预防作用相似。阿托伐他汀和瑞舒伐他汀同样降低了PCI患者CA-AKI的总发生率。阿托伐他汀与瑞舒伐他汀预防PCI术后CA-AKI的效果也相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of short-term treatment with atorvastatin versus rosuvastatin for preventing contrast-associated acute kidney injury in patients undergoing coronary angiography/percutaneous coronary intervention: a systematic review and meta-analysis.

The effect of atorvastatin compared with rosuvastatin on the prevention of contrast-associated acute kidney injury (CA-AKI) after percutaneous coronary intervention (PCI) has been heterogeneous in different studies, which may be due to the small size of the initial studies. This systematic review and meta-analysis aimed to compare the effect of atorvastatin versus rosuvastatin on preventing CA-AKI in patients undergoing PCI. The databases PubMed, Embase, Google Scholar, Cochrane Library, and Web of Science were searched by two independent investigators from 2000 to 2024 to find articles that evaluated the effect of atorvastatin versus rosuvastatin on the prevention of CA-AKI in cardiac patients undergoing PCI. An absolute increase of serum creatinine (SCr) ≥0.3 mg/dl or an increase of ≥50% from baseline within 48 to 72 hours after contrast exposure was defined as CA-AKI. This systematic review and meta-analysis were conducted according to the PRISMA guidelines. Eight studies involving 3,998 Patients who underwent PCI were included. A pooled estimate of 8 studies showed that the overall incidence of CA-AKI after PCI in patients receiving statins, regardless of type, was 8.5 % (95% CI: 7.6, 9.3%). Subgroup analysis showed that the incidence of CA-AKI in patients receiving atorvastatin and rosuvastatin was 8.5% and 8.7%, respectively. The protective effect of atorvastatin on preventing CA-AKI in cardiac patients undergoing PCI was similar to that of rosuvastatin. Both atorvastatin and rosuvastatin similarly reduced the overall incidence of CA-AKI in patients undergoing PCI. The effects of atorvastatin and rosuvastatin on preventing CA-AKI after PCI were also similar.

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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
367
审稿时长
1 months
期刊介绍: Journal of Cardiovascular Pharmacology is a peer reviewed, multidisciplinary journal that publishes original articles and pertinent review articles on basic and clinical aspects of cardiovascular pharmacology. The Journal encourages submission in all aspects of cardiovascular pharmacology/medicine including, but not limited to: stroke, kidney disease, lipid disorders, diabetes, systemic and pulmonary hypertension, cancer angiogenesis, neural and hormonal control of the circulation, sepsis, neurodegenerative diseases with a vascular component, cardiac and vascular remodeling, heart failure, angina, anticoagulants/antiplatelet agents, drugs/agents that affect vascular smooth muscle, and arrhythmias. Appropriate subjects include new drug development and evaluation, physiological and pharmacological bases of drug action, metabolism, drug interactions and side effects, application of drugs to gain novel insights into physiology or pathological conditions, clinical results with new and established agents, and novel methods. The focus is on pharmacology in its broadest applications, incorporating not only traditional approaches, but new approaches to the development of pharmacological agents and the prevention and treatment of cardiovascular diseases. Please note that JCVP does not publish work based on biological extracts of mixed and uncertain chemical composition or unknown concentration.
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