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术前 P2Y 受体抑制剂类型和停药时间如何影响出血?

How Do Type of Preoperative P2Y Receptor Inhibitor and Withdrawal Time Affect Bleeding?

机构信息

Department of Cardiac Surgery, Medical University of Graz, Austria; Department of Cardiovascular and Endovascular Surgery, Paracelsus Medical University, Salzburg, Austria.

Institute for Medical Informatics, Statistics, and Documentation, Medical University of Graz, Graz, Austria.

出版信息

Ann Thorac Surg. 2021 Jan;111(1):77-84. doi: 10.1016/j.athoracsur.2020.04.126. Epub 2020 Jun 18.

Abstract

BACKGROUND

Despite recommendations for standardized preoperative waiting of at least 3, 5, and 7 days for ticagrelor, clopidogrel, and prasugrel, respectively, there is still substantial interinstitutional variation in preoperative discontinuation of dual antiplatelet therapy in patients needing coronary artery bypass grafting (CABG).

METHODS

In 299 patients undergoing CABG with or without valve intervention less than 7 days after last P2Y receptor inhibition, this study evaluated calculated red blood cell loss and Bleeding Academic Research Consortium type 4 (BARC-4) bleeding.

RESULTS

A total of 83% of patients underwent CABG less than 48 hours after last drug intake. Calculated blood loss was lower in patients taking clopidogrel as compared with prasugrel or ticagrelor (1063 mL [690 to 1394 mL] vs 1351 mL [876 to 1829 mL] vs 1330 mL [994 to 1691 mL]; P < .001). Overall, 135 (45%) patients sustained BARC-4 bleeding; the incidence differed among the groups (P = .015) and was significantly higher in prasugrel-treated patients, as compared with clopidogrel-treated patients. In multivariable linear regression analysis, European System for Cardiac Operative Risk Evaluation II (EuroSCORE II), aspirin dose, cardiopulmonary bypass time, drug withdrawal time, and type of P2Y receptor inhibitor were significantly associated with red blood cell loss. Compared with 0 to 24 hours, a period of more than 48 hours of preoperative discontinuation substantially reduced calculated blood loss by 37% to 48% and BARC-4 bleeding by 58% to 71%, depending on the P2Y receptor inhibitor.

CONCLUSIONS

Exposure to prasugrel and ticagrelor 24 hours or less before CABG increases both calculated blood loss and BARC-4 bleeding as compared with clopidogrel. Although discontinuation for longer than 48 hours substantially reduced calculated blood loss and BARC-4 bleeding across all P2Y receptor inhibitors, our single-center data further support strict adherence to the 2017 guidelines whenever justified by stable hemodynamics and nonjeopardized myocardium.

摘要

背景

尽管建议替格瑞洛、氯吡格雷和普拉格雷的术前停药等待时间分别至少为 3、5 和 7 天,但在需要冠状动脉旁路移植术(CABG)的患者中,双抗血小板治疗的术前停药仍然存在很大的机构间差异。

方法

在 299 例接受 CABG 加或不加瓣膜介入治疗的患者中,有 83%的患者在最后一次 P2Y 受体抑制后不到 7 天接受了 CABG。本研究评估了计算的红细胞丢失和 Bleeding Academic Research Consortium 类型 4(BARC-4)出血。

结果

共有 83%的患者在最后一次药物摄入后不到 48 小时内接受了 CABG。与普拉格雷或替格瑞洛相比,服用氯吡格雷的患者的计算出血量较低(1063ml[690-1394ml]比 1351ml[876-1829ml]比 1330ml[994-1691ml];P<0.001)。总体而言,135 名(45%)患者发生 BARC-4 出血;各组之间的发生率不同(P=0.015),且普拉格雷治疗组明显高于氯吡格雷治疗组。多变量线性回归分析显示,欧洲心脏手术风险评估系统 II(EuroSCORE II)、阿司匹林剂量、体外循环时间、药物停药时间和 P2Y 受体抑制剂类型与红细胞丢失显著相关。与 0 至 24 小时相比,术前停药超过 48 小时可使替格瑞洛和普拉格雷治疗的患者的计算出血量分别减少 37%至 48%和 BARC-4 出血减少 58%至 71%,而氯吡格雷治疗的患者则减少 25%至 35%。

结论

与氯吡格雷相比,替格瑞洛和普拉格雷在 CABG 前 24 小时或更短时间暴露会增加计算出血量和 BARC-4 出血。尽管所有 P2Y 受体抑制剂停药超过 48 小时均可显著减少计算出血量和 BARC-4 出血,但我们的单中心数据进一步支持在稳定血流动力学和非心肌危险的情况下,严格遵守 2017 年指南。

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