Comparison of ticagrelor and clopidogrel in anemic patients with acute coronary syndrome: efficacy and safety outcomes over one year.

IF 2.4 3区 医学 Q3 PHARMACOLOGY & PHARMACY
Tolga Onuk, Fuat Polat, Barış Yaylak, Şükrü Akyüz, Zeynep Kolak, Furkan Durak
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Abstract

Objective: This retrospective study aimed to investigate the potential impact of ticagrelor and clopidogrel treatment on cardiovascular outcomes in patients with anemia and acute coronary syndrome (ACS) and to provide insights into the optimal therapeutic approach for this vulnerable patient population.

Methods: A retrospective research design was employed, involving patients diagnosed with ST-segment elevation myocardial infarction (STEMI) or non-ST-segment elevation myocardial infarction (NSTEMI) between 2014 and 2021. Inclusion criteria required a hemoglobin level below 12 mg/dL and a minimum 12-month P2Y12 inhibitor treatment. Comprehensive clinical, biochemical, and echocardiographic data were collected from the hospital's electronic repository. The primary efficacy endpoint was major adverse cardiovascular events (MACE), encompassing total mortality, cardiovascular mortality, reinfarction, ischemic stroke, and hemorrhagic stroke. Major hemorrhage was the primary safety endpoint. Secondary outcomes included total mortality, cardiovascular mortality, reinfarction, ischemic stroke, and hemorrhagic stroke, individually.

Results: Patients treated with ticagrelor (n = 118) and clopidogrel (n = 538) were compared. No significant difference was observed in major adverse cardiovascular events (MACE) and major bleeding between ticagrelor and clopidogrel treatment groups (MACE: clopidogrel 10.0% vs. ticagrelor 11.0%, p = 0.75; major bleeding: clopidogrel 2.8%, ticagrelor 2.5%, p = 0.88). Patients with hemoglobin levels ≤ 8 mg/dL demonstrated significantly higher MACE and major bleeding rates in the ticagrelor group (p = 0.008 and p = 0.002, respectively). Among patients aged ≥ 75 years, ticagrelor treatment was associated with a higher risk of major bleeding (p = 0.04).

Conclusions: Ticagrelor and clopidogrel exhibited comparable efficacy and safety outcomes in anemic ACS patients over a one-year period. Although ticagrelor demonstrated superiority in reducing ischemic events, it is crucial to recognize the limitations of retrospective studies in informing clinical practice. This study offers valuable insights into tailoring antiplatelet therapy for anemic ACS patients and provides guidance for personalized treatment strategies, acknowledging the hypothesis-generating nature of retrospective analyses.

Abstract Image

在急性冠状动脉综合征贫血患者中比较替卡格雷和氯吡格雷:一年的疗效和安全性结果。
研究目的这项回顾性研究旨在探讨替卡格雷和氯吡格雷治疗对贫血合并急性冠状动脉综合征(ACS)患者心血管预后的潜在影响,并为这一脆弱患者群体的最佳治疗方法提供见解:采用回顾性研究设计,纳入2014年至2021年期间诊断为ST段抬高型心肌梗死(STEMI)或非ST段抬高型心肌梗死(NSTEMI)的患者。纳入标准要求血红蛋白水平低于 12 mg/dL,并接受至少 12 个月的 P2Y12 抑制剂治疗。综合临床、生化和超声心动图数据由医院的电子资料库收集。主要疗效终点是主要心血管不良事件(MACE),包括总死亡率、心血管死亡率、再梗死、缺血性卒中和出血性卒中。大出血是主要的安全性终点。次要结果包括总死亡率、心血管死亡率、再梗死、缺血性中风和出血性中风:结果:比较了接受替卡格雷(118例)和氯吡格雷(538例)治疗的患者。在主要不良心血管事件(MACE)和大出血方面,ticagrelor治疗组和氯吡格雷治疗组之间未观察到明显差异(MACE:氯吡格雷10.0% vs. ticagrelor 11.0%,p = 0.75;大出血:氯吡格雷2.8%,ticagrelor 2.5%,p = 0.88)。血红蛋白水平≤8 mg/dL的患者中,ticagrelor组的MACE和大出血发生率明显更高(分别为p = 0.008和p = 0.002)。在年龄≥75岁的患者中,替卡格雷治疗与较高的大出血风险相关(p = 0.04):结论:在一年的时间里,替卡格雷和氯吡格雷对贫血的ACS患者具有相似的疗效和安全性。虽然替卡格雷在减少缺血事件方面表现出优势,但必须认识到回顾性研究在指导临床实践方面的局限性。这项研究为贫血性 ACS 患者量身定制抗血小板疗法提供了宝贵的见解,并为个性化治疗策略提供了指导,同时也承认回顾性分析具有假设生成的性质。
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来源期刊
CiteScore
5.40
自引率
3.40%
发文量
170
审稿时长
3-8 weeks
期刊介绍: The European Journal of Clinical Pharmacology publishes original papers on all aspects of clinical pharmacology and drug therapy in humans. Manuscripts are welcomed on the following topics: therapeutic trials, pharmacokinetics/pharmacodynamics, pharmacogenetics, drug metabolism, adverse drug reactions, drug interactions, all aspects of drug development, development relating to teaching in clinical pharmacology, pharmacoepidemiology, and matters relating to the rational prescribing and safe use of drugs. Methodological contributions relevant to these topics are also welcomed. Data from animal experiments are accepted only in the context of original data in man reported in the same paper. EJCP will only consider manuscripts describing the frequency of allelic variants in different populations if this information is linked to functional data or new interesting variants. Highly relevant differences in frequency with a major impact in drug therapy for the respective population may be submitted as a letter to the editor. Straightforward phase I pharmacokinetic or pharmacodynamic studies as parts of new drug development will only be considered for publication if the paper involves -a compound that is interesting and new in some basic or fundamental way, or -methods that are original in some basic sense, or -a highly unexpected outcome, or -conclusions that are scientifically novel in some basic or fundamental sense.
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