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首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >High-dose aspirin in addition to daily low-dose aspirin decreases platelet activation in patients before and after percutaneous coronary intervention.
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High-dose aspirin in addition to daily low-dose aspirin decreases platelet activation in patients before and after percutaneous coronary intervention.

机译:在每日经皮冠状动脉介入治疗前后,高剂量阿司匹林和每日低剂量阿司匹林可降低患者的血小板活化。

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摘要

BACKGROUND: Activated platelets play a major role in acute vessel closure after coronary angioplasty. Although aspirin is the routine therapy during angioplasty, it only incompletely prevents acute closure. This might be due to suboptimal dosing. OBJECTIVE: First, to study the effect of additional high-dose aspirin on platelet activation during coronary angioplasty. Second, to assess the potential of the new PFA-100 analyzer to evaluate the effect of different doses of aspirin in patients undergoing angioplasty. METHODS: Fifty-one patients on 100 mg aspirin/day for at least 1 month were randomized to continuation of 100 mg aspirin/day only (Group A=24 patients), or to this regime plus a bolus of 1000 mg of aspirin given 1 day before angioplasty (Group B=27 patients). Results were compared with 15 controls. Platelet function was measured before angioplasty by the PFA-100 analyzer; platelet activation was measured by flow cytometry just before and 1 h after angioplasty. RESULTS: At baseline, Group A had significantly more activated platelets than the control group (P<.001). High-dose aspirin in Group B resulted in significantly lower platelet activation as compared with both controls (P<.001) and Group A (P<.001). During angioplasty, the number of activated platelets decreased significantly in Group A (P<.001), while there was no change in Group B (P=.6). The PFA-100 analyzer was unable to detect differences between the two treatment groups. CONCLUSIONS: The addition of high-dose aspirin to daily low-dose aspirin, 1 day before coronary angioplasty, significantly reduced the platelet activation state before and after intervention. The PFA-100 analyzer did not detect differences in the effect of low- versus high-dose aspirin on platelet function.
机译:背景:活化的血小板在冠状动脉成形术后急性血管关闭中起主要作用。尽管阿司匹林是血管成形术中的常规治疗方法,但仅能完全预防急性闭合。这可能是由于剂量欠佳。目的:首先,研究大剂量阿司匹林对冠状动脉成形术中血小板活化的影响。其次,评估新型PFA-100分析仪评估不同剂量阿司匹林对血管成形术患者的疗效的潜力。方法:51名每天服用阿司匹林100毫克,持续至少1个月的患者被随机分配为仅继续每天服用100毫克阿司匹林(A组= 24名患者),或随机接受此方案加大剂量的1000毫克阿司匹林给予1血管成形术前一天(B组= 27例患者)。将结果与15个对照组进行比较。在PFA-100分析仪进行血管成形术之前测量血小板功能。在血管成形术之前和之后1小时通过流式细胞术测量血小板活化。结果:在基线时,A组的活化血小板明显多于对照组(P <.001)。与对照组(P <.001)和A组(P <.001)相比,B组的大剂量阿司匹林导致血小板活化明显降低。在血管成形术期间,活化的血小板数量在A组中显着减少(P <.001),而B组则没有变化(P = .6)。 PFA-100分析仪无法检测到两个治疗组之间的差异。结论:在冠状动脉成形术前1天每天向小剂量阿司匹林中添加大剂量阿司匹林可显着降低干预前后的血小板活化状态。 PFA-100分析仪未检测到小剂量和大剂量阿司匹林对血小板功能的影响存在差异。

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