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在冠状动脉搭桥手术期间,使用肝素涂层体外循环可降低单核细胞组织因子促凝活性。

Induction of monocyte tissue factor procoagulant activity during coronary artery bypass surgery is reduced with heparin-coated extracorporeal circuit.

作者信息

Barstad R M, Ovrum E, Ringdal M A, Oystese R, Hamers M J, Veiby O P, Rolfsen T, Stephens R W, Sakariassen K S

机构信息

Nycomed Pharma AS, Oslo, Norway.

出版信息

Br J Haematol. 1996 Sep;94(3):517-25. doi: 10.1111/j.1365-2141.1996.tb08989.x.

DOI:10.1111/j.1365-2141.1996.tb08989.x
PMID:8790153
Abstract

The possible activation of monocytes to express tissue factor procoagulant activity (TF-PCA) during CPB (cardiopulmonary bypass) was investigated. 22 patients undergoing myocardial revascularization were randomly assigned to two groups. In group C, heparin-coated circuits (Duraflo II) and reduced systemic heparinization (ACT > 250s) were used. In group NC, non-coated circuits and standard heparin administration (ACT > 480s) were used. Adherent monocytes retrieved from the oxygenators immediately after bypass arrest showed a 2-3-fold increase in TF-PCA when compared to circulating cells pre-CPB (P < 0.01). When cell PCA was expressed as percent change from pre-CPB (baseline) values, circulating monocytes in group NC at CPB-arrest showed a 2-fold increase in PCA compared to group C (P < 0.05). Moreover, the percent increase in PCA of oxygenator-retrieved monocytes was 7-fold in group NC and 2-fold in group C (P < 0.008 and P < 0.004, respectively). Thus, heparin-coating of the extracorporeal circuit reduced induction of adherent cell TF-PCA by 70% (P < 0.05). Thus, monocyte TF-PCA may cause activation of the extrinsic coagulation pathway during CPB surgery. It is apparent that heparin-coating enhanced biocompatibility of extracorporeal circuits. Reduced systemic heparinization in group C proved to be safe. However, further reduction of heparin administration may not be advisable, since monocytes were still activated in the coated oxygenator.

摘要

研究了体外循环(CPB)期间单核细胞表达组织因子促凝活性(TF-PCA)的可能性。22例行心肌血运重建术的患者被随机分为两组。C组使用肝素涂层回路(Duraflo II)并减少全身肝素化(活化凝血时间>250秒)。NC组使用非涂层回路和标准肝素给药(活化凝血时间>480秒)。体外循环停止后立即从氧合器中回收的贴壁单核细胞与CPB前的循环细胞相比,TF-PCA增加了2-3倍(P<0.01)。当将细胞PCA表示为相对于CPB前(基线)值的变化百分比时,CPB停止时NC组的循环单核细胞PCA比C组增加了2倍(P<0.05)。此外,NC组氧合器回收的单核细胞PCA增加百分比为7倍,C组为2倍(分别为P<0.008和P<0.004)。因此,体外循环回路的肝素涂层使贴壁细胞TF-PCA的诱导减少了70%(P<0.05)。因此,单核细胞TF-PCA可能在CPB手术期间引起外源性凝血途径的激活。显然,肝素涂层增强了体外循环回路的生物相容性。C组减少全身肝素化被证明是安全的。然而,进一步减少肝素给药可能不可取,因为在涂层氧合器中单核细胞仍被激活。

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