<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-17T04:56:07Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:11351/13016" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:11351/13016</identifier><datestamp>2025-10-24T10:17:50Z</datestamp><setSpec>com_2072_378070</setSpec><setSpec>com_2072_378040</setSpec><setSpec>col_2072_378092</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Moderate alcohol-associated hepatitis: A real-world multicenter study</dc:title>
   <dc:creator>Muñoz, Karen</dc:creator>
   <dc:creator>Caldentey, Vicente</dc:creator>
   <dc:creator>Idalsoaga, Francisco</dc:creator>
   <dc:creator>Díaz, Luis Antonio</dc:creator>
   <dc:creator>Dunn, Winston</dc:creator>
   <dc:creator>Mehta, Heer</dc:creator>
   <dc:creator>Ventura-Cots, Meritxell</dc:creator>
   <dc:subject>Hepatitis - Mortalitat</dc:subject>
   <dc:subject>Alcoholisme - Complicacions</dc:subject>
   <dc:subject>Hepatitis - Prognosi</dc:subject>
   <dc:subject>ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Diagnosis::Prognosis</dc:subject>
   <dc:subject>DISEASES::Digestive System Diseases::Liver Diseases::Hepatitis::Hepatitis, Alcoholic</dc:subject>
   <dc:subject>Other subheadings::Other subheadings::Other subheadings::Other subheadings::/mortality</dc:subject>
   <dc:subject>TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::diagnóstico::pronóstico</dc:subject>
   <dc:subject>ENFERMEDADES::enfermedades del sistema digestivo::enfermedades hepáticas::hepatitis::hepatitis alcohólica</dc:subject>
   <dc:subject>Otros calificadores::Otros calificadores::Otros calificadores::Otros calificadores::/mortalidad</dc:subject>
   <dcterms:abstract>Moderate alcohol-associated hepatitis; Mortality; Survival</dcterms:abstract>
   <dcterms:abstract>Hepatitis moderada associada a l'alcohol; Mortalitat; Supervivència</dcterms:abstract>
   <dcterms:abstract>Hepatitis moderada asociada al alcohol; Mortalidad; Supervivencia</dcterms:abstract>
   <dcterms:abstract>Background: &#xd;
Severe alcohol-associated hepatitis (sAH) is a well-characterized disease with high short-term mortality. However, there is limited research on those with a “less severe condition” (moderate AH). This study aims to characterize in-depth patients with moderate AH (mAH), including the performance of mortality scoring systems, key prognostic factors, and survival over time.&#xd;
Methods: &#xd;
A multicenter retrospective cohort study (2009–2019) included patients with mAH (MELD score ≤20 at admission). Cox regression and receiver operating characteristic curves with AUC were used for analysis.&#xd;
Results: &#xd;
We included 1845 patients with AH (20 centers, 8 countries) between 2009 and 2019. mAH was defined as a MELD score ≤20 at admission. Twenty-four percent met the criteria for an mAH episode. Patients with mAH tend to be older and have a higher proportion of females, with a median MELD of 17 (15–19), Maddrey discriminant function (mDF) of 33 (22–40), the trajectory of serum bilirubin of 0.83 (0.60–1.21), and neutrophil-to-lymphocyte ratio (NLR) of 5 (2.96–8.60). The primary causes of death in mAH included multiple organ failure (34.1%) and infections (16.6%). The cumulative survival rates at 30, 90, and 180 days were 94.3%, 90.4%, and 88.2%, respectively. In multivariable analysis, age was the only significant predictor of 30-day mortality (HR 1.49, 95% CI: 1.27–1.76, p&lt;0.001). Mortality prediction models showed poor performance, with AUC for MELD (0.671), mDF (0.726), trajectory of serum bilirubin (0.733), and NLR (0.697).&#xd;
Conclusions: &#xd;
Patients with moderate AH exhibited a mortality of 11.8% at 6 months, primarily driven by multiple organ failure and infections. These patients also exhibit a different clinical profile compared to those with sAH. Tailored models and therapeutic strategies are needed to improve long-term outcomes in mAH.</dcterms:abstract>
   <dcterms:abstract>Marco Arrese receives support from the Chilean government through the Fondo Nacional de Desarrollo Científico y Tecnológico (FONDECYT 1241450).</dcterms:abstract>
   <dcterms:dateAccepted>2025-10-24T10:17:50Z</dcterms:dateAccepted>
   <dcterms:available>2025-10-24T10:17:50Z</dcterms:available>
   <dcterms:created>2025-10-24T10:17:50Z</dcterms:created>
   <dcterms:issued>2025-04-30T06:39:26Z</dcterms:issued>
   <dcterms:issued>2025-04-30T06:39:26Z</dcterms:issued>
   <dcterms:issued>2025-04</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>http://hdl.handle.net/11351/13016</dc:identifier>
   <dc:relation>Hepatology Communications;9(4)</dc:relation>
   <dc:relation>https://doi.org/10.1097/HC9.0000000000000673</dc:relation>
   <dc:rights>Attribution 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>Wolters Kluwer Health</dc:publisher>
   <dc:source>Scientia</dc:source>
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