灾难性抗磷脂综合征的抗凝和抗纤溶药物管理。

IF 1.1 Q3 ANESTHESIOLOGY
Jee Ha Park, Nazia Siddiqui, William K Hrebec, Trevor J Szymanski, Santiago Uribe-Marquez, Kyle G Miletic, Sandeep Krishnan
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引用次数: 0

摘要

抗磷脂抗体综合征(APS)是一种自身免疫性疾病,表现为高凝状态,并导致 PTT 延长的实验室假象。最严重的形式是灾难性抗磷脂抗体综合征(CAPS),表现为多个器官系统迅速形成血栓,导致多器官缺血。治疗 CAPS 的主要方法是抗凝和全身使用皮质类固醇。由于 CAPS 具有促血栓形成的性质,抗纤维蛋白溶解剂以前一直被认为是 CAPS 的相对禁忌药物;CAPS 复杂的凝血谱可能会导致难以评估抗纤维蛋白溶解剂治疗的风险和益处。此外,如果 CAPS 患者需要使用心肺旁路术(CPB)进行手术,那么在延长 ACT 的情况下提供适当的抗凝治疗将是一项独特的挑战。我们介绍了一例需要进行心脏移植的 32 岁产后女性 CAPS 患者,她在术中安全地接受了抗纤维蛋白溶解治疗,并在围手术期进行血浆置换后成功地在 CPB 期间进行了抗凝治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Management of Anticoagulation and Antifibrinolytics in Catastrophic Antiphospholipid Syndrome.

Antiphospholipid syndrome (APS) is an autoimmune disorder that presents with hypercoagulability and results in a lab artifact of prolonged PTT. The most severe form is catastrophic antiphospholipid antibody syndrome (CAPS), which manifests as rapidly progressing thromboses in multiple organ systems leading to multi-organ ischemia. The mainstay management CAPS is anticoagulation and systemic corticosteroids. Antifibrinolytic agents have previously been thought to be relatively contraindicated in CAPS due to the pro-thrombotic nature of the disease; the complex coagulation profile of CAPS can make it difficult to assess the risks and benefits of antifibrinolytic therapy. Also, should a patient with CAPS require cardiopulmonary bypass (CPB) for surgery, it poses a unique challenge in providing appropriate anticoagulation in the setting of prolonged ACT. We present a case of a 32-year-old postpartum female with CAPS requiring heart transplant who safely received intraoperative antifibrinolytic therapy and was successfully anticoagulated during CPB after perioperative plasmapheresis.

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来源期刊
CiteScore
3.60
自引率
14.30%
发文量
31
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