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Predicting Acute Pancreatitis Severity: Comparison of Prognostic Scores

BACKGROUND: Acute pancreatitis has a broad clinical spectrum, from mild illness to multiple organ failure and death. Prognostic scores have been developed or adapted to predict disease severity. This study aimed to compare the prognostic scores according to sensitivity and specificity, receiver oper...

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Autores principales: Simoes, Marco, Alves, Patricia, Esperto, Helder, Canha, Catarina, Meira, Elisa, Ferreira, Erica, Gomes, Manuel, Fonseca, Isabel, Barbosa, Benilde, Costa, Jose Nascimento
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5139846/
https://www.ncbi.nlm.nih.gov/pubmed/27957018
http://dx.doi.org/10.4021/gr364w
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author Simoes, Marco
Alves, Patricia
Esperto, Helder
Canha, Catarina
Meira, Elisa
Ferreira, Erica
Gomes, Manuel
Fonseca, Isabel
Barbosa, Benilde
Costa, Jose Nascimento
author_facet Simoes, Marco
Alves, Patricia
Esperto, Helder
Canha, Catarina
Meira, Elisa
Ferreira, Erica
Gomes, Manuel
Fonseca, Isabel
Barbosa, Benilde
Costa, Jose Nascimento
author_sort Simoes, Marco
collection PubMed
description BACKGROUND: Acute pancreatitis has a broad clinical spectrum, from mild illness to multiple organ failure and death. Prognostic scores have been developed or adapted to predict disease severity. This study aimed to compare the prognostic scores according to sensitivity and specificity, receiver operating characteristic curves and area under the curve. Statistical correlation with disease severity, length of hospital stay, mortality and complication rates. METHODS: Retrospective analysis of the clinical data of patients admitted to an Internal Medicine ward with the diagnosis of acute pancreatitis over a ten year period. Evaluation of prognostic scores: Ranson, Glasgow-Imrie, Balthazar, APACHE II (admission and at 48 hours) and C-reactive protein (48 hours), was carried out as well as statistical analysis using Microsoft Excel 2007® and SPSS 16®. The confidence interval used was 95%. RESULTS: Data from 193 clinical files was collected. However, 67 were excluded due to lack of information. According to the Atlanta criteria, 90 cases were deemed as mild and 36 severe. The mortality rate was 6% and the local complication rate was 9.3%. Ranson, Glasgow and APACHE II scores had significant correlation with mortality. Apart from C-reactive protein levels at 48 hours, all scores had significant correlation with disease severity. The scores with best area under the curve correlation were APACHE II (48 hours): 0.892, Ranson: 0.879, and APACHE II (admission): 0.861. CONCLUSIONS: The most accurate prognostic scores in this study were APACHE II (48 hours) and Ranson. APACHE II at admission was a good indicator, impaired only by high false positive ratio.
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spelling pubmed-51398462016-12-12 Predicting Acute Pancreatitis Severity: Comparison of Prognostic Scores Simoes, Marco Alves, Patricia Esperto, Helder Canha, Catarina Meira, Elisa Ferreira, Erica Gomes, Manuel Fonseca, Isabel Barbosa, Benilde Costa, Jose Nascimento Gastroenterology Res Original Article BACKGROUND: Acute pancreatitis has a broad clinical spectrum, from mild illness to multiple organ failure and death. Prognostic scores have been developed or adapted to predict disease severity. This study aimed to compare the prognostic scores according to sensitivity and specificity, receiver operating characteristic curves and area under the curve. Statistical correlation with disease severity, length of hospital stay, mortality and complication rates. METHODS: Retrospective analysis of the clinical data of patients admitted to an Internal Medicine ward with the diagnosis of acute pancreatitis over a ten year period. Evaluation of prognostic scores: Ranson, Glasgow-Imrie, Balthazar, APACHE II (admission and at 48 hours) and C-reactive protein (48 hours), was carried out as well as statistical analysis using Microsoft Excel 2007® and SPSS 16®. The confidence interval used was 95%. RESULTS: Data from 193 clinical files was collected. However, 67 were excluded due to lack of information. According to the Atlanta criteria, 90 cases were deemed as mild and 36 severe. The mortality rate was 6% and the local complication rate was 9.3%. Ranson, Glasgow and APACHE II scores had significant correlation with mortality. Apart from C-reactive protein levels at 48 hours, all scores had significant correlation with disease severity. The scores with best area under the curve correlation were APACHE II (48 hours): 0.892, Ranson: 0.879, and APACHE II (admission): 0.861. CONCLUSIONS: The most accurate prognostic scores in this study were APACHE II (48 hours) and Ranson. APACHE II at admission was a good indicator, impaired only by high false positive ratio. Elmer Press 2011-10 2011-09-20 /pmc/articles/PMC5139846/ /pubmed/27957018 http://dx.doi.org/10.4021/gr364w Text en Copyright 2011, Simoes et al. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Simoes, Marco
Alves, Patricia
Esperto, Helder
Canha, Catarina
Meira, Elisa
Ferreira, Erica
Gomes, Manuel
Fonseca, Isabel
Barbosa, Benilde
Costa, Jose Nascimento
Predicting Acute Pancreatitis Severity: Comparison of Prognostic Scores
title Predicting Acute Pancreatitis Severity: Comparison of Prognostic Scores
title_full Predicting Acute Pancreatitis Severity: Comparison of Prognostic Scores
title_fullStr Predicting Acute Pancreatitis Severity: Comparison of Prognostic Scores
title_full_unstemmed Predicting Acute Pancreatitis Severity: Comparison of Prognostic Scores
title_short Predicting Acute Pancreatitis Severity: Comparison of Prognostic Scores
title_sort predicting acute pancreatitis severity: comparison of prognostic scores
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5139846/
https://www.ncbi.nlm.nih.gov/pubmed/27957018
http://dx.doi.org/10.4021/gr364w
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