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Ultrasonographic evaluation of gastrointestinal graft‐versus‐host disease after hematopoietic stem cell transplantation
Gastrointestinal graft‐versus‐host disease (GI‐GVHD) is a major and life‐threatening complication of hematopoietic stem cell transplantation (HSCT). This study evaluated the efficacy of ultrasonography (US) for assessing and monitoring GI‐GVHD. GI tract was evaluated by US in 81 patients. US finding...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744723/ https://www.ncbi.nlm.nih.gov/pubmed/26009803 http://dx.doi.org/10.1111/ctr.12570 |
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author | Nishida, Mutsumi Shigematsu, Akio Sato, Megumi Kudo, Yusuke Omotehara, Satomi Horie, Tatsunori Iwai, Takahito Endo, Tomoyuki Iguchi, Akihiro Shibuya, Hitoshi Hatanaka, Kanako Shimizu, Chikara Teshima, Takanori |
author_facet | Nishida, Mutsumi Shigematsu, Akio Sato, Megumi Kudo, Yusuke Omotehara, Satomi Horie, Tatsunori Iwai, Takahito Endo, Tomoyuki Iguchi, Akihiro Shibuya, Hitoshi Hatanaka, Kanako Shimizu, Chikara Teshima, Takanori |
author_sort | Nishida, Mutsumi |
collection | PubMed |
description | Gastrointestinal graft‐versus‐host disease (GI‐GVHD) is a major and life‐threatening complication of hematopoietic stem cell transplantation (HSCT). This study evaluated the efficacy of ultrasonography (US) for assessing and monitoring GI‐GVHD. GI tract was evaluated by US in 81 patients. US findings were positive in 43 patients, including 11 false positive, and negative in 38 patients. Sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of US for the diagnosis of GI‐GVHD were 100%, 78%, 74%, 100%, and 86%, respectively. Diffuse wall thickening of the ileum was the most frequent finding in patients with GI‐GVHD. Severity of GI‐GVHD was correlated with the thickness of internal low echoic layer of the wall, the echogenicity of mesenteric fat tissue, and the intensity of Doppler signaling. We classified US findings of GI‐GVHD into four US grades. There was a significant correlation between clinical stage of GI‐GVHD and the US grade. These ultrasonographic abnormalities were improved with clinical improvement of GI‐GVHD upon treatment. Thus, US is an effective and efficient non‐invasive means of identifying the extent and severity of GI‐GVHD and monitoring response to treatment. |
format | Online Article Text |
id | pubmed-4744723 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47447232016-02-18 Ultrasonographic evaluation of gastrointestinal graft‐versus‐host disease after hematopoietic stem cell transplantation Nishida, Mutsumi Shigematsu, Akio Sato, Megumi Kudo, Yusuke Omotehara, Satomi Horie, Tatsunori Iwai, Takahito Endo, Tomoyuki Iguchi, Akihiro Shibuya, Hitoshi Hatanaka, Kanako Shimizu, Chikara Teshima, Takanori Clin Transplant Original Articles Gastrointestinal graft‐versus‐host disease (GI‐GVHD) is a major and life‐threatening complication of hematopoietic stem cell transplantation (HSCT). This study evaluated the efficacy of ultrasonography (US) for assessing and monitoring GI‐GVHD. GI tract was evaluated by US in 81 patients. US findings were positive in 43 patients, including 11 false positive, and negative in 38 patients. Sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of US for the diagnosis of GI‐GVHD were 100%, 78%, 74%, 100%, and 86%, respectively. Diffuse wall thickening of the ileum was the most frequent finding in patients with GI‐GVHD. Severity of GI‐GVHD was correlated with the thickness of internal low echoic layer of the wall, the echogenicity of mesenteric fat tissue, and the intensity of Doppler signaling. We classified US findings of GI‐GVHD into four US grades. There was a significant correlation between clinical stage of GI‐GVHD and the US grade. These ultrasonographic abnormalities were improved with clinical improvement of GI‐GVHD upon treatment. Thus, US is an effective and efficient non‐invasive means of identifying the extent and severity of GI‐GVHD and monitoring response to treatment. John Wiley and Sons Inc. 2015-06-30 2015-08 /pmc/articles/PMC4744723/ /pubmed/26009803 http://dx.doi.org/10.1111/ctr.12570 Text en © 2015 The Authors. Clinical Transplantation Published by John Wiley &Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Nishida, Mutsumi Shigematsu, Akio Sato, Megumi Kudo, Yusuke Omotehara, Satomi Horie, Tatsunori Iwai, Takahito Endo, Tomoyuki Iguchi, Akihiro Shibuya, Hitoshi Hatanaka, Kanako Shimizu, Chikara Teshima, Takanori Ultrasonographic evaluation of gastrointestinal graft‐versus‐host disease after hematopoietic stem cell transplantation |
title | Ultrasonographic evaluation of gastrointestinal graft‐versus‐host disease after hematopoietic stem cell transplantation |
title_full | Ultrasonographic evaluation of gastrointestinal graft‐versus‐host disease after hematopoietic stem cell transplantation |
title_fullStr | Ultrasonographic evaluation of gastrointestinal graft‐versus‐host disease after hematopoietic stem cell transplantation |
title_full_unstemmed | Ultrasonographic evaluation of gastrointestinal graft‐versus‐host disease after hematopoietic stem cell transplantation |
title_short | Ultrasonographic evaluation of gastrointestinal graft‐versus‐host disease after hematopoietic stem cell transplantation |
title_sort | ultrasonographic evaluation of gastrointestinal graft‐versus‐host disease after hematopoietic stem cell transplantation |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744723/ https://www.ncbi.nlm.nih.gov/pubmed/26009803 http://dx.doi.org/10.1111/ctr.12570 |
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