Fatima Elmustafa, Abdelhaleem Sideeg, Mahima Tyagi, Akshaya Srikanth Bhagavathula, Mangesh Pagadala, Juan P Arab, Ashwani K Singal
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引用次数: 0
Abstract
Background: The Lille score is an established tool to guide corticosteroid (CS) response and treatment in severe alcohol-associated hepatitis (AH), MELD score >20. However, its use in clinical trials has remained inconsistent. We performed this meta-analysis to compare mortality and infection rates between studies using Lille-guided versus those using CS not guided by the Lille score.
Methods: We performed a systematic review and meta-analysis of randomized controlled trials (2007-2025) evaluating treatment arms using CS in severe AH. Pooled mortality and infection rates at 28, 90, and 180 days were calculated for Lille-guided and non-Lille-guided arms.
Results: Fourteen corticosteroid-treated arms from 13 trials (N=1,294) were included, of which four studies (n=437) used CS guided by the Lille score. Mortality was lower in Lille-guided arms compared with non-Lille-guided arms at 28 days: [8 (2-14) vs 21 (13-29)] %, P=0.01, and at 90 days [15 (10-20) vs 40 (25-56)] %, P<0.001, but similar at 180 days [35 (16-54) vs 48 (34-62)] %, P=0.27. Infection rates at corresponding time points were 14 (11-17), 26 (14-38), and 32 (19-44), without differences between Lille- and non-Lille-guided CS arms. Substantial heterogeneity existed across studies, mainly due to differences in the publication year of the 28-day mortality outcome.
Conclusion: Lille-guided CS use is associated with lower mortality across follow-up periods without a significant difference in infection rates. These findings support the use of the Lille score to guide CS therapy in patients with severe AH.
期刊介绍:
Clinical and Translational Gastroenterology (CTG), published on behalf of the American College of Gastroenterology (ACG), is a peer-reviewed open access online journal dedicated to innovative clinical work in the field of gastroenterology and hepatology. CTG hopes to fulfill an unmet need for clinicians and scientists by welcoming novel cohort studies, early-phase clinical trials, qualitative and quantitative epidemiologic research, hypothesis-generating research, studies of novel mechanisms and methodologies including public health interventions, and integration of approaches across organs and disciplines. CTG also welcomes hypothesis-generating small studies, methods papers, and translational research with clear applications to human physiology or disease.
Colon and small bowel
Endoscopy and novel diagnostics
Esophagus
Functional GI disorders
Immunology of the GI tract
Microbiology of the GI tract
Inflammatory bowel disease
Pancreas and biliary tract
Liver
Pathology
Pediatrics
Preventative medicine
Nutrition/obesity
Stomach.