Pharmacodynamic effects of cangrelor in patients with acute or chronic coronary syndrome undergoing percutaneous coronary intervention: the POMPEII Registry.

IF 7.6 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Giuseppe Gargiulo, Plinio Cirillo, Luca Sperandeo, Domenico Simone Castiello, Lina Manzi, Imma Forzano, Domenico Florimonte, Fiorenzo Simonetti, Mario Enrico Canonico, Marisa Avvedimento, Roberta Paolillo, Alessandra Spinelli, Federica Buongiorno, Luigi Di Serafino, Carmen Anna Maria Spaccarotella, Anna Franzone, Raffaele Piccolo, Eugenio Stabile, Marco Valgimigli, Giovanni Esposito
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引用次数: 0

Abstract

Background: Cangrelor is approved for oral P2Y12 inhibitor-naïve patients undergoing percutaneous coronary intervention (PCI). Pharmacodynamic (PD) investigations in various clinical settings, with various assays, have shown contrasting data in terms of the extent of platelet inhibition and rates of high residual platelet reactivity (HRPR).

Aims: We aimed to assess the PD effects of cangrelor in all patients receiving it during PCI.

Methods: PharmacOdynaMic Effects of Cangrelor in PatiEnts wIth Acute or chronIc Coronary Syndrome Undergoing Percutaneous Coronary Intervention (POMPEII Registry; ClinicalTrials.gov: NCT04790032) is an investigator-initiated, prospective study assessing PD effects at 4 timepoints with 3 assays. Clinical outcomes at 30 days were also assessed.

Results: From March 2021 to June 2024, 150 patients undergoing PCI and receiving cangrelor were enrolled (64 patients underwent elective PCI; 30 had non-ST-elevation acute coronary syndrome; and 56 had ST-segment elevation myocardial infarction [STEMI], of whom 24 were pretreated with ticagrelor). Most patients switched from cangrelor to either clopidogrel or ticagrelor. Inhibition of platelet aggregation was moderate during cangrelor infusion (light transmittance aggregometry with adenosine diphosphate 20 μM: 57.6±16.5%), with rates of 3.2% for HRPR and 1.3% for bailout tirofiban. Rates of HRPR were relevant at 3 h (37.9%) and 4-6 h (15.3%), and HRPR occurred significantly more frequently in patients switching to clopidogrel compared with ticagrelor. Rates of ischaemic and bleeding events were low.

Conclusions: Cangrelor provided effective platelet inhibition in most patients with ACS or CCS undergoing PCI, including those with STEMI who were pretreated with ticagrelor. Switching from cangrelor to an oral P2Y12 inhibitor, mainly clopidogrel, exposed a large number of patients to a variable period of on-treatment HRPR.

经皮冠状动脉介入治疗急性或慢性冠状动脉综合征患者的康格洛的药效学效应:庞培登记。
背景:canrelor被批准用于经皮冠状动脉介入治疗(PCI)的口服P2Y12 inhibitor-naïve患者。药效学(PD)研究在不同的临床环境中,通过各种分析,显示了血小板抑制程度和高残余血小板反应率(HRPR)方面的对比数据。目的:我们的目的是评估在PCI期间接受康格洛治疗的所有患者的PD效果。方法:康格乐在急性或慢性冠状动脉综合征患者经皮冠状动脉介入治疗中的药效学影响(POMPEII Registry;ClinicalTrials.gov: NCT04790032)是一项由研究者发起的前瞻性研究,通过3项分析在4个时间点评估PD的影响。还评估了30天的临床结果。结果:从2021年3月至2024年6月,纳入了150例接受PCI治疗并服用康格洛的患者(64例患者接受了选择性PCI;非st段抬高急性冠状动脉综合征30例;st段抬高型心肌梗死(STEMI) 56例,其中替格瑞洛预处理24例。大多数患者从康格瑞转为氯吡格雷或替格瑞。在康格瑞洛输注期间,血小板聚集的抑制是中度的(二磷酸腺苷20 μM的透光率:57.6±16.5%),HRPR的抑制率为3.2%,替罗非班的抑制率为1.3%。HRPR的发生率在3 h(37.9%)和4-6 h(15.3%)时相关,并且与替格瑞洛相比,改用氯吡格雷的患者发生HRPR的频率更高。缺血性和出血事件发生率低。结论:对于大多数接受PCI治疗的ACS或CCS患者,包括STEMI患者,替格瑞洛可有效抑制血小板。从angrelor切换到口服P2Y12抑制剂,主要是氯吡格雷,使大量患者暴露于治疗期间的可变HRPR。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Eurointervention
Eurointervention CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
10.30
自引率
4.80%
发文量
380
审稿时长
3-8 weeks
期刊介绍: EuroIntervention Journal is an international, English language, peer-reviewed journal whose aim is to create a community of high quality research and education in the field of percutaneous and surgical cardiovascular interventions.
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