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首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >PFA-100 and flow cytometry: can they challenge aggregometry to assess antiplatelet agents, other than GPIIbIIIa blockers, in coronary angioplasty?
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PFA-100 and flow cytometry: can they challenge aggregometry to assess antiplatelet agents, other than GPIIbIIIa blockers, in coronary angioplasty?

机译:PFA-100和流式细胞仪:在GPIIbIIIa阻滞剂之外,他们是否可以挑战凝集分析法评估冠状动脉成形术中的抗血小板药物?

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INTRODUCTION: Platelet response to inhibitors varies widely, leading to a higher risk of abrupt closure events in insufficiently treated-coronary heart disease patients. The aim of this study was to compare, in patients under various antiplatelet regimens, three platelet function assays: aggregometry, PFA-100 and flow cytometry. These assays stand for available tests, as "ready-to-use" device (PFA-100) and sophisticated assay (cytometry). We chose the setting of percutaneous coronary intervention as a standardized procedure to determine which test was appropriate to detect the effect of (1) an aspirin bolus in patients under long-term aspirin treatment, and (2) ticlopidin in case of stent implantation. METHODS: Fifty patients under oral aspirin treatment were randomized to receive a bolus of 500 mg aspirin before angioplasty (n=25). Ticlopidin was given at a 500 mg loading dose in the case of stent implantation (n=38). Platelet function was assessed before, at 2 and 24 h after angioplasty. RESULTS: Considering aspirin antiplatelet effect, the following was observed: (1) a lack of further inhibition after the bolus whatever assay was used and (2) a disagreement between aggregometry and PFA-100 to classify patients as being poor or good aspirin responders (kappa were 0.11 and 0.28 between ADP 4 or 6 microM aggregation, respectively, and PFA-100). Another finding was the good performance of flow cytometry, which evaluated GPIIbIIIa activation, and aggregometry, to detect ticlopidin the day after the loading dose. In contrast, PFA-100 was insensitive to ticlopidin. CONCLUSION: Current assays are not interchangeable to monitor antiplatelet treatment in daily practice.
机译:简介:血小板对抑制剂的反应差异很大,导致未充分治疗的冠心病患者突然关闭事件的风险更高。这项研究的目的是在各种抗血小板方案下的患者中比较三种血小板功能测定:凝集测定,PFA-100和流式细胞术。这些检测代表可用的检测,如“即用型”设备(PFA-100)和复杂的检测(细胞计数)。我们选择经皮冠状动脉介入治疗的设置作为标准程序,以确定哪种测试适合检测(1)长期接受阿司匹林治疗的患者中的阿司匹林推注,以及(2)支架植入情况下的替洛匹定的效果。方法:将50例接受口服阿司匹林治疗的患者随机分组,在血管成形术前接受500 mg阿司匹林的推注(n = 25)。在支架植入的情况下,以500 mg负荷剂量给予环氯丁定(n = 38)。在血管成形术之前,2和24 h评估血小板功能。结果:考虑到阿司匹林抗血小板作用,观察到以下情况:(1)推注后无论采用何种测定法都没有进一步的抑制作用;(2)凝集测定法和PFA-100在将患者归类为不良或良好的阿司匹林反应方面存在分歧( ADP 4或6 microM聚合与PFA-100之间的Kappa分别为0.11和0.28。另一个发现是流式细胞仪的良好性能,流式细胞仪评估了GPIIbIIIa的激活和凝集测定法,可在加载剂量后的第二天检测出替匹必定。相反,PFA-100对卵磷脂没有敏感性。结论:目前的检测方法不能互换以监测日常实践中的抗血小板治疗。

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