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2645. Severe Human Parainfluenza Virus-associated Pneumonia in Adults, Seoul, South Korea, 2010-2019
BACKGROUND: Human parainfluenza virus (HPIV) is a major cause of acute respiratory tract infections such as croup in children and pneumonia in immunocompromised patients. HPIV infections are generally regarded as mild and self-limiting in adults, however, HPIV-associated pneumonia is increasingly re...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677876/ http://dx.doi.org/10.1093/ofid/ofad500.2257 |
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author | Park, Joung Ha Hong, Sang-Bum Huh, Jin Won Jung, Jiwon Kim, Min Jae Chong, Yong Pil Sung, Heungsup Doh, Kyung Hyun Kim, Sung-Han Lee, Sang-Oh Kim, Yang Soo Lim, Chae-Man Koh, Younsuck Choi, Sang-Ho |
author_facet | Park, Joung Ha Hong, Sang-Bum Huh, Jin Won Jung, Jiwon Kim, Min Jae Chong, Yong Pil Sung, Heungsup Doh, Kyung Hyun Kim, Sung-Han Lee, Sang-Oh Kim, Yang Soo Lim, Chae-Man Koh, Younsuck Choi, Sang-Ho |
author_sort | Park, Joung Ha |
collection | PubMed |
description | BACKGROUND: Human parainfluenza virus (HPIV) is a major cause of acute respiratory tract infections such as croup in children and pneumonia in immunocompromised patients. HPIV infections are generally regarded as mild and self-limiting in adults, however, HPIV-associated pneumonia is increasingly reported in adults. To the best of our knowledge, data on the epidemiological and clinical characteristics of severe HPIV-associated pneumonia in adults are limited. Therefore, we investigated the epidemiological and clinical characteristics and outcomes of severe HPIV-associated pneumonia over ten years in a large cohort of critically ill adults with severe pneumonia requiring intensive care. METHODS: This sutdy was performed as a part of a prospective observational cohort study regarding severe virus-associated pneumonia at the 28-bed medical intensive care unit (ICU) at a 2,700-bed hospital, in Seoul, South Korea. Patients with severe HPIV-associated pneumonia were enrolled in this study, and the clinical data of these patients were analyzed. To describe the clinical outcomes of severe HPIV-associated pneumonia, we compared the HPIV-associated pneumonia outcomes with those of severe influenza virus-associated pneumonia. RESULTS: A total of 143 adult patients with severe HPIV-associated pneumonia were identified. HPIV is the most common cause (25.2%) of severe viral hospital-acquired pneumonia (HAP), and it is the third most common cause (15.7%) of severe viral community-acquired pneumonia. The median age of the patients was 61.6 years old. Almost patients (97.2%) had comorbidities, and hematologic malignancy (35.0%), diabetes mellitus (23.8%), and structural lung disease (21.0%) were common cormobidities. About half of the patients (54.5%) had co-infections at the time of ICU admission. The 90-day mortality was comparable with that of severe influenza virus-associated pneumonia (55.2% vs 48.4%, p = 0.22). The use of ribavirin was not associated with lower mortality. Fungal co-infections were associated with higher mortality (82.4% [14/17]). [Figure: see text] [Figure: see text] CONCLUSION: In conclusion, HPIV was the leading cause of severe viral HAP with substantial mortality, comparable to that of influenza virus-associated penumonia. Fungal co-infections contributed to the high mortality rates. DISCLOSURES: All Authors: No reported disclosures |
format | Online Article Text |
id | pubmed-10677876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106778762023-11-27 2645. Severe Human Parainfluenza Virus-associated Pneumonia in Adults, Seoul, South Korea, 2010-2019 Park, Joung Ha Hong, Sang-Bum Huh, Jin Won Jung, Jiwon Kim, Min Jae Chong, Yong Pil Sung, Heungsup Doh, Kyung Hyun Kim, Sung-Han Lee, Sang-Oh Kim, Yang Soo Lim, Chae-Man Koh, Younsuck Choi, Sang-Ho Open Forum Infect Dis Abstract BACKGROUND: Human parainfluenza virus (HPIV) is a major cause of acute respiratory tract infections such as croup in children and pneumonia in immunocompromised patients. HPIV infections are generally regarded as mild and self-limiting in adults, however, HPIV-associated pneumonia is increasingly reported in adults. To the best of our knowledge, data on the epidemiological and clinical characteristics of severe HPIV-associated pneumonia in adults are limited. Therefore, we investigated the epidemiological and clinical characteristics and outcomes of severe HPIV-associated pneumonia over ten years in a large cohort of critically ill adults with severe pneumonia requiring intensive care. METHODS: This sutdy was performed as a part of a prospective observational cohort study regarding severe virus-associated pneumonia at the 28-bed medical intensive care unit (ICU) at a 2,700-bed hospital, in Seoul, South Korea. Patients with severe HPIV-associated pneumonia were enrolled in this study, and the clinical data of these patients were analyzed. To describe the clinical outcomes of severe HPIV-associated pneumonia, we compared the HPIV-associated pneumonia outcomes with those of severe influenza virus-associated pneumonia. RESULTS: A total of 143 adult patients with severe HPIV-associated pneumonia were identified. HPIV is the most common cause (25.2%) of severe viral hospital-acquired pneumonia (HAP), and it is the third most common cause (15.7%) of severe viral community-acquired pneumonia. The median age of the patients was 61.6 years old. Almost patients (97.2%) had comorbidities, and hematologic malignancy (35.0%), diabetes mellitus (23.8%), and structural lung disease (21.0%) were common cormobidities. About half of the patients (54.5%) had co-infections at the time of ICU admission. The 90-day mortality was comparable with that of severe influenza virus-associated pneumonia (55.2% vs 48.4%, p = 0.22). The use of ribavirin was not associated with lower mortality. Fungal co-infections were associated with higher mortality (82.4% [14/17]). [Figure: see text] [Figure: see text] CONCLUSION: In conclusion, HPIV was the leading cause of severe viral HAP with substantial mortality, comparable to that of influenza virus-associated penumonia. Fungal co-infections contributed to the high mortality rates. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10677876/ http://dx.doi.org/10.1093/ofid/ofad500.2257 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Abstract Park, Joung Ha Hong, Sang-Bum Huh, Jin Won Jung, Jiwon Kim, Min Jae Chong, Yong Pil Sung, Heungsup Doh, Kyung Hyun Kim, Sung-Han Lee, Sang-Oh Kim, Yang Soo Lim, Chae-Man Koh, Younsuck Choi, Sang-Ho 2645. Severe Human Parainfluenza Virus-associated Pneumonia in Adults, Seoul, South Korea, 2010-2019 |
title | 2645. Severe Human Parainfluenza Virus-associated Pneumonia in Adults, Seoul, South Korea, 2010-2019 |
title_full | 2645. Severe Human Parainfluenza Virus-associated Pneumonia in Adults, Seoul, South Korea, 2010-2019 |
title_fullStr | 2645. Severe Human Parainfluenza Virus-associated Pneumonia in Adults, Seoul, South Korea, 2010-2019 |
title_full_unstemmed | 2645. Severe Human Parainfluenza Virus-associated Pneumonia in Adults, Seoul, South Korea, 2010-2019 |
title_short | 2645. Severe Human Parainfluenza Virus-associated Pneumonia in Adults, Seoul, South Korea, 2010-2019 |
title_sort | 2645. severe human parainfluenza virus-associated pneumonia in adults, seoul, south korea, 2010-2019 |
topic | Abstract |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677876/ http://dx.doi.org/10.1093/ofid/ofad500.2257 |
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