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In vitro hypercoagulability and ongoing in vivo activation of coagulation and fibrinolysis in COVID‐19 patients on anticoagulation

机译:在抗凝治疗抗凝患者凝血和纤维蛋白溶解的体外高凝率和持续的

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Background COVID‐19 is associated with a substantial risk of venous thrombotic events, even in the presence of adequate thromboprophylactic therapy. Objectives We aimed to better characterize the hypercoagulable state of COVID‐19 patients in patients receiving anticoagulant therapy. Methods We took plasma samples of 23 patients with COVID‐19 who were on prophylactic or intensified anticoagulant therapy. Twenty healthy volunteers were included to establish reference ranges. Results COVID‐19 patients had a mildly prolonged prothrombin time, high von Willebrand factor levels and low ADAMTS13 activity. Most rotational thromboelastometry parameters were normal, with a hypercoagulable maximum clot firmness in part of the patients. Despite detectable anti‐activated factor X activity in the majority of patients, ex vivo thrombin generation was normal, and in vivo thrombin generation elevated as evidenced by elevated levels of thrombin‐antithrombin complexes and D‐dimers. Plasma levels of activated factor VII were lower in patients, and levels of the platelet activation marker soluble CD40 ligand were similar in patients and controls. Plasmin‐antiplasmin complex levels were also increased in patients despite an in vitro hypofibrinolytic profile. Conclusions COVID‐19 patients are characterized by normal in vitro thrombin generation and enhanced clot formation and decreased fibrinolytic potential despite the presence of heparin in the sample. Anticoagulated COVID‐19 patients have persistent in vivo activation of coagulation and fibrinolysis, but no evidence of excessive platelet activation. Ongoing activation of coagulation despite normal to intensified anticoagulant therapy indicates studies on alternative antithrombotic strategies are urgently required.
机译:背景技术Covid-19与静脉血栓形成事件的大量风险有关,即使在适当的缩蛋白疗法的存在下也是如此。目的我们旨在更好地表征接受抗凝治疗患者的Covid-19患者的高凝状态。方法采用23例Covid-19患者的血浆样本,他是预防性或加剧的抗凝血治疗。包括二十个健康的志愿者,建立参考范围。结果Covid-19患者具有温和延长的凝血酶原时间,高von Willebrand因子水平和低adamts13活性。大多数旋转血栓性参数是正常的,具有超哥最大凝块的坚固性,部分患者。尽管在大多数患者中具有可检测的抗激活因子X活性,但前体内凝血酶产生正常,并且在体内凝血酶产生升高,如凝血酶抗凝血酶复合物和D-二聚体水平所证明的。激活因子VII的血浆水平较低,患者和对照等血小板活化标志物可溶性CD40配体的水平。尽管体外溶解型剖面,患者也增加了纤溶酶 - 抗胰蛋白复合物水平。结论Covid-19患者的特征在于正常的体外凝血酶产生和增强的凝块形成,并且尽管样品中存在肝素存在,但纤维蛋白溶解潜力降低。抗凝的Covid-19患者在体内激活凝血和纤维蛋白溶解的持续性,但没有过度血小板激活的证据。持续激活凝血,尽管加剧抗凝治疗正常表明迫切需要研究替代抗血栓形成策略。

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