A Histologic Scoring System for Prognosis of Patients With Alcoholic Hepatitis

被引:312
|
作者
Altamirano, Jose [1 ]
Miquel, Rosa [2 ]
Katoonizadeh, Aezam [4 ]
Abraldes, Juan G. [3 ,6 ]
Duarte-Rojo, Andres [7 ,9 ]
Louvet, Alexandre [10 ]
Augustin, Salvador [12 ]
Mookerjee, Rajeshwar P. [13 ]
Michelena, Javier [1 ]
Smyrk, Thomas C. [8 ]
Buob, David [11 ]
Leteurtre, Emmanuelle [11 ]
Rincon, Diego [14 ]
Ruiz, Pablo [1 ]
Garcia-Pagan, Juan Carlos [1 ,3 ]
Guerrero-Marquez, Carmen [15 ]
Jones, Patricia D. [16 ,17 ]
Barritt, A. Sidney [16 ,17 ]
Arroyo, Vicente [1 ]
Bruguera, Miquel [1 ]
Banares, Rafael [14 ]
Gines, Pere [1 ]
Caballeria, Juan [1 ]
Roskams, Tania [4 ]
Nevens, Frederik [5 ]
Jalan, Rajiv [13 ]
Mathurin, Philippe [10 ]
Shah, Vijay H. [7 ]
Bataller, Ramon [1 ,16 ,17 ]
机构
[1] Hosp Clin Barcelona, Liver Unit, Inst Invest Biomed August Pi & Sunyer, CIBER Enfermedades Hepat & Digestivas, Barcelona, Spain
[2] Hosp Clin Barcelona, Pathol Unit, Inst Invest Biomed August Pi & Sunyer, CIBER Enfermedades Hepat & Digestivas, Barcelona, Spain
[3] Hosp Clin Barcelona, Hepat Hemodynam Lab, Inst Invest Biomed August Pi & Sunyer, CIBER Enfermedades Hepat & Digestivas, Barcelona, Spain
[4] Katholieke Univ Leuven, Dept Morphol & Mol Pathol, Univ Hosp Gasthuisberg, Louvain, Belgium
[5] Katholieke Univ Leuven, Div Hepatol, Univ Hosp Gasthuisberg, Louvain, Belgium
[6] Univ Alberta, Dept Med, Div Gastroenterol, Edmonton, AB, Canada
[7] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN USA
[8] Mayo Clin, Dept Pathol, Rochester, MN USA
[9] Univ Arkansas Med Sci, Div Gastroenterol & Hepatol, Little Rock, AR 72205 USA
[10] Univ Lille, CHRU, Serv Hepatogastroenterol, Lille, France
[11] Univ Lille, CHRU, Inst Pathol, Lille, France
[12] Univ Autonoma Barcelona, Liver Unit, Dept Internal Med, Hosp Univ Vall dHebron,Inst Recerca VHIR, E-08193 Barcelona, Spain
[13] Royal Free Hosp, UCL Inst Hepatol, London NW3 2QG, England
[14] Univ Complutense, CIBER Enfermedades Hepat & Digestivas, Sch Med, Liver Unit,Gastroenterol & Hepatol Div,IISGM,Hosp, E-28040 Madrid, Spain
[15] Univ Complutense, CIBER Enfermedades Hepat & Digestivas, Sch Med, Pathol Dept,Hosp Gen Univ Gregorio Maranon,IISG, E-28040 Madrid, Spain
[16] Univ N Carolina, Dept Med, Div Gastroenterol & Hepatol, Chapel Hill, NC USA
[17] Univ N Carolina, Dept Nutr, Div Gastroenterol & Hepatol, Chapel Hill, NC USA
关键词
Alcoholic Hepatitis; Alcoholic Liver Disease; Histologic Classification; Liver Biopsy; LIVER-DISEASE; CIRRHOSIS; MANAGEMENT; MORTALITY; CHOLESTASIS; DIAGNOSIS; VALIDATION; FEATURES; STEROIDS; THERAPY;
D O I
10.1053/j.gastro.2014.01.018
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & 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 kappa 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 < .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.
引用
收藏
页码:1231 / +
页数:15
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