At the time of the diagnosis of acute liver failure was made, the need for liver transplantation was explained to the patient’s relatives. Hepatic encephalopathy was assessed using the West Haven criteria of altered mental state [13] and the Glasgow Coma Scale in accordance with the recommendation

of a working party on studies in hepatic encephalopathy [14]. Two investigators, who had extensive clinical experience in hepatic encephalopathy, confirmed all cases of encephalopathy by reviewing the clinical course of the patient during hospitalization. All patients underwent computerized tomography Inhibitors,research,lifescience,medical (CT) examination to determine liver volume on admission and at least Inhibitors,research,lifescience,medical once a week thereafter. The study was performed according to the selleck chem Vismodegib guidelines of the Declaration of Helsinki and the study protocol was approved by the ethics committee at our institution. Written informed consent was obtained from each patient or their relative if the patient was unable to give consent. Artificial liver support On-line HDF Blood access Inhibitors,research,lifescience,medical was established with a double-lumen catheter (table 1 Vas-Cath®, Niagara®; Bard, Salt Lake City, UT, USA) inserted into a central vein with an internal jugular vein approach.

On-line HDF was performed as previously described [15,16]. In brief, in the on-line solution preparation system, substitution fluid was prepared continuously Inhibitors,research,lifescience,medical by ultrafiltration of dialysate, enabling its use as substitution fluid. In our on-line system, two ultrafilters (EF-01, FLX-18GW,

polyester-polymer alloy [PEPA] membranes; Nikkiso, Tokyo, Japan) were used for cold sterilization of the dialysate (AK-Solita® FL; Ajinomoto Pharma, Tokyo, Japan) in hemodialysis Inhibitors,research,lifescience,medical (HD), and one ultrafilter (EF-01, FLX-18GW, PEPA; Nikkiso) was added when using substitution fluid (Figure ​(Figure1).1). Sterile substitution fluid produced on-line from the dialysate was infused pre-filter with a substitution fluid pump and Cilengitide tubing set (PRS-12, NV-A300PA; Nikkiso) (pre-dilution). HDF was performed using filters containing 1.5 m2 of polysulfone membranes (APS-15E; Asahi Kasei Medical Co., Tokyo, Japan). Pore size was 85 Å. A HD control device and tubing set (model DBG-02, NV-Y888PC; Nikkiso) were used. An AK-Solita FL was set to prepare 700 mL/min of dialysate. Substitution fluid flow rates ranged from 300 to 350 mL/min, so that actual dialysate flow rates during HDF ranged from 350 to 400 mL/min. Blood flow rates ranged from 300 to 350 mL/min. At the start, the duration of on-line HDF was set so that the amount of hemocatharsis (blood flow rate × time) was three times the estimated body fluid volume (actual body weight ×0.6).