Department of Internal Medicine, Health Sciences University of Hokkaido, Hokkaido, Japan; Department of Clinical Laboratory, Iwate Prefectural Chubu Hospital, Iwate, Japan.
Department of Internal Medicine, Health Sciences University of Hokkaido, Hokkaido, Japan.
Thromb Res. 2020 Nov;195:158-164. doi: 10.1016/j.thromres.2020.07.020. Epub 2020 Jul 14.
Direct oral anticoagulants targeting factor Xa (DXaIs) are administered as prophylaxis for various venothrombotic diseases without routine monitoring required. However, assessment of their anticoagulant effects is necessary to prevent severe events, including major bleeding and/or refractory thrombosis.
We examined the correlation of ratio of inhibited thrombin generation (RITG), determined using a novel assay based on dilute prothrombin time (dPT), with coagulant markers and laboratory test results to show drug effects. In addition, RITG usefulness as a confirmation test for DXaI therapy was investigated.
Citrated plasma samples were obtained from patients treated with rivaroxaban (n = 882), apixaban (n = 1214), or edoxaban (n = 820) at 4 different institutions in Japan. Laboratory tests, including prothrombin time (PT), activated partial thromboplastin time (APTT), D-dimer, and plasma concentrations of DXaIs, were conducted, with drug concentrations divided into peak and trough groups, within and after 5 h of administration.
In each DXaI group, RITG was positively correlated with PT, APTT, and drug concentration, and negatively with D-dimer. RITG fluctuation during the peak and trough periods reflected the anticoagulant activity characteristic of each DXaI, which was different from blood concentration fluctuations. RITG showed a significant decrease in cases with thrombosis, while that was increased in those with hemorrhage.
We developed RITG, a novel measurement method based on dPT. RITG represents residual coagulation ability in plasma samples, and is useful for assessment of bleeding and thrombotic tendencies in DXaI patients. RITG can be utilized to confirm the effectiveness of oral anticoagulation therapy with DXaI agents.
针对因子 Xa(DXaIs)的直接口服抗凝剂(DOACs)无需常规监测即可用于预防各种静脉血栓栓塞性疾病。然而,为了预防包括大出血和/或难治性血栓形成在内的严重事件,评估其抗凝效果是必要的。
我们检查了基于稀释凝血酶原时间(dPT)的新型测定法测定的抑制凝血酶生成比(RITG)与凝血标志物和实验室检测结果的相关性,以显示药物作用。此外,还研究了 RITG 作为 DXaI 治疗确认试验的有用性。
从日本 4 个不同机构接受利伐沙班(n=882)、阿哌沙班(n=1214)或依度沙班(n=820)治疗的患者中获得枸橼酸盐血浆样本。进行了凝血酶原时间(PT)、活化部分凝血活酶时间(APTT)、D-二聚体和 DXaIs 血浆浓度等实验室检测,并在给药后 5 小时内和之后将药物浓度分为峰值和谷值组。
在每个 DXaI 组中,RITG 与 PT、APTT 和药物浓度呈正相关,与 D-二聚体呈负相关。峰值和谷值期间 RITG 的波动反映了每种 DXaI 的抗凝活性特征,与血液浓度波动不同。在血栓形成病例中 RITG 显著下降,而在出血病例中 RITG 增加。
我们开发了一种基于 dPT 的新型 RITG 测量方法。RITG 代表血浆样本中的残留凝血能力,可用于评估 DXaI 患者的出血和血栓倾向。RITG 可用于确认 DXaI 药物口服抗凝治疗的有效性。