Singh Sukhi, Malm Carl Johan, Ramström Sofia, Hesse Camilla, Jeppsson Anders
Department of Molecular and Clinical Medicine Institute of Medicine Sahlgrenska Academy University of Gothenburg Gothenburg Sweden.
School of Medical Sciences Örebro University Örebro Sweden.
Res Pract Thromb Haemost. 2018 Sep 30;2(4):718-725. doi: 10.1002/rth2.12149. eCollection 2018 Oct.
Temporarily improved platelet reactivity may reduce the bleeding in patients on antiplatelet therapy who have ongoing bleeding or who are in need of acute surgery. Adrenaline can bind to adrenergic α-receptors on platelets and potentially enhance platelet reactivity.
To assess if adrenaline can improve adenosine diphosphate (ADP)-induced platelet aggregation and activation in blood samples from patients on dual antiplatelet therapy with acetylsalicylic acid (ASA) and the ADP-receptor antagonist ticagrelor.
Blood samples were collected from a total of forty acute coronary syndrome patients on dual antiplatelet therapy with ASA and ticagrelor. ADP-induced platelet aggregation (by impedance aggregometry) and activation (by flow cytometry) were assessed before and after supplementation with adrenaline and/or platelet concentrate.
Adrenaline supplementation (770 nmol L) increased median ADP-induced aggregation from 15 (25-75th percentiles: 10-20) to 26 (18-38) aggregation units. The effect was independent of concomitant platelet supplementation. Adrenaline also increased ADP-induced platelet activation: from 40% (36-54%) to 83% (74-88%) platelets with active fibrinogen receptor (binding PAC-1) and from 13% (7-21%) to 35% (18-50%) P-selectin-expressing platelets.
Adrenaline potentiated ADP-induced platelet aggregation and activation in blood samples from ticagrelor-treated patients. Adrenaline infusion may be a new method to enhance platelet function in ticagrelor-treated patients who are in need of acute surgery or have ongoing bleeding. In vivo studies are needed to confirm the present results.
暂时改善血小板反应性可能会减少接受抗血小板治疗且有持续出血或需要进行急诊手术的患者的出血情况。肾上腺素可与血小板上的肾上腺素能α受体结合,并可能增强血小板反应性。
评估肾上腺素是否能改善接受乙酰水杨酸(ASA)和ADP受体拮抗剂替格瑞洛双重抗血小板治疗的患者血样中ADP诱导的血小板聚集和活化。
共采集了40例接受ASA和替格瑞洛双重抗血小板治疗的急性冠脉综合征患者的血样。在补充肾上腺素和/或血小板浓缩物之前和之后,评估ADP诱导的血小板聚集(通过阻抗聚集法)和活化(通过流式细胞术)。
补充肾上腺素(770 nmol/L)后,ADP诱导的聚集中位数从15(第25-75百分位数:10-20)个聚集单位增加到26(18-38)个聚集单位。该效应与同时补充血小板无关。肾上腺素还增加了ADP诱导的血小板活化:具有活性纤维蛋白原受体(结合PAC-1)的血小板从40%(36-54%)增加到83%(74-88%),表达P-选择素的血小板从13%(7-21%)增加到35%(18-50%)。
肾上腺素增强了替格瑞洛治疗患者血样中ADP诱导的血小板聚集和活化。对于需要急诊手术或有持续出血的替格瑞洛治疗患者,输注肾上腺素可能是一种增强血小板功能的新方法。需要进行体内研究以证实目前的结果。