Observational Study
Copyright ©The Author(s) 2018.
World J Hepatol. Mar 27, 2018; 10(3): 379-387
Published online Mar 27, 2018. doi: 10.4254/wjh.v10.i3.379
Table 1 Baseline general conditions of patients recruited
CharacteristicHepatic failure, n = 211
Male/female107/104
Age in year, mean and standard deviation59 ± 4.7
(median range)(36-74)
BMI, kg/m225.43 ± 4.1
Cause of liver disease, n211
Previous alcohol abuse139
Hepatic venous outflow tract obstruction14
Cryptogenic12
Liver primary tumor46
Child-Pugh class; number211
A132
B54
C25
Table 2 Baseline metabolic parameters of 211 patients recruited
Labs parameter (normal values)Average of 211 patients (range)
Hemoglobin (14-16 g/dL)11.1 (7.5-12.3)
Platelets counts (150-400 × 1000/μL)97 (65-423)
Serum protein (g/dL)7.6 (3.4-10.1)
Serum bilirubin (0.1-1.3 mg/dL)1.7 (0.9-12)
Alanine aminotransferase (8-55 IU/L)77 (24-452)
Aspartate aminotransferase (8-48 IU/L)71 (34-715)
International normalized ratio (INR)1.8 (1.0-4.9)
Serum creatinine (0.6-1.2 mg/dL)1.0 (0.6-2.1)
Serum albumin (3.7-5.0 g/dL)3.5 (1.5-5.1)
Ammonium (40-80 μg/dL)97 (45-134)
Folate (3.89-26.0 ng/mL)2.3 (1.9-12.3)
Iron free level (40-150 μg/dL)26.5 (12-89)
Ferritine (20-200 ng/mL)235 (126-456)
Vitamin B12 ( 205-870 pg/mL)189 (121-245)
Vitamin D-OH25 (30-100 ng/mL)41 (12-130)
Table 3 Synopsis of the tests at baseline
Test (range)Results
Hamilton rating scale (0-66)18.5 ± 4.5
PSQI (0-5)3.4 ± 0.5
ESS (0-24)11 ± 2.1
IRLSSGFulfillment of criteria:
211/211
IRSL (0-40)0-10 (mild) = 22
11-20 (moderate) = 76
21-30 (severe) = 109
31-40 (very severe) = 4
Table 4 Synopsis of pramipexole titration
PatientsBaseline75th day105th d135th day165th day205th day
2110.18 mg
2110.7 mg
2110.88 mg
1701.4 mg
1341.4 mg
360.88 mg
1101.4 mg
600.7 mg
Table 5 Synopsis of gabapentin titration
Patients45th day75th day105th day135th day165th day205th day
41100 mg
41300 mg
35300 mg
6400 mg
30300 mg
11500 mg
27300 mg
14600 mg
16300 mg
25600 mg
Table 6 Results for pramipexole therapy during follow-up of 170 patients
Test (range)135th day165th day205th day
Hamilton rating scale (0-66)9.2 ± 0.18.7 ± 1.39.0 ± 1.1
(-9.3 ± 3.0; < 0.01)(-9.8 ± 1.7; < 0.01)(-9.5 ± 0.2; < 0.01)
PSQI (0-5)2.2 ± 0.71.9 ± 0.72.3 ± 0.7
(-1.2 ± 0.2; < 0.05)(-1.32 ± 0.2; < 0.05)(-1.1 ± 0.2; < 0.05)
ESS (0-24)8. 3 ± 0.78. 5 ± 0.48 .7 ± 1.1
(-7.1 ± 0.4; < 0.01)(-7.3 ± 0.7; < 0.01)(-7.7 ± 0.2; < 0.01)
IRSL (0-40)0-10 (mild) = 51134110
11-20 (moderate) = 1001245
21-30 (severe) = 191415
31-40 (very severe) = 000
Table 7 Results for gabapentin therapy during follow-up of 41 patients
Test (range)135th day165th day205th day
Hamilton rating scalec(0-66)9.7 ± 0.49.7 ± 0.510.0 ± 0.7
(-9.8 ± 0.2; < 0.01)(-9.8 ± 0.3; < 0.01)(-9.9 ± 1.2; < 0.01)
PSQI (0-5)2.7 ± 0.72.9 ± 0.33.0 ± 0.5
(+ 0.7 ± 0.2; NS)(+0.5 ± 0.2; NS)(+0.6 ± 0.3; NS)
ESS (0-24)9 9 ± 0.79. 5 ± 0.412 .7 ± 1.1
(-0.7 ± 1.0; NS)(-0.5 ± 0.1; NS)(-3.3 ± 0.1; < 0.05)
IRSL (0-40)0-10 (mild) = 211817
11-20 (moderate) = 141922
21-30 (severe) = 642
31-40 (very severe) = 000
Table 8 Analysis of factors for association with the presence of augmentation
FactornUnivariate
Multivariate
OR (95%CI)P valueOR (95%CI)P value
Age1701.07 (0.7-1.2)0.241.1 (0.9-1.3)0.20
BMI1701.3 (0.9-1.5)0.451.6 (1.0-1.9)0.40
IRLS1701.5 (1.1-2.2)0.361.7 (1.2-2.2)0.57
Alcohol abuse1392.3 (0.9-4.1)< 0.0013.75 (2.7-6.2)< 0.001
Daily pramipexole1703.6 (2.1-6.8)< 0.0017.2 (4.1-15.2)< 0.001
Treatment duration, > 75 d/< 75 d1702.3 (1.3-4.2)0.0366.6 (3.1-11.2)0.01
ALT1701.3 (0.9-1.6)0.213.1 (1.7-3.9)0.54
AST1701.6 (0.8-1.7)0.502.7 (0.7-4.2)0.76
Iron-free level1702.9 (0.9-4.1)0.015.05 (1.1-12.2)0.06
Vit. B121704.25 (1.3-9.7)0.016.9 (4.7-7.6)0.01
Folate1704.1 (3.1-13.6)0.015.7 (4.2-8.2)0.01
Vit. D-OH251704.8 (3.4-12.9)0.015.67 (2.4-8.9)0.01