Improvement of hepatorenal syndrome with extracorporeal albumin dialysis mars: Results of a prospective, randomized, controlled clinical trial

In hepatorenal syndrome (HRS), renal insufficiency is often progressive, and the prognosis is extremely poor under standard medical therapy. The molecular adsorbent recirculating system (MARS) is a modified dialysis method using an albumin-containing dialysate that is recirculated and perfused onlin...

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Published inLiver transplantation Vol. 6; no. 3; pp. 277 - 286
Main Authors Mitzner, Stefan R., Stange, Jan, Klammt, Sebastian, Risler, Teut, Erley, Christiane M., Bader, Brigitte D., Berger, Elke D., Lauchart, Werner, Peszynski, Piotr, Freytag, Jens, Hickstein, Heiko, Loock, Jan, Löhr, Johannes-Mathias, Liebe, Stefan, Emmrich, Jörg, Korten, Gero, Schmidt, Reinhard
Format Journal Article
LanguageEnglish
Published Elsevier Inc 01.05.2000
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Summary:In hepatorenal syndrome (HRS), renal insufficiency is often progressive, and the prognosis is extremely poor under standard medical therapy. The molecular adsorbent recirculating system (MARS) is a modified dialysis method using an albumin-containing dialysate that is recirculated and perfused online through charcoal and anion-exchanger columns. MARS enables the selective removal of albumin-bound substances. A prospective controlled trial was performed to determine the effect of MARS treatment on 30-day survival in patients with type I HRS at high risk (bilirubin level,15 mg/dL) compared with standard treatment. Thirteen patients with cirrhosis with type I HRS were included from 1997 to 1999. All were Child's class C, with Child-Turcotte-Pugh scores of 12.4 ± 1.0, United Network for Organ Sharing status 2A, and total bilirubin values of 25.7 ± 14.0 mg/dL. Eight patients were treated with the MARS method in addition to hemodiafiltration (HDF) and standard medical therapy, and 5 patients were in the control group (HDF and standard medical treatment alone). None of these patients underwent liver transplantation or received a transjugular intrahepatic portosystemic shunt or vasopressin analogues during the observation period. In the MARS group, 5.2 ± 3.6 treatments (range, 1 to 10 treatments) were performed for 6 to 8 hours daily per patient. A significant decrease in bilirubin and creatinine levels ( P < .01) and increase in serum sodium level and prothrombin activity ( P < .01) were observed in the MARS group. Mortality rates were 100% in the control group at day 7 and 62.5% in the MARS group at day 7 and 75% at day 30, respectively ( P < .01). We conclude that the removal of albumin-bound substances with the MARS method can contribute to the treatment of type I HRS.
ISSN:1527-6465
1527-6473
DOI:10.1053/lv.2000.6355