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A new measure for in vivo thrombin activity in comparison with in vitro thrombin generation potential in patients with hyper- and hypocoagulability

机译:高凝和低凝患者的体内凝血酶活性与体外凝血酶生成潜力比较的新方法

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摘要

The thrombin generation potential is an in vitro measure for the capacity of an individual to generate thrombin and recognized as a reflection of a hypo- or hypercoagulable status. Measurement of the in vivo thrombin activity, however, may be of clinical significance. We evaluated a new assay for in vivo thrombin activity and compared it to the in vitro thrombin generation potential in patients with hemophilia A (N = 15), oral anticoagulation for atrial fibrillation (AF) (N = 20), subjects with active cancer (N = 21), and healthy volunteers (N = 10). Thrombin activity was measured with a commercially available oligonucleotide enzyme capture assay in argatroban-stabilized plasma samples. Thrombin generation potential was determined with a commercially available assay in citrated plasma. Thrombin activity was detected in 17 (30.4 %) patients (mean 0.30 mU/ml [SD 0.80]), and in 39 patients (69.6 %) no thrombin activity was present. In cancer patients, thrombin activity was detected in 11 patients (52 %) (range 0.14–5.00 mU/ml) and was particularly increased in 3 patients with vessel-invasive tumors (1.2, 1.5, and 5.0 mU/ml). In AF patients, thrombin activity was only measureable in two patients (10 %) (recent hematoma [0.4 mU/ml] and recent ischemic stroke [1.5 mU/ml]). Thrombin activity was detected in four patients (27 %) with hemophilia (range 0.29–1.75 mU/ml), all of whom had received a factor VIII infusion on the same day. Thrombin activity did not correlate with any of the parameters of the thrombin generation potential. Only patients in acute procoagulatory states or after clotting factor replacement had elevated in vivo thrombin activity, which was, however, unrelated to the in vitro thrombin generation potential.
机译:凝血酶的产生潜力是对个体产生凝血酶的能力的体外测量,并被认为是低或高凝状态的反映。然而,体内凝血酶活性的测量可能具有临床意义。我们评估了一种新的体内凝血酶活性测定方法,并将其与血友病A(N = 15),房颤口服抗凝(AF)(N = 20),患有活动性癌症的患者(N = 15)的体外凝血酶产生潜力进行了比较。 N = 21)和健康的志愿者(N = 10)。用市售的寡核苷酸酶捕获测定法在阿加曲班稳定的血浆样品中测量凝血酶活性。凝血酶的产生潜力是通过在柠檬酸盐血浆中的市售测定法确定的。在17(30.4%)名患者中检测到凝血酶活性(平均0.30 mU / ml [SD 0.80]),在39名患者中(69.6%)没有凝血酶活性。在癌症患者中,有11名患者(52%)(范围0.14–5.00 mU / ml)检测到凝血酶活性,并且在3例血管浸润性肿瘤(1.2、1.5和5.0mU / ml)患者中尤其明显。在房颤患者中,凝血酶活性仅可在两名患者中测量(10%)(近期血肿[0.4mU / ml]和最近的缺血性中风[1.5mU / ml])。在四名血友病患者(范围为0.29-1.75 mU / ml)中检测到凝血酶活性(27%),所有患者均在同一天接受了VIII因子输注。凝血酶活性与凝血酶生成潜能的任何参数都不相关。仅处于急性促凝状态或凝血因子替代后的患者体内凝血酶活性升高,但与体外凝血酶生成潜能无关。

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