Retrospective Cohort Study
Copyright ©The Author(s) 2022.
World J Hepatol. Mar 27, 2022; 14(3): 570-582
Published online Mar 27, 2022. doi: 10.4254/wjh.v14.i3.570
Table 1 Diagnostic criteria for kidney dysfunction in cirrhosis (Wong et al[22], 2011)
Diagnosis
Definition
AKIRise in serum creatinine of > 50% from baseline or rise of sCr by > 26.4 mmol/L (> 0.3 mg/dL) in < 48 h; HRS type 1 is a specific form of AKI
CKDeGFR of < 60 mL/min for > 3 mo calculated using MDRD6 formula; HRS type 2 is a specific form of CKD
ACKDRise in serum creatinine of > 50% from baseline or rise of sCr by > 26.4 mmol/L (> 0.3 mg/dL) in < 48 h in a patient with cirrhosis whose eGFR is < 60 ml/min for > 3 mo calculated using MDRD6 formula
Table 2 Definition and classification of acute kidney injury for patients with liver cirrhosis according to the International Club of Ascites (Angeli et al[23], 2015)
Baseline sCr
A sCr value obtained in 3 mo prior to hospital admission, with preference to the value dated the closest to hospital admission. In patients without a previous sCr value, the value on admission should be used
AKI definitionIncrease in sCr ≥ 0.3 mg/dL (≥ 26.5 µmol/L) within 48 h; or the percentage increase in sCr ≥ 50%, which occurred in the last 7 d
Stage 1 AKIIncrease in sCr ≥ 0.3 mg/dL (26.5 µmol/L) or an increase of 1.5 to 2 times the baseline value
Stage 2 AKIIncrease of sCr 2 to 3 times the baseline value
Stage 3 AKIIncrease in sCr > 3 times the baseline or sCr ≥ 4.0 mg/dL (353.6 µmol/L), with acute increase in sCr ≥ 0.3 mg/dL (26.5 µmol/L) or onset of RRT
Table 3 Diagnostic criteria and hepatorenal syndrome subtypes (Angeli et al[23], 2015)
Diagnostic criteria for HRS
HRS subtype
1) Presence of cirrhosis or ascites; 2) sCr > 1.5 mg/dL or 133 µmoles/L; 3) No improvement in sCr (below 1.5 mg/dL) after at least 48 h of diuretic withdrawal and volume expansion with albumin; 4) Absence of shock; 5) Has not undergone recent treatment with nephrotoxic drugs; 6) Absence of parenchymal kidney disease as indicated by proteinuria less than 500 mg/d, microhematuria (less than 50 erythrocytes/high-magnification field), and/or abnormal renal ultrasound findingsHRS type 1-Rapidly progressive renal failure defined as the doubling of initial serum creatinine to a level greater than 2.5 mg/dL or 220 µmoles/L in less than 3 wk, and associated with a very poor prognosis; HRS type 2-Moderate renal failure (sCr > 1.5 mg/dL or 133 µmoles/L), following a stable or slowly progressive course, often associated with refractory ascites
Table 4 Acute kidney injury stages according to International Club of Ascites criteria (n = 145)
Overall incidence (n = 88)
Stage 1 (n = 22)
Stage 2 (n = 36)
Stage 3/RRT (n = 30/12)
60.6%15.1%24.8%20.6/8.7%
Table 5 Patients’ preoperative baseline information according to the occurrence of acute kidney injury after deceased-donor liver transplantation (n = 145)

No AKI (n = 57)
AKI (n = 88)
P value
Male gender, n (%)29 (50.8)49 (55.6)0.441
Age (yr), mean (± SD)53.2 (± 13.56)56.2 (± 13.26)0.352
BMI, mean (± SD)18.2(± 4.54)22.7 (± 4.92)0.065
Biological MELD score, mean (± SD)21.67 (± 2.15)26.05 (± 3.05)< 0.001
Previous ascites, n (%)24 (42.1)52 (59.0)0.013
Previous encephalopathy, n (%)18 (31.5)39 (44.3)0.025
Previous upper digestive bleeding, n (%)21 (36.8)45 (51.1)0.018
Preexisting KD, n (%)15 (26.3)60 (68.1)< 0.001
HCC, n (%)20 (35.0)37 (42.0)0.069
Systemic arterial hypertension, n (%)28 (49.1)46 (52.2)0.083
Diabetes mellitus, n (%)23 (40.3)43 (48.8)0.254
Table 6 Donor and graft characteristics according to the occurrence of acute kidney injury after deceased-donor liver transplantation (n = 145)

No AKI (n = 57)
AKI (n = 88)
P value
Donor > 60 yr, n (%)16 (28.0)31 (35.2)0.346
Donor BMI > 27-30 kg/m2, n (%)14(24.5)28 (31.8)0.039
Graft macrosteatosis > 30%, n (%)11 (19.2)32 (36.3)0.024
GCIT > 8 h, n (%)00-
GWIT > 40-45 min38 (66.6)54 (61.3)0.349
Donor ICU stay > 4 d, n (%)11 (19.2)22 (25.0)0.088
Donor controlled sepsis, n (%)05 (8.7)11 (12.5)0.061
History of alcoholism of donor, n (%)08 (14.0)15 (17.0)0.255
Donor sCr > 1.2 mg/dL, n (%) 16 (28.0)31 (35.2)0.024
Donor hypotensive episodes (< 60 mmHg) > 1 h, n (%)10 (17.5)18 (20.4)0.127
Donor serum bilirubin > 2.0 mg/dL, n (%)25 (43.8)48 (54.5)0.087
Donor serum ALT > 170 U/L, n (%)11 (19.2)22 (25.0)0.073
Donor serum AST > 140 U/L, n (%)05 (8.7)13 (14.7)0.023
Use of dopamine doses > 10 microg/kg per min, n (%)10 (17.5)13 (14.7)0.176
Donor peak serum sodium > 155 mEq/L, n (%)02 (3.5)5 (5.6)0.219
ECD (3 or more factors above), n (%)07 (12.2)31 (35.2)< 0.001
Table 7 Intraoperative events in 145 deceased-donor liver transplantations according to the occurrence of postoperative acute kidney injury

Without AKI (n = 57)
With AKI (n = 88)
P value
IOAH (bleeding/PRS), n (%)14 (24.5)54 (61.3)< 0.001
MBT, n (%)5 (8.7)15 (17.0)< 0.001
Vasoactive drugs, n (%)38(66.6)48 (54.5)0.197
Cryoprecipitate transfusion, n (%)10 (17.5)18 (20.4)0.169
Piggy-back clamping, n (%)30 (52.6)48 (54.5)0.072
SL (mmol/L) at the end of LT, mean (± SD)1.4 (± 0.3)2.8 (± 0.7)< 0.001
Lower serum fibrinogen (mg/dL), mean (± SD)242 (± 34)214 (± 24)0.090
Table 8 Logistic regression analysis of risk factors for acute kidney injury after deceased-donor liver transplantation (n = 145)
Logistic regression
Beta coeficient
OR
95%CI
P value
Biological MELD score ≥ 250.1941.9991.5862.503< 0.001
Pre-existing KD, n (%)0.1151.2790.9161.686< 0.001
ECD (3 or more factors above)0.9111.1910.7111.7870.002
IOAH (bleeding/PRS), n (%)0.1691.9351.5052.344< 0.001
MBT, n (%)0.1251.8301.4282.241< 0.001
SL (mmol/L) ≥ 2.0 at the end of LT0.1102.0011.6162.421< 0.001