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局部凝血酶的最新进展。

Recent developments in topical thrombins.

作者信息

Kessler Craig M, Ortel Thomas L

机构信息

Department of Laboratory Medicine, Georgetown University , Washington, DC, USA.

出版信息

Thromb Haemost. 2009 Jul;102(1):15-24. doi: 10.1160/TH09-01-0034.

Abstract

Managing blood loss is part of the surgeon's responsibility during surgical procedures, and a variety of therapeutic strategies are available to help accomplish this. Topical haemostatic agents are among the agents used to control surgical bleeding and locally arrest blood flow. Bovine thrombin is a commonly used topical haemostatic agent; however, its use has been associated with potential risks, including well-documented cases of antibody-mediated coagulopathy. This coagulopathy develops as a consequence of antibody formation directed against bovine thrombin, other bovine coagulation proteins, and their human orthologs. The fact that a coagulopathy can result in association with the use of bovine plasma-derived thrombin preparations prompted the FDA to require pharmaceutical companies to place a black-box warning in their prescribing information for products containing bovine plasma-derived thrombin. Recently, human plasma-derived thrombin and recombinant human thrombin have been approved by the FDA with the expectation that they will be less immunogenic than the bovine-derived product. In clinical studies, purified human plasma-derived thrombin and recombinant thrombin have demonstrated equivalent efficacy and safety, with improved immunogenicity profiles compared with bovine-derived thrombin agents. Well-designed and adequately powered clinical trials should be conducted to indicate whether human thrombin products would improve the risk-benefit and cost-benefit profiles for surgeries complicated by excessive bleeding.

摘要

在外科手术过程中,控制失血是外科医生职责的一部分,并且有多种治疗策略可用于实现这一目标。局部止血剂是用于控制手术出血和局部止血的药物之一。牛凝血酶是一种常用的局部止血剂;然而,其使用存在潜在风险,包括有充分记录的抗体介导的凝血病病例。这种凝血病是由于针对牛凝血酶、其他牛凝血蛋白及其人类同源物形成抗体而导致的。使用牛血浆源性凝血酶制剂可能导致凝血病这一事实促使美国食品药品监督管理局(FDA)要求制药公司在其含牛血浆源性凝血酶产品的处方信息中添加黑框警告。最近,人血浆源性凝血酶和重组人凝血酶已获FDA批准,期望它们的免疫原性低于牛源性产品。在临床研究中,纯化的人血浆源性凝血酶和重组凝血酶已证明具有等效的疗效和安全性,与牛源性凝血酶制剂相比,免疫原性特征有所改善。应开展设计良好且有足够效力的临床试验,以表明人凝血酶产品是否会改善因出血过多而复杂化的手术的风险效益和成本效益情况。

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