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   <dc:title>A histologic scoring system for prognosis of patients with Alcoholic hepatitis</dc:title>
   <dc:creator>Altamirano, José</dc:creator>
   <dc:creator>Miquel Morera, Rosa</dc:creator>
   <dc:creator>Katoonizadeh, Aezam</dc:creator>
   <dc:creator>Abraldes, Juan G.</dc:creator>
   <dc:creator>Duarte Rojo, Andrés</dc:creator>
   <dc:creator>Louvet, Alexandre</dc:creator>
   <dc:creator>Augustin, Salvador</dc:creator>
   <dc:creator>Mookerjee, Rajeshwar P.</dc:creator>
   <dc:creator>Michelena Vegas, Xabier</dc:creator>
   <dc:creator>Smyrk, Thomas C.</dc:creator>
   <dc:creator>Buob, David</dc:creator>
   <dc:creator>Leteurtre, Emmanuelle</dc:creator>
   <dc:creator>Rincón, Diego</dc:creator>
   <dc:creator>Ruiz, Pablo</dc:creator>
   <dc:creator>García Pagán, Juan Carlos</dc:creator>
   <dc:creator>Guerrero Marquez, Carmen</dc:creator>
   <dc:creator>Jones, Patricia D.</dc:creator>
   <dc:creator>Barritt, A.S 4th.</dc:creator>
   <dc:creator>Arroyo, Vicente</dc:creator>
   <dc:creator>Bruguera i Cortada, Miquel, 1942-</dc:creator>
   <dc:creator>Bañares, Rafael</dc:creator>
   <dc:creator>Ginès i Gibert, Pere</dc:creator>
   <dc:creator>Caballeria Rovira, Joan</dc:creator>
   <dc:creator>Roskams, Tania</dc:creator>
   <dc:creator>Nevens, Frederick</dc:creator>
   <dc:creator>Jalan, Rajiv</dc:creator>
   <dc:creator>Mathurin, Philippe</dc:creator>
   <dc:creator>Shah, Vijay H.</dc:creator>
   <dc:creator>Bataller Alberola, Ramón</dc:creator>
   <dc:subject>Hepatitis</dc:subject>
   <dc:subject>Alcoholisme</dc:subject>
   <dc:subject>Pronòstic mèdic</dc:subject>
   <dc:subject>Malalties del fetge</dc:subject>
   <dc:subject>Hepatitis</dc:subject>
   <dc:subject>Alcoholism</dc:subject>
   <dc:subject>Prognosis</dc:subject>
   <dc:subject>Liver diseases</dc:subject>
   <dc:description>BACKGROUND &amp; AIMS: There is no histologic classification system to determine prognoses of patients with alcoholic hepatitis (AH). We identified histologic features associated with disease severity and created a histologic scoring system to predict short-term (90-day) mortality. METHODS: We analyzed data from 121 patients admitted to the Liver Unit (Hospital Clinic, Barcelona, Spain) from January 2000 to January 2008 with features of AH and developed a histologic scoring system to determine the risk of death using logistic regression. The system was tested and updated in a test set of 96 patients from 5 academic centers in the United States and Europe, and a semiquantitative scoring system called the Alcoholic Hepatitis Histologic Score (AHHS) was developed. The system was validated in an independent set of 109 patients. Interobserver agreement was evaluated by weighted κ statistical analysis. RESULTS: The degree of fibrosis, degree of neutrophil infiltration, type of bilirubinostasis, and presence of megamitochondria were independently associated with 90-day mortality. We used these 4 parameters to develop the AHHS to identify patients with a low (0-3 points), moderate (4-5 points), or high (6-9 points) risk of death within 90 days (3%, 19%, and 51%, respectively; P &lt; .0001). The AHHS estimated 90-day mortality in the training and test sets with an area under the receiver operating characteristic value of 0.77 (95% confidence interval, 0.71-0.83). Interrater agreement values were 0.65 for fibrosis, 0.86 for bilirubinostasis, 0.60 for neutrophil infiltration, and 0.46 for megamitochondria. Interestingly, the type of bilirubinostasis predicted the development of bacterial infections. CONCLUSIONS: We identified histologic features associated with the severity of AH and developed a patient classification system that might be used in clinical decision making.</dc:description>
   <dc:date>2019-02-12T12:50:48Z</dc:date>
   <dc:date>2019-02-12T12:50:48Z</dc:date>
   <dc:date>2014-01-15</dc:date>
   <dc:date>2019-02-12T12:50:48Z</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
   <dc:identifier>0016-5085</dc:identifier>
   <dc:identifier>https://hdl.handle.net/2445/128168</dc:identifier>
   <dc:identifier>638865</dc:identifier>
   <dc:identifier>24440674</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Versió postprint del document publicat a: https://doi.org/10.1053/j.gastro.2014.01.018</dc:relation>
   <dc:relation>Gastroenterology, 2014, vol. 146, num. 5, p. 1231-1239</dc:relation>
   <dc:relation>https://doi.org/10.1053/j.gastro.2014.01.018</dc:relation>
   <dc:rights>(c) AGA Institute, 2014</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>22 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Elsevier</dc:publisher>
   <dc:source>Articles publicats en revistes (Medicina)</dc:source>
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