“…Currently, EBP uses a series of hemofilters to remove hydrophilic or hydrophobic solutes through the mechanism of convection, diffusion or adsorption, and the solute removal spectrum of a hemofilter is significantly dependent on its own membrane/adsorbent structure and treatment dose [ 6 ]. Multiple hemofilters, such as Toraymyxin hemofilter (Toray Industries, Tokyo, Japan), the CytoSorb hemofilter (CytoSorbents Corporation, New Jersey, USA) and the oXiris hemofilter (Baxter, Meyzieu, France), have been used to treat critically ill patients in current clinical practice aiming to eliminate endotoxins and/or cytokines despite the lack of solid evidence of survival benefit [ 3 , 7 ]. The failure of EBP therapies to improve survival in these patients could be attributed to the inadequate timing for treatment initiation, inadequate patient selection, inadequate therapeutic target selection and insufficient clearance of inflammatory mediators [ 3 , 5 ].…”