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Clinical characteristics and outcomes of severe rhinovirus-associated pneumonia identified by bronchoscopic bronchoalveolar lavage in adults: Comparison with severe influenza virus-associated pneumonia

BACKGROUND: Rhinoviruses (RVs) may cause pneumonia, but the characteristics of RV-associated pneumonia have not been adequately evaluated. OBJECTIVE: We aimed to compare characteristics, complications, and outcomes between severe RV- and influenza virus (IFV)-associated pneumonia in adults. STUDY DE...

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Autores principales: Choi, Sang-Ho, Huh, Jin Won, Hong, Sang-Bum, Lee, Ju Young, Kim, Sung-Han, Sung, Heungsup, Do, Kyung-Hyun, Lee, Sang-Oh, Kim, Mi-Na, Jeong, Jin-Yong, Lim, Chae-Man, Kim, Yang Soo, Woo, Jun Hee, Koh, Younsuck
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106464/
https://www.ncbi.nlm.nih.gov/pubmed/25542469
http://dx.doi.org/10.1016/j.jcv.2014.11.010
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author Choi, Sang-Ho
Huh, Jin Won
Hong, Sang-Bum
Lee, Ju Young
Kim, Sung-Han
Sung, Heungsup
Do, Kyung-Hyun
Lee, Sang-Oh
Kim, Mi-Na
Jeong, Jin-Yong
Lim, Chae-Man
Kim, Yang Soo
Woo, Jun Hee
Koh, Younsuck
author_facet Choi, Sang-Ho
Huh, Jin Won
Hong, Sang-Bum
Lee, Ju Young
Kim, Sung-Han
Sung, Heungsup
Do, Kyung-Hyun
Lee, Sang-Oh
Kim, Mi-Na
Jeong, Jin-Yong
Lim, Chae-Man
Kim, Yang Soo
Woo, Jun Hee
Koh, Younsuck
author_sort Choi, Sang-Ho
collection PubMed
description BACKGROUND: Rhinoviruses (RVs) may cause pneumonia, but the characteristics of RV-associated pneumonia have not been adequately evaluated. OBJECTIVE: We aimed to compare characteristics, complications, and outcomes between severe RV- and influenza virus (IFV)-associated pneumonia in adults. STUDY DESIGN: We used prospective cohort data of adult patients with severe pneumonia who had been admitted to the medical intensive care unit of a tertiary care hospital over a 4-year period. The clinical features and outcomes of 27 patients with RV-positive bronchoscopic bronchoalveolar lavage (BAL) fluid were compared to those of 51 pneumonia patients with IFV-positive BAL fluid or IFV-positive nasopharyngeal specimens. RESULTS: Of 356 patients who underwent bronchoscopic BAL and respiratory virus polymerase chain reaction (PCR), RV was the most commonly identified virus (8.1%) from BAL fluid. Patients with RV-associated pneumonia were more likely to be immunocompromised than patients with IFV-associated pneumonia (81.5% vs. 33.3%, p < 0.001). Bacterial coinfection tended to be less common in the RV group (18.5% vs. 37.3%, p = 0.09). Although septic shock was less common in the RV group (29.6% vs. 54.9%, p = 0.03), other clinical manifestations, laboratory findings, and radiologic patterns were similar between the groups. The 28-day mortality of patients with severe RV- and IFV-associated pneumonia was similarly high (29.6% vs. 35.3% respectively, p = 0.61). CONCLUSIONS: Severe RV-associated pneumonia patients were more likely to be immunocompromised and less likely to present septic shock. Overall clinical features were similar and mortalities of both groups were comparably high. Studies of larger cohorts encompassing mild to moderate pneumonia patients are needed.
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spelling pubmed-71064642020-03-31 Clinical characteristics and outcomes of severe rhinovirus-associated pneumonia identified by bronchoscopic bronchoalveolar lavage in adults: Comparison with severe influenza virus-associated pneumonia Choi, Sang-Ho Huh, Jin Won Hong, Sang-Bum Lee, Ju Young Kim, Sung-Han Sung, Heungsup Do, Kyung-Hyun Lee, Sang-Oh Kim, Mi-Na Jeong, Jin-Yong Lim, Chae-Man Kim, Yang Soo Woo, Jun Hee Koh, Younsuck J Clin Virol Article BACKGROUND: Rhinoviruses (RVs) may cause pneumonia, but the characteristics of RV-associated pneumonia have not been adequately evaluated. OBJECTIVE: We aimed to compare characteristics, complications, and outcomes between severe RV- and influenza virus (IFV)-associated pneumonia in adults. STUDY DESIGN: We used prospective cohort data of adult patients with severe pneumonia who had been admitted to the medical intensive care unit of a tertiary care hospital over a 4-year period. The clinical features and outcomes of 27 patients with RV-positive bronchoscopic bronchoalveolar lavage (BAL) fluid were compared to those of 51 pneumonia patients with IFV-positive BAL fluid or IFV-positive nasopharyngeal specimens. RESULTS: Of 356 patients who underwent bronchoscopic BAL and respiratory virus polymerase chain reaction (PCR), RV was the most commonly identified virus (8.1%) from BAL fluid. Patients with RV-associated pneumonia were more likely to be immunocompromised than patients with IFV-associated pneumonia (81.5% vs. 33.3%, p < 0.001). Bacterial coinfection tended to be less common in the RV group (18.5% vs. 37.3%, p = 0.09). Although septic shock was less common in the RV group (29.6% vs. 54.9%, p = 0.03), other clinical manifestations, laboratory findings, and radiologic patterns were similar between the groups. The 28-day mortality of patients with severe RV- and IFV-associated pneumonia was similarly high (29.6% vs. 35.3% respectively, p = 0.61). CONCLUSIONS: Severe RV-associated pneumonia patients were more likely to be immunocompromised and less likely to present septic shock. Overall clinical features were similar and mortalities of both groups were comparably high. Studies of larger cohorts encompassing mild to moderate pneumonia patients are needed. Elsevier B.V. 2015-01 2014-11-15 /pmc/articles/PMC7106464/ /pubmed/25542469 http://dx.doi.org/10.1016/j.jcv.2014.11.010 Text en Copyright © 2014 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Choi, Sang-Ho
Huh, Jin Won
Hong, Sang-Bum
Lee, Ju Young
Kim, Sung-Han
Sung, Heungsup
Do, Kyung-Hyun
Lee, Sang-Oh
Kim, Mi-Na
Jeong, Jin-Yong
Lim, Chae-Man
Kim, Yang Soo
Woo, Jun Hee
Koh, Younsuck
Clinical characteristics and outcomes of severe rhinovirus-associated pneumonia identified by bronchoscopic bronchoalveolar lavage in adults: Comparison with severe influenza virus-associated pneumonia
title Clinical characteristics and outcomes of severe rhinovirus-associated pneumonia identified by bronchoscopic bronchoalveolar lavage in adults: Comparison with severe influenza virus-associated pneumonia
title_full Clinical characteristics and outcomes of severe rhinovirus-associated pneumonia identified by bronchoscopic bronchoalveolar lavage in adults: Comparison with severe influenza virus-associated pneumonia
title_fullStr Clinical characteristics and outcomes of severe rhinovirus-associated pneumonia identified by bronchoscopic bronchoalveolar lavage in adults: Comparison with severe influenza virus-associated pneumonia
title_full_unstemmed Clinical characteristics and outcomes of severe rhinovirus-associated pneumonia identified by bronchoscopic bronchoalveolar lavage in adults: Comparison with severe influenza virus-associated pneumonia
title_short Clinical characteristics and outcomes of severe rhinovirus-associated pneumonia identified by bronchoscopic bronchoalveolar lavage in adults: Comparison with severe influenza virus-associated pneumonia
title_sort clinical characteristics and outcomes of severe rhinovirus-associated pneumonia identified by bronchoscopic bronchoalveolar lavage in adults: comparison with severe influenza virus-associated pneumonia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106464/
https://www.ncbi.nlm.nih.gov/pubmed/25542469
http://dx.doi.org/10.1016/j.jcv.2014.11.010
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