Department of Laboratory Haematology, Austin Health, Melbourne, Vic, Australia.
Department of Laboratory Haematology, Austin Health, Melbourne, Vic, Australia.
Pathology. 2021 Aug;53(5):623-627. doi: 10.1016/j.pathol.2020.10.017. Epub 2021 Jan 30.
Dabigatran is an orally administrated anticoagulant that directly inhibits thrombin. However, the drug can affect routine coagulation tests such as prothrombin time (PT), activated partial thromboplastin time (APTT) and thrombin time (TT), as well as haemostasis assays, (e.g., clot-based coagulation factor assays). There are limited data on the effect of dabigatran on some fibrinogen measurements and on D-dimer assays, both important components in the laboratory assessment of disseminated intravascular coagulation (DIC). The objectives of this study were: (1) to determine the effects of various concentrations of dabigatran on fibrinogen and D-Dimer assays; and (2) to compare the von Clauss method of fibrinogen measurement using two reagents with differing thrombin concentrations (35 UNIH/mL and 100 UNIH/mL) and PT-derived fibrinogen measurement in the presence of the drug. Aliquots of pooled normal plasma were spiked with different concentrations of dabigatran to reflect in vivo on-therapy levels as well as levels observed in cases of massive accumulation of the drug. Of the routine coagulation assays, in ascending order of sensitivity to dabigatran were PT, APTT and TT. The von Clauss method of measuring fibrinogen using a reagent with low thrombin concentration was affected even at drug levels corresponding to in vivo trough concentrations, whereas the reagent with higher thrombin concentration was only affected at drug levels that were above observed peak concentrations in patients taking 150 mg of the drug twice daily. PT-derived fibrinogen was affected at approximately in vivo peak drug concentrations. The D-dimer assay was affected only at drug concentrations well above peak drug levels. Attempts at in vitro neutralisation of the drug with DOAC-Stop resulted in 'correction' of some of these measurements depending on drug concentration. Like the routine coagulation assays, there is a dabigatran concentration dependent effect on the accuracy of fibrinogen and D-dimer assays. Falsely low fibrinogen results due to dabigatran may confound the assessment of DIC and diagnostic laboratories need to evaluate the performance of their own reagents.
达比加群是一种口服抗凝剂,可直接抑制凝血酶。然而,该药会影响常规凝血测试,如凝血酶原时间(PT)、活化部分凝血活酶时间(APTT)和凝血时间(TT),以及止血检测(如基于凝块的凝血因子检测)。关于达比加群对某些纤维蛋白原测量值和 D-二聚体检测的影响,数据有限,这些都是弥散性血管内凝血(DIC)实验室评估的重要组成部分。本研究的目的是:(1)确定不同浓度的达比加群对纤维蛋白原和 D-二聚体检测的影响;(2)比较两种不同凝血酶浓度(35 UNIH/mL 和 100 UNIH/mL)的 Von Clauss 纤维蛋白原检测方法和在药物存在下使用 PT 衍生的纤维蛋白原检测方法。将不同浓度的达比加群加入混合正常血浆中,以反映体内治疗水平和药物大量蓄积时的水平。在常规凝血检测中,对达比加群的敏感性依次为 PT、APTT 和 TT。使用低凝血酶浓度试剂的 Von Clauss 纤维蛋白原检测方法甚至在药物水平对应于体内谷浓度时就受到影响,而高凝血酶浓度试剂仅在药物水平高于接受 150 mg 达比加群每日两次的患者观察到的峰值浓度时受到影响。PT 衍生的纤维蛋白原在大约体内药物峰值浓度时受到影响。D-二聚体检测仅在药物浓度明显高于峰值药物水平时受到影响。使用 DOAC-Stop 进行体外中和药物的尝试,根据药物浓度“纠正”了这些测量中的一些。与常规凝血检测一样,纤维蛋白原和 D-二聚体检测的准确性也存在达比加群浓度依赖性。由于达比加群导致的假性纤维蛋白原降低可能会混淆 DIC 的评估,诊断实验室需要评估其自身试剂的性能。