1.Acute-on-chronic liver failure: a new syndrome in cirrhosis.
Clinical and Molecular Hepatology 2016;22(1):1-6
Patients with cirrhosis who are hospitalized for an acute decompensation (AD) and also have organ failure(s) are at high risk of short-term death. These patients have a syndrome called Acute-on-Chronic Liver Failure (ACLF). ACLF is now considered as a new syndrome that it is distinct from "mere" AD not only because of the presence of organ failure(s) and high short-term mortality but also because of younger age, higher prevalence of alcoholic etiology of cirrhosis, higher prevalence of some precipitants (such as bacterial infections, active alcoholism), and more intense systemic inflammatory response. ACLF is a new syndrome also because severe sepsis or severe alcoholic hepatitis do not account for 100% of the observed cases; in fact, almost 50% of the cases are of "unknown" origin. In other words, severe sepsis, severe alcoholic hepatitis and ACLF of "unknown origin" are subcategories of the syndrome.
Acute-On-Chronic Liver Failure/complications/mortality/*pathology
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Age Factors
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Cytokines/metabolism
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Hepatitis, Alcoholic/complications
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Humans
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Liver Cirrhosis/*complications/diagnosis
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Sepsis/complications
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Severity of Illness Index
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Survival Rate
2.Pathophysiology and Management of Alcoholic Liver Disease: Update 2016.
Felix STICKEL ; Christian DATZ ; Jochen HAMPE ; Ramon BATALLER
Gut and Liver 2017;11(2):173-188
Alcoholic liver disease (ALD) is a leading cause of cirrhosis, liver cancer, and acute and chronic liver failure and as such causes significant morbidity and mortality. While alcohol consumption is slightly decreasing in several European countries, it is rising in others and remains high in many countries around the world. The pathophysiology of ALD is still incompletely understood but relates largely to the direct toxic effects of alcohol and its main intermediate, acetaldehyde. Recently, novel putative mechanisms have been identified in systematic scans covering the entire human genome and raise new hypotheses on previously unknown pathways. The latter also identify host genetic risk factors for significant liver injury, which may help design prognostic risk scores. The diagnosis of ALD is relatively easy with a panel of well-evaluated tests and only rarely requires a liver biopsy. Treatment of ALD is difficult and grounded in abstinence as the pivotal therapeutic goal; once cirrhosis is established, treatment largely resembles that of other etiologies of advanced liver damage. Liver transplantation is a sound option for carefully selected patients with cirrhosis and alcoholic hepatitis because relapse rates are low and prognosis is comparable to other etiologies. Still, many countries are restrictive in allocating donor livers for ALD patients. Overall, few therapeutic options exist for severe ALD. However, there is good evidence of benefit for only corticosteroids in severe alcoholic hepatitis, while most other efforts are of limited efficacy. Considering the immense burden of ALD worldwide, efforts of medical professionals and industry partners to develop targeted therapies in ALF has been disappointingly low.
Acetaldehyde
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Adrenal Cortex Hormones
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Alcohol Drinking
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Alcoholics*
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Biopsy
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Carcinoma, Hepatocellular
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Diagnosis
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End Stage Liver Disease
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Fibrosis
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Genome, Human
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Hepatitis, Alcoholic
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Humans
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Liver
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Liver Cirrhosis
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Liver Diseases, Alcoholic*
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Liver Transplantation
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Malnutrition
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Mortality
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Prognosis
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Recurrence
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Risk Factors
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Tissue Donors
3.Comparison of Model for End-stage Liver Disease Score with Discriminant Function and Child-Turcotte-Pugh Scores for Predicting Short-term Mortality in Korean Patients with Alcoholic Hepatitis.
Jae Yoon JEONG ; Joo Hyun SOHN ; Byoung Kwan SON ; Chang Hee PAIK ; Seok Hwan KIM ; Dong Soo HAN ; Yong Chul JEON ; Min Ho LEE ; Dong Hoo LEE ; Choon Suk KEE
The Korean Journal of Gastroenterology 2007;49(2):93-99
BACKGROUND/AIMS: Alcoholic hepatitis is an acute or acute-on-chronic inflammatory syndrome associated with significant morbidity and mortality. Traditionally, Maddrey discriminant function (DF) score and Child-Turcott- Pugh (CTP) score have been used for stratifying the prognosis of alcoholic hepatitis. Recently, the model for end-stage liver disease (MELD) score has been applied to alcoholic hepatitis and some investigators consider MELD score as a better prognostic indicator for severe alcoholic hepatitis. Therefore, this analysis was aimed to compare MELD score with DF and CTP scores for predicting the short-term mortality in Korean patients with alcoholic hepatitis. METHODS: The medical records of patients hospitalized with alcoholic hepatitis between January 1, 1999 and December 31, 2004 at Hanyang University Guri-Hospital were analyzed retrospectively. RESULTS: Of the 138 medical records reviewed, 74 cases fulfilled the inclusion criteria (61 males and 13 females; mean age 47.1 years). Twelve patients (16.2%) died within 90 days after admission. Univariate analysis demonstrated that variables such as ascites, hepatic encephalopathy, splenomegaly, international normalized ratio, CTP, and DF scores were significantly correlated with increased 90-day mortality while MELD score was not. According to the multivariate analysis, only CTP score was statistically significant (p=0.012) while DF and MELD scores were not significant for predicting 90-day mortality. The survival analysis with Cox regression test showed higher DF and CTP scores, but not MELD score, significantly increased the risk of in-hospital mortality. CONCLUSIONS: This study demonstrates that DF and CTP scores are independent predictors of short-term mortality in patients with alcoholic hepatitis.
Adult
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Female
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Follow-Up Studies
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Hepatitis, Alcoholic/diagnosis/*mortality
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Humans
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Korea
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Liver Diseases/diagnosis/mortality
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Male
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Middle Aged
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Predictive Value of Tests
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Prognosis
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ROC Curve
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*Severity of Illness Index
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Survival Analysis
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Time Factors