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首页> 外文期刊>Liver transplantation: official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society >Use of Thromboelastography PlateletMapping (TM) to Monitor Antithrombotic Therapy in a Patient with Budd-Chiari Syndrome
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Use of Thromboelastography PlateletMapping (TM) to Monitor Antithrombotic Therapy in a Patient with Budd-Chiari Syndrome

机译:血栓弹力描记术血小板映射(TM)监测Budd-Chiari综合征患者的抗血栓形成治疗

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摘要

Budd-Chiari syndrome (BCS) is the end result of a number of disease states resulting in hepatic venous outflow obstruction. We report a Janus kinase 2-homozygous patient with BCS who thrombosed a transjugular intrahepatic portosystemic shunt (TIPS) despite treatment with warfarin (international normalized ratio = 3.0), aspirin, and clopidogrel. PlateletMapping (TM) (Haemonetics Corp.) is a novel point-of-care assay of platelet function based on thromboelastography (TEG) that has the ability to detect platelet inhibition (%) by antiplatelet therapy. Initial PlateletMapping (TM) traces showed no platelet inhibition by aspirin or clopidogrel but demonstrated adequate suppression of plasmatic coagulation. On this basis, the aspirin dose was doubled, and this resulted in a significant increase in platelet inhibition (45%). To further suppress platelet activity, the patient was started on tirofiban, a glycoprotein IIb/IIIa inhibitor. Repeat PlateletMapping (TM) revealed 100% inhibition of platelets by both pathways, and this coincided with angiographic evidence of TIPS blood flow. Subsequently, the patient developed bleeding from the venous access sites. TEG demonstrated poor underlying plasmatic coagulation with a prolonged R time of 9.2 minutes (normal = 2-8 minutes), and the international normalized ratio was found to be supratherapeutic (> 4). Treatment with fresh frozen plasma stopped the bleeding without compromising the platelet inhibition. This case demonstrates that increased platelet activation may contribute to the development of thromboses in BCS. Despite the standard dose of dual antiplatelet therapy, there was minimal inhibition in platelet function, and anticoagulation with warfarin alone was not adequate to prevent thrombotic events. PlateletMapping (TM) was used to assess and then optimize the antiplatelet treatment while facilitating the management of complications without an increased risk of thrombosis. Liver Transpl 16:38-41, 2010.
机译:Budd-Chiari综合征(BCS)是导致肝静脉流出阻塞的多种疾病的最终结果。我们报告了尽管使用了华法林(国际标准化比例= 3.0),阿司匹林和氯吡格雷治疗,但仍经颈静脉肝内门体分流术(TIPS)栓塞了经颈静脉肝内门体分流术(TIPS)的BCS Janus激酶2纯合患者。 PlateletMapping(TM)(Haemonetics Corp.)是一种基于血栓弹力图(TEG)的新颖的血小板功能即时检测方法,具有通过抗血小板疗法检测血小板抑制(%)的能力。最初的PlateMapping(TM)痕迹显示阿司匹林或氯吡格雷对血小板没有抑制作用,但对血浆凝结有充分的抑制作用。在此基础上,阿司匹林的剂量增加了一倍,这导致血小板抑制作用显着增加(45%)。为进一步抑制血小板活性,患者开始使用糖蛋白IIb / IIIa抑制剂替罗非班。重复PlateletMapping(TM)显示两种途径均对血小板有100%的抑制作用,这与TIPS血流的血管造影证据相吻合。随后,患者从静脉通路部位出血。 TEG表现出不良的血浆血浆凝集,R时间延长了9.2分钟(正常= 2-8分钟),并且国际标准化比率被认为是超治疗的(> 4)。用新鲜的冷冻血浆进行治疗可在不损害血小板抑制的情况下停止出血。这种情况表明,血小板活化的增加可能有助于BCS中血栓形成的发展。尽管采用双重抗血小板治疗的标准剂量,但对血小板功能的抑制作用极小,仅用华法令抗凝治疗不足以预防血栓形成事件。使用PlateletMapping(TM)评估然后优化抗血小板治疗,同时促进并发症的管理而不会增加血栓形成的风险。肝运输16:38-41,2010。

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