中等强度阿托伐他汀和依泽替米贝联合治疗与高强度阿托伐他汀单药治疗在经皮冠状动脉介入治疗患者中的应用:评估RACING的普遍性。

IF 5.3 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Seung-Jun Lee, Jae Hong Joo, Sohee Park, Choongki Kim, Dong-Woo Choi, Yong-Joon Lee, Sung-Jin Hong, Chul-Min Ahn, Jung-Sun Kim, Byeong-Keuk Kim, Young-Guk Ko, Donghoon Choi, Yangsoo Jang, Chung-Mo Nam, Myeong-Ki Hong
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引用次数: 0

摘要

目的:使用瑞舒伐他汀,race(他汀单药降脂与他汀/依泽替米联合降脂治疗高危心血管疾病的疗效和安全性随机比较)试验显示,在动脉粥样硬化性心血管疾病患者中,中等强度他汀与依泽替米联合降脂比高强度他汀单药更有效。本研究调查了在日常临床实践中,联合降脂治疗是否对阿托伐他汀而非瑞舒伐他汀的患者有益。方法与结果:采用治疗加权稳定逆概率法,从全国队列数据库中筛选出32993例药物洗脱支架(DES)植入术后使用阿托伐他汀的患者:6 215例阿托伐他汀20 mg +依泽替米贝10 mg(联合降脂治疗),25 778例阿托伐他汀40-80 mg单药治疗。根据race试验设计,主要终点是心血管死亡、心肌梗死、冠状动脉血运重建术、心力衰竭住院治疗或非致死性卒中的3年综合情况。联合降脂治疗与主要终点发生率较低相关(12.9% vs.高强度阿托伐他汀单药组15.1%;风险比[HR] 0.81, 95%可信区间[CI] 0.74-0.88, p结论:在临床实践中,使用依折替米贝和中强度阿托伐他汀联合降脂方法与良好的临床结果、药物依从性以及DES植入治疗患者新发糖尿病需要药物的发生率降低相关。试验注册:ClinicalTrial.gov (NCT04715594)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combination therapy with moderate-intensity atorvastatin and ezetimibe vs. high-intensity atorvastatin monotherapy in patients treated with percutaneous coronary intervention in practice: assessing RACING generalizability.

Aims: Using rosuvastatin, the RACING (randomized comparison of efficacy and safety of lipid-lowering with statin monotherapy versus statin/ezetimibe combination for high-risk cardiovascular diseases) trial showed the beneficial effects of combining moderate-intensity statin with ezetimibe compared with high-intensity statin monotherapy in patients with atherosclerotic cardiovascular disease. This study investigated whether the beneficial effects of combination lipid-lowering therapy extend to patients treated with atorvastatin, not rosuvastatin, in daily clinical practice.

Methods and results: Using stabilized inverse probability of treatment weighting, a total of 31 993 patients who were prescribed atorvastatin after drug-eluting stent (DES) implantation were identified from a nationwide cohort database: 6215 patients with atorvastatin 20 mg plus ezetimibe 10 mg (combination lipid-lowering therapy) and 25 778 patients with atorvastatin 40-80 mg monotherapy. The primary endpoint was the 3-year composite of cardiovascular death, myocardial infarction, coronary artery revascularization, hospitalization for heart failure treatment, or non-fatal stroke in accordance with the RACING trial design. Combination lipid-lowering therapy was associated with a lower incidence of the primary endpoint (12.9% vs. 15.1% in high-intensity atorvastatin monotherapy; hazard ratio [HR] 0.81, 95% confidence interval [CI] 0.74-0.88, P < 0.001). Compared with high-intensity atorvastatin monotherapy, combination lipid-lowering therapy was also significantly associated with lower rates of statin discontinuation (10.0% vs. 8.4%, HR 0.81, 95% CI 0.73-0.90, P < 0.001) and new-onset diabetes requiring medication (8.8% vs. 7.0%, HR 0.80, 95% CI 0.70-0.92, P = 0.002).

Conclusion: In clinical practice, a combined lipid-lowering approach utilizing ezetimibe and moderate-intensity atorvastatin was correlated with favourable clinical outcomes, drug compliance, and a reduced incidence of new-onset diabetes requiring medications in patients treated with DES implantation. Trial registration:  ClinicalTrial.gov (NCT04715594).

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来源期刊
European Heart Journal - Cardiovascular Pharmacotherapy
European Heart Journal - Cardiovascular Pharmacotherapy Medicine-Cardiology and Cardiovascular Medicine
CiteScore
10.10
自引率
14.10%
发文量
65
期刊介绍: The European Heart Journal - Cardiovascular Pharmacotherapy (EHJ-CVP) is an international, peer-reviewed journal published in English, specifically dedicated to clinical cardiovascular pharmacology. EHJ-CVP publishes original articles focusing on clinical research involving both new and established drugs and methods, along with meta-analyses and topical reviews. The journal's primary aim is to enhance the pharmacological treatment of patients with cardiovascular disease by interpreting and integrating new scientific developments in this field. While the emphasis is on clinical topics, EHJ-CVP also considers basic research articles from fields such as physiology and molecular biology that contribute to the understanding of cardiovascular drug therapy. These may include articles related to new drug development and evaluation, the physiological and pharmacological basis of drug action, metabolism, drug interactions, and side effects.
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