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      Management of Sepsis in Patients With Cirrhosis: Current Evidence and Practical Approach : Hepatology

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          American College of Chest Physicians/Society of Critical Care Medicine Consensus Conference

          (1992)
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            Resuscitation Fluids

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              Extracorporeal albumin dialysis with the molecular adsorbent recirculating system in acute-on-chronic liver failure: the RELIEF trial.

              Acute-on-chronic liver failure (ACLF) is a frequent cause of death in cirrhosis. Albumin dialysis with the molecular adsorbent recirculating system (MARS) decreases retained substances and improves hemodynamics and hepatic encephalopathy (HE). However, its survival impact is unknown. In all, 189 patients with ACLF were randomized either to MARS (n=95) or to standard therapy (SMT) (n=94). Ten patients (five per group) were excluded due to protocol violations. In addition, 23 patients (MARS: 19; SMT: 4) were excluded from per-protocol (PP) analysis (PP population n=156). Up to 10 6-8-hour MARS sessions were scheduled. The main endpoint was 28-day ITT and PP survival. There were no significant differences at inclusion, although the proportion of patients with Model for Endstage Liver Disease (MELD) score over 20 points and with spontaneous bacterial peritonitis (SBP) as a precipitating event was almost significantly greater in the MARS group. The 28-day survival was similar in the two groups in the ITT and PP populations (60.7% versus 58.9%; 60% versus 59.2% respectively). After adjusting for confounders, a significant beneficial effect of MARS on survival was not observed (odds ratio [OR]: 0.87, 95% confidence interval [CI] 0.44-1.72). MELD score and HE at admission and the increase in serum bilirubin at day 4 were independent predictors of death. At day 4, a greater decrease in serum creatinine (P=0.02) and bilirubin (P=0.001) and a more frequent improvement in HE (from grade II-IV to grade 0-I; 62.5% versus 38.2%; P=0.07) was observed in the MARS group. Severe adverse events were similar.
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                Author and article information

                Journal
                Hepatology
                Hepatology
                Wiley
                02709139
                July 2019
                July 2019
                June 27 2019
                : 70
                : 1
                : 418-428
                Affiliations
                [1 ]Division of Gastroenterology and Hepatology; Mayo Clinic College of Medicine and Science; Rochester MN
                [2 ]Division of Pulmonary and Critical Care Medicine; Mayo Clinic College of Medicine and Science; Rochester MN
                [3 ]Multidisciplinary Epidemiology and Translational Research in Intensive Care (METRIC); Mayo Clinic College of Medicine and Science; Rochester MN
                Article
                10.1002/hep.30412
                30516866
                5dcfd3b4-a0f4-4df3-8013-c21d79c7a80a
                © 2019

                http://doi.wiley.com/10.1002/tdm_license_1.1

                http://onlinelibrary.wiley.com/termsAndConditions#vor

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