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首页> 外文期刊>Thrombosis and Haemostasis: Journal of the International Society on Thrombosis and Haemostasis >Rivaroxaban differentially influences ex vivo global coagulation assays based on the administration time.
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Rivaroxaban differentially influences ex vivo global coagulation assays based on the administration time.

机译:利伐沙班根据给药时间不同地影响离体全身凝血测定。

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摘要

It was the objective of this study to quantify the effects of rivaroxaban administration on global coagulation parameters associated with routine clinical procedures, we collected plasma samples from patients undergoing major orthopaedic surgery receiving rivaroxaban at various time points after drug administration. Forty-seven patients received rivaroxaban (10 mg daily) for venous thromboembolism prophylaxis. Blood samples were collected at four different time points: A) before surgery; B) before drug administration at day 4-5 after surgery (steady state of rivaroxaban); C) 2 hours (h) after drug administration and D) 12 h after drug administration. The prothrombin time (PT), activated partial thromboplastin time (aPTT), thrombin time (TT), antithrombin (AT) level, fibrinogen level by Clauss method (FibC), and derived fibrinogen (dFIB) level were assessed with various reagents. At 2 h after rivaroxaban administration, the PT and aPTT clotting times were significantly prolonged to different extents up to 1.4 fold, whereas 12 h after drug administration, no significant effect was observed. Rivaroxaban administration had no influence on the TT or the FibC concentration. The dFIB assay was differentially affected by rivaroxaban when different reagents were tested. The AT assay dependent on thrombin activity was not influenced by rivaroxaban, whereas the AT levels dependent on factor Xa activity were significantly increased by rivaroxaban. Clinicians should be aware of the time-dependent influence of rivaroxaban on factor Xa-dependent routine coagulation assays. Therefore, routine coagulation parameters should be assessed directly before drug administration to keep the interaction of rivaroxaban low.
机译:这项研究的目的是量化利伐沙班给药对与常规临床程序相关的整体凝血参数的影响,我们从药物治疗后各个时间点接受大型外科手术的患者接受利伐沙班的血浆样品收集。 47例患者接受了利伐沙班(每日10 mg)预防静脉血栓栓塞。在四个不同的时间点采集血样:A)手术前; B)在手术后第4-5天给药前(利伐沙班的稳态); C)给药后2小时(h)和D)给药后12小时。用各种试剂评估凝血酶原时间(PT),活化的部分凝血活酶时间(aPTT),凝血酶时间(TT),抗凝血酶(AT)水平,Clauss方法的纤维蛋白原水平(FibC)和衍生的纤维蛋白原(dFIB)水平。利伐沙班给药后2小时,PT和aPTT凝血时间显着延长至1.4倍,不同程度,而药物给药后12小时,未观察到明显的作用。利伐沙班给药对TT或FibC浓度没有影响。当测试不同的试剂时,利伐沙班对dFIB测定有不同的影响。利伐沙班不影响依赖于凝血酶活性的AT测定,而利伐沙班显着增加依赖于因子Xa活性的AT水平。临床医生应注意利伐沙班对依赖Xa因子的常规凝血分析的时间依赖性影响。因此,应在给药前直接评估常规凝血参数,以保持利伐沙班的低相互作用。

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