Wexels Fredrik, Dahl Ola E, Pripp Are H, Seljeflot Ingebjørg
1 Department of Radiology, Vestre Viken Hospital Trust, Drammen, Norway.
2 Faculty of Medicine, University of Oslo, Oslo, Norway.
Clin Appl Thromb Hemost. 2017 Jul;23(5):416-421. doi: 10.1177/1076029617700999. Epub 2017 Mar 24.
Increasing number of patients with clinically suspected venous thromboembolism is referred to radiological departments for definitive diagnosis. A simple assay to exclude the diagnosis and avoid radiological examinations is needed. We have reported correlations between D-dimer and prothrombin fragment 1 + 2 measured in plasma and urine. To further develop an analysis based on urine, more understanding of thrombin generation in these patients is needed. The aim of this study was to compare ex vivo thrombin generation with in vivo markers in plasma and urine in patients with and without venous thromboembolism. Urine and blood samples were collected from patients with suspected venous thromboembolism. Commercially available enzyme-linked immunosorbent assay (ELISA) kits were used to analyze the samples for in vivo thrombin generation. The ex vivo thrombogram parameters were measured by the calibrated automated thrombogram assay. Venous thromboembolism was verified with compression ultrasound of the lower extremity deep veins or with computer tomography of the pulmonary arteries. Venous thromboembolism was diagnosed in 117 of 591 patients, and they had significantly higher levels of urine and plasma prothromin fragment 1 + 2, D-dimer, lag time, time to peak, and endogenous thrombin potential when adjusted for covariates. The pattern of ex vivo and in vivo thrombin generation in patients with suspected venous thromboembolism was comparable when adjusted for covariates. Prothrombin fragment 1 + 2 in plasma and urine reflects thrombin generation ex vivo in the same manner. This indicates that urine may be an alternative substrate to quantify a procoagulant state.
临床上疑似静脉血栓栓塞的患者数量不断增加,他们被转诊至放射科进行明确诊断。因此需要一种简单的检测方法来排除该诊断并避免进行放射学检查。我们已经报道了血浆和尿液中D - 二聚体与凝血酶原片段1 + 2之间的相关性。为了进一步开展基于尿液的分析,需要对这些患者体内的凝血酶生成有更多了解。本研究的目的是比较有和没有静脉血栓栓塞的患者血浆和尿液中体外凝血酶生成与体内标志物的情况。从疑似静脉血栓栓塞的患者中采集尿液和血液样本。使用市售的酶联免疫吸附测定(ELISA)试剂盒分析样本以检测体内凝血酶生成情况。通过校准自动血栓图测定法测量体外血栓图参数。通过下肢深静脉压迫超声或肺动脉计算机断层扫描来证实静脉血栓栓塞。591例患者中有117例被诊断为静脉血栓栓塞,在对协变量进行校正后,他们的尿液和血浆凝血酶原片段1 + 2、D - 二聚体、延迟时间、达到峰值的时间和内源性凝血酶潜力水平显著更高。在对协变量进行校正后,疑似静脉血栓栓塞患者的体外和体内凝血酶生成模式具有可比性。血浆和尿液中的凝血酶原片段1 + 2以相同方式反映体外凝血酶生成情况。这表明尿液可能是量化促凝状态的一种替代底物。