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

被引:410
作者
Banares, Rafael [1 ,2 ]
Nevens, Frederik [3 ]
Larsen, Fin Stolze [4 ]
Jalan, Rajiv [5 ]
Albillos, Agustin [6 ,7 ]
Dollinger, Matthias [8 ]
Saliba, Faouzi [9 ,10 ,11 ]
Sauerbruch, Tilman [12 ]
Klammt, Sebastian [13 ]
Ockenga, Johann [14 ]
Pares, Albert [15 ,16 ]
Wendon, Julia [17 ]
Bruennler, Tanja [18 ]
Kramer, Ludwig [19 ]
Mathurin, Philippe [20 ]
de la Mata, Manuel [21 ,22 ]
Gasbarrini, Antonio [23 ]
Muellhaupt, Beat [24 ,25 ]
Wilmer, Alexander [3 ]
Laleman, Wim [3 ]
Eefsen, Martin [4 ]
Sen, Sambit [5 ]
Zipprich, Alexander [8 ]
Tenorio, Teresa [6 ]
Pavesi, Marco [26 ]
Schmidt, Hartmut H. -J. [27 ]
Mitzner, Steffen [13 ]
Williams, Roger [28 ]
Arroyo, Vicente [15 ,16 ]
机构
[1] Hosp Gen Univ Gregorio Maranon, Liver Unit, IiSGM, Madrid 28007, Spain
[2] Univ Complutense, Sch Med, E-28040 Madrid, Spain
[3] Univ Hosp Gasthuisberg KU, Dept Liver & Biliopancreat Dis, Louvain, Belgium
[4] Rigshosp Univ Hosp, Dept Hepatol, Copenhagen, Denmark
[5] Royal Free Hosp, UCL Med Sch, Inst Liver & Digest Hlth, London NW3 2QG, England
[6] Hosp Ramon & Cajal, Dept Gastroenterol, IRYCIS, E-28034 Madrid, Spain
[7] Univ Alcala de Henares, Sch Med, Madrid, Spain
[8] Martin Luther Univ Hosp, Dept Med 1, Halle, Germany
[9] Hop Paul Brousse, Ctr Hepatobiliaire, Villejuif, France
[10] Univ Paris 11, UMR S 785, Villejuif, France
[11] INSERM, U785, Villejuif, France
[12] Univ Bonn, Bonn, Germany
[13] Univ Rostock, Dept Med, Div Nephrol, D-18055 Rostock, Germany
[14] Charite, Berlin, Germany
[15] IDIBAPS, Liver Unit, Barcelona, Spain
[16] Univ Barcelona, Sch Med, Barcelona, Spain
[17] Kings Coll Hosp London, Liver Unit, London, England
[18] Notfallzentrum Barmherzige Bruder, Regensburg, Germany
[19] Hietzing Hosp, Dept Med 1, Vienna, Austria
[20] Serv MAD Hop Claude Huriez CHRU, Lille, France
[21] UGC Digestivo Hosp Univ Reina Sofia, Cordoba, Spain
[22] Inst Maimonides Invest Biomed Cordoba IMIBIC, Cordoba, Spain
[23] Liver Unit Policlin A, Rome, Italy
[24] Univ Zurich Hosp, Swiss HPB Hepatopancreatobiliary Ctr, Zurich, Switzerland
[25] Univ Zurich Hosp, Dept Gastroenterol & Hepatol, Zurich, Switzerland
[26] CLIF Consortium Data Management, Barcelona, Spain
[27] Klin & Poliklin Transplantat Med, Munster, Germany
[28] Fdn Liver Res, Inst Hepatol, London, England
关键词
HEPATIC-ENCEPHALOPATHY; SEVERE SEPSIS; MANAGEMENT; CIRRHOSIS; TRANSPLANTATION; PROMETHEUS; MORTALITY; DIAGNOSIS; PRURITUS; SURVIVAL;
D O I
10.1002/hep.26185
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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. Conclusion: At scheduled doses, a beneficial effect on survival of MARS therapy in patients with ACLF could not be demonstrated. However, MARS has an acceptable safety profile, has significant dialysis effect, and nonsignificantly improves severe HE. (HEPATOLOGY 2013)
引用
收藏
页码:1153 / 1162
页数:10
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