Département de cardiologie, Hôpital universitaire nord, Aix-Marseille Univ., Marseille, France.
Thromb Res. 2013 Jul;132(1):e15-8. doi: 10.1016/j.thromres.2013.04.030. Epub 2013 May 30.
The level of platelet reactivity (PR) inhibition obtained after P2Y12-ADP receptor antagonist loading dose (LD) is associated with the ischemic and bleeding risk following percutaneous coronary intervention (PCI) in acute coronary syndromes (ACS).
We aimed to evaluate the level of PR inhibition achieved by a 180 mg LD of ticagrelor and the rate of high on-treatment platelet reactivity (HTPR) in ACS patients undergoing PCI.
We performed a multicentre prospective observational study enrolling ACS patients undergoing PCI. Patients were included if they were admitted for ST-elevation myocardial infarction or non ST-elevation ACS. To assess PR, a VASP index was measured at least 6 and within 24 hours following a 180 mg LD of ticagrelor. HTPR was defined as a VASP index ≥50%.
One hundred and fifteen patients were included: 31.3% of STEMI, 49.6% of NSTEMI and 19.1% of unstable angina. Following ticagrelor LD the mean VASP index was 17±14%. However the response to ticagrelor was not uniform with a small inter-individual variability: inter quartile range: 7.6-22.8% and a rate of HTPR of 3.5%. A high number of patients, 65.6%, had a VASP index <16%. None of the baseline characteristics of the study population was associated with PR. In addition, PR was similar in STEMI, NSTEMI and unstable angina (p=0.9).
In ACS patients the level of PR inhibition achieved by a 180 mg loading dose of ticagrelor is not uniform and the rate of HTPR is 3.5%. A high proportion of patients exhibited a VASP index <16%.
在急性冠脉综合征(ACS)患者行经皮冠状动脉介入治疗(PCI)后,血小板反应性(PR)抑制水平与缺血和出血风险相关。
我们旨在评估 ACS 患者 PCI 中使用 180mg 替格瑞洛负荷剂量(LD)后达到的 PR 抑制水平和高反应性血小板(HTPR)发生率。
我们进行了一项多中心前瞻性观察研究,纳入了接受 PCI 的 ACS 患者。纳入标准为 ST 段抬高型心肌梗死或非 ST 段抬高型 ACS 患者。为了评估 PR,在接受替格瑞洛 180mg LD 后至少 6 小时且 24 小时内测量了 VASP 指数。HTPR 定义为 VASP 指数≥50%。
共纳入 115 例患者:31.3%为 ST 段抬高型心肌梗死,49.6%为非 ST 段抬高型心肌梗死,19.1%为不稳定型心绞痛。替格瑞洛 LD 后平均 VASP 指数为 17±14%。然而,替格瑞洛的反应并不均匀,个体间变异性较小:四分位间距为 7.6-22.8%,HTPR 发生率为 3.5%。大多数患者(65.6%)的 VASP 指数<16%。研究人群的基线特征均与 PR 无关。此外,STEMI、NSTEMI 和不稳定型心绞痛患者的 PR 相似(p=0.9)。
ACS 患者中,使用 180mg 替格瑞洛负荷剂量达到的 PR 抑制水平不一致,HTPR 发生率为 3.5%。很大一部分患者的 VASP 指数<16%。