Division of Cardiology, ASL VCO, Verbania, Italy.
Department of Cardiology, Policlinico Casilino, Rome, Italy.
Thromb Haemost. 2018 May;118(5):852-863. doi: 10.1055/s-0038-1635578. Epub 2018 Apr 4.
Early escalation from clopidogrel to new generation P2Y12 inhibitors is common practice in patients with ST-elevation myocardial infarction (STEMI) treated with primary percutaneous coronary intervention (pPCI). Real-world data about this strategy, however, are limited.
From 2012 to 2015, 1,057 consecutive STEMI patients treated with pPCI in an Italian hub-and-spoke network were prospectively included in an observational registry (RENOVAMI, ClinicalTrials.gov Identifier: NCT01760382). We compared the prevalence, predictive factors and in-hospital outcomes of patients escalated to a new generation P2Y12 inhibitor within the first 24 hours from pPCI with those continuing on admission antiplatelet therapy.
In the first 24 hours after pPCI, 165 patients (15.6%) were escalated from clopidogrel to a new generation P2Y12 inhibitor, while de-escalation to clopidogrel was occasional (19 patients, 1.8%) and switch between new generation P2Y12 inhibitors was rare (8 patients, 0.8%, all from ticagrelor to prasugrel). Drug eluting stent use (adjusted odds ratio [OR], 2.19, 95% confidence interval [CI], 1.55-3.08, = 0.0002) and impaired renal function (adjusted OR, 0.19, 95% CI, 0.05-0.77, = 0.02) were the only independent predictive factors for the decision to escalate. After adjustment for potential confounders, escalation did not predict in-hospital outcomes, whereas the overall use of new generation P2Y12 inhibitors was correlated with a better in-hospital survival (adjusted hazard ratio, 0.47, 95% CI, 0.25-0.91, = 0.03). Moreover, escalation did not influence bleeding rates.
In this prospective registry of STEMI patients treated with pPCI and contemporary antiplatelet therapy, early escalation to a new generation P2Y12 inhibitor appeared safe and did not significantly affect in-hospital bleeding rates.
在接受直接经皮冠状动脉介入治疗(pPCI)的 ST 段抬高型心肌梗死(STEMI)患者中,早期将氯吡格雷升级为新一代 P2Y12 抑制剂是常见做法。然而,关于这种策略的真实数据有限。
在意大利的一个中心辐射网络中,2012 年至 2015 年,1057 例连续 STEMI 患者接受 pPCI 治疗,前瞻性纳入观察性登记研究(RENOVAMI,临床试验.gov 标识符:NCT01760382)。我们比较了在 pPCI 后 24 小时内升级为新一代 P2Y12 抑制剂的患者与继续接受入院抗血小板治疗的患者的发生率、预测因素和住院期间结局。
在 pPCI 后 24 小时内,165 例(15.6%)患者从氯吡格雷升级为新一代 P2Y12 抑制剂,而降级至氯吡格雷的情况很少见(19 例,1.8%),新一代 P2Y12 抑制剂之间的转换也很少见(8 例,0.8%,均由替格瑞洛转为普拉格雷)。药物洗脱支架的使用(调整后的比值比[OR],2.19,95%置信区间[CI],1.55-3.08, = 0.0002)和肾功能不全(调整后的 OR,0.19,95%CI,0.05-0.77, = 0.02)是决定升级的唯一独立预测因素。在调整了潜在混杂因素后,升级与住院期间结局无关,而新一代 P2Y12 抑制剂的总体使用率与住院期间生存的改善相关(调整后的风险比,0.47,95%CI,0.25-0.91, = 0.03)。此外,升级并未影响出血发生率。
在接受 pPCI 和当代抗血小板治疗的 STEMI 患者的前瞻性登记研究中,早期升级为新一代 P2Y12 抑制剂似乎是安全的,并且不会显著影响住院期间出血的发生率。