Literature DB >> 28574999

Predictors of renal function recovery among patients undergoing renal replacement therapy following orthotopic liver transplantation.

Maria Claudia Cruz Andreoli1, Nádia Karina Guimarães de Souza1, Adriano Luiz Ammirati1, Thais Nemoto Matsui1, Fabiana Dias Carneiro1, Ana Claudia Mallet de Souza Ramos1, Ilson Jorge Iizuca1, Maria Paula Vilela Coelho2, Rogério Carballo Afonso2, Ben-Hur Ferraz-Neto2, Marcio Dias de Almeida2, Marcelino Durão1, Marcelo Costa Batista1, Julio Cesar Monte1, Virgílio Gonçalves Pereira1, Oscar Pavão Dos Santos1, Bento Cardoso Dos Santos1.   

Abstract

Renal dysfunction frequently occurs during the periods preceding and following orthotopic liver transplantation (OLT), and in many cases, renal replacement therapy (RRT) is required. Information regarding the duration of RRT and the rate of kidney function recovery after OLT is crucial for transplant program management. We evaluated a sample of 155 stable patients undergoing post-intensive care hemodialysis (HD) from a patient population of 908 adults who underwent OLT. We investigated the average time to renal function recovery (duration of RRT required) and determined the risk factors for remaining on dialysis > 90 days after OLT. Log-rank tests were used for univariate analysis, and Cox proportional hazards models were used to identify factors associated with the risk of remaining on HD. The results of our analysis showed that of the 155 patients, 28% had pre-OLT diabetes mellitus, 21% had pre-OLT hypertension, and 40% had viral hepatitis. Among the patients, the median MELD (Model for End-Stage Liver Disease) score was 27 (interquartile range [IQR] 22-35). When they were listed for liver transplantation, 32% of the patients had serum creatinine (Scr) levels > 1.5 mg/dL or were on HD, and 50% had serum creatinine (Scr) levels > 1.5 mg/dL or were on HD at the time of OLT. Of the transplanted patients, 25% underwent pre-OLT intermittent HD, and 14% and 41% underwent continuous renal replacement therapy (CRRT) pre-OLT and post-OLT, respectively. At 90 days post-OLT, 118 (76%) patients had been taken off dialysis, and 16 (10%) patients had died while undergoing HD. The median recovery time of these post-OLT patients was 33 (IQR 27-39) days. In the multivariate analysis, fulminant hepatic failure as the cause of liver disease (p<0.001), the absence of pre-OLT hypertension (p = 0.016), a lower intraoperative fresh-frozen plasma (FFP) transfusion volume (p = 0.019) and not undergoing pre-OLT intermittent HD (p = 0.032) were associated with performing RRT for less than 90 days. Therefore, a high proportion of OLT patients showed improved renal function after OLT, and those who were diagnosed with fulminant hepatic failure, had no pre-OLT hypertension, received a lower transfused volume of intraoperative FFP and did not undergo pre-OLT intermittent HD had a higher probability of recovery.

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Year:  2017        PMID: 28574999      PMCID: PMC5456041          DOI: 10.1371/journal.pone.0178229

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


Introduction

In the MELD (Model for End-Stage Liver Disease) score era of organ allocation, which considers serum levels of creatinine and bilirubin and the international normalized ratio of the prothrombin time, patients are prioritized based on measures of preoperative renal dysfunction. Between 5% and 35% of liver transplant patients require perioperative dialysis for renal replacement therapy (RRT) [1]. Information regarding a patient’s RRT duration requirements and probability of kidney function recovery is crucial for transplant program management. Patients with liver disease and advanced irreversible renal disease are typically considered for a combined liver and kidney transplant [2, 3]. In contrast, patients with acute kidney injury (AKI) can have improved renal function after orthotopic liver transplantation (OLT) and thus are considered for isolated liver transplantation. AKI patients may remain on RRT post-transplant for various periods of time, and some may never spontaneously recover renal function. These patients will then need a kidney transplant [4]. Isolated liver transplant recipients who remain on RRT during the post-transplant period have lower survival rates than those who undergo subsequent kidney transplantation [5, 6]. However, given the shortage of available organs, it is essential to determine the optimal length of time a physician should wait before deciding that a patient undergoing post-OLT RRT has an irreversible AKI and thus needs kidney transplantation. This approach may avoid unnecessary transplantation in a patient whose native kidney function could eventually improve. We investigated a group of 155 stable patients undergoing post-intensive care dialysis following OLT to evaluate the average time to renal function recovery (duration of RRT) and factors associated with remaining on dialysis > 90 days after OLT in an urban tertiary medical center in São Paulo, Brazil. We consider renal function recovery the suspension of dialysis, and the average time to renal function recovery (duration of RRT) refers to the interval between the date of OLT and the date of the last hemodialysis session performed.

Materials and methods

Study population

In this retrospective study, we evaluated a sample of 155 stable patients undergoing post-intensive care dialysis from a patient population of 908 adults who underwent OLT between June 1, 2005, and December 31, 2011, at Albert Einstein Jewish Hospital, São Paulo, Brazil, an urban tertiary medical center. All the patients required RRT [intermittent hemodialysis (HD)] for presumed AKI during the postoperative period. Combined liver-kidney transplant recipients were excluded from the study due to the possibility of concurrent chronic kidney disease. For each patient, the following data were collected: age; gender; pre-transplant diabetes mellitus and hypertension status; etiology of liver disease (viral hepatitis, alcoholic cirrhosis, fulminant hepatic failure or other); MELD score; history of hepatocellular carcinoma; pre-OLT continuous renal replacement therapy (CRRT) and pre-OLT intermittent HD; history and volume of intraoperative packed red blood cells, fresh-frozen plasma (FFP), and cryoprecipitate and platelet transfusion; length of intensive care unit (ICU) stay during transplant hospitalization; and duration of pre-OLT RRT. CRRT was performed as continuous venovenous hemodiafiltration (CVVHDF) with the Prismaflex® system (Gambro, Lakewood, CO, USA) in hemodynamically unstable patients in the ICU. The need for early liver retransplantation (re-OLT) or post-OLT CRRT was noted. Additionally, the presence of serum creatinine (Scr) levels > 1.5 mg/dL or the need for RRT at the time of listing for liver transplantation or at the time of transplant was determined. The etiology of renal dysfunction was not assessed in our study due to its frequent inaccuracy. Tacrolimus levels were routinely monitored and were kept within the therapeutic range. We evaluated the average time to renal function recovery in OLT patients undergoing post-intensive care hemodialysis (HD) and determined the risk factors for remaining on dialysis > 90 days after OLT. Renal function recovery was defined as no longer needing RRT. Patients were censored at the time of recovery of kidney function, death on HD, or at the end of follow-up.

Statistical analysis

Unadjusted post-transplant survival was estimated using Kaplan-Meier curves and compared using log-rank tests. Multivariate Cox proportional hazards models were used to evaluate factors associated with renal function recovery, and the results are presented as hazard ratios (HRs) and 95% confidence intervals (CIs) for those remaining on HD after 90 days. The data were analyzed using SPSS (Statistical Package for the Social Science) 17.0 for Windows. Statistical significance was set at p < 0.05. Continuous and categorical variables were expressed as medians [quartile 1 (Q1) to quartile 3 (Q3)] and as counts and percentages, respectively. Approval was obtained from the local ethics committee, and formal informed consent was waived due to the observational nature of the study (Ethics Committee: Hospital Israelita Albert Einstein - Sao Paulo – Brazil; Approval Number: 37516814.3.0000.0071). The clinical and research activities reported here are consistent with the Principles of the Declaration of Istanbul as outlined in the “Declaration of Istanbul on Organ Trafficking and Transplant Tourism”.

Results

Baseline characteristics

A total of 155 adult recipients [male: female 99:56; median age 53.1 (45.0 – 60.3) years] were included in our study. Of the patients, 43 (27.7%) had pre-transplant diabetes mellitus, and 32 (20.6%) had pre-transplant hypertension; viral hepatitis was the cause of liver disease for 62 (40.0%). The median MELD score was 27 (22-35). Overall, 47 (31.5%) patients had Scr levels > 1.5 mg/dL or were on HD at the time of listing, and 78 (50.4%) patients had Scr levels > 1.5 mg/dL or were on HD at the time of OLT. Twenty-six patients (16.8%) needed early re-OLT: 20 (77%) for primary nonfunction, 5 (19%) for hepatic artery thrombosis and 1 (4%) for hyperacute rejection. Twenty-eight patients (18.1%) had a history of hepatocellular carcinoma. Of the patients, 21 (13.5%) underwent pre-OLT CRRT, 38 (24.5%) underwent pre-OLT intermittent HD and 63 (40.6%) underwent post-OLT CRRT (undergoing CRRT and intermittent HD were not mutually exclusive). The median intraoperative transfusion volumes were 2 (0-3) U packed red blood cells and 0 (0-5) U FFP; 22 (14.2%) and 47 (30.3%) of the patients received intraoperative cryoprecipitate and platelet transfusions, respectively. The median length of ICU stay during transplant hospitalization was 7 (4-14) days. One hundred nine (70.3%) patients did not undergo pre-OLT RRT, and 37 (23.9%) underwent ≤ 14 days and 9 (5.8%) underwent > 14 days of pre-OLT RRT (Table 1). The median length of pre-OLT RRT was 5 (2-11) days. Table 1 also shows the baseline characteristics of the stable patients undergoing post-OLT RRT by renal function recovery status.
Table 1

Baseline characteristics of stable patients undergoing RRT post-OLT according to renal recovery status (N = 155).

Population characteristicsRenal function recovery ≤ 90 daysTotal
No (N = 37)Yes (N = 118)
Age (years)55.1 (48.8 – 61.2)52.8 (42.5 – 59.4)53.1 (45.0 – 60.3)
Gender
    Male20 (20.2%)79 (79.8%)99 (63.9%)
    Female17 (30.4%)39 (69.6%)56 (36.1%)
Pre-OLT diabetes mellitus
    No25 (22.3%)87 (77.7%)43 (27.7%)
    Yes12 (27.9%)31 (72,1%)112 (72.3%)
Pre-OLT hypertension
    No26 (21,1%)97 (78.9%)123 (79.4%)
    Yes11 (34.4%)21 (65.6%)32 (20.6%)
Etiology of liver disease
    Viral hepatitis17 (27.4%)45 (72.6%)62 (40.0%)
    Alcoholic cirrhosis2 (11.1%)16 (88.9%)18 (11.6%)
    Fulminant hepatic failure1 (5.9%)16 (94.1%)17 (11.0%)
    Other17 (29.3%)41 (70.7%)58 (37.4%)
MELD26 (24 – 36)28 (20 – 35)27 (22-35)
Scr level > 1.5 mg/dL or undergoing RRT at the time of listing*
    Scr level ≤ 1.5 mg/dL26 (25.5%)76 (74.5%)102 (68.5%)
    Scr level > 1.5 mg/dL9 (22.5%)31 (77.5%)40 (26.8%)
    RRT2 (28.6%)5 (71.4%)7 (4.7%)
Scr level > 1.5 mg/dL or undergoing RRT at the time of transplant
    level ≤ 1.5 mg/dL14 (18.2%)63 (81.8%)77 (49.7%)
    Scr level > 1.5 mg/dL6 (20%)24 (80.0%)30 (19.4%)
    RRT17 (35.4%)31 (64.6%)48 (31.0%)
Early re-OLT
    No34 (26.4%)95 (73.6%)129 (83.2%)
    Yes3 (11.5%)23 (88.5%)26 (16.8%)
Hepatocellular carcinoma
    No30 (23.6%)97 (76.4%)127 (81.9%)
    Yes7 (25.0%)21 (75.0%)28 (18.1%)
Pre-OLT CRRT
    No31 (23.1%)103 (76.9%)134 (86.5%)
    Yes6 (28.6%)15 (71.4%)21 (13.5%)
Pre-OLT intermittent HD
    No23 (19.7%)94 (80.3%)117 (75.5%)
    Yes14 (36.8%)24 (63.2%)38 (24.5%)
Post-OLT CRRT
    No17 (18.5%)75 (81.5%)92 (59.4%)
    Yes20 (31.7%)43 (68.3%)63 (40.6%)
Intraoperative packed red blood cells (U)3 (1 – 4)2 (0 – 3)2 (0 – 3)
Intraoperative fresh-frozen plasma (U)4 (0 – 8)0 (0 – 4)0 (0 – 5)
Intraoperative cryoprecipitate transfusion
    No32 (24.1%)101 (75.9%)133 (85.8%)
    Yes5 (22.7%)17 (77.3%)22 (14.2%)
Intraoperative platelet transfusion
    No21 (19.4%)87 (80.6%)108 (69.7%)
    Yes16 (34.0%)31 (66.0%)47 (30.3%)
Length of ICU stay11 (6 – 25)6.5 (4 – 12)7 (4 – 14)
Pre-OLT days of RRT
    No20 (18.3%)89 (81.7%)109 (70.3%)
    ≤ 14 days12 (32.4%)25 (67.6%)37 (23.9%)
    > 14 days5 (55.6%)4 (44.4%)9 (5.8%)

Data are displayed as median (interquartile range - IQR) or as count (percentage). RRT, renal replacement therapy; OLT, Orthotopic liver transplantation; MELD, Model for End-Stage Liver Disease; Scr, serum creatinine; CRRT, continuous renal replacement therapy; HD, hemodialysis; ICU, intensive care unit.

*N = 149

Data are displayed as median (interquartile range - IQR) or as count (percentage). RRT, renal replacement therapy; OLT, Orthotopic liver transplantation; MELD, Model for End-Stage Liver Disease; Scr, serum creatinine; CRRT, continuous renal replacement therapy; HD, hemodialysis; ICU, intensive care unit. *N = 149 At 90 days post-OLT, 118 (76%) patients had been removed from dialysis, and 16 (10%) patients had died while undergoing HD (Fig 1). At the one-year follow-up, a total of 129 (83%) patients had been removed from dialysis, 19 (12%) patients had died while undergoing HD, 2 (1%) patients had subsequently received a kidney transplant, and only 5 (3%) patients were currently undergoing HD. The median recovery time of the post-OLT patients was 33 (27–39) days. For the patients whose renal function recovered, 225 days was the longest duration of HD.
Fig 1

Time to renal function recovery.

Risk factors for renal function recovery

Univariate Cox regression analyses revealed that age; etiology of liver disease; pre-OLT hypertension status; Scr level > 1.5 mg/dL or undergoing RRT at the time of transplant; transfusion of intraoperative packed red blood cells, FFP and intraoperative platelets; undergoing pre-OLT intermittent HD and post-OLT CRRT; and the duration of pre-OLT RRT were important predictors of renal function recovery (Table 2). These variables were included in a multivariate model.
Table 2

Univariate Cox regression analysis of renal function recovery.

 Median time until renal function recovery95% confidence intervalLog-rank p
LowerUpper
General33.026.639.4
GenderFemale32.026.337.70.632
Male34.022.945.1
Age (years)≤ 53.128.021.834.20.106
> 53.143.027.258.8
Etiology of liver diseaseAlcoholic cirrhosis32.027.936.10.008
Fulminant hepatic failure23.019.226.8
Other41.026.056.0
Viral hepatitis34.024.243.8
Pre-OLT diabetes mellitusNo31.025.336.70.354
Yes41.022.859.2
Pre-OLT hypertensionNo32.027.336.70.035
Yes42.011.572.5
Scr level > 1.5 mg/dL or in RRT at the time of listingScr ≤ 1.5 mg/dL32.026.137.90.881
Scr > 1.5 mg/dL38.023.952.1
RRT44.024.463.6
MELD≤ 2732.024.040.00.712
> 2733.022.044.0
Scr level > 1.5 mg/dL or undergoing RRT at the time of transplantScr ≤ 1.5 mg/dL29.023.334.70.049
Scr > 1.5 mg/dL29.03.454.6
RRT43.019.266.8
Early re-OLT No32.021.542.50.183
Yes33.029.936.1
Intraoperative packed red blood cellsNo23.018.127.90.006
Yes41.030.551.5
Intraoperative fresh-frozen plasmaNo29.023.734.30.005
Yes40.025.654.4
Intraoperative cryoprecipitate transfusionNo32.025.738.30.659
Yes34.014.553.5
Intraoperative platelet transfusionNo29.022.635.40.045
Yes38.024.052.0
Length of ICU stay≤ 7 days29.023.734.30.276
> 7 days37.030.343.7
Hepatocellular carcinomaNo33.025.340.70.734
Yes33.023.642.4
Pre-OLT CRRTNo32.026.737.30.384
Yes41.032.649.4
Pre-OLT intermittent HDNo31.025.636.40.032
Yes44.016.871.2
Post-OLT CRRTNo29.024.933.10.096
Yes41.028.153.9
Pre-OLT days of RRTNo31.026.235.80.066
≤ 14 days40.034.445.6
> 14 days *------

RRT, renal replacement therapy; OLT, orthotopic liver transplantation; MELD, Model for End-Stage Liver Disease; Scr, serum creatinine; CRRT, continuous renal replacement therapy; HD, hemodialysis; ICU, intensive care unit.

* Nine patients had > 14 days of pre-OLT RRT; of these, 4 recovered renal function, i.e., 55.5% were censored, which makes it impossible to estimate the median time to renal function recovery in this group.

RRT, renal replacement therapy; OLT, orthotopic liver transplantation; MELD, Model for End-Stage Liver Disease; Scr, serum creatinine; CRRT, continuous renal replacement therapy; HD, hemodialysis; ICU, intensive care unit. * Nine patients had > 14 days of pre-OLT RRT; of these, 4 recovered renal function, i.e., 55.5% were censored, which makes it impossible to estimate the median time to renal function recovery in this group. In the multivariate analysis, fulminant hepatic failure as the cause of liver disease (HR = 3.39, 95% CI = 1.81 to 6.35, p < 0.001); the absence of pre-OLT hypertension (HR = 1.82, 95% CI = 1.12 to 2.96, p = 0.016); lower intraoperative FFP transfusion volume (HR = 0.94, 95% CI = 0.89 to 0.99, p = 0.019) and not undergoing pre-OLT intermittent HD (HR = 1.68, 95% CI = 1.05 to 2.7, p = 0.032) were associated with performing RRT for less than 90 days. Not undergoing post-OLT CRRT was also a marginally significant predictor of removal from dialysis (HR = 1.43, 95% CI = 0.95 to 2.14, p = 0.088; Table 3).
Table 3

Multivariate Cox regression analysis of renal function recovery.

HR95% confidence intervalP
LowerUpper
Etiology of liver diseaseAlcoholic cirrhosis1.530.842.780.168
Fulminant hepatic failure3.391.816.35<0.001
Other1.070.691.670.761
Viral hepatitis (reference)------
Pre-OLT hypertensionYes (reference)------
No1.821.122.960.016
Intraoperative cryoprecipitate transfusion0.940.890.990.019
Pre-OLT intermittent HDYes (reference)------
No1.681.052.700.032
Post-OLT CRRTYes (reference)------
No1.430.952.140.088

OLT, orthotopic liver transplantation; HD, hemodialysis; CRRT, continuous renal replacement therapy.

OLT, orthotopic liver transplantation; HD, hemodialysis; CRRT, continuous renal replacement therapy.

Discussion

Renal failure in cirrhotic patients is a challenging complication with a significant impact on mortality both before and after OLT [6, 7]. As the Scr level is a component of the MELD score, the number of patients with renal dysfunction who undergo OLT and the proportion of OLTs performed in combination with kidney transplants have increased [8, 9]. Patients with normal or mild impairment of renal function pre-OLT whose status deteriorates during the perioperative period may need RRT. A key point of this scenario is that it is important to determine the nature of renal dysfunction and anticipate whether kidney function could recover after post-OLT liver function recovery. In the present study, we evaluated 155 stable post-OLT patients who did not have chronic irreversible renal disease diagnosed preoperatively and required RRT (HD) post-intensive care hospitalization. Our objective was to describe the average time to renal recovery and identity the factors associated with remaining on RRT > 90 days after OLT among patients undergoing RRT. We observed that at 90 days post-OLT, 21 patients (14%) were undergoing RRT, and after 1 year, only 5 (3%) remained on dialysis. The proportion of patients in our study who recovered renal function was higher than that observed in a previous, larger study [4]. We did not aim to investigate the incidence of post-OLT RRT in our center, as we did not evaluate patients who required RRT in the intensive care unit environment post-OLT. Many of those critical patients underwent continuous dialysis modalities and might have had an increased risk of mortality. Our focus was on patients who were stable on dialysis and no longer needed intensive care but had an undetermined renal function prognosis. Age; etiology of liver disease; pre-OLT hypertension status; Scr level > 1.5 mg/dL or undergoing RRT at the time of transplant; transfusion of intraoperative packed red blood cells, FFP and intraoperative platelets; undergoing pre-OLT intermittent HD and post-OLT CRRT; and the duration of pre-OLT RRT were significant predictors of the need for RRT > 90 days after OLT in the univariate analysis. However, in the multivariate analysis, fulminant hepatic failure; the absence of pre-OLT hypertension; lower intraoperative FFP transfusion volume; and not undergoing pre-OLT intermittent HD were associated with performing RRT for less than 90 days. A previous study found that the duration of renal dysfunction pre-OLT (defined as Scr level ≥ 1.5 mg/dL) was correlated with creatinine elevation 6 and 12 months following liver transplantation [10]. Similar results have been found among patients with kidney dysfunction for more than 12 weeks prior to OLT (pretransplant Scr level ≥ 2 mg/dL); in a previous study, these patients had increased risk of poor post-transplant renal outcomes (estimated glomerular filtration rate ≥ 20 mL/minute within 3 years post-transplant) [11]. Our data are in accordance with a study that evaluated 1041 liver transplant recipients who were on RRT at the time of OLT. In this study, 707 recipients (67.9%) had spontaneous recovery of renal function after liver transplantation, and those who recovered spontaneously had a significantly shorter course of RRT during the pre-transplant period (15.6 versus 36.6 days, p < 0.001) [4]. Similarly, Sharma et al. found that among surviving recipients who underwent acute RRT before OLT without subsequent kidney transplant, the majority recovered renal function within 6 months, and longer pre-OLT RRT duration was significantly associated with increased risk of renal nonrecovery (HR = 1.04 per day, 95% CI = 1.02 to 1.05, p < 0.001) [12]. Fulminant hepatic failure is defined as the rapid development of acute liver injury with severe impairment of synthetic function and hepatic encephalopathy in a patient without obvious previous liver disease [13]. AKI is common in patients with fulminant hepatic failure. Based on a retrospective analysis of data from 1604 patients with acute liver failure, Tujius et al. found that 70% developed AKI, 30% received RRT, and, in accordance with previous reports, outcomes were negatively affected by AKI [14, 15]. The need for RRT has also been identified as an independent prognostic factor of poor outcomes after OLT for fulminant hepatic failure [16]. Conversely, Leithead et al. did not find an association between perioperative AKI or RRT and chronic kidney disease in patients who received transplants due to acute liver failure [17]. They proposed that the failure of perioperative renal dysfunction to impact long-term posttransplant renal outcomes in patients with acute liver failure could reflect the duration of renal impairment as the duration of renal dysfunction appears to be a key determinant of chronic renal impairment in patients who receive transplants due to chronic liver disease [10, 17]. Nevertheless, it was observed that patients with fulminant hepatic failure and AKI rarely developed chronic kidney disease, which corroborates our finding that fulminant hepatic failure is a predictor of the need for RRT < 90 days after OLT [14]. Intraoperative blood transfusion is known to affect postoperative renal outcomes in OLT patients [18-20]. A biologically plausible explanation for this association is that kidney hypoperfusion secondary to intraoperative bleeding represents an additional renal insult in patients with pre-OLT AKI. In fact, Sirivatanauksorn et al. retrospectively observed that prolonged intraoperative hypotension and postoperative hypotension were independent risk factors for AKI after OLT [21]. Therefore, bleeding secondary to intraoperative coagulopathy could have contributed to our finding that the need for FFP transfusion was negatively associated with post-OLT recovery of renal function. According to our data, pre-OLT hypertension was also associated with a higher probability of remaining on dialysis > 90 days post-OLT. Rueggeberg et al. observed that pretransplant hypertension was a risk factor for AKI after OLT [18]. Although we did not perform pre-OLT kidney biopsies to provide histological evidence of the degree of associated hypertensive nephrosclerosis in this subgroup of patients, it was not surprising that a classic risk factor for chronic kidney disease in the general population could also impact patients with subsequent AKI, as a similar association was previously observed in diabetic patients who underwent OLT [11, 12]. A previous study found that among patients who developed end-stage renal disease after OLT, only 27% who underwent HD were alive 6 years after the onset of renal failure; this finding is substantially lower than the 71.4% survival rate among those who subsequently received a kidney transplant [22]. Likewise, a Canadian registry study found significantly decreased survival in post-OLT patients who underwent RRT compared with matched nontransplant chronic dialysis control patients, with 5-year patient survival rates of 17% and 43% for the post-OLT patients and controls, respectively (p = 0.01) [23]. Thus, given the increasing frequency of renal transplant referrals for recipients of nonrenal solid-organ transplants [24], two decisions must be made: the appropriate time to list OLT patients undergoing RRT for a subsequent kidney transplant and whether they should be prioritized for kidney transplantation. There is concern that recipients of OLT alone who undergo RRT may prematurely be considered part of the group of patients with end-stage renal disease who need subsequent kidney transplantation. This approach could compromise the pool of renal organs for those with end-stage renal disease alone. Percutaneous renal biopsy may be helpful for determining the therapeutic strategy in patients with liver function improvement and lower risk of bleeding. According to the RIFLE (Risk, Injury, Failure, Loss, and End-stage kidney disease) definition of AKI, end-stage renal disease is the complete loss of kidney function (i.e., need for RRT) for more than 3 months [25]. Based on this criterion, the renal transplant community is authorized to list postoperative OLT patients for kidney transplantation after 3 months of RRT. In fact, according to a previous report, within a year of transplant, a small percentage of OLT patients had already undergone subsequent kidney transplantation [26]. However, how long after liver transplantation should kidney transplantation be performed? Hepatorenal syndrome, which is thought to be reversible with OLT alone, may contribute to the requirement for long-term RRT post-transplant. A previous study indicated that among 2112 adult deceased-donor OLT recipients who received acute RRT for ≤ 90 days pre-OLT, a nonrecovery rate of only 8.9% was observed among those who survived 6 months following OLT [12]. In contrast, in a series of 130 patients with hepatorenal syndrome who underwent OLT, 7 (6%) were found to have developed irreversible kidney failure post-transplant, and 5 died within 1 year [27]. Based on these unfavorable results, the authors recommend a minimum 60-day waiting period prior to considering subsequent kidney transplantation, regardless of donor type [27]. Nevertheless, our data suggest a longer period may be appropriate before adding a patient to the kidney transplant list to assure opportune kidney allocation, and a minimum 3-month waiting period is suggested; this approach may be particularly appropriate for patients who have had a diagnosis of fulminant hepatic failure, had no pre-OLT hypertension, received a lower transfused volume of intraoperative FFP and did not undergo pre-OLT intermittent HD. Our data provide practical information for transplant doctors that allows them to stratify patients in terms of the factors predicting whether they will no longer need RRT.
  27 in total

1.  Development of a risk stratification model for predicting acute renal failure in orthotopic liver transplantation recipients.

Authors:  A Rueggeberg; S Boehm; F Napieralski; A R Mueller; P Neuhaus; K J Falke; H Gerlach
Journal:  Anaesthesia       Date:  2008-09-17       Impact factor: 6.955

Review 2.  Renal failure in cirrhosis.

Authors:  Pere Ginès; Robert W Schrier
Journal:  N Engl J Med       Date:  2009-09-24       Impact factor: 91.245

3.  Renal dysfunction after orthotopic liver transplantation.

Authors:  Y Sirivatanauksorn; T Parakonthun; N Premasathian; S Limsrichamrern; P Mahawithitwong; P Kositamongkol; C Tovikkai; S Asavakarn
Journal:  Transplant Proc       Date:  2014-04       Impact factor: 1.066

4.  Postliver transplant acute renal injury and failure by the RIFLE criteria in patients with normal pretransplant serum creatinine concentrations: a matched study.

Authors:  Jie Chen; Terry Singhapricha; Ke-Qin Hu; Johnny C Hong; Randolph H Steadman; Ronald W Busuttil; Victor W Xia
Journal:  Transplantation       Date:  2011-02-15       Impact factor: 4.939

Review 5.  Acute kidney injury after liver, heart, and lung transplants: dialysis modality, predictors of renal function recovery, and impact on survival.

Authors:  Phuong-Thu T Pham; Carmen Slavov; Phuong-Chi T Pham
Journal:  Adv Chronic Kidney Dis       Date:  2009-07       Impact factor: 3.620

Review 6.  Renal Function and Transplantation in Liver Disease.

Authors:  Sandesh Parajuli; David Foley; Arjang Djamali; Didier Mandelbrot
Journal:  Transplantation       Date:  2015-09       Impact factor: 4.939

7.  Transplantation: impact of pretransplant renal insufficiency.

Authors:  Ranjeeta Bahirwani; Mical S Campbell; Tim Siropaides; James Markmann; Kim Olthoff; Abraham Shaked; Roy D Bloom; K Rajender Reddy
Journal:  Liver Transpl       Date:  2008-05       Impact factor: 5.799

Review 8.  Renal disease in recipients of nonrenal solid organ transplantation.

Authors:  Akinlolu O Ojo
Journal:  Semin Nephrol       Date:  2007-07       Impact factor: 5.299

9.  Simultaneous liver-kidney transplantation: evaluation to decision making.

Authors:  C L Davis; S Feng; R Sung; F Wong; N P Goodrich; L B Melton; K R Reddy; M K Guidinger; A Wilkinson; J Lake
Journal:  Am J Transplant       Date:  2007-05-26       Impact factor: 8.086

10.  Increasing referral for renal transplant evaluation in recipients of nonrenal solid-organ transplants: a single-center experience.

Authors:  Arun Chandrakantan; Angelo M de Mattos; David Naftel; Apryl Crosswy; James Kirklin; John J Curtis
Journal:  Clin J Am Soc Nephrol       Date:  2006-03-29       Impact factor: 8.237

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  1 in total

1.  Continuous Renal Replacement Therapy after Liver Transplantation: Peri-Operative Associated Factors and Impact on Survival.

Authors:  Gennaro Martucci; Matteo Rossetti; Sergio Li Petri; Rossella Alduino; Riccardo Volpes; Giovanna Panarello; Salvatore Gruttadauria; Gaetano Burgio; Antonio Arcadipane
Journal:  J Clin Med       Date:  2022-06-30       Impact factor: 4.964

  1 in total

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