Department of Cardiology and Angiology II, University Heart Center Freiburg, Bad Krozingen, Germany.
Thromb Haemost. 2018 Feb;118(2):362-368. doi: 10.1160/TH17-07-0466. Epub 2018 Jan 29.
Reticulated platelets are associated with impaired antiplatelet response to irreversibly acting P2Y-receptor inhibitors. However, the impact of reticluated platelets (RP) on the reversibly acting injectable P2Y-receptor inhibitor cangrelor is unknown. Thus, this study sought to investigate the influence of RP on cangrelor and transitioning strategies to oral P2Y-receptor inhibitors.
This study randomized 110 patients undergoing elective percutaneous coronary intervention with use of cangrelor to different oral transitioning strategies loading with prasugrel 60 mg or ticagrelor 180 mg at the start of cangrelor ( = 45 each) or loading with clopidogrel 600 mg after discontinuation of cangrelor ( = 20). ADP-induced platelet reactivity was assessed by impedance aggregometry. Reticulated platelets were analysed by an automated whole blood flow cytometry and described as immature platelet count.
There was no correlation of reticulated platelets and ADP-induced platelet reactivity in patients under treatment with cangrelor ( = 0.06, = 0.47). This finding was consistent in all three transitioning strategies. On day 1 following treatment with cangrelor, the correlation of reticulated platelets and platelet reactivity was detectable again in patients receiving thienopyridines but not ticagrelor (all patients = 0.37, < 0.001; clopidogrel: = 0.59, = 0.01; prasugrel: = 0.47, < 0.001; ticagrelor = 0.22, = 0.13).
Platelet inhibition is not influenced by levels of reticulated platelets during infusion of cangrelor independent of oral P2Y-receptor inhibitor transitioning strategy. These findings underline the potency of cangrelor as immediate and reversibly acting P2Y-receptor inhibitor.
网织血小板与不可逆作用的 P2Y 受体抑制剂的抗血小板反应受损有关。然而,网织血小板(RP)对可逆转作用的注射用 P2Y 受体抑制剂坎格瑞洛的影响尚不清楚。因此,本研究旨在探讨 RP 对坎格瑞洛的影响以及向口服 P2Y 受体抑制剂转换的策略。
本研究将 110 例行择期经皮冠状动脉介入治疗的患者随机分为不同的口服转换策略组,在开始使用坎格瑞洛时分别给予普拉格雷 60mg 或替格瑞洛 180mg(每组 45 例)或在停用坎格瑞洛后给予氯吡格雷 600mg(20 例)。通过阻抗聚集法评估 ADP 诱导的血小板反应性。通过自动化全血流式细胞术分析网织血小板,并描述为不成熟血小板计数。
在接受坎格瑞洛治疗的患者中,网织血小板与 ADP 诱导的血小板反应性之间无相关性(r=0.06,p=0.47)。这一发现在所有三种转换策略中均一致。在接受坎格瑞洛治疗后的第 1 天,再次在接受噻吩吡啶类药物但未接受替格瑞洛的患者中检测到网织血小板与血小板反应性之间的相关性(所有患者 r=0.37,p<0.001;氯吡格雷:r=0.59,p=0.01;普拉格雷:r=0.47,p<0.001;替格瑞洛:r=0.22,p=0.13)。
在坎格瑞洛输注期间,血小板抑制不受网织血小板水平的影响,与口服 P2Y 受体抑制剂转换策略无关。这些发现强调了坎格瑞洛作为一种即时和可逆转作用的 P2Y 受体抑制剂的效力。