Wand Saskia, Adam Elisabeth Hannah, Wetz Anna Julienne, Meybohm Patrick, Kunze-Szikszay Nils, Zacharowski Kai, Popov Aron Frederick, Moritz Anton, Moldenhauer Lisa, Kaiser Julia, Bauer Martin, Weber Christian Friedrich
1 Department of Anesthesiology, University Medical Center Göttingen, Göttingen, Germany.
2 Department of Anesthesia, Intensive Care Medicine and Pain Therapy, University Hospital Frankfurt, Frankfurt am Main, Germany.
Clin Appl Thromb Hemost. 2018 Jan;24(1):179-185. doi: 10.1177/1076029617693939. Epub 2017 Feb 23.
We aimed to identify the prevalence of acetylsalicylic acid (ASA) nonresponse in patients after coronary artery bypass graft (CABG) surgery and the possible consequences for the rate of major cardiovascular events. This prospective, observational, bicentric cohort study was conducted in two German University hospitals. A total of 400 patients (200 in each study center) undergoing elective CABG surgery were enrolled after written informed consent. Platelet function was analyzed on day 3 (d3) and day 5 (d5) postoperatively following stimulation with arachidonic acid (ASPItest) and with thrombin receptor-activating peptide 6 (TRAPtest) using multiple electrode aggregometry (Multiplate). Individuals with an ASPItest ≥40 AU·min were categorized as ASA nonresponders. A 1-year follow-up recorded the combined end point of cardiovascular events, hospital admissions, or deaths related to cardiovascular disease. The prevalence of ASA nonresponse was 51.5% on d3, and it significantly increased to 71.3% on d5 ( P = .0049). The area under the aggregation curve in the TRAPtest ( P < .0001), the platelet count on d5 ( P = .009), and the cardiopulmonary bypass time ( P = .01) were identified as independent predictors of an ASA nonresponse. A 1-year follow-up recorded 54 events fulfilling criteria for the combined end point with no difference between ASA responders and nonresponders. This study indicates a high incidence of perioperative ASA nonresponse in patients following CABG. No effect on the incidence of cardiovascular events was recorded in the 1-year follow-up. Therefore, a randomized dosage adjustment trial should elucidate whether a tailored ASA treatment after CABG surgery represents a useful concept.
我们旨在确定冠状动脉旁路移植术(CABG)后患者中乙酰水杨酸(ASA)无反应的发生率以及对主要心血管事件发生率的可能影响。这项前瞻性、观察性、双中心队列研究在两家德国大学医院进行。共有400例接受择期CABG手术的患者在签署书面知情同意书后入组。术后第3天(d3)和第5天(d5),使用多电极聚集仪(Multiplate),在花生四烯酸(ASPItest)和凝血酶受体激活肽6(TRAPtest)刺激后分析血小板功能。ASPItest≥40 AU·min的个体被归类为ASA无反应者。1年随访记录心血管事件、住院或与心血管疾病相关死亡的联合终点。d3时ASA无反应的发生率为51.5%,d5时显著增加至71.3%(P = .0049)。TRAPtest中的聚集曲线下面积(P < .0001)、d5时的血小板计数(P = .009)和体外循环时间(P = .01)被确定为ASA无反应的独立预测因素。1年随访记录了54例符合联合终点标准的事件,ASA反应者和无反应者之间无差异。本研究表明CABG术后患者围手术期ASA无反应的发生率很高。1年随访中未记录到对心血管事件发生率的影响。因此,一项随机剂量调整试验应阐明CABG术后个体化ASA治疗是否是一个有用的概念。