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Etiologic spectrum and occurrence of coinfections in children hospitalized with community-acquired pneumonia
BACKGROUND: Co-infections are common in childhood community acquired pneumonia (CAP). However, their etiological pattern and clinical impact remains inconclusive. METHODS: Eight hundred forty-six consecutive children with CAP were evaluated prospectively for the presence of viral and bacterial patho...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738861/ https://www.ncbi.nlm.nih.gov/pubmed/29262797 http://dx.doi.org/10.1186/s12879-017-2891-x |
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author | Jiang, Wujun Wu, Min Zhou, Jing Wang, Yuqing Hao, Chuangli Ji, Wei Zhang, Xinxing Gu, Wenjing Shao, Xuejun |
author_facet | Jiang, Wujun Wu, Min Zhou, Jing Wang, Yuqing Hao, Chuangli Ji, Wei Zhang, Xinxing Gu, Wenjing Shao, Xuejun |
author_sort | Jiang, Wujun |
collection | PubMed |
description | BACKGROUND: Co-infections are common in childhood community acquired pneumonia (CAP). However, their etiological pattern and clinical impact remains inconclusive. METHODS: Eight hundred forty-six consecutive children with CAP were evaluated prospectively for the presence of viral and bacterial pathogens. Nasopharyngeal aspirates were examined by direct immunofluorescence assay or polymerase chain reaction (PCR) for viruses. PCR of nasopharyngeal aspirates and enzyme-linked immunosorbent assays were performed to detect M. pneumoniae. Bacteria was detected in blood, bronchoalveolar lavage specimen, or pleural fluid by culture. RESULTS: Causative pathogen was identified in 70.1% (593 of 846) of the patients. The most commonly detected pathogens were respiratory syncytial virus (RSV) (22.9%), human rhinovirus (HRV) (22.1%), M. pneumoniae (15.8%). Coinfection was identified in 34.6% (293 of 846) of the patients. The majority of these (209 [71.3%] of 293) were mixed viral-bacterial infections. Age < 6 months (odds ratio: 2.1; 95% confidence interval: 1.2–3.3) and admission of PICU (odds ratio: 12.5; 95% confidence interval: 1.6–97.4) were associated with mix infection. Patients with mix infection had a higher rate of PICU admission. CONCLUSIONS: The high mix infection burden in childhood CAP underscores a need for the enhancement of sensitive, inexpensive, and rapid diagnostics to accurately identify pneumonia pathogens. |
format | Online Article Text |
id | pubmed-5738861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57388612018-01-02 Etiologic spectrum and occurrence of coinfections in children hospitalized with community-acquired pneumonia Jiang, Wujun Wu, Min Zhou, Jing Wang, Yuqing Hao, Chuangli Ji, Wei Zhang, Xinxing Gu, Wenjing Shao, Xuejun BMC Infect Dis Research Article BACKGROUND: Co-infections are common in childhood community acquired pneumonia (CAP). However, their etiological pattern and clinical impact remains inconclusive. METHODS: Eight hundred forty-six consecutive children with CAP were evaluated prospectively for the presence of viral and bacterial pathogens. Nasopharyngeal aspirates were examined by direct immunofluorescence assay or polymerase chain reaction (PCR) for viruses. PCR of nasopharyngeal aspirates and enzyme-linked immunosorbent assays were performed to detect M. pneumoniae. Bacteria was detected in blood, bronchoalveolar lavage specimen, or pleural fluid by culture. RESULTS: Causative pathogen was identified in 70.1% (593 of 846) of the patients. The most commonly detected pathogens were respiratory syncytial virus (RSV) (22.9%), human rhinovirus (HRV) (22.1%), M. pneumoniae (15.8%). Coinfection was identified in 34.6% (293 of 846) of the patients. The majority of these (209 [71.3%] of 293) were mixed viral-bacterial infections. Age < 6 months (odds ratio: 2.1; 95% confidence interval: 1.2–3.3) and admission of PICU (odds ratio: 12.5; 95% confidence interval: 1.6–97.4) were associated with mix infection. Patients with mix infection had a higher rate of PICU admission. CONCLUSIONS: The high mix infection burden in childhood CAP underscores a need for the enhancement of sensitive, inexpensive, and rapid diagnostics to accurately identify pneumonia pathogens. BioMed Central 2017-12-20 /pmc/articles/PMC5738861/ /pubmed/29262797 http://dx.doi.org/10.1186/s12879-017-2891-x Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Jiang, Wujun Wu, Min Zhou, Jing Wang, Yuqing Hao, Chuangli Ji, Wei Zhang, Xinxing Gu, Wenjing Shao, Xuejun Etiologic spectrum and occurrence of coinfections in children hospitalized with community-acquired pneumonia |
title | Etiologic spectrum and occurrence of coinfections in children hospitalized with community-acquired pneumonia |
title_full | Etiologic spectrum and occurrence of coinfections in children hospitalized with community-acquired pneumonia |
title_fullStr | Etiologic spectrum and occurrence of coinfections in children hospitalized with community-acquired pneumonia |
title_full_unstemmed | Etiologic spectrum and occurrence of coinfections in children hospitalized with community-acquired pneumonia |
title_short | Etiologic spectrum and occurrence of coinfections in children hospitalized with community-acquired pneumonia |
title_sort | etiologic spectrum and occurrence of coinfections in children hospitalized with community-acquired pneumonia |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738861/ https://www.ncbi.nlm.nih.gov/pubmed/29262797 http://dx.doi.org/10.1186/s12879-017-2891-x |
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