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The Lille model: A new tool for therapeutic strategy in patients with severe alcoholic hepatitis treated with steroids
Author(s) -
Louvet Alexandre,
Naveau Sylvie,
Abdelnour Marcelle,
Ramond MarieJosé,
Diaz Emmanuel,
Fartoux Laetitia,
Dharancy Sébastien,
Texier Frédéric,
Hollebecque Antoine,
Serfaty Lawrence,
Boleslawski Emmanuel,
Deltenre Pierre,
Canva Valérie,
Pruvot FrançoisRené,
Mathurin Philippe
Publication year - 2007
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1002/hep.21607
Subject(s) - medicine , alcoholic hepatitis , cohort , logistic regression , gastroenterology , receiver operating characteristic , bilirubin , cutoff , hepatitis , renal function , surgery , alcoholic liver disease , cirrhosis , quantum mechanics , physics
Early identification of patients with severe (discriminant function ≥ 32) alcoholic hepatitis (AH) not responding to corticosteroids is crucial. We generated a specific prognostic model (Lille model) to identify candidates early on for alternative therapies. Three hundred twenty patients with AH prospectively treated by corticosteroids were included in the development cohort and 118 in its validation. Baseline data and a change in bilirubin at day 7 were tested. The model was generated by logistic regression. The model combining six reproducible variables (age, renal insufficiency, albumin, prothrombin time, bilirubin, and evolution of bilirubin at day 7) was highly predictive of death at 6 months ( P < 0.1). The area under the receiver operating characteristic (AUROC) curve of the Lille model was 0.89 ± 0.02, higher than the Child‐Pugh (0.62 ± 0.04, P < 0.00001) or Maddrey scores (0.66 ± 0.04, P < 0.00001). In the validation cohort, its AUROC was 0.85 ± 0.04, still higher than the other models, including MELD (0.72 ± 0.05, P = 0.01) and Glasgow scores (0.67 ± 0.05, P = 0.0008). Patients above the ideal cutoff of 0.45 showed a marked decrease in 6‐month survival as compared with others: 25% ± 3.8% versus 85% ± 2.5%, P < 0.0001. This cutoff was able to identify approximately 75% of the observed deaths. Conclusion: In the largest cohort to date of patients with severe AH, we demonstrate that the term “nonresponder” can now be extended to patients with a Lille score above 0.45, which corresponds to 40% of cases. Early identification of subjects with substantial risk of death according to the Lille model will improve management of patients suffering from severe AH and will aid in the design of future studies for alternative therapies. (H EPATOLOGY 2007.)