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Is Follow-Up Endoscopy Necessary in Upper Gastrointestinal Cytomegalovirus Disease?
Gastrointestinal (GI) cytomegalovirus (CMV) disease is a major cause of morbidity and mortality in immunocompromised patients. Diagnosis of GI CMV disease mostly relies on endoscopy examination and histopathologic findings. There are limited data on the need for follow-up endoscopy with histopatholo...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902479/ https://www.ncbi.nlm.nih.gov/pubmed/27175637 http://dx.doi.org/10.1097/MD.0000000000003389 |
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author | Seo, Myeongsook Kim, Do Hoon Gong, Eun Jeong Ahn, Ji Yong Lee, Jeong Hoon Jung, Kee Wook Choi, Kee Don Song, Ho June Lee, Gin Hyug Jung, Hwoon-Yong Kim, Jin-Ho Lee, Sang-Oh Choi, Sang-Ho Kim, Yang Soo Woo, Jun Hee Kim, Sung-Han |
author_facet | Seo, Myeongsook Kim, Do Hoon Gong, Eun Jeong Ahn, Ji Yong Lee, Jeong Hoon Jung, Kee Wook Choi, Kee Don Song, Ho June Lee, Gin Hyug Jung, Hwoon-Yong Kim, Jin-Ho Lee, Sang-Oh Choi, Sang-Ho Kim, Yang Soo Woo, Jun Hee Kim, Sung-Han |
author_sort | Seo, Myeongsook |
collection | PubMed |
description | Gastrointestinal (GI) cytomegalovirus (CMV) disease is a major cause of morbidity and mortality in immunocompromised patients. Diagnosis of GI CMV disease mostly relies on endoscopy examination and histopathologic findings. There are limited data on the need for follow-up endoscopy with histopathologic examination in patients with upper gastrointestinal (UGI) CMV disease. All adult patients with confirmed and probable UGI CMV disease at a tertiary hospital over a 16-year period whose follow-up endoscopy was available were enrolled. The patients were classified as endoscopic responders if they showed complete or partial improvement on follow-up endoscopy, and as endoscopic nonresponders if there was no improvement or worsening. CMV tissue clearance was defined as absence of any visible CMV inclusion bodies, negative CMV immunohistochemistry and negative CMV polymerase chain reaction in follow-up biopsy tissues. During the study period, 77 patients with UGI CMV disease were analyzed. The median time to follow-up endoscopy was 19 days (interquartile range, 14–27). Of these 77 patients, 52 (68%) were classified as responders, and the remaining 25 (32%) as nonresponders. GI bleeding was more common in the nonresponders than the responders (36% vs 12%, respectively; P = 0.02). There was no significant difference in CMV tissue clearance between the responders and nonresponders (56% vs 69%, respectively; P = 0.38), median durations of treatment (20 days vs 21 days, respectively; P = 0.48), and relapse rates (10% vs 8%, respectively; P > 0.99). Multivariate analysis showed that the only independent predictive factor for relapse of CMV antigenemia or CMV GI disease was multiorgan CMV disease (odds ratio = 12.4, 95% confidence interval 1.6–97.9; P = 0.02). Endoscopic responses were obtained in about two-thirds of patients with UGI CMV disease 2 or 3 weeks after antiviral therapy. However, these follow-up endoscopic findings neither reflected CMV tissue clearance nor predicted disease relapse. These findings suggest that the routine follow-up endoscopy may not be warranted in patients with UGI CMV disease. |
format | Online Article Text |
id | pubmed-4902479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-49024792016-06-27 Is Follow-Up Endoscopy Necessary in Upper Gastrointestinal Cytomegalovirus Disease? Seo, Myeongsook Kim, Do Hoon Gong, Eun Jeong Ahn, Ji Yong Lee, Jeong Hoon Jung, Kee Wook Choi, Kee Don Song, Ho June Lee, Gin Hyug Jung, Hwoon-Yong Kim, Jin-Ho Lee, Sang-Oh Choi, Sang-Ho Kim, Yang Soo Woo, Jun Hee Kim, Sung-Han Medicine (Baltimore) 4900 Gastrointestinal (GI) cytomegalovirus (CMV) disease is a major cause of morbidity and mortality in immunocompromised patients. Diagnosis of GI CMV disease mostly relies on endoscopy examination and histopathologic findings. There are limited data on the need for follow-up endoscopy with histopathologic examination in patients with upper gastrointestinal (UGI) CMV disease. All adult patients with confirmed and probable UGI CMV disease at a tertiary hospital over a 16-year period whose follow-up endoscopy was available were enrolled. The patients were classified as endoscopic responders if they showed complete or partial improvement on follow-up endoscopy, and as endoscopic nonresponders if there was no improvement or worsening. CMV tissue clearance was defined as absence of any visible CMV inclusion bodies, negative CMV immunohistochemistry and negative CMV polymerase chain reaction in follow-up biopsy tissues. During the study period, 77 patients with UGI CMV disease were analyzed. The median time to follow-up endoscopy was 19 days (interquartile range, 14–27). Of these 77 patients, 52 (68%) were classified as responders, and the remaining 25 (32%) as nonresponders. GI bleeding was more common in the nonresponders than the responders (36% vs 12%, respectively; P = 0.02). There was no significant difference in CMV tissue clearance between the responders and nonresponders (56% vs 69%, respectively; P = 0.38), median durations of treatment (20 days vs 21 days, respectively; P = 0.48), and relapse rates (10% vs 8%, respectively; P > 0.99). Multivariate analysis showed that the only independent predictive factor for relapse of CMV antigenemia or CMV GI disease was multiorgan CMV disease (odds ratio = 12.4, 95% confidence interval 1.6–97.9; P = 0.02). Endoscopic responses were obtained in about two-thirds of patients with UGI CMV disease 2 or 3 weeks after antiviral therapy. However, these follow-up endoscopic findings neither reflected CMV tissue clearance nor predicted disease relapse. These findings suggest that the routine follow-up endoscopy may not be warranted in patients with UGI CMV disease. Wolters Kluwer Health 2016-05-13 /pmc/articles/PMC4902479/ /pubmed/27175637 http://dx.doi.org/10.1097/MD.0000000000003389 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 4900 Seo, Myeongsook Kim, Do Hoon Gong, Eun Jeong Ahn, Ji Yong Lee, Jeong Hoon Jung, Kee Wook Choi, Kee Don Song, Ho June Lee, Gin Hyug Jung, Hwoon-Yong Kim, Jin-Ho Lee, Sang-Oh Choi, Sang-Ho Kim, Yang Soo Woo, Jun Hee Kim, Sung-Han Is Follow-Up Endoscopy Necessary in Upper Gastrointestinal Cytomegalovirus Disease? |
title | Is Follow-Up Endoscopy Necessary in Upper Gastrointestinal Cytomegalovirus Disease? |
title_full | Is Follow-Up Endoscopy Necessary in Upper Gastrointestinal Cytomegalovirus Disease? |
title_fullStr | Is Follow-Up Endoscopy Necessary in Upper Gastrointestinal Cytomegalovirus Disease? |
title_full_unstemmed | Is Follow-Up Endoscopy Necessary in Upper Gastrointestinal Cytomegalovirus Disease? |
title_short | Is Follow-Up Endoscopy Necessary in Upper Gastrointestinal Cytomegalovirus Disease? |
title_sort | is follow-up endoscopy necessary in upper gastrointestinal cytomegalovirus disease? |
topic | 4900 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902479/ https://www.ncbi.nlm.nih.gov/pubmed/27175637 http://dx.doi.org/10.1097/MD.0000000000003389 |
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