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About:
Pathogen screening and prognostic factors in children with severe ARDS of pulmonary origin
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An Entity of Type :
schema:ScholarlyArticle
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wasabi.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
title
Pathogen screening and prognostic factors in children with severe ARDS of pulmonary origin
Creator
Kageyama, Tsutomu
Suzuki, Tadaki
Nakajima, Noriko
Furuya, Hiroyuki
Kawachi, Shoji
Nunoi, Hiroyuki
Bich, Thuy
Dao, Huu
Dien, |
Do Msc, Thu
Hai, |
Huong, |
Le, Thanh
Nam, |
Phan, Huu
Phd, Phung
Phuc, |
Ta, Anh
Tran, Minh
Tuan, |
source
Medline; PMC
abstract
BACKGROUND: Acute respiratory distress syndrome (ARDS) is one of the most lethal diseases encountered in the pediatric intensive care unit (PICU). The etiological pathogens and prognostic factors of severe ARDS of pulmonary origin in children with respiratory virus infections were prospectively investigated. METHODS: Enrolled children fulfilled the following criteria: (1) PICU admission; (2) age of 1 month to 16 years; (3) diagnosis of infectious pneumonia and respiratory virus infection; and (4) development of severe ARDS within 72 h after PICU admission. Pathogens were detected in the blood and tracheal lavage fluid using molecular techniques and a conventional culture system. The serum levels of inflammatory mediators on the day of PICU admission were examined. RESULTS: Fifty‐seven patients (32 boys; median age, 9 months) were enrolled. Multiple virus infections, co‐infection with bacteria/fungus, and bacteremia/fungemia were observed in 60%, 49%, and 32% of children, respectively. Adenovirus‐B, measles virus, and cytomegalovirus were detected predominantly in tracheal lavage fluid. There were no statistically significant differences between non‐survivors and survivors regarding the types of pathogen, incidence of multiple virus infection, gender, age, clinical features, and treatment. The serum levels of interferon (IFN)‐γ and the IFN‐γ/interleukin (IL)‐10 ratio were higher in non‐survivors. CONCLUSIONS: IFN‐γ upregulation as detected on the day of PICU admission was found to be one of the possible prognostic factors affecting a fatal outcome. These results suggest that modulation of inflammatory responses is critical for the clinical management of children with ARDS.
has issue date
2017-07-13
(
xsd:dateTime
)
bibo:doi
10.1002/ppul.23694
bibo:pmid
28703486
has license
cc-by-nc
sha1sum (hex)
82dcb53e236df1adb5c3c9f5291dc4e8eabb354a
schema:url
https://doi.org/10.1002/ppul.23694
resource representing a document's title
Pathogen screening and prognostic factors in children with severe ARDS of pulmonary origin
has PubMed Central identifier
PMC5697698
has PubMed identifier
28703486
schema:publication
Pediatr Pulmonol
resource representing a document's body
covid:82dcb53e236df1adb5c3c9f5291dc4e8eabb354a#body_text
is
schema:about
of
named entity 'pediatric intensive care unit'
named entity 'clinical management'
named entity 'lavage'
named entity 'investigated'
named entity 'Methods'
named entity 'factors'
named entity 'diseases'
named entity 'features'
named entity 'age'
named entity 'interleukin'
named entity 'ARDS'
covid:arg/82dcb53e236df1adb5c3c9f5291dc4e8eabb354a
named entity 'inflammatory mediators'
named entity 'conventional'
named entity 'measles virus'
named entity 'median age'
named entity 'Acute respiratory distress syndrome (ARDS)'
named entity 'IFN-γ'
named entity 'factors'
named entity 'day'
named entity 'statistically'
named entity 'admission'
named entity 'respiratory'
named entity 'severe'
named entity 'Acute respiratory distress syndrome'
named entity 'tracheal'
named entity 'statistically significant'
named entity 'co-infection'
named entity 'IFN-γ'
named entity 'pathogen'
named entity 'molecular techniques'
named entity 'PICU'
named entity 'interferon (IFN)-γ'
named entity 'pediatric intensive care unit'
named entity 'inflammatory mediators'
named entity 'etiological'
named entity 'virus infection'
named entity 'serum levels'
named entity 'bacteremia'
named entity 'Pathogen'
named entity 'ARDS'
named entity 'lethal'
named entity 'diagnosis'
named entity 'IFN-γ'
named entity 'IL-10'
named entity 'immunoglobulin'
named entity 'IL-10'
named entity 'PICU'
named entity 'measles'
named entity 'immunocompetent'
named entity 'fungemia'
named entity 'IFN-γ'
named entity 'ARDS'
named entity 'chemokines'
named entity 'Cytokines'
named entity 'PEEP'
named entity 'serum levels'
named entity 'anti-inflammatory'
named entity 'mm Hg'
named entity 'ARDS'
named entity 'sample size'
named entity 'R-squared'
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