Table 1

Variables evaluated in the univariate analysis for the different endpoints examined

 Stage 4
MTTTp ValueCPA≥6%CPA≥7.2%HVPG≥10 mm HgDecompensation
Cold/warm ischaemia time (min)680/46688/41NSNSNSNSNS
Treatment allocation (evaluated)54 (49)49 (48)<0.001<0.001<0.001<0.001<0.001
Stopped azathioprineNA16 (33%)<0.001<0.001<0.0010.0120.013
Tacrolimus trough concentrations (ng/mL)
 5 days7.750.0020.0020.010.0170.01
 15 days*8.56.10.0030.0010.010.0010.01
 30 days*7.96.70.010.010.040.020.01
Conc. HCC1713NSNSNSNS0.03
Conc. ALD1012NSNSNSNSNS
Age48.9 years50 yearsNSNSNSNSNS
Donor age48.5 years44 years0.010.010.010.040.02
Gender mismatch1717NSNSNSNSNS
Rejection episodes42640.0020.00330.040.033NS
Rejection treatment (courses)21300.0020.010.030.038NS
HDNH178<0.001<0.001<0.001<0.001<0.001
CMV viraemia treated710NSNSNSNSNS
Viral load logIU/mL (median)
 Pre-LT5.295.36NSNSNSNSNS
 3 m post-LT6.66.39NSNSNSNSNS
Genotype 1/1b41%41%NSNSNSNSNS
Antiviral treatment19110.010.010.010.0010.001
SVR33NSNANANANA
DM
 Pre-LT1313NSNSNSNSNS
 Post-LT (last follow-up)19150.0130.0380.044NSNS
  • *Median trough levels derived from all measurements up to days 15 and 30 post-LT.

  • ALD, alcoholic liver disease; CMV, cytomegalovirus; CPA, collagen proportionate area; DM, diabetes mellitus; HCC, hepatocellular carcinoma; HDNH, histological de novo hepatitis; HVPG, hepatic venous pressure gradient; LT, liver transplantation; MT, monotherapy; NA, non-applicable; NS, non-significant; SVR, sustained virological response; TT, triple therapy.