Videm V, Fosse E, Mollnes T E, Ellingsen O, Pedersen T, Karlsen H
Institute for Experimental Medical Research, University of Oslo, Norway.
J Thorac Cardiovasc Surg. 1989 May;97(5):764-70.
Complement activation was studied in vitro with six different membrane and bubble oxygenators for cardiopulmonary bypass. There was a similar increase in terminal (C5 to C9) activation with all oxygenators (p less than 0.001), ranging from 281% (117% to 444%) to 453% (225% to 680%) after 60 minutes (median and 95% confidence intervals). C3 activation was not observed with a hollow fiber membrane and a soft shell bubble oxygenator. On the other hand, a capillary membrane, a sheet membrane, a nonporous membrane, and a hard shell bubble oxygenator all induced a similar increase in C3 activation (p less than 0.01), ranging from 107% (23% to 346%) to 272% (88% to 395%) after 60 minutes. The differences in C3 activation could not be explained by the blood contact materials or any other single factor known to induce activation, which suggests that overall complement activation during cardiopulmonary bypass is a multifactorial effect. The tubing set per se induced only minor C3 activation but contributed to the overall formation of terminal complement complex. The study further indicates that an arterial line blood filter prevents activated neutrophils from being reinfused to the patient and should be used regardless of type of oxygenator.
使用六种不同的膜式和鼓泡式氧合器对体外循环中的补体激活进行了研究。所有氧合器的终末(C5至C9)激活均有类似增加(p<0.001),60分钟后增加幅度在281%(117%至444%)至453%(225%至680%)之间(中位数和95%置信区间)。中空纤维膜式和软壳鼓泡式氧合器未观察到C3激活。另一方面,毛细管膜式、片状膜式、无孔膜式和硬壳鼓泡式氧合器均诱导C3激活出现类似增加(p<0.01),60分钟后增加幅度在107%(23%至346%)至272%(88%至395%)之间。C3激活的差异无法用血液接触材料或任何其他已知可诱导激活的单一因素来解释,这表明体外循环期间的总体补体激活是一种多因素效应。管路本身仅诱导轻微的C3激活,但有助于终末补体复合物的总体形成。该研究进一步表明,动脉血滤器可防止活化的中性粒细胞重新输注给患者,无论氧合器类型如何均应使用。