Original Article
Copyright ©2010 Baishideng.
World J Gastroenterol. May 14, 2010; 16(18): 2227-2234
Published online May 14, 2010. doi: 10.3748/wjg.v16.i18.2227
Table 1 MARS treatment protocols for acute liver failure in Finland
EtiologyMARS treatment initiation criteriaTreatment protocol
Acute liver failureRapid deterioration of hepatic synthetic function and clinical condition despite conservative standard medical therapy22-h sessions daily until:
And one of the following criteria:(1) Native liver recovers
(1) Ingestion of a lethal dose of a known hepatotoxin (e.g. Amanita, paracetamol)(2) Suitable transplant organ is found
(2) The patient fulfills the criteria for highly urgent liver transplantation(3) Irreversible multi-organ damage occurs
Table 2 Mean pre-treatment 15D scores in different encephalopathy grade groups (mean ± SD)
Pre-treatment encephalopathy grade15D score
00.532 ± 0.151
10.461 ± 0.188
20.403 ± 0.177
30.079 ± 0.077
40.016
Table 3 Baseline data for the MARS and control groups
MARS groupHistorical control groupP value
Pre-treatment demographic & clinical data
Number of patients9017
Age (yr)45 (14-81)42 (21-72)0.714
Sex (male)37 (41%)7 (41%)0.996
Body mass index (kg/m2)26 (17-40)26 (21-37)0.372
MARS sessions/patient2 (1-9)0
Mechanically ventilated30 (33%)6 (35%)0.875
Vasoactive infusion used27 (30%)9 (56%)0.041
Renal insufficiency29 (32%)7 (41%)0.474
MELD-score31 (5-50)30 (19-51)0.225
Mean encephalopathy grade1.7 ± 1.62.1 ± 1.70.335
Contra-indication to Ltx prior to treatment11 (12%)4 (24%)0.253
Became untransplantable during treatment7 (8%)3 (18%)0.195
Number of transplanted patients26 (29%)8 (47%)0.162
Pre-treatment key laboratory values
Platelets (× 109/L)138 (11-410)142 (51-448)0.919
NH4 ion (μmol/L)68 (8-512)90 (14-241)0.559
Bilirubin (μmol/L)215 (4-761)381 (38-880)0.057
Creatinine (μmol/L)75 (35-1318)78 (38-275)0.946
FV (%)32 (5-142)38 (7-71)0.865
Table 4 The survival, cost, and HRQoL data of MARS-treated and control patients
Subgroups according to outcome3-yr survival
Cost (€)
HRQoL
n%Mean (d)nMeanMinMaxnPre-treatment meanPost-treatment mean
MARS groupAll ALF patients90783179 74511 961370 573900.300.70
Alive at 3 yr702478 72411 961370 573700.340.89
Dead2063783 24332 496171 157200.150.00
Contraindication to Ltx1839
Alive at 3 yr7452 49230 325112 58570.380.85
Dead1114564 41432 49695 666110.130.00
No contraindication - no Ltx4685
Alive at 3 yr391541 95711 961137 235390.400.93
Dead7110189 47170.090.00
Transplanted2692
Alive at 3 yr245210 01296 984370 573240.220.84
Dead21691171 15720.470.00
Control groupAll ALF patients174116105 82016 862262 481170.270.36
Contraindication to Ltx0
Dead79745 08917 591105 91770.270.00
No contraindication - no Ltx100
Alive at 3 yr2277 16216 862137 46220.270.85
Transplanted63
Alive at 3 yr54170 578117 444262 48150.320.87
Dead3283180 285129 120250 77230.190.00
Table 5 Base case results for MARS
Cost (€)Incremental cost (€)QALYsIncremental QALYsCost per QALY (€)Incremental cost per QALY
MARS93 2141.440.6664 732MARS dominates SMT
Control group (SMT only)104 14210 9280.78133 858