Comparative effectiveness and safety of dual antiplatelet therapy with ticagrelor vs. clopidogrel in older adults with acute coronary syndrome: a target trial emulation study.

IF 6.1 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Carole A Marxer, Paul Hjemdahl, Juan J Carrero, Edouard L Fu
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引用次数: 0

Abstract

Aims: There is conflicting trial evidence on the comparative effects of dual antiplatelet therapy (DAPT) with ticagrelor vs. clopidogrel in older patients with acute coronary syndromes (ACS). We aimed to assess the risk of major adverse cardiovascular events (MACE) and major bleeding in ACS patients ≥75 years initiating ticagrelor vs. clopidogrel treatment.

Methods and results: We used healthcare data from the Stockholm region (2011-2021) to emulate a hypothetical target trial comparing ticagrelor vs. clopidogrel. MACE was defined as a composite of cardiovascular death, myocardial infarction, or stroke. Patients were followed for 12 months. Inverse probability of treatment weighting was used to adjust for 46 baseline confounders. We used weighted Cox proportional hazards regression to estimate hazard ratios (HRs) with 95% confidence intervals (CIs) and the weighted Aalen-Johansen estimator to estimate absolute risks (AR).Among 4637 older patients [median age, 81 years (IQR, 77-85)], 49% initiated DAPT with ticagrelor and 51% with clopidogrel. After weighting, all confounders were balanced. Ticagrelor was associated with a lower one-year MACE risk than clopidogrel (11.1% vs. 14.9%), corresponding to an AR difference of -3.8% (95%CI, -6.8, -0.8). The HR for ticagrelor vs. clopidogrel was 0.73 (95%CI, 0.56-0.95). There was no difference in the risk of major bleeding with one-year absolute risks of 4.3% with ticagrelor vs. 4.8% with clopidogrel, and a HR of 0.89 (95%CI, 0.63-1.27).

Conclusion: In ACS patients aged ≥75 years, ticagrelor was associated with a lower risk of MACE than clopidogrel. There were no differences in major bleeding, although the confidence interval was wide.

替格瑞洛与氯吡格雷双重抗血小板治疗老年人急性冠脉综合征的有效性和安全性比较:一项目标试验模拟研究
目的:关于替格瑞洛与氯吡格雷双重抗血小板治疗(DAPT)对老年急性冠脉综合征(ACS)患者的比较效果的试验证据存在矛盾。我们的目的是评估≥75岁ACS患者开始替格瑞洛与氯吡格雷治疗的主要不良心血管事件(MACE)和主要出血的风险。方法和结果:我们使用斯德哥尔摩地区(2011-2021年)的医疗数据来模拟比较替格瑞洛和氯吡格雷的假设目标试验。MACE定义为心血管死亡、心肌梗死或中风的复合。随访12个月。使用治疗加权逆概率来调整46个基线混杂因素。我们使用加权Cox比例风险回归来估计95%置信区间的风险比(hr),并使用加权aallen - johansen估计来估计绝对风险(AR)。在4,637例老年患者(中位年龄81岁[IQR 77-85])中,49%的患者开始使用替格瑞洛DAPT, 51%的患者开始使用氯吡格雷DAPT。加权后,平衡所有混杂因素。替格瑞洛的1年MACE风险低于氯吡格雷(11.1% vs. 14.9%),对应的AR差异为-3.8% (95%CI -6.8, -0.8)。替格瑞洛与氯吡格雷的HR为0.73 (95%CI 0.56-0.95)。替格瑞洛组和氯吡格雷组的1年ARs大出血风险无差异,分别为4.3%和4.8%,HR为0.89 (95%CI 0.63-1.27)。结论:在年龄≥75岁的ACS患者中,替格瑞洛发生MACE的风险低于氯吡格雷。尽管置信区间很宽,但在大出血方面没有差异。
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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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