Weerwind P W, van der Veen F H, Lindhout T, de Jong D S, Cahalan P T
Department of Extra Corporeal Circulation, University Hospital Nijmegen, The Netherlands.
Int J Artif Organs. 1998 May;21(5):291-8.
In this study the intrinsic thrombogenicity of the extracorporeal circuits and the benefit of heparin-bonded circuits in an extracorporeal life support system without full systemic heparinization and with minimal interference of the so called material-independent factors was tested in four calves. In two circuits (group A) all blood-contacting surfaces were coated with end-point-attached heparin and the other two were non-coated (group B). Under standardized conditions the calves were perfused at a blood flow rate of 2 L/min. After only one bolus injection of heparin (250 IU/kg body weight) before cannulation, plasma heparin activity rapidly decreased in both groups: half life of about 55 minutes. This decrease of the heparin activity was accompanied by a fall of the activated clotting time (ACT) level to baseline values. The experiments using a heparin-coated circuit, had a runtime of more than 360 minutes, whereas the experiments using a non-coated circuit had to be terminated after a runtime of 255 minutes, because massive fibrin formation was noticed in the circuit. This formation was accompanied by a rapid increase in the line pressure, measured just before the inlet of the oxygenator. The macroscopic inspections after terminating the experiments and rinsing the circuit showed a clean circuit in group A. The fibrinopeptide A (FPA) level increased faster during perfusion with the non-coated circuit than in the heparin coated circuit. Lung histopathological examinations of the lungs of the animals in group A showed no fibrin deposition, whereas most of the blood vessels of the lung preparations of the animals in group B were partially or completely occluded with fibrin. These results suggest that heparin-bonding greatly reduces the thrombogenicity of the extracorporeal circuit, and therefore it can reduce the need for systemic heparinization in an extracorporeal life support system.
在本研究中,对4头小牛测试了体外循环回路的内在血栓形成性,以及在体外生命支持系统中使用肝素涂层回路的益处,该系统未进行全身肝素化且所谓的材料无关因素干扰最小。在两个回路(A组)中,所有血液接触表面均涂有末端连接肝素,另外两个回路未涂层(B组)。在标准化条件下,以2 L/min的血流速率对小牛进行灌注。插管前仅一次性注射肝素(250 IU/kg体重)后,两组血浆肝素活性均迅速下降:半衰期约为55分钟。肝素活性的这种下降伴随着活化凝血时间(ACT)水平降至基线值。使用肝素涂层回路的实验运行时间超过360分钟,而使用未涂层回路的实验在运行255分钟后必须终止,因为在回路中发现大量纤维蛋白形成。这种形成伴随着在氧合器入口前测量的管路压力迅速增加。实验结束并冲洗回路后的宏观检查显示A组回路清洁。灌注过程中,未涂层回路的纤维蛋白肽A(FPA)水平比肝素涂层回路升高得更快。A组动物肺部的组织病理学检查显示无纤维蛋白沉积,而B组动物肺部标本的大多数血管部分或完全被纤维蛋白阻塞。这些结果表明,肝素结合可大大降低体外循环回路的血栓形成性,因此可减少体外生命支持系统中全身肝素化的需求。