首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Effects of pretreatment with clopidogrel on platelet and coagulation activation in patients undergoing elective coronary stenting.
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Effects of pretreatment with clopidogrel on platelet and coagulation activation in patients undergoing elective coronary stenting.

机译:氯吡格雷预处理对择期冠状动脉支架置入术患者血小板和凝血激活的影响。

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BACKGROUND: Current data suggest that pretreatment with clopidogrel (in addition to aspirin) prior to elective percutaneous coronary intervention (PCI) might be associated with a reduced incidence of subsequent adverse ischemic events. The aim of this placebo-controlled study was to find out whether an extended pretreatment period with clopidogrel before an elective PCI might confer a superior inhibition of the platelet activation and aggregation than clopidogrel given not until PCI. METHODS: Twenty patients with stable angina being already on aspirin were randomly assigned to receive the loading dose of 300 mg clopidogrel, either 24 h before or immediately after stent implantation. At several time points before and after PCI, the activation of both the platelet and the coagulation system was determined by measuring beta-thromboglobulin (beta-TG) and prothrombin fragment f1.2 (f1.2), respectively, in venous blood and in blood emerging from a microvascular injury (shed blood). RESULTS: Pretreatment withclopidogrel before PCI exhibited a slight reduction of beta-TG (from 178 to 139 ng/ml, p=0.085) and of f1.2 (from 0.81 to 0.75 nmol/l, p=0.045) in venous blood. Heparin administration (at the beginning of PCI) resulted in a 65% inhibition of ss-TG (from 10,590 to 2833 ng/ml) and 90% inhibition of f1.2 formation (from 38.7 to 4.2 nmol/l) in shed blood of patients with clopidogrel pretreatment. The extent of inhibition was, however, comparable to that observed in patients without clopidogrel pretreatment (beta-TG: from 8025 to 2812 ng/ml, 76% inhibition, p=0.47; f1.2: from 34.9 to 3.8 nmol/l, 86% inhibition, p=0.80). After PTT normalisation (6 h after PCI), levels of beta-TG and f1.2 both in venous blood and in shed blood did not differ between the two treatment regimens up to 48 h after PCI. CONCLUSION: Pretreatment with clopidogrel did not result in a pronounced inhibition of the platelet and coagulation system activation in patients on aspirin undergoing elective coronary stent implantation.
机译:背景:目前的数据表明,在选择性经皮冠状动脉介入治疗(PCI)之前用氯吡格雷(除阿司匹林外)进行预处理可能与减少随后的不良缺血事件的发生率有关。这项安慰剂对照研究的目的是确定在选择PCI之前使用氯吡格雷延长治疗周期是否可能比在PCI之前给予氯吡格雷更好地抑制血小板活化和聚集。方法:将20例已经接受阿司匹林治疗的稳定型心绞痛患者随机分配在支架植入前24小时或之后立即接受300 mg氯吡格雷的负荷剂量。在PCI前后的几个时间点,分别通过测量静脉血和静脉血中的β-凝血球蛋白(beta-TG)和凝血酶原片段f1.2(f1.2)来确定血小板和凝血系统的激活。微血管损伤引起的血液(流血)。结果:PCI前用氯吡格雷预处理后静脉血中β-TG(从178降至139 ng / ml,p = 0.085)和f1.2(从0.81至0.75 nmol / l,p = 0.045)略有降低。给予肝素(在PCI开始时)可导致流血的ss-TG受到65%的抑制(从10,590 ng至2833 ng / ml)和90%抑制f1.2形成(从38.7至4.2 nmol / l)。氯吡格雷预处理的患者。但是,抑制程度与未进行氯吡格雷预处理的患者相当(β-TG:8025至2812 ng / ml,76%抑制,p = 0.47; f1.2:34.9至3.8nmol / l,抑制率为86%,p = 0.80)。 PTT正常化后(PCI后6小时),两种治疗方案在PCI术后48小时内,静脉血和流血中的β-TG和f1.2的水平没有差异。结论:阿司匹林行择期冠状动脉支架植入术的患者,氯吡格雷预处理并没有明显抑制血小板和凝血系统的活化。

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