Gehrie Eric, Tormey Christopher
From the Department of Laboratory Medicine, Yale University School of Medicine, New Haven, Connecticut.
Arch Pathol Lab Med. 2015 May;139(5):687-92. doi: 10.5858/arpa.2013-0677-RS.
Warfarin, the most commonly used of the vitamin K antagonists, has been a mainstay of oral anticoagulation for decades. However, its usage is limited by morbidity and mortality secondary to bleeding as well as a cumbersome therapeutic monitoring process. In the past several years, a number of competing novel oral anticoagulants (NOACs) have been developed, each of which aspires to match or exceed warfarin's effectiveness while mitigating bleeding risk and eliminating therapeutic monitoring requirements. At present, 1 oral direct thrombin inhibitor and 2 direct factor Xa inhibitors are approved by the US Food and Drug Administration. Here, we compare the clinical efficacy and safety profiles of these new drugs. In addition, we discuss various laboratory assays that may be useful to measure these drugs in certain clinical circumstances. Finally, we discuss emerging strategies to reverse these agents in an emergency. The purpose of this article is to provide a framework for practicing pathologists to advise clinicians on NOAC laboratory measurement and management of NOAC-associated bleeding.
华法林是最常用的维生素K拮抗剂,几十年来一直是口服抗凝治疗的中流砥柱。然而,其使用受到出血继发的发病率和死亡率以及繁琐的治疗监测过程的限制。在过去几年中,已经开发出了多种竞争性新型口服抗凝药(NOAC),每一种都力求在降低出血风险并消除治疗监测要求的同时,达到或超过华法林的疗效。目前,1种口服直接凝血酶抑制剂和2种直接Xa因子抑制剂已获美国食品药品监督管理局批准。在此,我们比较这些新药的临床疗效和安全性。此外,我们还讨论了在某些临床情况下可能有助于检测这些药物的各种实验室检测方法。最后,我们讨论在紧急情况下逆转这些药物作用的新出现的策略。本文的目的是为执业病理学家提供一个框架,以便就NOAC的实验室检测以及NOAC相关出血的管理向临床医生提供建议。