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Small Bowel Abnormalities in Patients with Compensated Liver Cirrhosis
BACKGROUND: Although capsule endoscopy is available as a minimally invasive imaging technique that contributes significantly to the detection of small bowel lesions, there are only a very few published descriptions of small bowel abnormalities in patients with portal hypertension. AIMS: The aim of t...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3661038/ https://www.ncbi.nlm.nih.gov/pubmed/23247799 http://dx.doi.org/10.1007/s10620-012-2502-z |
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author | Aoyama, Taiki Oka, Shiro Aikata, Hiroshi Nakano, Makoto Watari, Ikue Naeshiro, Noriaki Yoshida, Shigeto Tanaka, Shinji Chayama, Kazuaki |
author_facet | Aoyama, Taiki Oka, Shiro Aikata, Hiroshi Nakano, Makoto Watari, Ikue Naeshiro, Noriaki Yoshida, Shigeto Tanaka, Shinji Chayama, Kazuaki |
author_sort | Aoyama, Taiki |
collection | PubMed |
description | BACKGROUND: Although capsule endoscopy is available as a minimally invasive imaging technique that contributes significantly to the detection of small bowel lesions, there are only a very few published descriptions of small bowel abnormalities in patients with portal hypertension. AIMS: The aim of this study was to characterize the occurrence of small bowel lesions by means of capsule endoscopy in patients with portal hypertension, particularly those with compensated liver cirrhosis and associated anemia. METHODS: Sixty consecutive patients who met our criteria underwent capsule endoscopy. The frequency, type, and distribution of small bowel lesions were determined, and clinical factors associated with the lesions were examined. RESULTS: Small bowel abnormalities were found in 40 patients (67 %), including erythema (n = 32, 53 %), erosion (n = 10, 17 %), angioectasia (n = 9, 15 %), varices (n = 4, 7 %), and villous edema (n = 4, 7 %). Most lesions were located in the proximal or middle small bowel. Factors associated with the lesions were Child–Pugh class B (vs. class A, P = 0.0023), ascites (vs. no ascites, P = 0.0085), and portal hypertensive gastropathy (vs. no portal hypertensive gastropathy, P = 0.0434). CONCLUSIONS: We found capsule endoscopy to be a useful diagnostic modality for detecting clinically significant small bowel lesions in patients with compensated liver cirrhosis. Based on our results, we suggest that this procedure should be especially considered for patients with Child–Pugh class B disease, ascites, and/or portal hypertensive gastropathy if they show evidence of gastrointestinal blood loss and/or iron-deficiency anemia. |
format | Online Article Text |
id | pubmed-3661038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-36610382013-05-22 Small Bowel Abnormalities in Patients with Compensated Liver Cirrhosis Aoyama, Taiki Oka, Shiro Aikata, Hiroshi Nakano, Makoto Watari, Ikue Naeshiro, Noriaki Yoshida, Shigeto Tanaka, Shinji Chayama, Kazuaki Dig Dis Sci Original Article BACKGROUND: Although capsule endoscopy is available as a minimally invasive imaging technique that contributes significantly to the detection of small bowel lesions, there are only a very few published descriptions of small bowel abnormalities in patients with portal hypertension. AIMS: The aim of this study was to characterize the occurrence of small bowel lesions by means of capsule endoscopy in patients with portal hypertension, particularly those with compensated liver cirrhosis and associated anemia. METHODS: Sixty consecutive patients who met our criteria underwent capsule endoscopy. The frequency, type, and distribution of small bowel lesions were determined, and clinical factors associated with the lesions were examined. RESULTS: Small bowel abnormalities were found in 40 patients (67 %), including erythema (n = 32, 53 %), erosion (n = 10, 17 %), angioectasia (n = 9, 15 %), varices (n = 4, 7 %), and villous edema (n = 4, 7 %). Most lesions were located in the proximal or middle small bowel. Factors associated with the lesions were Child–Pugh class B (vs. class A, P = 0.0023), ascites (vs. no ascites, P = 0.0085), and portal hypertensive gastropathy (vs. no portal hypertensive gastropathy, P = 0.0434). CONCLUSIONS: We found capsule endoscopy to be a useful diagnostic modality for detecting clinically significant small bowel lesions in patients with compensated liver cirrhosis. Based on our results, we suggest that this procedure should be especially considered for patients with Child–Pugh class B disease, ascites, and/or portal hypertensive gastropathy if they show evidence of gastrointestinal blood loss and/or iron-deficiency anemia. Springer US 2012-12-18 2013 /pmc/articles/PMC3661038/ /pubmed/23247799 http://dx.doi.org/10.1007/s10620-012-2502-z Text en © The Author(s) 2012 https://creativecommons.org/licenses/by-nc/2.5/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Article Aoyama, Taiki Oka, Shiro Aikata, Hiroshi Nakano, Makoto Watari, Ikue Naeshiro, Noriaki Yoshida, Shigeto Tanaka, Shinji Chayama, Kazuaki Small Bowel Abnormalities in Patients with Compensated Liver Cirrhosis |
title | Small Bowel Abnormalities in Patients with Compensated Liver Cirrhosis |
title_full | Small Bowel Abnormalities in Patients with Compensated Liver Cirrhosis |
title_fullStr | Small Bowel Abnormalities in Patients with Compensated Liver Cirrhosis |
title_full_unstemmed | Small Bowel Abnormalities in Patients with Compensated Liver Cirrhosis |
title_short | Small Bowel Abnormalities in Patients with Compensated Liver Cirrhosis |
title_sort | small bowel abnormalities in patients with compensated liver cirrhosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3661038/ https://www.ncbi.nlm.nih.gov/pubmed/23247799 http://dx.doi.org/10.1007/s10620-012-2502-z |
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