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首页> 外文期刊>ASAIO journal >Newly designed CRRT membranes for sepsis and SIRS-a pragmatic approach for bedside intensivists summarizing the more recent advances: A systematic structured review
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Newly designed CRRT membranes for sepsis and SIRS-a pragmatic approach for bedside intensivists summarizing the more recent advances: A systematic structured review

机译:新型设计用于脓毒症和SIRS的CRRT膜-一种床边强化医生的实用方法,总结了最近的进展:系统的结构综述

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摘要

In recent years, after all the attention has been focused on the dose for continuous renal replacement therapy (CRRT) in sepsis and systemic inflammation response syndrome (SIRS), the relatively negative results of all those studies did urge our expectations on new approaches regarding CRRT in sepsis and SIRS. So far, after the failure of the major randomized studies on dose, attention is now drawn to new membranes that could better eliminate massive amounts of unbound mediators in wider spectrum and also in greater magnitude Nevertheless, for septic acute kidney injury, the recommended dose will remain 35 ml/kg/h until the IVOIRE (hIgh VOlume in Intensive Care) study will be published. In this new armamentarium, we have distinguished the first tools that can still be called membranes ranging from AN69 Surface Treated (ST), SEPTEX, polymethylmetacrylate, to Oxiris that can still run with a CRRT device. Polymyxin B is still a kind of membrane although it has a larger surface, but it can run in a hemoperfusion system and is also much more selective. Adsorptive columns and sorbents are not anymore membranes but are seen as cartridges as the surface is extremely huge when compared with that of membranes (more than 500 m). They can still run in a hemoperfusion device. At the very end, we do have apheresis or selective plasma exchange (also very close to sorbents and columns) but we have very few data up to now regarding sepsis. Regarding spectrum, CytoSorb seems to be very promising although it is not able to capture endotoxin and IL-10. Oxiris is also promising as it can capture endotoxin and cytokines. AN69 ST is very powerful to capture numerous cytokines and especially high-mobility group box 1 protein (a very upstream cytokine). Polymethylmetacrylate has also the power to capture endotoxin and numerous other cytokines probably with a larger magnitude than Oxiris although this is not proven. Lastly, high-porosity membranes (Septex) may play a role especially when used in continuous venovenous hemodialysis mode. At the end, if we look for a more enlarged spectrum and a higher magnitude, CytoSorb might be seen as the most promising although not having the ability to fix endotoxin. Future studies will tell us which membrane or sorbent will be most useful in the adjunctive treatment for sepsis.
机译:近年来,在所有注意力都集中在败血症和全身炎症反应综合征(SIRS)的连续肾脏替代疗法(CRRT)的剂量之后,所有这些研究的相对阴性结果确实促使我们对CRRT的新方法寄予期望在败血症和SIRS中。迄今为止,在主要的剂量随机研究失败之后,现在人们开始关注可以更好地消除更广谱和更大范围内大量未结合介体的新膜。然而,对于败血症性急性肾损伤,推荐剂量应为保持35毫升/千克/小时,直到IVOIRE(重症监护中的高剂量)研究发表为止。在这个新的武器库中,我们区分了仍可以称为膜的首批工具,范围从AN69表面处理(ST),SEPTEX,聚甲基丙烯酸甲酯到仍然可以使用CRRT设备运行的Oxiris。多粘菌素B尽管具有较大的表面,但仍是一种膜,但它可以在血液灌流系统中运行并且选择性更高。吸附柱和吸附剂不再是膜,而是膜盒,因为与膜(大于500 m)相比,其表面非常大。他们仍然可以在血液灌流装置中运行。最后,我们确实进行了单采血液分离术或选择性血浆交换(也非常接近吸附剂和色谱柱),但是到目前为止,关于败血症的数据很少。关于光谱,尽管CytoSorb无法捕获内毒素和IL-10,但它似乎非常有前途。 Oxiris也很有希望,因为它可以捕获内毒素和细胞因子。 AN69 ST具有强大的功能,可以捕获多种细胞因子,尤其是高迁移率的第1组盒蛋白(非常上游的细胞因子)。聚甲基丙烯酸甲酯还具有捕获内毒素和许多其他细胞因子的能力,尽管这种作用尚未得到证实,但其含量可能比Oxiris大。最后,高孔隙率膜(Septex)可能会发挥作用,尤其是在连续静脉血液透析模式下使用时。最后,如果我们寻找更大的光谱和更大的幅度,尽管没有固定内毒素的能力,CytoSorb可能被认为是最有前途的。未来的研究将告诉我们哪种膜或吸附剂在败血症的辅助治疗中最有用。

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