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Evaluation of the antithrombotic abilities of non-vitamin K antagonist oral anticoagulants using the Total Thrombus-formation Analysis System((R))

机译:使用总血栓形成分析系统评估非维生素K拮抗剂口腔抗凝血剂的抗血栓形成能力((R))

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The Total Thrombus-formation Analysis System (T-TAS(A (R))) is a novel automated microchip flow-chamber system for the quantitative evaluation of thrombus formation under blood flow conditions. T-TAS(A (R)) uses two types of microchip to evaluate thrombus formation: the AR-chip quantifies white thrombus formation and the PL-chip quantifies platelet thrombus formation. We assessed the antithrombotic abilities of various non-vitamin K antagonist oral anticoagulants (NOACs) using T-TAS(A (R)). One hundred and three consecutive patients who were hospitalized with cardiovascular diseases were enrolled. We divided the patients into 2 groups; a control group that did not receive an anticoagulant (non-AC group) and an anticoagulant group (AC group). The AC group was further divided into warfarin, dabigatran, rivaroxaban and apixaban groups. We performed common coagulation tests and evaluated the area under the flow pressure curve (AR-AUC and PL-AUC) to quantify antithrombotic ability using T-TAS(A (R)) at the trough. There were no significant differences in patient characteristics between the non-AC and AC groups. Only 55.1 % of patients in the AC group achieved the target blood pressure (BP) of less than 130/80 mmHg. Compared with the non-AC group, AR-AUC was significantly decreased in the AC, warfarin, dabigatran and apixaban groups. Only the rivaroxaban group did not show a significant decrease in AR-AUC. NOACs showed a significant decrease in PL-AUC compared with the non-AC group. In conclusion, T-TAS(A (R)) was a useful tool for evaluating anticoagulation activity. NOACs was significantly effective as an antiplatelet agent. BP control should be a higher priority than the selection of an anticoagulant drug, especially NOACs.
机译:总血栓形成分析系统(T-TAS(A(R))是一种新型自动微芯片流量室系统,用于在血流条件下进行血栓形成的定量评估。 T-TAS(A(R))使用两种类型的微芯片来评估血栓形成:AR芯片量化白色血栓形成和PL芯片量化血小板血栓形成。我们使用T-Tas评估各种非维生素K拮抗剂口腔抗凝血剂(NOAC)的抗血栓形成能力(A(R))。注册了一百一三,连续三名患有心血管疾病住院的患者。我们将患者分为2组;没有接受抗凝血剂(非AC组)和抗凝血组(AC组)的对照组。 AC组进一步分为Warfarin,Dabigatran,Rivaroxaban和Apixaban组。我们进行了常用的凝血试验,并评估了流量曲线(AR-AUC和PL-AUC)下的面积,以定量使用在槽中的T-TAS(A(R))的抗血栓能力。非AC和AC组之间的患者特性没有显着差异。只有55.1%的AC组患者达到目标血压(BP)小于130/80 mmHg。与非AC组相比,AR-AUC在AC,Warfarin,Dabigatran和Apixaban组中显着降低。只有Rivaroxaban集团没有显示AR-AUC的显着降低。与非AC组相比,Noacs显示Pl-Auc的显着降低。总之,T-TAS(A(R))是评估抗凝活性的有用工具。 Noacs作为抗血小板剂显着有效。 BP控制应该是比选择抗凝血药物,尤其是Noacs的优先级。

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