Pathogen screening and prognostic factors in children with severe ARDS of pulmonary origin

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 inves...

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Veröffentlicht in:Pediatric pulmonology 2017-11, Vol.52 (11), p.1469-1477
Hauptverfasser: Phung, Thuy Thi Bich, Suzuki, Tadaki, Phan, Phuc Huu, Kawachi, Shoji, Furuya, Hiroyuki, Do, Huong Thu, Kageyama, Tsutomu, Ta, Tuan Anh, Dao, Nam Huu, Nunoi, Hiroyuki, Tran, Dien Minh, Le, Hai Thanh, Nakajima, Noriko
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container_end_page 1477
container_issue 11
container_start_page 1469
container_title Pediatric pulmonology
container_volume 52
creator Phung, Thuy Thi Bich
Suzuki, Tadaki
Phan, Phuc Huu
Kawachi, Shoji
Furuya, Hiroyuki
Do, Huong Thu
Kageyama, Tsutomu
Ta, Tuan Anh
Dao, Nam Huu
Nunoi, Hiroyuki
Tran, Dien Minh
Le, Hai Thanh
Nakajima, Noriko
description 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.
doi_str_mv 10.1002/ppul.23694
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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.</description><identifier>ISSN: 8755-6863</identifier><identifier>EISSN: 1099-0496</identifier><identifier>DOI: 10.1002/ppul.23694</identifier><identifier>PMID: 28703486</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Bacterial Infections - blood ; Bacterial Infections - immunology ; Bacterial Infections - microbiology ; Child ; Child, Preschool ; Coinfection - blood ; Coinfection - immunology ; Coinfection - microbiology ; critical care ; Cytokines - blood ; Cytokines - immunology ; Female ; Hospitalization ; Humans ; IFN‐γ ; Infant ; Infections ; Intensive Care Units, Pediatric ; Lung - microbiology ; Male ; Mycoses - blood ; Mycoses - immunology ; Mycoses - microbiology ; Original ; Pathogens ; pneumonia ; Prognosis ; Respiratory Distress Syndrome - blood ; Respiratory Distress Syndrome - immunology ; Respiratory Distress Syndrome - microbiology ; Respiratory Tract Infections - blood ; Respiratory Tract Infections - immunology ; Respiratory Tract Infections - microbiology ; respiratory virus infection ; Trachea - microbiology ; Virus Diseases - blood ; Virus Diseases - immunology ; Virus Diseases - microbiology</subject><ispartof>Pediatric pulmonology, 2017-11, Vol.52 (11), p.1469-1477</ispartof><rights>2017 The Authors. Published by Wiley Periodicals, Inc.</rights><rights>2017 The Authors. Pediatric Pulmonology Published by Wiley Periodicals, Inc.</rights><rights>2017 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4484-e1f9d2c37ba76c4a9150db76433cd4c6836af4895307389b7f2f21ab9154a0623</citedby><cites>FETCH-LOGICAL-c4484-e1f9d2c37ba76c4a9150db76433cd4c6836af4895307389b7f2f21ab9154a0623</cites><orcidid>0000-0003-1824-0603</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fppul.23694$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fppul.23694$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,1417,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28703486$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Phung, Thuy Thi Bich</creatorcontrib><creatorcontrib>Suzuki, Tadaki</creatorcontrib><creatorcontrib>Phan, Phuc Huu</creatorcontrib><creatorcontrib>Kawachi, Shoji</creatorcontrib><creatorcontrib>Furuya, Hiroyuki</creatorcontrib><creatorcontrib>Do, Huong Thu</creatorcontrib><creatorcontrib>Kageyama, Tsutomu</creatorcontrib><creatorcontrib>Ta, Tuan Anh</creatorcontrib><creatorcontrib>Dao, Nam Huu</creatorcontrib><creatorcontrib>Nunoi, Hiroyuki</creatorcontrib><creatorcontrib>Tran, Dien Minh</creatorcontrib><creatorcontrib>Le, Hai Thanh</creatorcontrib><creatorcontrib>Nakajima, Noriko</creatorcontrib><title>Pathogen screening and prognostic factors in children with severe ARDS of pulmonary origin</title><title>Pediatric pulmonology</title><addtitle>Pediatr Pulmonol</addtitle><description>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. 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Medical Complete (Alumni)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Pediatric pulmonology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Phung, Thuy Thi Bich</au><au>Suzuki, Tadaki</au><au>Phan, Phuc Huu</au><au>Kawachi, Shoji</au><au>Furuya, Hiroyuki</au><au>Do, Huong Thu</au><au>Kageyama, Tsutomu</au><au>Ta, Tuan Anh</au><au>Dao, Nam Huu</au><au>Nunoi, Hiroyuki</au><au>Tran, Dien Minh</au><au>Le, Hai Thanh</au><au>Nakajima, Noriko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pathogen screening and prognostic factors in children with severe ARDS of pulmonary origin</atitle><jtitle>Pediatric pulmonology</jtitle><addtitle>Pediatr Pulmonol</addtitle><date>2017-11</date><risdate>2017</risdate><volume>52</volume><issue>11</issue><spage>1469</spage><epage>1477</epage><pages>1469-1477</pages><issn>8755-6863</issn><eissn>1099-0496</eissn><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.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28703486</pmid><doi>10.1002/ppul.23694</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-1824-0603</orcidid><oa>free_for_read</oa></addata></record>
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subjects Bacterial Infections - blood
Bacterial Infections - immunology
Bacterial Infections - microbiology
Child
Child, Preschool
Coinfection - blood
Coinfection - immunology
Coinfection - microbiology
critical care
Cytokines - blood
Cytokines - immunology
Female
Hospitalization
Humans
IFN‐γ
Infant
Infections
Intensive Care Units, Pediatric
Lung - microbiology
Male
Mycoses - blood
Mycoses - immunology
Mycoses - microbiology
Original
Pathogens
pneumonia
Prognosis
Respiratory Distress Syndrome - blood
Respiratory Distress Syndrome - immunology
Respiratory Distress Syndrome - microbiology
Respiratory Tract Infections - blood
Respiratory Tract Infections - immunology
Respiratory Tract Infections - microbiology
respiratory virus infection
Trachea - microbiology
Virus Diseases - blood
Virus Diseases - immunology
Virus Diseases - microbiology
title Pathogen screening and prognostic factors in children with severe ARDS of pulmonary origin
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