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艾美赛珠单抗成功用于一名患有难治性获得性血友病A且需要经皮冠状动脉介入治疗的急性冠状动脉综合征患者。

Successful use of emicizumab in a patient with refractory acquired hemophilia A and acute coronary syndrome requiring percutaneous coronary intervention.

作者信息

Dane Kathryn E, Lindsley John P, Streiff Michael B, Moliterno Alison R, Khalid Mian K, Shanbhag Satish

机构信息

The Johns Hopkins Hospital Department of Pharmacy Baltimore Maryland.

Division of Hematology Department of Medicine Johns Hopkins University School of Medicine Baltimore Maryland.

出版信息

Res Pract Thromb Haemost. 2019 Apr 9;3(3):420-423. doi: 10.1002/rth2.12201. eCollection 2019 Jul.

Abstract

ABSTRACT

We report a patient with a high-titer factor VIII inhibitor refractory to immunosuppression. He initially presented with myocardial infarction requiring percutaneous coronary intervention (PCI) with bare metal stent placement. Despite Feiba prophylaxis, inadequate hemostasis prompted premature discontinuation of dual antiplatelet therapy (DAPT). Fifteen weeks later, the patient presented with a left anterior descending artery in-stent restenosis. This case report examines the Key Clinical Question of how to manage in-stent restenosis in a patient with acquired hemophilia A (AHA). After multidisciplinary discussions including hematology, cardiology, cardiac surgery, laboratory medicine, and pharmacy, emicizumab was initiated to facilitate PCI. Four weeks after emicizumab initiation, the patient underwent successful PCI with drug-eluting stent placement. Five months after discharge, he remains without signs or symptoms of cardiac disease or bleeding on DAPT and emicizumab. This case provides evidence of the potential of emicizumab for bleeding prophylaxis in AHA.

摘要

摘要

我们报告了一名对免疫抑制难治的高滴度凝血因子VIII抑制剂患者。他最初因心肌梗死就诊,需要进行经皮冠状动脉介入治疗(PCI)并植入裸金属支架。尽管使用了非旁路9因子预防,但止血不足促使过早停用双联抗血小板治疗(DAPT)。15周后,患者出现左前降支动脉支架内再狭窄。本病例报告探讨了如何处理获得性血友病A(AHA)患者支架内再狭窄这一关键临床问题。经过血液学、心脏病学、心脏外科、检验医学和药学等多学科讨论后,开始使用艾美赛珠单抗以促进PCI。开始使用艾美赛珠单抗四周后,患者成功接受了药物洗脱支架植入的PCI。出院五个月后,他在接受DAPT和艾美赛珠单抗治疗时仍无心脏病或出血的迹象或症状。本病例提供了艾美赛珠单抗在AHA中预防出血潜力的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c84/6611359/64b9ee05ab39/RTH2-3-420-g001.jpg

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