Hasper D, Schefold J C, Jörres A
Klinik für Nephrologie und Internistische Intensivmedizin, Charité-Universitätsmedizin Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, 13353, Berlin, Deutschland,
Med Klin Intensivmed Notfmed. 2015 May;110(4):272-7. doi: 10.1007/s00063-014-0415-7. Epub 2014 Sep 24.
The activation of multiple pro- and anti-inflammatory mediators is a key feature in the pathophysiology of sepsis. Many of these mediators may directly contribute to organ dysfunction and determine disease severity. So far our ability to modulate these upregulated mediator pathways is very limited. Therefore the adsorption of such mediators via an extracorporeal circuit may be a beneficial intervention during sepsis.
Recent technical innovations have made this intervention feasible. Both systems for exclusive mediator adsorption and for adsorption beside a conventional renal replacement therapy are now available. Some of the membranes can adsorb a broad range of mediators by rather unspecific binding, whereas others specifically adsorb endotoxin or mediators.
Whilst biochemical efficacy could be demonstrated by some of the systems, controlled and randomized studies demonstrating improved clinical endpoints are still lacking. Therefore the use of such therapies outside clinical studies cannot yet be recommended.
多种促炎和抗炎介质的激活是脓毒症病理生理学的关键特征。其中许多介质可能直接导致器官功能障碍并决定疾病严重程度。到目前为止,我们调节这些上调的介质途径的能力非常有限。因此,通过体外循环吸附此类介质可能是脓毒症期间一种有益的干预措施。
最近的技术创新使这种干预成为可能。现在既有用于专门介质吸附的系统,也有用于在传统肾脏替代治疗之外进行吸附的系统。一些膜可以通过相当非特异性的结合吸附多种介质,而其他膜则特异性吸附内毒素或介质。
虽然一些系统已证明具有生化功效,但仍缺乏能证明临床终点得到改善的对照和随机研究。因此,目前还不推荐在临床研究之外使用此类疗法。