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Vol. 22.
(May - June 2021)
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Vol. 22.
(May - June 2021)
Original article
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Renal and brain failure predict mortality of patients with acute-on-chronic liver failure admitted to the intensive care unit
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Osvely Méndez-Guerreroa, Daniel A. Calle-Rodasa, Eduardo Cervantes-Alvareza,c, Elisa Alatorre-Arenasa, Juanita Pérez-Escobara, Nalu Navarro-Alvareza,b,d,
,1
, Aldo Torrea,
,1
a Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Department of Gastroenterology, Mexico City, Mexico
b Universidad Panamericana School of Medicine, Campus México, Mexico City, Mexico
c PECEM, Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico City, Mexico
d Department of Surgery, University of Colorado Anschutz Medical Campus, Denver, CO, United States
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Table 1. Population baseline characteristics based on ACLF grading (n = 148).
Table 2. General characteristics based on outcome.
Table 3. Clinical predictors of 28 and 90 day mortality. Bivariate and multivariate Cox regression analysis.
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Abstract
Introduction and Objectives

Acute on Chronic Liver Failure (ACLF) is characterized by organ failure and high 28-day mortality. Identifying clinical predictors associated with early mortality could have implications for the treatment of patients with ACLF.

Patients and methods

Patients diagnosed with chronic liver failure that developed ACLF based on the EASL-CLIF Consortium definition admitted to the Intensive care unit of a tertiary hospital between 2012–2018 were included. Bivariate and multivariate Cox regression analyses were performed to identify factors associated with mortality.

Results

148 patients (55% female) were diagnosed with ACLF of which 55% (n = 82) had ACLF grade 3, 28% (n = 41) grade 2 and 17% (n = 25) grade 1. The median age was 54 years (41-63). Hepatitis C virus (HCV) was the most frequent etiology in 29.8% (n = 44) of the patients with bacterial infection being the most predominant precipitant factor in 58.1% (n = 86). Ninety-day global cumulative survival was only 18%. When divided by grade, mortality reached to 10% in ACLF 3. Moreover, in the multivariate Cox regression analysis, renal failure (HR 3.26, 95% CI (2.13–4.99), brain failure (HR 1.37, 95% CI 1.09–2.04) and male sex (HR 1.62, 95% CI 1.10–2.40) were independent predictors of 28- and 90-day mortality.

Conclusions

ACLF is a frequent syndrome among chronic liver disease patients. Brain and renal failure are significantly associated with higher mortality and are independent predictors of 28 and 90-day mortality.

Keywords:
ACLF
Mortality predictors
Brain failure
Renal failure
Mexico
Full Text
1Introduction

Acute on chronic liver failure (ACLF) is a clinical syndrome manifesting as an acute insult on an already compromised liver with a chronic disease that is associated with organ failure and high short-term mortality [1].

Multiple organ dysfunction is a common cause of morbidity and mortality in intensive care units (ICUs) [2] and in patients with ACLF [3]. It is known that bacterial infections which are the most common precipitant in ACLF patients, are associated with a bad prognosis [1,4], and with the development of organ failure(s) [5–7]. ACLF events are classified based on the number of organ failure (s) (OFs), grade 1 (less severe) to grade 3 (most severe) and it is universally known that short-term survival worsens with increasing ACLF grades [1,8].

Moreover, not only the number of organs involved but the type of organ affected, has an impact on mortality [9,10]. Hepatic encephalopathy (HE) grade 3–4 has been associated with high mortality in ACLF patients in the United States [9], while in Europe, renal failure in ACLF patients has a high short-term mortality [11]. Renal failure has also been demonstrated to be a negative predictor of ACLF resolution [12]. Whereas liver failure within the CLIF-C ACLF score, has been proven to independently predict a severe course [13].

While most of the information we currently have regarding ACLF comes from the European, American and Asian cohorts, information on ACLF and predictors of mortality on Latin American population are completely lacking [1,14,15]. Here we present our 6-year single-center experience of patients admitted to the ICU that fulfill the criteria for ACLF, and describe the clinical factors and type of organ failures that are independent predictors of 28 and 90-day mortality.

2Methods2.1Patients

Patients with cirrhosis that were admitted to the intensive care unit (ICU) due to a decompensation event between 2012 to 2018 and fulfilled criteria for ACLF diagnosis within the first 6 days of hospitalization were included. The diagnosis of liver cirrhosis was based on histological, clinical signs of hepatic decompensation (HE, variceal bleeding, jaundice, ascites and/or hepatorenal syndrome) ultrasonography, and/or endoscopic findings. Liver disease severity was assessed using the following scores: Child-pugh, Model for End-Stage liver disease (MELD) [16,17]. We excluded patients younger than 18 years old, pregnant, and patients diagnosed with hepatocellular carcinoma, as well as those who received a liver transplant during the 90-day follow-up after the diagnosis of ACLF. The present study was approved by the ethics committee and was performed according to the ethical guidelines of the 1975 Declaration of Helsinki. The requirement for obtaining informed consent from patients was waived because of the retrospective nature of the study.

2.2ACLF and organ failure definitions

ACLF was diagnosed according to the EASL-CLIF Consortium criteria [1]. Grading of ACLF was performed according to the CANONIC study [1] with the following classification: ACLF 1: patients with renal failure (creatinine ≥2.0 mg/dl) or a non-renal organ failure plus renal dysfunction (creatinine between 1.5–1.9 mg/dl) and/or HE grade I–II. ACLF 2: Patients with 2 organ failures; ACLF 3: Patients with 3 or more organ failures. Organ Failure(s) were defined as follows: Liver (serum bilirubin ≥12.0 mg/dl), renal (creatinine ≥2 mg/dl or renal replacement), brain (HE III–IV grade), coagulation (INR ≥ 2.5), circulatory (vasopressor use for circulatory failure indication) and lung (SpO2/FiO2 ≤ 214 or mechanical Ventilation for lung failure).

2.3Infections

The following diagnostic criteria for infection were used: suggestive findings on chest radiographs was diagnostic of pneumonia [18], Spontaneous Bacterial Peritonitis (SBP) was based on an increased number of polymorphonuclear neutrophils in ascitic fluid (>250/mm3) [19] ;more than 15 white blood cells in urine per high power field with either positive urine gram stain or culture was diagnostic of urinary tract infection [20]; and acute cholangitis was suspected clinically by the Charcot triad (pain, fever, jaundice) and confirmed by means of biliary tract dilatation or obstruction [21]. Nosocomial infections were those diagnosed after 48 h of admission, and community acquired (CA) within 48 h of admission. Diagnosis of other infections were made according to conventional criteria [22].

2.4Data collection

The following data were collected from the charts: patient demographics including age, sex, cirrhosis etiology, ascites according to the International Club of Ascites [23], HE according to the West-Haven criteria [24], vital signs, biochemical profile including complete blood count (CBC), liver function tests, use of vasopressors, need for renal replacement therapy, mechanical ventilation and precipitating factors (Infection, GI bleeding, HE, Alcohol) affecting ACLF development and mortality. Patients were followed for up to 90-days. If patients were discharged before 90-days, the follow-up was performed by reviewing the medical records, contacting the patient, a close relative or legal representative, or in person during a scheduled follow-up appointment.

2.5Statistical analysis

All results were expressed as mean ± standard deviation (SD) or median and interquartile range (percentile 25 to percentile 75) according to the normal distribution of the data. The quantitative variable distribution was performed using asymmetry values, kurtosis, and Kolmogorov–Smirnov test. Categorical variables were reported in frequencies and percentages and compared using Pearson’s Chi-squared test. The comparison among ACLF grades was performed using ANOVA when the continuous variables were normally distributed or a non-parametric test (Kruskal–Wallis) for those variables with asymmetric distribution. We constructed a Cox regression analysis to evaluate the possible predictors/associations with ACLF mortality. We used a stepwise approach and included only clinically meaningful variables in the final model to understand what factors were independently associated with 28 and 90-day mortality. Collinearity between explanatory variables was tested using the Variance Inflation Factor, highly correlated variables were excluded from the analysis to prevent issues with multicollinearity. Survival curves were done using a Kaplan–Meier plot and were compared with the log-rank test. All analyses were performed using SPSS (Statistical Package for the Social Sciences) version 22 and GraphPad Prism version 8 software. A p-value of <0.05 was considered statistically significant.

3Results3.1General demographics

From 2012–2018 a total of 938 cirrhotic patients were seen in the emergency department and admitted to the ICU due to a decompensation event. Of those 938 patients, 599 had decompensated cirrhosis (DC), 263 developed ACLF and 76 patients were excluded for the following reasons (57 had hepatocellular carcinoma, 13 had extra-hepatic cancer (colon, stomach, pancreas) and 6 had HIV infection). From the 263 patients fulfilling ACLF inclusion criteria, 115 were excluded (92 had incomplete data and 23 received liver transplantation during the 90 days following the diagnosis of ACLF). Thus, a total of 148 patients were included in this study, with the majority fulfilling ACLF criteria either at the time of admission or during the first 6 days of admission to the ICU (Fig. 1).

Fig. 1.

Study inclusion flowchart. From 2012 to 2018, 938 patients with liver cirrhosis were admitted to the emergency department for some decompensation event (variceal bleeding, infection, hepatic encephalopathy, among others) of which 148 patients diagnosed with ACLF were analyzed.

(0.18MB).

The median age for our cohort was 54 years old (interquartile range 41–63 years). Sex frequency was very similar, with females constituting 55% (n = 81) of the population. The underlying causes of cirrhosis were virus 29.8% (n = 44), cryptogenic 17.6% (n = 26), alcohol 13.5% (n = 20), Autoimmune Hepatitis (AIH) 11.5% (n = 17), Primary Biliary Cirrhosis (PBC) 8.1% (n = 12), and non-alcoholic fatty liver disease (NAFLD) 7.4% (n = 11). Based on the liver disease severity scores, the majority of the patients were severely ill, had MELD score >15 (69.6%; n = 103), 68.2% (n = 101) had Child-Pugh C, 28.4 % (n = 42) had Child-Pugh B and only 3.4% (n = 5) had Child-Pugh A. In addition, more than half of the patients 55% (n = 82) had ACLF grade 3, 28% (n = 41) grade 2, and only 17% (n = 25) grade 1 (Supplementary Table S1).

The most common precipitating events were infection 58.1% (n = 86), GI bleeding 8.1% (n = 12), Hepatic Encephalopathy (HE) 2.7% (n = 4) and alcohol 2.7% (n = 4). Interestingly in 28.4% (n = 42) of the patients, the precipitant was unknown (Supplementary Table S1).

3.2Clinical and biochemical characteristics and organ failure prevalence based on ACLF grading

Patients were further classified into ACLF grade, and clinical and biochemical characteristics were analyzed (Table 2). There were no statistical differences in age, sex or etiology among the different ACLF grades (p = 0.535), (p = 0.982), (p = 0.332) respectively. However, we found a significant difference among them in the presence of HE (p = 0.001), bilirubin (p = 0.002), creatinine (p = 0.001), INR (p = 0.007), leukocytes (p = 0.024), Child-Pugh score (p = 0.017) vasopressor use (P = 0.001) and SpO2/FiO2 ≤ 214 (p = 0.042). The majority of patients with ACLF grade 3 accounted for these differences, with 68.3% (n = 56) presenting with HE grades III–IV, a median of serum bilirubin of 19.1 mg/dl, creatinine of 2.41 mg/dl, INR of 2.1 mg/dl and total leukocyte count of 12.7 × 109/l. Sixty four percent (n = 53) of patients with ACLF-3 presented with severe circulatory failure with a MAP ≤ 70 (mmHg), and almost all of these patients, 97.6% (n = 80) required vasopressors. Likewise, mechanical ventilation was required in more than half of ACLF-3 patients 59.69% (n = 49), of which in 46.34% (n = 38) was indicated by HE. As we expected, the ACLF and CLIF-C OF scores were significantly different among groups with a proportional increase according to the degree of ACLF severity (p = 0.001) (Table 1).

Table 1.

Population baseline characteristics based on ACLF grading (n = 148).

Characteristics  Grade 1n = 25  Grade 2n = 41  Grade 3n = 82 
Age (years)  57 (47–59)  56 (47–64)  50.5 (40–63  0.535 
Female sex – n.(%)  14 (56%)  22 (53.7%)  45 (54.9%)  0.982 
Etiology – n. (%)         
Viral  7 (28%)  16 (39%)  21 (25.6%)  0.332
Alcohol  5 (20%)  4 (9.8%)  11 (13.4%) 
AIH  2 (8%)  4 (9.8%)  11 (13.4%) 
PBC  2 (8%)  1 (2.4%)  9 (11%) 
NASH  3 (12%)  4 (9.8%)  4 (4.9%) 
Cryptogenic  2 (8%)  7 (17%)  17 (20.7%) 
Overlap syndrome  1 (4%)  2 (5%)  3 (3.6%) 
Others  3 (12%)  3 (7.3%|  6 (7.2%) 
Child-Pugh – n. (%)
A  3 (12%)  0 (0%)  2 (2.4%)  0.017
B  2 (8%)  13 (31.7%)  27 (32.9 
C  20 (80%)  28 (68.3%)  53 (64.6%) 
MELD score         
≤15  5 (20%)  14 (34.1%)  26 (31.7%)  0.459
>15  20 (80%)  27 65.9%)  56 (68.3%) 
CLIF-C OF  10 (10–11)  12 (11–13)  15(13–16)  0.001 
ACLF score  49 ± 6.64  55.8 ± 9.69  64.7 ± 9.15  0.001 
HE – n. (%)         
No HE  4 (16%)  8 (19.5%)  4 (4.9%)  0.001
I–II  18 (72%)  18 (43.9%)  22 (26.8%) 
III–IV  3 (12%)  15 (36.6%)  56 (68.3%) 
Ascites – n.(%)  21 (84%)  31 (75.6%)  66 (80.5%)  0.694 
Serum bilirubin (mg/dl)  6.5 (3.7–10.3)  9.2 (6.4–17.8)  19.1 (6.2–34)  0.002 
Serum creatinine (mg/dl)  1.29 (0.93–1.75)  1.49(1.1–1.9)  2.41 (2.1–3.8)  0.001 
INR  1.7(1.6–2)  1.7(1.5–2.1)  2.1 (1.6–2.8)  0.007 
Sodium (mmol/l)  133 (132–137)  133 (131–138)  134 (131–138)  0.838 
Leukocytes (×109/l)  10.3 (4.3–13.8)  11.6 (4.8–16.9)  12.7 (8.6–16.8)  0.024 
Renal replacement  0 (0%)  2 (4.9%)  6 (7.3%)  0.427 
MAP ≤ 70 (mmHg)  14 (56%)  20 (48.8%)  53 (64.6%)  0.229 
Vasopressor use  12 (48%)  31 (75.6%)  80 (97.6%)  0.001 
SpO2/FiO2 ≤ 214  0 (0%)  5 (12.2%)  15 (18.3%)  0.042 
Mechanical Ventilation         
HE  2 (8%)  4 (9.7%)  38 (46.34%)  0.081
Respiratory failure  0 (0%)  6 (14.6%)  3 (3.65%) 
Both  1 (4%)  1 (1.9%)  8(9.7%) 

The data are presented in frequency (n.) and percentage (%), median and interquartile range, mean and standard deviation (SD)(±). Abbreviations. ACLF (Acute on chronic liver failure), AIH (Autoimmune Hepatitis), PBC (Primary Biliary Cholangitis), NAFLD (non-alcoholic fatty liver disease), MELD (Model for End-stage Liver Disease), CLIF-C OF(Chronic Liver Failure -Organ Failure), Mg (milligram), HE (Hepatic encephalopathy), dl (deciliter) mmol/l (milliosmoles/liter), MAP (Mean arterial pressure), SpO2 (Oxygen saturation), FiO2 (Fractional inspired oxygen).

Table 2.

General characteristics based on outcome.

Characteristics  Diedn = 124  Survivedn = 24  p 
Age (years)  55 (44–64)  48 (39–58)  0.089 
Male sex – n.(%)  59 (47.6%)  8 (33.3%)  0.199 
CLIF-C OF  13 (12–15)  11 (10–12)  0.001 
ACLF score  61.45 ± 10.36  50.08 ± 7.52  0.001 
ACLF Grade       
Grade 1  13 (10.5%)  12 (50%)  0.001
Grade 2  35 (28.2%)  6 (25%) 
Grade 3  76 (61.3%)  6 (25%) 
Organ failures       
Liver  60 (48.4%)  9 (37.5%)  0.377 
Renal  74 (59.7%)  4 (16.7%)  0.001 
Brain  70 (56.5%)  5 (20.8%)  0.002 
Coagulation  33 (26.6%)  3 (12.5%)  0.195 
Circulatory  108 (87.1%)  15 (62.5%)  0.007 
Lung  16 (12.9%)  4 (16.7%)  0.744 
Sodium (mmol/l)  135 ± 6.3  134 ± 4.9  0.613 
Leukocytes (×109/l)  12.5 (7.7–16.8)  9.1 (4.4–14.9)  0.073 
Infection  74 (59.7%)  12 (50%)  0.498 

The data are presented in frequency (n.) and percentage (%), median and interquartile range (P25–P75), mean and standard deviation (SD) (±). Bivariate analysis by means of U Mann–Whitney test, T-student and chi square test. Abbreviations. CLIF-C OF (Chronic Liver Failure - Organ Failure) ACLF (Acute on chronic liver failure).

The most prevalent OF was the circulation with 83.1% (n = 123) of the total cases, followed by renal 52.7% (n = 78), brain 50.7% (n = 75), liver 46.6% (n = 69), coagulation 24.3% (n = 36) and lung failure 13.5% (n = 20), of cases respectively (Fig. 2).

Fig. 2.

Frequency of organ failures based on ACLF grading. Circulatory, renal and brain failure were the most prevalent organ failures. According to the ACLF grade, circulatory failure was the most prevalent in all ACLF grades. Lung failure was not present in grade 1 and renal failure was more prevalent in grade 3 compared to grade 2 and 1.

(0.09MB).

When patients were divided according to ACLF severity, it was interesting to note that in ACLF 1 there was no lung failure. Meanwhile, the failures that occurred most frequently in grade 3 ACLF were the circulatory 97.6% (n = 80) and renal failure 82.9% (n = 68) (Fig. 2).

3.3Survival and mortality according to ACLF grading

The global 90-day survival for patients with ACLF was 18% (Fig. 3-A) and the median overall survival was 19 days 95% CI (11.96–26.03). When survival was analyzed according to ACLF severity, we found that the higher the ACLF grade, the lower the survival (Fig. 3-B). Survival for patients with ACLF-3 was extremely low 10%, while survival for grades 2 and 1, was 22% and 45% respectively. Likewise, the median survival in grade 3 was 6 days, 95% CI (3.3–8.6), grade 2 was 28 days, 95% CI (22.7–33.29) and grade 1 was 90 days 95% CI (82.3–97.65). There was a statistical difference in the survival curves between ACLF grades (p = 0.001) (Fig. 3-B).

Fig. 3.

Survival and mortality in patiens with ACLF. (A) Graphic representation of cumulative survival during the 90-day follow up. After 90 days, only 18% of the cohort was still alive. (B) Survival was greater in patients with grade 1 and decreased as the degree of ACLF increases (log rank, p:0.001). Green line: Grade 1, blue line: Grade 2, and red line: Grade 3. (C) Percentage of 7, 28- and 90-day mortality based on ACLF grading.

(0.23MB).

When mortality was analyzed globally, it was clear that most of the patients died within the first 7 days 35.8% (n = 53); 29.7% (n = 44) of patients died by 28 days and 18.2% (n = 27) by 90 days.

According to the ACLF grade, as expected, ACLF grade 3 patients had higher mortality within the first 7 days [59.2% (n = 45)], compared to grade 2 [17.1% (n = 6)] and grade 1 [15.4% (n = 2)]. The same applied for 28 and 90 days with 31.6% (n = 24) and 9.2% (n = 7) of cases respectively (Fig. 3-C).

We next evaluated which organ failure was associated with lower survival. When comparing patients with and without each of the different organ failures, it was clear that having brain, circulatory, liver, renal or coagulation failure was associated with lower survival (P < 0.05) (Fig. 4-A–E). The median survival was lower in patients with the presence of any of the specified organ failure than in those without (12 days, 95% CI (4.50–19.49) vs 27 days, 95% CI (19.74–34.25) brain), (14 days, 95% CI (4.80–23.19) vs 45 days, 95% CI (2.61–87.38) circulatory) (11 days, 95% CI (0.9–23.44) vs 26 days, 95% CI (17.29–34.71) liver), (6 days, 95% CI (4.07–7.92) vs 45 days, 95% CI (28.23–61.77) renal) (6 days 95% CI (2.08–9.92) vs 25 days, 95% CI (18.76–31.23) coagulation) (Fig. 4A–E) respectively. Lung failure was associated with the lowest median survival, however, there was no significant difference between patients with and without the failure (2.23 days, 95% CI (1–8.38) vs 20 days, 95% CI (12.52–27.47) (Fig. 4-F).

Fig. 4.

Kaplan–Meier survival curve in patients based on the type of organ failure. Patients with the following organ failures (A) brain failure (B) circulatory failure (C) liver failure (D) renal failure and (E) coagulation failure, have lower survival (log rank, p:0.001) - (log rank, p:0.02) compared to those without any of these organs. (F) No differences were found between patients with lung failure and those without (log rank, p:0.415).

(0.29MB).
3.4Factors associated with increased 28 and 90-day mortality

We first divided patients between those who died (n = 124) and those who survived (n = 24) (Table 3). No significant differences were found in age, however the majority of patients who died were female (52.4% vs 47.6%). As expected, patients that died, had a significantly higher CLIF-C OF [13 (12–15) vs 11 (10–12) p = 0.001], and ACLF scores (61.45 ± 10.36 vs 50.08 ± 7.52) p = 0.001, when compared to those who survived. The majority of the patients that died had ACLF grade 3 [76 (61.3%) vs 6 (25%), p = 0.001] and a significantly greater proportion of circulatory failure [108 (87.1%) vs 15 (62.5%), p = 0.007], renal failure [74 (59.7%) vs 4 (16.7%), p = 0.001] and brain failure [70 (56.5%) vs 5 (20.8%), p = 0.002]. No significant differences were observed in coagulation failure [33 (26.6%) vs 3 (12.5%), p = 0.195], liver failure [60 (48.4%) vs 9 (37.5%), p = 0.377] and lung failure [16 (12.9%) vs 4 (16.7%), p = 0.744] between patients that died and those who survived. While no difference in infection was observed between dead and surviving patients [(74 (59.7%) vs 12 (50%), p = 0.498], leukocyte count was significantly higher in patients that died compared to those who survived [12.5 × 109/L (7.7–16.8) vs 9.1 × 109/L (4.4–14.9), p = 0.073] (Table 2).

Table 3.

Clinical predictors of 28 and 90 day mortality. Bivariate and multivariate Cox regression analysis.

Parameters  Bivariate analysis,Crude HR (95% CI)(90 days mortality)  p Value  Multivariate analysis, HR (95% CI)*P value of the model(28-day mortality)  pValue  Multivariate analysis, HR (95% CI)*P value of the model(90-day mortality)  pValue 
General characteristics
Age (years)  1.0 (0.99–1.01)  0.543  1.62 (1.10–2.40) *0.0010.0151.78 (1.23–2.56)*0.0010.002
Male sex  1.42 (1.02–2.03)  0.049 
Leukocytes  1.03 (1.01–1.06)  0.005 
Infection  1.18 (0.83–1.70)  0.344 
ACLF characteristics
ACLF Score  1.05 (1.03–1.07)  0.001         
CLIF-C OF  1.32 (1.21–1.44)  0.001         
ACLF Grade             
Grade 1  1 (reference)  0.210         
Grade 2  2.04 (1.07–3.87)  0.029         
Grade 3  4.25 (2.34–7.71)  0.001         
Organ failures
Liver  1.58 (1.11–2.26)  0.011         
Renal  2.91 (2.01–4.22)  0.001  3.26 (2.13–4.99)*0.001  0.001  3.06 (2.08–4.51)*0.001  0.001 
Brain  1.67 (1.17–2.39)  0.005  1.37 (1.09–2.04)*0.001  0.049  1.43 (1.03–2.07)*0.001  0.05 
Coagulation  1.73 (1.16–2.58)  0.007         
Circulatory  1.81 (1.07–3.07)  0.026         
Lung  1.23 (0.73–2.09)  0.428         

Bivariate and multivariate analysis using Cox proportional risks. Abbreviations. HR (Hazard ratio), CI (Confidence interval), ACLF (Acute on chronic liver failure), CLIF-OF (Chronic Liver Failure - Organ Failure).

Based on these data, we next performed a bivariate analysis to determine the clinical parameters associated with 90 day-mortality (Table 3). We found that male sex HR 1.42 (1.02–2.03) p = 0.049 and leukocyte count HR 1.03 (1.01–1.06) p = 0.005, were associated with high 90-day mortality. Likewise, ACLF HR 1.05 (1.03–1.07) p = 0.001 and CLIF-C OF HR 1.32 (1.21–1.44) p = 0.001 scores, ACLF 3 HR 4.25 (2.34–7.71) p = 0.001, ACLF 2 HR 2.04 (1.07–3.87) P = 0.029 as well as the presence of all organ failures: liver HR 1.58 (1.11–2.26) p = 0.011, renal HR 2.91 (2.01–4.22) p = 0.001, brain HR 1.67 (1.17–2.39) p = 0.005, coagulation HR 1.73 (1.16–2.58) p = 0.007 and circulatory HR 1.81 (1.07–3.07) p = 0.026 were all associated with high 90-day mortality. We next performed a multivariate regression analysis using Cox proportional hazard ratio, to determine which factors were independently associated with 28 and 90-day mortality. Results are shown in Table 4. Based on this model, we determined that male sex, brain and renal organ failures were independent predictors of 28 and 90-day mortality in patients with ACLF (Table 3). Of the three factors mentioned above, renal failure (HR 3.26 95% CI (2.13–4.99), p < 0.001, proved superior compared to male sex (HR 1.62 95% CI (1.10–2.40), p = 0.015 and brain failure (HR 1.37 95% CI (1.09–2.04), p = 0.049) in predicting 28 day mortality. Meanwhile, the same variables were also independent predictors of 90-day mortality; with renal failure (HR 3.06 95% CI (2.08–4.51), p < 0.001 still being superior compared to male sex (HR 1.78 95% CI (1.23–2.56), p < 0.002) and brain failure (HR 1.43 95% CI (1.03–2.07), p = 0.05 in predicting 90-day mortality (Table 3).

4Discussion

To our knowledge, this is the first study to report an independent cohort with detailed analysis of ACLF syndrome in the Mexican population.

In Latin America, only 2 studies have described ACLF patients. The first one was a prospective Brazilian cohort of 192 patients with decompensated cirrhosis, 24% of those developing ACLF [25]. The second one was performed in Argentina [26], where 29% of patients admitted for AD were diagnosed with ACLF. When compared with the CANONIC study, despite race differences, it seems that the overall prevalence in Latin America remains pretty much within the range of 20–30%.

However, there seems to be a difference in the mortality rate, which vary significantly between races. For instance, mortality rate in Europe according to the CANONIC, is 33% and 51% at 28-days and 90 days [1], while in Asia is 41% and 63% [27] respectively. On the other hand, in the American continent we have data from the USA indicating that ACLF mortality ranges from 26% to 40% at day 28 and day 90 [28].

Based on the gathered information, it is clear that our ACLF population differs significantly from Europeans, Asians and Americans. ACLF in the Mexican population is a well-defined entity characterized by an extremely high 28-day (70.3%) and 90-day (81.8%) mortality which doubles the one generally observed in other cohorts. In addition, our population comprises patients usually presenting with a more severe disease state as determined by their higher MELD and ACLF-scores prompting their ICU admission.

When comparing the etiology of the underlying chronic disease with those reported in the CANONIC study, we observed that we have the same 2 most prevalent causes (HCV and alcohol), with the main difference being that in the European population, alcohol (60.3%) was almost 6 times higher than HCV (13%). In our population, HCV (29.8%) doubled the alcohol proportion (13.5%), possibly because HCV in Mexico is the most common cause of cirrhosis [29]. Another likely contributing factor is that the hospital where our study was conducted is a reference center for treating HCV infection.

However, while prevalence according to ACLF degree in studies conducted in Latin America [25,26] matches that of the CANONIC [1], with ACLF grade 1 being the most prevalent group, we found very different results. Most of our patients presented with more advanced cirrhosis stage (Child-Pugh C 68.2%) and had more organ failure(s) with a great majority presenting with ACLF grade 3.

The precipitating factors described in the literature vary widely depending on the geographical area. In the region of Asia and the Pacific, on which the guidelines of Asian Pacific Association for the Study of the Liver (APASL) are based, the main ACLF precipitant is HBV. In European countries, these viral etiologies are replaced mostly by non-viral insults, such as bacterial infections [15] similarly to what was reported in Latin America (Brazil and Argentina) and what we found in our population. Despite that, our population’s mortality is still extremely high.

We found a significant association between high 90-day mortality and several clinical factors including leukocyte count, as well as ACLF and CLIF-C OF scores and ACLF grade 3. Those factors were increased in patients that died, compared to those that survived, indicating the critically ill population that this cohort comprises. In addition, having any of the 6 organ failures recognized by the CANONIC for the definition of ACLF was also associated with a higher 90-day mortality. Of all those, lung failure was the only organ not associated with 90-day mortality (p = 0.428, HR 1.23, 95% CI: 0.73–2.09. Whereas renal, brain, coagulation and circulatory failure were all associated with a HR between 2.91 and 1.58 of 90-day mortality.

Indeed, the most affected organ in our cohort was the circulatory system (83.1%) even among the different grades of ACLF (48% in ACLF 1, 75.6% in ACLF 2, and 97.6% in ACLF 3). In comparison, in the CANONIC study, the kidney was the most affected organ (55.8%) followed by the liver (43.6%); while in North America the brain (55.7%) was the most frequent one.

The multivariate analysis leads us to identify that 3 specific factors were independently associated with 28 and 90-day mortality. The first one is male sex (p = 0.015, HR 1.62, 95% CI: 1.10–2.40) and (p = 0.002, HR 1.78, 95% CI: 1.23–2.56) for 28 and 90 days respectively, which we attribute to the fact that females seek earlier medical attention and are more compliant to medical treatment. Additionally, all those with alcoholic etiology (87%, n = 20) are men of whom 94.4% (n = 17) died. Although the sample size is too small to take into account the type of etiology as a prognostic factor, a trend in this variable was also found.

The other two factors that independently predicted 28 and 90-day mortality were renal and brain failure (p = 0.001, HR 3.26, 95% CI: 2.13–4.99) and (p = 0.049, HR 1.37, 95% CI: 1.09–2.04) for 28 and (p = 0.001, HR 3.06, 95% CI: 2.08–4.51) and (p = 0.05, HR 1.43, 95% CI: 1.03–2.07) for 90 day respectively.

Recently, Sawhney et al., demonstrated that ACLF survival, diminishes in relation to the presence of HE (ACLF with HE 35/53, [66%]; ACLF without HE, 16/48 [33%]; p = 0,002) and the grade of HE, grade 0–1, 16/48 [33%]; grade 2, 19/32 [59%]; grade 3–4, 16/21 [76%]; p = 0.002) [6]. Similar results were shown by Cordoba et al., and an additional association with increased systemic inflammatory response in ACLF patients with HE was found, as assessed by elevated C reactive protein levels (ACLF without HE, 27 (12–49 mg/dl); ACLF with HE, 32 (16–60 mg/dl); p < 0.0001) [30]. These findings support the ones in our study, where patient prognosis is negatively affected by the presence of brain failure as determined by the presence of grade III/IV HE. In addition, our results also indicate that patients that died have a more severe systemic inflammatory response compared to those who survived as indicated by higher leukocyte count p = 0.073, 12.5 × 109/l (7.7–16.8) vs 9.1 × 109/l (4.4–14.9) despite no significant differences in the presence of infection p = 0.498, 74 (59.7%) vs 12 (50%). Renal failure as demonstrated in the CANONIC has also been associated with a worse mortality and with a severe systemic inflammatory response [1].

The relation between the three independent predictors of mortality (male sex, brain and renal failure) with the systemic inflammatory response observed in patients that died, deserve further attention since it could have implications in the physiopathology of ACLF.

Limitations to our study include its retrospective nature and the fact that we only describe patients treated in a single third-level center, where there is a larger number of patients with this condition. Therefore, it is not possible to generalize the prevalence nationwide.

This study provides a comprehensive analysis of the clinical characteristics of the ACLF syndrome in Mexico, which due to its high mortality rate is considered an important area of ​​research. We have identified three important independent prognostic factors associated with higher 28 and 90-day mortality, which could allow us to prioritize ACLF patients for general supportive care, disease-specific therapy, management of complications and, if needed, a timely referral for liver transplantation. Additional studies are needed to understand its pathophysiology and to develop novel diagnostic markers and therapeutic options for ACLF patients.

In conclusion, ACLF patients admitted to the ICU have a very high short-term mortality, especially when patients are male and present with brain and renal failure.AbbreviationsACLFAcute on chronic liver failureHEHepatic encephalopathyICUIntensive care unitCLIF-C OFChronic Liver Failure - Organ FailureOFOrgan failureCBCComplete blood countSDStandard deviationSPSSStatistical Package for the Social SciencesAIHAutoimmune HepatitisPBCPrimary Biliary CholangitisNAFLDNon-alcoholic fatty liver diseaseMELDModel for End-stage Liver DiseaseMAPmean arterial pressureEASL-CLIFEuropean Association for the Study of the Liver – Chronic Liver FailureHCVHepatitis C virusAPASLAsian Pacific Association for the Study of the LiverICUIntensive care unit

AbbreviationsACLF

Acute on chronic liver failure

HE

Hepatic encephalopathy

ICU

Intensive care unit

CLIF-C OF

Chronic Liver Failure - Organ Failure

OF

Organ failure

CBC

Complete blood count

SD

Standard deviation

SPSS

Statistical Package for the Social Sciences

AIH

Autoimmune Hepatitis

PBC

Primary Biliary Cholangitis

NAFLD

Non-alcoholic fatty liver disease

MELD

Model for End-stage Liver Disease

MAP

mean arterial pressure

EASL-CLIF

European Association for the Study of the Liver – Chronic Liver Failure

HCV

Hepatitis C virus

APASL

Asian Pacific Association for the Study of the Liver

ICU

Intensive care unit

Conflict of interest

The authors have no conflicts of interest to declare.

Author contributions

OMG: study concept and design, acquisition of data, analysis and interpretation of data, drafting of the manuscript, statistical analysis.

DACR, EC, EAA, JPE: acquisition of data and drafting of the manuscript, administrative, technical and material support

NNA, AT: Study concept and design, drafting of the manuscript, critical revision of the manuscript and study supervision

Funding

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Acknowledgments

The authors thanks National Autonomous University of Mexico. Master’s and Doctoral Program in Medical, Dental and Health Sciences and National Council of Science and Technology (CONACyT) for the support provided.

Appendix A
Supplementary data

The following are Supplementary data to this article:

References
[1]
R. Moreau, R. Jalan, P. Gines, M. Pavesi, P. Angeli, J. Cordoba, et al.
Acute-on-chronic liver failure is a distinct syndrome that develops in patients with acute decompensation of cirrhosis.
Gastroenterology, 144 (2013), pp. 1426-1437
[2]
A. Soo, D.J. Zuege, G.H. Fick, D.J. Niven, L.R. Berthiaume, H.T. Stelfox, et al.
Describing organ dysfunction in the intensive care unit: a cohort study of 20,000 patients.
[3]
R. Jalan, V. Stadlbauer, S. Sen, L. Cheshire, Y.M. Chang, R.P. Mookerjee.
Role of predisposition, injury, response and organ failure in the prognosis of patients with acute-on-chronic liver failure: a prospective cohort study.
Crit Care, 16 (2012), pp. R227
[4]
J.G. O’Leary, K.R. Reddy, G. Garcia-Tsao, S.W. Biggins, F. Wong, M.B. Fallon, et al.
NACSELD acute-on-chronic liver failure (NACSELD-ACLF) score predicts 30-day survival in hospitalized patients with cirrhosis.
Hepatology, 67 (2018), pp. 2367-2374
[5]
D.L. Shawcross, Y. Sharifi, J.B. Canavan, A.D. Yeoman, R.D. Abeles, N.J. Taylor, et al.
Infection and systemic inflammation, not ammonia, are associated with grade 3/4 hepatic encephalopathy, but not mortality in cirrhosis.
J Hepatol, 54 (2011), pp. 640-649
[6]
R. Sawhney, P. Holland-Fischer, M. Rosselli, R.P. Mookerjee, B. Agarwal, R. Jalan.
Role of ammonia, inflammation, and cerebral oxygenation in brain dysfunction of acute-on-chronic liver failure patients.
Liver Transplant, 22 (2016), pp. 732-742
[7]
P. Bellot, J.C. García-Pagán, R. Francés, J.G. Abraldes, M. Navasa, M. Pérez-Mateo, et al.
Bacterial DNA translocation is associated with systemic circulatory abnormalities and intrahepatic endothelial dysfunction in patients with cirrhosis.
Hepatology, 52 (2010), pp. 2044-2052
[8]
A.P.C. da Silva Boteon, A. Chauhan, Y.L. Boteon, S. Tillakaratne, B. Gunson, A.M. Elsharkawy, et al.
Predictive factors for 28-day mortality in acute-on-chronic liver failure patients admitted to the intensive care unit.
Dig Liver Dis, 51 (2019), pp. 1416-1422
[9]
J.S. Bajaj, J.G. O’Leary, P. Tandon, F. Wong, G. Garcia-Tsao, P.S. Kamath, et al.
Hepatic encephalopathy is associated with mortality in patients with cirrhosis independent of other extrahepatic organ failures.
Clin Gastroenterol Hepatol, 15 (2017), pp. 565-574.e4
[10]
M. Premkumar, P. Saxena, D. Rangegowda, S. Baweja, R. Mirza, P. Jain, et al.
Coagulation failure is associated with bleeding events and clinical outcome during systemic inflammatory response and sepsis in acute-on-chronic liver failure: an observational cohort study.
Liver Int, 39 (2019), pp. 694-704
[11]
R. Moreau, R. Jalan, P. Gines, M. Pavesi, P. Angeli, J. Cordoba, et al.
Acute-on-chronic liver failure is a distinct syndrome that develops in patients with acute decompensation of cirrhosis.
Gastroenterology, 144 (2013), pp. 1426-1437.e9
[12]
A. Ferrarese, P. Feltracco, S. Barbieri, U. Cillo, P. Burra, M. Senzolo.
Outcome of critically ill cirrhotic patients admitted to the ICU: the role of ACLF.
J Hepatol, 70 (2019), pp. 801-803
[13]
T. Gustot, J. Fernandez, E. Garcia, F. Morando, P. Caraceni, C. Alessandria, et al.
Clinical course of acute-on-chronic liver failure syndrome and effects on prognosis.
Hepatology, 62 (2015), pp. 243-252
[14]
J.S. Bajaj, J.G. O’Leary, K.R. Reddy, F. Wong, S.W. Biggins, H. Patton, et al.
Survival in infection-related acute-on-chronic liver failure is defined by extrahepatic organ failures.
Hepatology, 60 (2014), pp. 250-256
[15]
H. Singh, C.G. Pai.
Defining acute-on-chronic liver failure: East, West or Middle ground?.
World J Hepatol, 7 (2015), pp. 2571-2577
[16]
G.V. Papatheodoridis, E. Cholongitas, E. Dimitriadou, G. Touloumi, V. Sevastianos, A.J. Archimandritis.
MELD vs Child-Pugh and creatinine-modified Child-Pugh score for predicting survival in patients with decompensated cirrhosis.
World J Gastroenterol, 11 (2005), pp. 3099-3104
[17]
Y. Peng, X. Qi, J. Dai, H. Li, X. Guo.
Child-Pugh versus MELD score for predicting the in-hospital mortality of acute upper gastrointestinal bleeding in liver cirrhosis.
Int J Clin Exp Med, 8 (2015), pp. 751-757
[18]
J. Franco.
Community-acquired pneumonia.
Radiol Technol, 88 (2017), pp. 621-636
[19]
B. Velkey, E. Vitális, Z. Vitális.
Spontaneous bacterial peritonitis.
Orv Hetil, 158 (2017), pp. 50-57
[20]
S.B. Dubbs, S.K. Sommerkamp.
Evaluation and management of urinary tract infection in the emergency department.
Emerg Med Clin North Am, 37 (2019), pp. 707-723
[21]
A. Sokal, A. Sauvanet, B. Fantin, V. de Lastours.
Acute cholangitis: diagnosis and management.
J Visc Surg, 156 (2019), pp. 515-525
[22]
Mandell, Douglas and Bennett´s. Principles and Practice of Infectious Diseases. Chapter 75: Sepsis, severe sepsis and septic shock; page: 915-935. 8th edition.
[23]
T. Aldo, P. Mauricio, D.A. Suárez, J.C. Román, D. Violante.
Guías clínicas de diagnóstico y tratamiento de la ascitis Fisiopatología y diagnóstico de la ascitis.
Rev Gastroenterol Mex, 74 (2009), pp. 387-391
[24]
D.K. Atluri, R. Prakash, K.D. Mullen.
Pathogenesis, diagnosis, and treatment of hepatic encephalopathy.
J Clin Exp Hepatol, 1 (2011), pp. 77-86
[25]
M.F. Ronsoni, M.L. Bazzo, L. Narciso-schiavon, L.L. Schiavon.
Single-centre validation of the EASL-CLIF consortium definition of acute- on-chronic liver failure and CLIF-SOFA for prediction of mortality in cirrhosis.
Liver Int, (2014), pp. 1-8
[26]
C. Dominguez, E. Romero, J. Graciano, J.L. Fernandez, L. Viola.
Prevalence and risk factors of acute-on-chronic liver failure in a single center from Argentina.
World J Hepatol, 8 (2016), pp. 1529-1534
[27]
J. Wu, Y.-Y. Li, J.-H. Hu, L. Jia, M. Shi, F.-P. Meng, et al.
Differential characteristics and prognosis of patients with hepatitis B virus-related acute-on-chronic liver failure defined by European Association for the Study of the Liver - Chronic Liver Failure criteria.
Hepatol Res, 48 (2018), pp. 153-164
[28]
R. Hernaez, J.R. Kramer, Y. Liu, A. Tansel, Y. Natarajan, K.B. Hussain, et al.
Prevalence and short-term mortality of acute-on-chronic liver failure: a national cohort study from the USA.
J Hepatol, 70 (2019), pp. 639-647
[29]
N. Méndez-Sánchez, A.R. Villa, N.C. Chávez-Tapia, G. Ponciano-Rodriguez, P. Almeda-Valdés, D. González, et al.
Trends in liver disease prevalence in Mexico from 2005 to 2050 through mortality data.
Ann Hepatol Off J Mex Assoc Hepatol, 4 (2005), pp. 52-55
[30]
J. Cordoba, M. Ventura-Cots, M. Simón-Talero, À Amorós, M. Pavesi, H. Vilstrup, et al.
Characteristics, risk factors, and mortality of cirrhotic patients hospitalized for hepatic encephalopathy with and without acute-on-chronic liver failure (ACLF).
J Hepatol, 60 (2014), pp. 275-281

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