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替格瑞洛拮抗剂 MEDI2452 在阿司匹林背景下应用替格瑞洛的猪中的止血作用。

Hemostatic effects of the ticagrelor antidote MEDI2452 in pigs treated with ticagrelor on a background of aspirin.

机构信息

Cardiovascular and Metabolic Diseases, Innovative Medicines and Early Development, AstraZeneca, Mölndal, Sweden.

Clinical Pharmacology and DMPK, MedImmune, Cambridge, UK.

出版信息

J Thromb Haemost. 2017 Jun;15(6):1213-1222. doi: 10.1111/jth.13680. Epub 2017 May 11.

Abstract

UNLABELLED

Essentials MEDI2452 is a specific antidote of the platelet P2Y receptor antagonist ticagrelor. Hemostatic effects of MEDI2452 were evaluated in pigs treated with ticagrelor and aspirin. MEDI2452 eliminated free ticagrelor within 5 min and gradually normalized platelet aggregation. Improvements in blood pressure (significant) and in blood-loss and survival (non-significant) were observed.

SUMMARY

Background Ticagrelor, a P2Y antagonist, is approved for the prevention of thromboembolic events. However, antiplatelet therapies carry a risk of bleeding. Objective To explore the hemostatic effects of MEDI2452, an antidote for ticagrelor. Methods Pigs, pre-treated with aspirin, were given an intravenous infusion of ticagrelor or vehicle. At the end of the infusion, a piece of a liver lobe was cut off and a bolus of MEDI2452 or vehicle was administered intravenously. Blood was collected to monitor blood loss, mean arterial blood pressure (MAP) was recorded and survival time was observed over 4 h. Blood samples for drug plasma exposures and platelet aggregation were collected. Results MEDI2452 eliminated the free concentrations of ticagrelor and its active metabolite AR-C124910XX within 5 min. ADP-induced platelet aggregation was close to normal at 60 min, which was not significantly different from aspirin alone. MEDI2452 numerically reduced ticagrelor-mediated effects: body-weight-adjusted blood loss in the 15- to 90-min interval, 12 (confidence interval [CI] 95% 7-28] vs. 17 (CI 95% 5-31) (ticagrelor and aspirin) vs. 5 (CI 95% 3-9) mL kg (aspirin alone), survival 70% (CI 95% 47-100) vs. 45% (CI 95% 21-92) (ticagrelor and aspirin) vs. 100% (CI 95% 100-100) (aspirin alone), and median survival time, 240 (CI 95% 180-240) vs. 169 (CI 95% 64-240) (ticagrelor and aspirin) vs. 240 (CI 95% 240-240) min (aspirin alone). Finally, MEDI2452 significantly attenuated the decline in MAP, 0.08 (CI 95% 0.07-0.09) vs. 0.141 (CI 95% 0.135-0.148) (ticagrelor and aspirin) vs. 0.04 (CI 95% 0.03-0.05) mmHg per min (aspirin alone) and maintained MAP at a significantly higher level, 73 (CI 95% 51-95) vs. 48 (CI 95% 25-70) (ticagrelor and aspirin) vs. 115 (CI 95% 94-136) mmHg (aspirin alone). Conclusion MEDI2452 eliminated free ticagrelor and AR-C124910XX within 5 min. This translated into a gradual normalization of ADP-induced platelet aggregation and significant improvement in blood pressure and numerical but non-significant improvements in blood-loss and survival.

摘要

未注明

Essentials MEDI2452 是血小板 P2Y 受体拮抗剂替格瑞洛的特定解毒剂。在接受替格瑞洛和阿司匹林治疗的猪中评估了 MEDI2452 的止血作用。MEDI2452 在 5 分钟内消除了游离的替格瑞洛,并逐渐使血小板聚集正常化。观察到血压(显著)和失血量及存活率(不显著)的改善。

摘要

背景替格瑞洛,一种 P2Y 拮抗剂,已被批准用于预防血栓栓塞事件。然而,抗血小板治疗有出血的风险。目的探讨 MEDI2452(替格瑞洛解毒剂)的止血作用。

方法用阿司匹林预处理猪,给予替格瑞洛或载体静脉输注。输注结束时,切下一块肝组织,并静脉给予 MEDI2452 或载体。采集血液以监测失血量,记录平均动脉血压(MAP),并在 4 小时内观察存活时间。采集血样以监测药物血浆暴露和血小板聚集。

结果 MEDI2452 在 5 分钟内消除了游离的替格瑞洛及其活性代谢物 AR-C124910XX。ADP 诱导的血小板聚集在 60 分钟时接近正常,与单独使用阿司匹林无显著差异。MEDI2452 数值上降低了替格瑞洛介导的作用:15-90 分钟时体重调整的失血量,12(置信区间[CI] 95% 7-28])与 17(CI 95% 5-31)(替格瑞洛和阿司匹林)与 5(CI 95% 3-9)mL·kg(单独使用阿司匹林),存活率 70%(CI 95% 47-100)与 45%(CI 95% 21-92)(替格瑞洛和阿司匹林)与 100%(CI 95% 100-100)(单独使用阿司匹林),中位数存活时间,240(CI 95% 180-240)与 169(CI 95% 64-240)(替格瑞洛和阿司匹林)与 240(CI 95% 240-240)min(单独使用阿司匹林)。最后,MEDI2452 显著减轻了 MAP 的下降,0.08(CI 95% 0.07-0.09)与 0.141(CI 95% 0.135-0.148)(替格瑞洛和阿司匹林)与 0.04(CI 95% 0.03-0.05)mmHg·min(单独使用阿司匹林),并维持 MAP 在一个显著更高的水平,73(CI 95% 51-95)与 48(CI 95% 25-70)(替格瑞洛和阿司匹林)与 115(CI 95% 94-136)mmHg(单独使用阿司匹林)。

结论 MEDI2452 在 5 分钟内消除了游离的替格瑞洛和 AR-C124910XX。这转化为 ADP 诱导的血小板聚集逐渐正常化,并显著改善血压,以及失血量和存活率的数值但不显著改善。

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