Borris Lars C, Breindahl Morten, Ryge Camilla, Sommer Helle M, Lassen Michael R
Department of Orthopaedics, Section of Traumatology, Arhus University Hospital, Arhus.
Thromb Res. 2007;121(3):369-76. doi: 10.1016/j.thromres.2007.05.002. Epub 2007 Jun 27.
Prothrombin fragment 1+2 measured in spot urine (uF1+2) is an indicator of thrombin generation. We examined whether measured levels of uF1+2 can be used to differentiate between patients who do and do not acquire sustained coagulation activation after total hip arthroplasty (THA).
We performed two separate studies in patients undergoing THA. Study 1 was a prospective pilot study aiming to roughly estimate the extent of pre- and postoperative fluctuations in the uF1+2 concentration. Study 2 was a larger prospective cohort study aiming to verify the findings of Study 1 and to examine the association between the uF1+2 concentrations and risk of vascular thrombotic complications (VTC) or death. Finally, we sought to define a cut-off concentration value that could be used to identify patients with a sustained uF1+2 elevation after the first postoperative week. The urine samples were analysed by ELISA. In both studies thromboprophylaxis was used for at least 7 days after the operation.
The operative trauma resulted in elevation of the uF1+2 level in all patients compared with the preoperative level and levels in the healthy volunteers. Ten out of 113 patients (8.8%) in the second study suffered VTC or death, assumed to be caused by a coagulation problem. Analysis of variance revealed the following statistically significant associations: pre- vs. postoperative log uF1+2 levels (P<0.0001), log uF1+2 levels comparing patients with and without events (P=0.004); and the individual log uF1+2 levels (P<0.0001). A cut-off value of uF1+2 concentration between 0.3 and 0.5 nmol/l had a sensitivity and a negative predictive value between100% and 90%, and specificity between 45% and 63% and overall accuracy between 50% and 65%. This value was obtained by the analysis of a receiver operating characteristic curve with the purpose of identifying patients with sustained coagulation activation on day 5 after operation.
Our studies suggest that measured levels of uF1+2 can be potentially used to assess the individual risk of VTC after THA and to test for non-invasive detection of sustained coagulation activation.
检测即时尿样中的凝血酶原片段1+2(uF1+2)是凝血酶生成的一个指标。我们研究了所检测的uF1+2水平是否可用于区分全髋关节置换术(THA)后出现持续性凝血激活和未出现持续性凝血激活的患者。
我们对接受THA的患者进行了两项独立研究。研究1是一项前瞻性初步研究,旨在大致估计术前和术后uF1+2浓度的波动程度。研究2是一项更大规模的前瞻性队列研究,旨在验证研究1的结果,并研究uF1+2浓度与血管血栓形成并发症(VTC)或死亡风险之间的关联。最后,我们试图确定一个临界浓度值,用于识别术后第一周后uF1+2持续升高的患者。尿样通过酶联免疫吸附测定(ELISA)进行分析。在两项研究中,术后均至少进行7天的血栓预防。
与术前水平及健康志愿者的水平相比,手术创伤导致所有患者的uF1+2水平升高。第二项研究中的113名患者中有10名(8.8%)发生了VTC或死亡,推测是由凝血问题引起的。方差分析显示了以下具有统计学意义的关联:术前与术后的uF1+2对数水平(P<0.0001)、有事件和无事件患者的uF1+2对数水平比较(P=0.004);以及个体uF1+2对数水平(P<0.0001)。uF1+2浓度的临界值在0.3至0.5 nmol/l之间,其敏感性和阴性预测值在100%至90%之间,特异性在45%至63%之间,总体准确性在50%至65%之间。该值是通过分析受试者工作特征曲线获得的,目的是识别术后第5天出现持续性凝血激活的患者。
我们的研究表明,所检测的uF1+2水平可能可用于评估THA后个体发生VTC的风险,并用于检测持续性凝血激活的非侵入性检测。