首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Prognostic values of the factor Xa-activated clotting time and endogenous thrombin potential in patients suspected of having disseminated intravascular coagulation.
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Prognostic values of the factor Xa-activated clotting time and endogenous thrombin potential in patients suspected of having disseminated intravascular coagulation.

机译:Xa因子激活的凝血时间和内源性凝血酶潜能在怀疑弥散性血管内凝血的患者中的预后价值。

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BACKGROUND: Widespread coagulation activation and intravascular fibrin formation are clinical features of disseminated intravascular coagulation (DIC). The endogenous thrombin potential (ETP) has been shown to be a useful marker for hypo- or hypercoagulability. The factor Xa-activated clotting time (XACT) represents plasma levels of procoagulant phospholipids. We investigated whether the ETP and XACT would be good prognostic markers in patients suspected of having DIC and whether these markers would show a significant correlation with the thrombin-antithrombin complex (TAT), a marker of in vivo coagulation activation. METHODS: One hundred twenty-nine patients suspected of having DIC were enrolled for the study. The TAT was measured by ELISA. The ETP and XACT were measured by calibrated automated thrombinography. The 28-day mortality was used as a predictor of clinical outcomes. RESULTS: In overt DIC, higher XACT (9.67 vs. 7.33 min) and higher TAT (26.15 vs. 11.56 ng/ml) results were obtained from the nonsurvivors than from the survivors. ETP levels were lower in the overt DIC group than in the no overt DIC group. In receiver operating characteristic analysis, which was conducted to predict the 28-day mortality, the areas under the receiver operating characteristic analysis curve were as follows: 0.71 (95% CI: 0.62-0.78) for the XACT, 0.70 (0.61-0.77) for the TAT, and 0.64 (0.55-0.72) for the ETP. For the diagnosis of overt DIC, the area under the curve of XACT, TAT and ETP were 0.77 (0.69-0.84), 0.64 (0.55-0.72) and 0.73 (0.64-0.80), respectively. The odds ratio of the XACT for the relative risk of 28-day mortality was 9.60 (3.53-26.11), and that of the TAT was 5.18 (2.11-12.72) and that of the ETP 7.66 (1.67-35.17). For the diagnosis of overt DIC, the odds ratio of XACT, TAT and ETP were 37.35 (4.86-286.89), 4.89 (1.93-12.43) and 4.89 (1.98-12.09), respectively. There was a negative correlation between the TAT and ETP (r=-0.223, P=0.012) and a positive correlation between the TAT and XACT (r=0.251, P=0.004). CONCLUSION: Our results suggest that the XACT and ETP may be useful diagnostic and prognostic markers for the DIC. Among various markers, the XACT serves as a good prediction of the 28-day mortality in patients suspected of having DIC.
机译:背景:广泛的凝血激活和血管内血纤蛋白形成是弥散性血管内凝血(DIC)的临床特征。内源性凝血酶潜能(ETP)已被证明是低凝或高凝的有用标志物。 Xa因子激活的凝血时间(XACT)代表血浆中促凝磷脂的水平。我们调查了在怀疑患有DIC的患者中ETP和XACT是否将是良好的预后标志物,以及这些标志物是否与体内凝血激活标志物凝血酶-抗凝血酶复合物(TAT)显着相关。方法:129例怀疑患有DIC的患者入选了该研究。通过ELISA测量TAT。 ETP和XACT通过校准的自动凝血酶谱仪测量。 28天的死亡率被用作临床结果的预测指标。结果:在公开的DIC中,与未幸存者相比,非幸存者获得了更高的XACT(9.67对7.33分钟)和更高的TAT(26.15对11.56 ng / ml)结果。显性DIC组的ETP水平低于非显性DIC组。在进行接收机工作特征分析以预测28天死亡率时,接收机工作特征分析曲线下的面积如下:XACT为0.71(95%CI:0.62-0.78),XACT为0.70(0.61-0.77) TAT为0.64(0.55-0.72)。对于显性DIC的诊断,XACT,TAT和ETP曲线下的面积分别为0.77(0.69-0.84),0.64(0.55-0.72)和0.73(0.64-0.80)。 XACT对28天死亡率的相对风险的比值比是9.60(3.53-26.11),TAT的比值比是5.18(2.11-12.72),而ETP的比值比是7.66(1.67-35.17)。对于显性DIC的诊断,XACT,TAT和ETP的优势比分别为37.35(4.86-286.89),4.89(1.93-12.43)和4.89(1.98-12.09)。 TAT与ETP之间呈负相关(r = -0.223,P = 0.012),而TAT与XACT之间呈正相关(r = 0.251,P = 0.004)。结论:我们的结果表明XACT和ETP可能是DIC的有用诊断和预后标志物。在各种标记中,XACT可很好地预测怀疑患有DIC的患者28天死亡率。

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