TY - JOUR
T1 - Utility and appropriateness of the fatty Liver Inhibition of progression ( FLIP) Algorithm and Steatosis, Activity, and Fibrosis ( SAF) Score in the evaluation of Biopsies of Nonalcoholic Fatty Liver Disease
AU - Cabibi, Daniela
AU - Montani, Matteo
AU - Brain, null
AU - Pareja, María Jesús
AU - Bury, Yvonne
AU - Lackner, Carolin
AU - Burt, Alastair
AU - Gouw, Annette
AU - Tiniakos, null
AU - Ziol, Marianne
AU - Wendum, Dominique
AU - Gouw, Annette
AU - Ratziu, Vlad
AU - Schirmacher, Peter
AU - Terracciano, Luigi
AU - Losi, Luisa
AU - Charlotte, Frederic
AU - David, Ezio
AU - Burt, Alastair
AU - Bedossa, Pierre
PY - 2014
Y1 - 2014
N2 - Biopsy is still the gold standard for the diagnosis of nonalcoholic steatohepatitis but thedefinition may vary among pathologists, a drawback especially in evaluation of biopsiesfor clinical trials. We previously developed a scoring system (steatosis, activity, fibrosis[SAF]) allowing the use of an algorithm (fatty liver inhibition of progression [FLIP])for the classification of liver injury in morbid obesity. The aim of this study was todetermine whether the use of the SAF score and FLIP algorithm can decrease interobservervariations among pathologists. In a first session, pathologists categorized 40 liverbiopsies of patients with nonalcoholic fatty liver disease (NAFLD) according to theirown experience. In a second reading session, each pathologist reclassified the same slidesby using the FLIP algorithm and SAF score, blinded to their first evaluation. Theexperiment was repeated with two different groups of pathologists at varying levels oftraining in liver pathology. The percentage of biopsy interpretation concordant with referenceevaluation increased from 77% to 97% in Group 1 and from 42% to 75% inGroup 2 after the use of the SAF score and FLIP algorithm. The strength of concordancein classification increased in Group 1 from moderate (j50.54) to substantial(j50.66) and from fair (j50.35) to substantial (j50.61) in Group 2 with applicationof the algorithm. With regard to the SAF score, concordance was substantial inGroup 1 for steatosis (j50.61), activity (j50.75), and almost perfect for fibrosis(j50.83 after pooling 1a, 1b, and 1c together into a single score F1). Similar trendswere observed in Group 2 (j50.54 for S, j50.68 for A, and j50.72 for F). Conclusion:The FLIP algorithm based on the SAF score should decrease interobserver variationsamong pathologists and are likely to be implemented in pathology practice.(HEPATOLOGY 2014;60:565-575)
AB - Biopsy is still the gold standard for the diagnosis of nonalcoholic steatohepatitis but thedefinition may vary among pathologists, a drawback especially in evaluation of biopsiesfor clinical trials. We previously developed a scoring system (steatosis, activity, fibrosis[SAF]) allowing the use of an algorithm (fatty liver inhibition of progression [FLIP])for the classification of liver injury in morbid obesity. The aim of this study was todetermine whether the use of the SAF score and FLIP algorithm can decrease interobservervariations among pathologists. In a first session, pathologists categorized 40 liverbiopsies of patients with nonalcoholic fatty liver disease (NAFLD) according to theirown experience. In a second reading session, each pathologist reclassified the same slidesby using the FLIP algorithm and SAF score, blinded to their first evaluation. Theexperiment was repeated with two different groups of pathologists at varying levels oftraining in liver pathology. The percentage of biopsy interpretation concordant with referenceevaluation increased from 77% to 97% in Group 1 and from 42% to 75% inGroup 2 after the use of the SAF score and FLIP algorithm. The strength of concordancein classification increased in Group 1 from moderate (j50.54) to substantial(j50.66) and from fair (j50.35) to substantial (j50.61) in Group 2 with applicationof the algorithm. With regard to the SAF score, concordance was substantial inGroup 1 for steatosis (j50.61), activity (j50.75), and almost perfect for fibrosis(j50.83 after pooling 1a, 1b, and 1c together into a single score F1). Similar trendswere observed in Group 2 (j50.54 for S, j50.68 for A, and j50.72 for F). Conclusion:The FLIP algorithm based on the SAF score should decrease interobserver variationsamong pathologists and are likely to be implemented in pathology practice.(HEPATOLOGY 2014;60:565-575)
UR - http://hdl.handle.net/10447/201352
M3 - Article
VL - 60
SP - 565
EP - 575
JO - HEPATOLOGY
JF - HEPATOLOGY
SN - 1527-3350
ER -