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Characteristics of Adenovirus Pneumonia in Korean Military Personnel, 2012–2016
Adenovirus (AdV) can cause severe pneumonia in non-immunocompromised host, but limited data exist on the distinctive characteristics of AdV pneumonia in non-immunocompromised patients. We evaluated distinctive clinico-laboratory and radiological characteristics and outcomes of AdV pneumonia (n = 179...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Academy of Medical Sciences
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5219995/ https://www.ncbi.nlm.nih.gov/pubmed/28049240 http://dx.doi.org/10.3346/jkms.2017.32.2.287 |
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author | Yoon, Hee Jhun, Byung Woo Kim, Hojoong Yoo, Hongseok Park, Sung Bum |
author_facet | Yoon, Hee Jhun, Byung Woo Kim, Hojoong Yoo, Hongseok Park, Sung Bum |
author_sort | Yoon, Hee |
collection | PubMed |
description | Adenovirus (AdV) can cause severe pneumonia in non-immunocompromised host, but limited data exist on the distinctive characteristics of AdV pneumonia in non-immunocompromised patients. We evaluated distinctive clinico-laboratory and radiological characteristics and outcomes of AdV pneumonia (n = 179), compared with non-AdV pneumonia (n = 188) in Korean military personnel between 2012 and 2016. AdV pneumonia patients had a higher rate of consolidation with ground-glass opacity (101/152) in lobar distribution (89/152) on computed tomography (CT) (P < 0.001). Laboratory findings showed a higher incidence of unusual blood profiles such as leukopenia (55/179, P < 0.001) or thrombocytopenia (100/179, P < 0.001). The patients had more systemic symptoms such as myalgia (82/179, P = 0.001) or diarrhea (23/179, P < 0.001), compared with non-AdV pneumonia patients. Bacterial co-infection was identified in 28.5% of AdV pneumonia. Most of the AdV isolates typed (69/72, 95.8%) were AdV-55. Patients with a pneumonia severity index ≥ class III were more commonly observed in AdV pneumonia patients compared with non-AdV pneumonia patients (11.2% vs. 2.1%, P < 0.001), and time to clinical stabilization from admission was longer in the AdV pneumonia patients compared with the non-AdV pneumonia patients (3.8 vs. 2.6 days, P < 0.001). Mechanical ventilation (n = 6) was only required in AdV pneumonia patients, one of whom died due to AdV-55. Our data showed that AdV pneumonia in non-immunocompromised patients had distinct characteristics and most of the isolates typed in our study were AdV-55. It is suggested that AdV-55 is an important pathogen of pneumonia in Korean military personnel. |
format | Online Article Text |
id | pubmed-5219995 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Korean Academy of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-52199952017-02-01 Characteristics of Adenovirus Pneumonia in Korean Military Personnel, 2012–2016 Yoon, Hee Jhun, Byung Woo Kim, Hojoong Yoo, Hongseok Park, Sung Bum J Korean Med Sci Original Article Adenovirus (AdV) can cause severe pneumonia in non-immunocompromised host, but limited data exist on the distinctive characteristics of AdV pneumonia in non-immunocompromised patients. We evaluated distinctive clinico-laboratory and radiological characteristics and outcomes of AdV pneumonia (n = 179), compared with non-AdV pneumonia (n = 188) in Korean military personnel between 2012 and 2016. AdV pneumonia patients had a higher rate of consolidation with ground-glass opacity (101/152) in lobar distribution (89/152) on computed tomography (CT) (P < 0.001). Laboratory findings showed a higher incidence of unusual blood profiles such as leukopenia (55/179, P < 0.001) or thrombocytopenia (100/179, P < 0.001). The patients had more systemic symptoms such as myalgia (82/179, P = 0.001) or diarrhea (23/179, P < 0.001), compared with non-AdV pneumonia patients. Bacterial co-infection was identified in 28.5% of AdV pneumonia. Most of the AdV isolates typed (69/72, 95.8%) were AdV-55. Patients with a pneumonia severity index ≥ class III were more commonly observed in AdV pneumonia patients compared with non-AdV pneumonia patients (11.2% vs. 2.1%, P < 0.001), and time to clinical stabilization from admission was longer in the AdV pneumonia patients compared with the non-AdV pneumonia patients (3.8 vs. 2.6 days, P < 0.001). Mechanical ventilation (n = 6) was only required in AdV pneumonia patients, one of whom died due to AdV-55. Our data showed that AdV pneumonia in non-immunocompromised patients had distinct characteristics and most of the isolates typed in our study were AdV-55. It is suggested that AdV-55 is an important pathogen of pneumonia in Korean military personnel. The Korean Academy of Medical Sciences 2017-02 2016-12-01 /pmc/articles/PMC5219995/ /pubmed/28049240 http://dx.doi.org/10.3346/jkms.2017.32.2.287 Text en © 2017 The Korean Academy of Medical Sciences. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Yoon, Hee Jhun, Byung Woo Kim, Hojoong Yoo, Hongseok Park, Sung Bum Characteristics of Adenovirus Pneumonia in Korean Military Personnel, 2012–2016 |
title | Characteristics of Adenovirus Pneumonia in Korean Military Personnel, 2012–2016 |
title_full | Characteristics of Adenovirus Pneumonia in Korean Military Personnel, 2012–2016 |
title_fullStr | Characteristics of Adenovirus Pneumonia in Korean Military Personnel, 2012–2016 |
title_full_unstemmed | Characteristics of Adenovirus Pneumonia in Korean Military Personnel, 2012–2016 |
title_short | Characteristics of Adenovirus Pneumonia in Korean Military Personnel, 2012–2016 |
title_sort | characteristics of adenovirus pneumonia in korean military personnel, 2012–2016 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5219995/ https://www.ncbi.nlm.nih.gov/pubmed/28049240 http://dx.doi.org/10.3346/jkms.2017.32.2.287 |
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