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Cytomegalovirus Diseases of the Gastrointestinal Tract

Cytomegalovirus (CMV) infection of the gastrointestinal (GI) tract can be fatal. However, very few studies have provided comprehensive analyses and specified the differences in symptoms observed in different parts of the GI tract. This study aimed to comprehensively analyze clinical manifestations a...

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Autores principales: Yeh, Pai-Jui, Wu, Ren-Chin, Chiu, Cheng-Tang, Lai, Ming-Wei, Chen, Chien-Ming, Pan, Yu-Bin, Su, Ming-Yao, Kuo, Chia-Jung, Lin, Wey-Ran, Le, Puo-Hsien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879032/
https://www.ncbi.nlm.nih.gov/pubmed/35215942
http://dx.doi.org/10.3390/v14020352
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author Yeh, Pai-Jui
Wu, Ren-Chin
Chiu, Cheng-Tang
Lai, Ming-Wei
Chen, Chien-Ming
Pan, Yu-Bin
Su, Ming-Yao
Kuo, Chia-Jung
Lin, Wey-Ran
Le, Puo-Hsien
author_facet Yeh, Pai-Jui
Wu, Ren-Chin
Chiu, Cheng-Tang
Lai, Ming-Wei
Chen, Chien-Ming
Pan, Yu-Bin
Su, Ming-Yao
Kuo, Chia-Jung
Lin, Wey-Ran
Le, Puo-Hsien
author_sort Yeh, Pai-Jui
collection PubMed
description Cytomegalovirus (CMV) infection of the gastrointestinal (GI) tract can be fatal. However, very few studies have provided comprehensive analyses and specified the differences in symptoms observed in different parts of the GI tract. This study aimed to comprehensively analyze clinical manifestations and management of GI CMV disease. This retrospective cohort study enrolled the patients who had CMV diseases of the GI tract proved by CMV immunohistochemistry stain from the pathology database in a 4000-bed tertiary medical center between January 2000 and May 2021. The patient characteristics, clinical manifestations, endoscopic features, treatments, outcomes, and prognostic factors were analyzed. A total of 356 patients were enrolled, including 46 infected in the esophagus, 76 in the stomach, 30 in the small intestine, and 204 in the colon. In total, 49.4% patients were immunocompromised. The overall in-hospital mortality rate was 20.8%: CMV enteritis had the highest rate (23.3%). Sixty percent of patients received antiviral treatment and 16% were administered both intravenous and oral anti-viral drugs (Combo therapy, minimal and mean treatment duration were 14 and 39.9 ± 25 days). Prognostic factors of in-hospital mortality included age, immune status, albumin level, platelet count, GI bleeding, time-to-diagnosis, and Combo therapy. In the survival analysis, immunocompetent patients receiving Combo therapy had the best survival curve, and immunocompromised patients receiving non-Combo therapy had the worst survival curve. Combo therapy ≥14 days resulted in a better outcome for both immunocompromised and immunocompetent patients. In conclusion, CMV GI diseases affect both immunocompromised and immunocompetent hosts, and a complete treatment course should be considered for patients with poor prognostic factors.
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spelling pubmed-88790322022-02-26 Cytomegalovirus Diseases of the Gastrointestinal Tract Yeh, Pai-Jui Wu, Ren-Chin Chiu, Cheng-Tang Lai, Ming-Wei Chen, Chien-Ming Pan, Yu-Bin Su, Ming-Yao Kuo, Chia-Jung Lin, Wey-Ran Le, Puo-Hsien Viruses Article Cytomegalovirus (CMV) infection of the gastrointestinal (GI) tract can be fatal. However, very few studies have provided comprehensive analyses and specified the differences in symptoms observed in different parts of the GI tract. This study aimed to comprehensively analyze clinical manifestations and management of GI CMV disease. This retrospective cohort study enrolled the patients who had CMV diseases of the GI tract proved by CMV immunohistochemistry stain from the pathology database in a 4000-bed tertiary medical center between January 2000 and May 2021. The patient characteristics, clinical manifestations, endoscopic features, treatments, outcomes, and prognostic factors were analyzed. A total of 356 patients were enrolled, including 46 infected in the esophagus, 76 in the stomach, 30 in the small intestine, and 204 in the colon. In total, 49.4% patients were immunocompromised. The overall in-hospital mortality rate was 20.8%: CMV enteritis had the highest rate (23.3%). Sixty percent of patients received antiviral treatment and 16% were administered both intravenous and oral anti-viral drugs (Combo therapy, minimal and mean treatment duration were 14 and 39.9 ± 25 days). Prognostic factors of in-hospital mortality included age, immune status, albumin level, platelet count, GI bleeding, time-to-diagnosis, and Combo therapy. In the survival analysis, immunocompetent patients receiving Combo therapy had the best survival curve, and immunocompromised patients receiving non-Combo therapy had the worst survival curve. Combo therapy ≥14 days resulted in a better outcome for both immunocompromised and immunocompetent patients. In conclusion, CMV GI diseases affect both immunocompromised and immunocompetent hosts, and a complete treatment course should be considered for patients with poor prognostic factors. MDPI 2022-02-08 /pmc/articles/PMC8879032/ /pubmed/35215942 http://dx.doi.org/10.3390/v14020352 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yeh, Pai-Jui
Wu, Ren-Chin
Chiu, Cheng-Tang
Lai, Ming-Wei
Chen, Chien-Ming
Pan, Yu-Bin
Su, Ming-Yao
Kuo, Chia-Jung
Lin, Wey-Ran
Le, Puo-Hsien
Cytomegalovirus Diseases of the Gastrointestinal Tract
title Cytomegalovirus Diseases of the Gastrointestinal Tract
title_full Cytomegalovirus Diseases of the Gastrointestinal Tract
title_fullStr Cytomegalovirus Diseases of the Gastrointestinal Tract
title_full_unstemmed Cytomegalovirus Diseases of the Gastrointestinal Tract
title_short Cytomegalovirus Diseases of the Gastrointestinal Tract
title_sort cytomegalovirus diseases of the gastrointestinal tract
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879032/
https://www.ncbi.nlm.nih.gov/pubmed/35215942
http://dx.doi.org/10.3390/v14020352
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