Clinical Study

A Randomized Multicenter Study Comparing a Tacrolimus-Based Protocol with and without Steroids in HCV-Positive Liver Allograft Recipients

Table 1

Baseline recipient and donor characteristics of the FAS population.

TAC/DACTAC/STR
𝑁 = 6 7 𝑁 = 6 8

Recipient age, mean (SD)53.1 (9.6)55.3 (6.5)
Male, no. (%)49 (73.1)45 (66.2)
Mean (SD) MELD score16.2 (6.3)14.5 (6.1)
HCV genotype:
17 (12.1)5 (8.3)
1a8 (13.8)4 (6.7)
1b28 (48.3)37 (61.7)
21 (1.7)1 (1.7)
2a/c1 (1.7)0
34 (6.9)5 (8.3)
3a6 (10.3)7 (11.7)
42 (3.4)1 (1.7)
4a1 (1.7)0
HCV-RNA positive*, no. (%)50 (84.7)55 (94.8)
Serum HCV-RNA, median (min; max) IU/mL5.05 (0.95; 6.61)5.09 (0.95; 6.12)
Donor age, mean (SD) years49.1 (19.0)50.6 (19.3)
Donor age <60 years, mean (SD) years41 (61.2)47 (64.7)
Donor age ≥60 years, mean (SD) years26 (38.8)24 (35.3)
Donor sex, male, no. (%)43 (64.2)32 (47.1)
Traumatic cause of donor death, no. (%)21 (33.3)20 (30.8)
Non-traumatic cause of donor death, no. (%)42 (66.7)45 (69.2)
Ischemic time, mean (SD), hours8.8 (3.3)8.0 (3.0)
Donor/recipient CMV serological status:
Donor +/recipient −, no. (%)8 (11.9)6 (8.8)
ABO identical, no. (%)66 (98.5)64 (94.1)

SD: standard deviation; HCV: hepatitis C virus; MELD: mean model for end-stage liver disease; CMV: cytomegalovirus.
*HCV-RNA above the limit of quantification at baseline.