首页> 美国卫生研究院文献>Lippincott Williams Wilkins Open Access >Correcting thrombin generation ex vivo using different haemostatic agents following cardiac surgery requiring the use of cardiopulmonary bypass
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Correcting thrombin generation ex vivo using different haemostatic agents following cardiac surgery requiring the use of cardiopulmonary bypass

机译:需要进行体外循环的心脏手术后使用不同的止血剂离体校正凝血酶的产生

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摘要

Recently, lower thrombin generation has been associated with excess bleeding post-cardiopulmonary bypass (CPB). Therefore, treatment to correct thrombin generation is a potentially important aspect of management of bleeding in this group of patients. The objective of the present study was to investigate the effects of fresh frozen plasma (FFP), recombinant factor VIIa (rFVIIa), prothrombin complex concentrate (PCC) and tissue factor pathway inhibitor (TFPI) inhibition on thrombin generation when added ex vivo to the plasma of patients who had undergone cardiac surgery requiring CPB. Patients undergoing elective cardiac surgery were recruited. Blood samples were collected before administration of heparin and 30 min after its reversal. Thrombin generation was measured in the presence and absence of different concentrations of FFP, rFVIIa, PCC and an anti-TFPI antibody. A total of 102 patients were recruited. Thrombin generation following CPB was lower compared with pre-CPB (median endogenous thrombin potential pre-CPB 339 nmol/l per min, post-CPB 155 nmol/l per min, P < 0.0001; median peak thrombin pre-CPB 35 nmol/l, post-CPB 11 nmol/l, P < 0.0001). Coagulation factors and anticoagulants decreased, apart from total TFPI, which increased (55–111 ng/ml, P < 0.0001), and VWF (144–170 IU/dl, P < 0.0001). Thrombin generation was corrected to pre-CPB levels by the equivalent of 15 ml/kg FFP, 45 μg/kg rFVIIa and 25 U/kg of PCC. Inhibition of TFPI resulted in an enhancement of thrombin generation significantly beyond pre-CPB levels. This study shows that FFP, rFVIIa, PCC and inhibition of TFPI correct thrombin generation in the plasma of patients who have undergone surgery requiring CPB. Inhibition of TFPI may be a further potential therapeutic strategy for managing bleeding in this group of patients.
机译:最近,凝血酶水平降低与体外循环(CPB)后出血过多有关。因此,在该组患者中,纠正凝血酶生成的治疗是控制出血的潜在重要方面。本研究的目的是研究新鲜冰冻血浆(FFP),重组因子VIIa(rFVIIa),凝血酶原复合物浓缩物(PCC)和组织因子途径抑制剂(TFPI)对凝血酶生成的抑制作用。接受CPB的心脏手术患者的血浆。招募接受择期心脏手术的患者。肝素给药前和逆转后30分钟采集血样。在存在和不存在不同浓度的FFP,rFVIIa,PCC和抗TFPI抗体的情况下测量凝血酶的生成。总共招募了102名患者。 CPB后的凝血酶生成量低于CPB前(CPB前339 nmol / l / min,CPB后155 nmol / l / min,P <0.0001; CPB前pre化酶中位数峰值35 nmol / l) ,CPB后为11 nmol / l,P <0.0001)。除总TFPI增加(55-111 ng / ml,P <0.0001)和VWF(144-170 IU / dl,P <0.0001)外,凝血因子和抗凝剂减少。凝血酶的生成被校正为CPB之前的水平,相当于15μml/ kg FFP,45μg/ kg rFVIIa和25μU/ kg PCC。 TFPI的抑制导致凝血酶的产生大大超过了CPB前水平。这项研究表明,FFP,rFVIIa,PCC和TFPI抑制作用可纠正接受CPB手术的患者血浆中的凝血酶生成。 TFPI的抑制可能是治疗该组患者出血的另一种潜在治疗策略。

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