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 |
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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 |
format | Article |
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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.</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. These results suggest that modulation of inflammatory responses is critical for the clinical management of children with ARDS.</description><subject>Bacterial Infections - blood</subject><subject>Bacterial Infections - immunology</subject><subject>Bacterial Infections - microbiology</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Coinfection - blood</subject><subject>Coinfection - immunology</subject><subject>Coinfection - microbiology</subject><subject>critical care</subject><subject>Cytokines - blood</subject><subject>Cytokines - immunology</subject><subject>Female</subject><subject>Hospitalization</subject><subject>Humans</subject><subject>IFN‐γ</subject><subject>Infant</subject><subject>Infections</subject><subject>Intensive Care Units, Pediatric</subject><subject>Lung - microbiology</subject><subject>Male</subject><subject>Mycoses - blood</subject><subject>Mycoses - immunology</subject><subject>Mycoses - microbiology</subject><subject>Original</subject><subject>Pathogens</subject><subject>pneumonia</subject><subject>Prognosis</subject><subject>Respiratory Distress Syndrome - blood</subject><subject>Respiratory Distress Syndrome - immunology</subject><subject>Respiratory Distress Syndrome - microbiology</subject><subject>Respiratory Tract Infections - blood</subject><subject>Respiratory Tract Infections - immunology</subject><subject>Respiratory Tract Infections - microbiology</subject><subject>respiratory virus infection</subject><subject>Trachea - microbiology</subject><subject>Virus Diseases - blood</subject><subject>Virus Diseases - immunology</subject><subject>Virus Diseases - microbiology</subject><issn>8755-6863</issn><issn>1099-0496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><recordid>eNp9kU1LxDAURYMoOo5u_AEScCdUkyZNk40gfsOAgx8bNyFN006kk9Sko_jvzTgqunH1Fu9w3uVdAPYwOsII5cd9v-iOcsIEXQMjjITIEBVsHYx4WRQZ44xsge0YnxFKO4E3wVbOS0QoZyPwNFXDzLfGwaiDMc66FipXwz741vk4WA0bpQcfIrQO6pnt6pDgNzvMYDSvJhh4end-D30DU4q5dyq8Qx9sa90O2GhUF83u1xyDx8uLh7PrbHJ7dXN2Osk0pZxmBjeizjUpK1UyTZXABaqrklFCdE0144SphnJREFQSLqqyyZscqypxVCGWkzE4WXn7RTU3tTZuCKqTfbDzFEZ6ZeXfjbMz2fpXWTBRMsGT4OBLEPzLwsRBPvtFcCmzxOksxxhTlqjDFaWDjzGY5ucCRnLZg1z2ID97SPD-70w_6PfjE4BXwJvtzPs_KjmdPk5W0g_YvZSV</recordid><startdate>201711</startdate><enddate>201711</enddate><creator>Phung, Thuy Thi Bich</creator><creator>Suzuki, Tadaki</creator><creator>Phan, Phuc Huu</creator><creator>Kawachi, Shoji</creator><creator>Furuya, Hiroyuki</creator><creator>Do, Huong Thu</creator><creator>Kageyama, Tsutomu</creator><creator>Ta, Tuan Anh</creator><creator>Dao, Nam Huu</creator><creator>Nunoi, Hiroyuki</creator><creator>Tran, Dien Minh</creator><creator>Le, Hai Thanh</creator><creator>Nakajima, Noriko</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1824-0603</orcidid></search><sort><creationdate>201711</creationdate><title>Pathogen screening and prognostic factors in children with severe ARDS of pulmonary origin</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4484-e1f9d2c37ba76c4a9150db76433cd4c6836af4895307389b7f2f21ab9154a0623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Bacterial Infections - blood</topic><topic>Bacterial Infections - immunology</topic><topic>Bacterial Infections - microbiology</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Coinfection - blood</topic><topic>Coinfection - immunology</topic><topic>Coinfection - microbiology</topic><topic>critical care</topic><topic>Cytokines - blood</topic><topic>Cytokines - immunology</topic><topic>Female</topic><topic>Hospitalization</topic><topic>Humans</topic><topic>IFN‐γ</topic><topic>Infant</topic><topic>Infections</topic><topic>Intensive Care Units, Pediatric</topic><topic>Lung - microbiology</topic><topic>Male</topic><topic>Mycoses - blood</topic><topic>Mycoses - immunology</topic><topic>Mycoses - microbiology</topic><topic>Original</topic><topic>Pathogens</topic><topic>pneumonia</topic><topic>Prognosis</topic><topic>Respiratory Distress Syndrome - blood</topic><topic>Respiratory Distress Syndrome - immunology</topic><topic>Respiratory Distress Syndrome - microbiology</topic><topic>Respiratory Tract Infections - blood</topic><topic>Respiratory Tract Infections - immunology</topic><topic>Respiratory Tract Infections - microbiology</topic><topic>respiratory virus infection</topic><topic>Trachea - microbiology</topic><topic>Virus Diseases - blood</topic><topic>Virus Diseases - immunology</topic><topic>Virus Diseases - microbiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Wiley-Blackwell Open Access Titles</collection><collection>Wiley Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & 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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