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Association between juxtapapillary diverticulum and acute cholangitis determined using laboratory data

The aim of this study was to evaluate the association between juxtapapillary diverticulum (JD) and acute cholangitis (AC), and to analyze laboratory data to reveal the underlying mechanism. We conducted a retrospective review of 139 patients who underwent endoscopic retrograde cholangiopancreatograp...

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Autores principales: Tomizawa, Minoru, Shinozaki, Fuminobu, Motoyoshi, Yasufumi, Sugiyama, Takao, Yamamoto, Shigenori, Sueishi, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4242068/
https://www.ncbi.nlm.nih.gov/pubmed/25429235
http://dx.doi.org/10.2147/CEG.S71539
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author Tomizawa, Minoru
Shinozaki, Fuminobu
Motoyoshi, Yasufumi
Sugiyama, Takao
Yamamoto, Shigenori
Sueishi, Makoto
author_facet Tomizawa, Minoru
Shinozaki, Fuminobu
Motoyoshi, Yasufumi
Sugiyama, Takao
Yamamoto, Shigenori
Sueishi, Makoto
author_sort Tomizawa, Minoru
collection PubMed
description The aim of this study was to evaluate the association between juxtapapillary diverticulum (JD) and acute cholangitis (AC), and to analyze laboratory data to reveal the underlying mechanism. We conducted a retrospective review of 139 patients who underwent endoscopic retrograde cholangiopancreatography (ERCP) between April 2008 and March 2013 for diagnosis or treatment of biliary tract conditions. The Wilcoxon signed-rank test was used for comparison of variables between patients with or without JD. The χ(2) test was used to analyze the association between JD and AC duct dilatation. Logistic regression analysis was performed to identify variables with strong correlation with AC. ERCP was attempted in 139 patients, but in one patient the endoscope did not reach the papilla of Vater because of a partial gastrectomy, and in two patients evaluation for JD was not possible because of duodenal or papilla of Vater cancer. Therefore, 136 patients were included in this study. JD was significantly associated with AC (P<0.0001) and bile-duct dilatation (P=0.0107), and AC was strongly associated with bile duct dilatation (P=0.0013). Alkaline phosphatase levels were significantly elevated in patients with JD (P=0.0237). In AC patients without JD, χ(2) for C-reactive protein was 4.48 (P=0.0342), whereas in AC patients with JD, χ(2) values for the white blood cell count, alkaline phosphatase, and aspartate aminotransferase were 2.62, 3.1, and 3.61, respectively (P=0.025, 0.015, and 0.0336, respectively). JD was strongly associated with AC. Logistic regression analysis suggested that bile flow was disturbed with JD.
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spelling pubmed-42420682014-11-26 Association between juxtapapillary diverticulum and acute cholangitis determined using laboratory data Tomizawa, Minoru Shinozaki, Fuminobu Motoyoshi, Yasufumi Sugiyama, Takao Yamamoto, Shigenori Sueishi, Makoto Clin Exp Gastroenterol Original Research The aim of this study was to evaluate the association between juxtapapillary diverticulum (JD) and acute cholangitis (AC), and to analyze laboratory data to reveal the underlying mechanism. We conducted a retrospective review of 139 patients who underwent endoscopic retrograde cholangiopancreatography (ERCP) between April 2008 and March 2013 for diagnosis or treatment of biliary tract conditions. The Wilcoxon signed-rank test was used for comparison of variables between patients with or without JD. The χ(2) test was used to analyze the association between JD and AC duct dilatation. Logistic regression analysis was performed to identify variables with strong correlation with AC. ERCP was attempted in 139 patients, but in one patient the endoscope did not reach the papilla of Vater because of a partial gastrectomy, and in two patients evaluation for JD was not possible because of duodenal or papilla of Vater cancer. Therefore, 136 patients were included in this study. JD was significantly associated with AC (P<0.0001) and bile-duct dilatation (P=0.0107), and AC was strongly associated with bile duct dilatation (P=0.0013). Alkaline phosphatase levels were significantly elevated in patients with JD (P=0.0237). In AC patients without JD, χ(2) for C-reactive protein was 4.48 (P=0.0342), whereas in AC patients with JD, χ(2) values for the white blood cell count, alkaline phosphatase, and aspartate aminotransferase were 2.62, 3.1, and 3.61, respectively (P=0.025, 0.015, and 0.0336, respectively). JD was strongly associated with AC. Logistic regression analysis suggested that bile flow was disturbed with JD. Dove Medical Press 2014-11-20 /pmc/articles/PMC4242068/ /pubmed/25429235 http://dx.doi.org/10.2147/CEG.S71539 Text en © 2014 Tomizawa et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Tomizawa, Minoru
Shinozaki, Fuminobu
Motoyoshi, Yasufumi
Sugiyama, Takao
Yamamoto, Shigenori
Sueishi, Makoto
Association between juxtapapillary diverticulum and acute cholangitis determined using laboratory data
title Association between juxtapapillary diverticulum and acute cholangitis determined using laboratory data
title_full Association between juxtapapillary diverticulum and acute cholangitis determined using laboratory data
title_fullStr Association between juxtapapillary diverticulum and acute cholangitis determined using laboratory data
title_full_unstemmed Association between juxtapapillary diverticulum and acute cholangitis determined using laboratory data
title_short Association between juxtapapillary diverticulum and acute cholangitis determined using laboratory data
title_sort association between juxtapapillary diverticulum and acute cholangitis determined using laboratory data
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4242068/
https://www.ncbi.nlm.nih.gov/pubmed/25429235
http://dx.doi.org/10.2147/CEG.S71539
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