Department of Endovascular Surgery, Tokyo Medical and Dental University, Tokyo, Japan; Department of Neurology and Neurological Science, Tokyo Medical and Dental University, Tokyo, Japan.
Department of Endovascular Surgery, Tokyo Medical and Dental University, Tokyo, Japan.
J Stroke Cerebrovasc Dis. 2022 Sep;31(9):106631. doi: 10.1016/j.jstrokecerebrovasdis.2022.106631. Epub 2022 Jul 16.
To investigate the associations of perioperative P2Y12 reaction units (PRU) measured using VerifyNow with ischemic and bleeding events, and to determine the PRU threshold in the setting of elective neuro-endovascular treatment (EVT) for intracranial/extracranial vascular disease in patients taking aspirin and clopidogrel.
Of the patients undergoing elective neuro-EVT while taking aspirin and clopidogrel, those taking both antiplatelet agents for 7 days or more and whose PRU and aspirin reaction units (ARU) were measured were included. The primary and safety outcomes were defined as symptomatic ischemic and major bleeding events within 30 days after EVT.
A total of 197 patients were available for the analyses. Higher PRU was associated with symptomatic ischemic events on multivariable logistic analysis (odds ratio per 10 increase 1.14 [95% confidence interval 1.03-1.27], p=0.011). Receiver operating characteristic curve analysis showed that PRU ≥212 was the threshold to predict symptomatic ischemic events (area under the curve=0.73; sensitivity, 62.5%; specificity, 82.0%). Lower PRU was also associated with major bleeding events (odds ratio per 10 increase 0.87 [0.78-0.96], p=0.004), and the threshold to predict major bleeding events was PRU ≤46 (area under the curve=0.76; sensitivity, 70.0%; specificity, 87.2%) CONCLUSIONS: The PRU value was associated with symptomatic ischemic and major bleeding events after elective neuro-EVT in patients taking aspirin and clopidogrel. PRU ≥212 and PRU ≤46 appeared to be the threshold values to predict symptomatic ischemic and major bleeding events, respectively.
本研究旨在探讨使用 VerifyNow 测定的围手术期 P2Y12 反应单位(PRU)与缺血性和出血性事件的相关性,并确定接受阿司匹林和氯吡格雷双联抗血小板治疗的患者行择期神经血管内治疗(EVT)治疗颅内/颅外血管疾病时的 PRU 阈值。
在接受择期神经 EVT 治疗且服用阿司匹林和氯吡格雷的患者中,纳入了接受双联抗血小板治疗 7 天或以上且 PRU 和阿司匹林反应单位(ARU)可测量的患者。主要终点和安全性终点定义为 EVT 后 30 天内发生症状性缺血性和主要出血性事件。
共纳入 197 例患者进行分析。多变量逻辑分析显示,较高的 PRU 与症状性缺血性事件相关(每增加 10 个单位,比值比为 1.14 [95%置信区间 1.03-1.27],p=0.011)。受试者工作特征曲线分析显示,PRU≥212 是预测症状性缺血性事件的阈值(曲线下面积为 0.73;敏感度为 62.5%,特异性为 82.0%)。较低的 PRU 也与主要出血性事件相关(每增加 10 个单位,比值比为 0.87 [0.78-0.96],p=0.004),预测主要出血性事件的阈值为 PRU≤46(曲线下面积为 0.76;敏感度为 70.0%,特异性为 87.2%)。
PRU 值与接受阿司匹林和氯吡格雷双联抗血小板治疗的患者行择期神经 EVT 后的症状性缺血性和主要出血性事件相关。PRU≥212 和 PRU≤46 似乎分别是预测症状性缺血性和主要出血性事件的阈值。