Risk factors for mortality in patients with alcoholic hepatitis and assessment of prognostic models: A population-based study

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Abstract

Background: Severe alcoholic hepatitis (AH) is associated with a substantial risk for short-term mortality. OBJECTIVES: To identify prognostic factors and validate well-known prognostic models in a Canadian population of patients hospitalized for AH. Methods: In the present retrospective study, patients hospitalized for AH in Calgary, Alberta, between January 2008 and August 2012 were included. Stepwise logistic regression models identified independent risk factors for 90-day mortality, and the discrimination of prognostic models (Model for End-stage Liver Disease [MELD] and Maddrey discriminant function [DF]) were examined using areas under the ROC curves. Results: A total of 122 patients with AH were hospitalized during the study period; the median age was 49 years (interquartile range [IQR] 42 to 55 years) and 60% were men. Median MELD score and Maddrey DF on admission were 21 (IQR 18 to 24) and 45 (IQR 26 to 62), respectively. Seventy-three percent of patients received corticosteroids and/or pentoxifylline, and the 90-day mortality was 17%. Independent predictors of mortality included older age, female sex, international normalized ratio, MELD score and Maddrey DF (all P<0.05). For discrimination of 90-day mortality, the areas under the ROC curves of the prognostic models (MELD 0.64; Maddrey DF 0.68) were similar (P>0.05). At optimal cut-offs of ≥22 for MELD score and ≥37 for Maddrey DF, both models excluded death with high certainty (negative predictive values 90% and 96%, respectively). Conclusions: In patients hospitalized for AH, well-known prognostic models can be used to predict 90-day mortality, particularly to identify patients with a low risk for death.

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Pang, J. X. Q., Ross, E., Borman, M. A., Zimmer, S., Kaplan, G. G., Heitman, S. J., … Myers, R. P. (2015). Risk factors for mortality in patients with alcoholic hepatitis and assessment of prognostic models: A population-based study. Canadian Journal of Gastroenterology and Hepatology, 29(3), 131–138. https://doi.org/10.1155/2015/814827

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