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早期给予肝素可减轻体外循环模拟过程中组织因子介导的凝血酶生成。

Early heparin administration attenuates tissue factor-mediated thrombin generation during simulated cardiopulmonary bypass.

作者信息

Morizumi Sei, Hiramatsu Yuji, Matsuzaki Kanji, Goto Yukinobu, Sato Shoko, Abe Masakazu, Kato Hideyuki, Matsubara Muneaki, Sakakibara Yuzuru

机构信息

Department of Cardiovascular Surgery, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.

出版信息

J Card Surg. 2014 Jan;29(1):35-40. doi: 10.1111/jocs.12254. Epub 2013 Nov 25.

Abstract

BACKGROUND

We tested the hypothesis that heparin administration prior to the emergence of tissue factor (TF) would increase plasma TF pathway inhibitor (TFPI) and attenuate TF-mediated thrombin generation during simulated cardiopulmonary bypass (CPB).

METHODS

Human blood was recirculated for 120 minutes using an oxygenator and roller pump. Four groups were examined: control group (heparin 3.75 U/mL, in donor blood, n = 7), rTF group (heparin + recombinant TF 1000 pg/mL, in donor blood, n = 7), TFPI boost group (heparin, in preheparinized donor blood, n = 8), and rTF + TFPI boost group (heparin + rTF, in preheparinized blood, n = 7). In the two TFPI boost groups, 50 U/kg of heparin was given to the donors intravenously five minutes before donation to boost plasma TFPI levels. Total plasma TFPI, thrombin-antithrombin complex, and prothrombin fragment F1+2 levels were measured before and during CPB.

RESULTS

Preheparinization increased total plasma TFPI levels by a factor of 8.0. Administration of rTF significantly enhanced the generation of F1+2 (p = 0.0002). The heparin-induced TFPI elevation reduced both thrombin-antithrombin complex and F1+2 to control levels in rTF + TFPI boost group (p = 0.0158 for thrombin-antithrombin complex, p < 0.0001 for F1+2 ). F1+2 levels were at all times lower than control levels in TFPI boost group (p < 0.0001).

CONCLUSIONS

Heparin-induced TFPI elevation attenuates TF-mediated thrombin generation. Early heparin administration prior to the emergence of plasma TF may represent a novel strategy for controlling thrombin generation by the extrinsic coagulation pathway during CPB.

摘要

背景

我们检验了这样一个假设,即在组织因子(TF)出现之前给予肝素会增加血浆TF途径抑制剂(TFPI),并在模拟体外循环(CPB)期间减弱TF介导的凝血酶生成。

方法

使用氧合器和滚压泵将人体血液再循环120分钟。检查了四组:对照组(供体血液中肝素浓度为3.75 U/mL,n = 7),rTF组(供体血液中肝素+重组TF 1000 pg/mL,n = 7),TFPI增强组(预肝素化供体血液中的肝素,n = 8),以及rTF + TFPI增强组(预肝素化血液中肝素+rTF,n = 7)。在两个TFPI增强组中,在献血前5分钟给供体静脉注射50 U/kg肝素以提高血浆TFPI水平。在CPB之前和期间测量血浆总TFPI、凝血酶 - 抗凝血酶复合物和凝血酶原片段F1 + 2水平。

结果

预肝素化使血浆总TFPI水平提高了8.0倍。给予rTF显著增强了F1 + 2的生成(p = 0.0002)。肝素诱导的TFPI升高使rTF + TFPI增强组中的凝血酶 - 抗凝血酶复合物和F1 + 2均降至对照水平(凝血酶 - 抗凝血酶复合物p = 0.0158,F1 + 2 p < 0.0001)。TFPI增强组中的F1 + 2水平在所有时间均低于对照水平(p < 0.0001)。

结论

肝素诱导的TFPI升高减弱了TF介导的凝血酶生成。在血浆TF出现之前早期给予肝素可能代表一种在CPB期间通过外源性凝血途径控制凝血酶生成的新策略。

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