New parameters for childhood ventilator associated pneumonia diagnosis

Summary Purpose Our aim is to determine whether the presence of soluble triggering receptor expressed on myeloid cells‐1 (s‐TREM‐1) of bronchoalveolar lavage fluid (BALF), serum procalcitonin levels (PCT), and Clinical Pulmonary Infection Score (CPIS) have diagnostic value in children with VAP. Meth...

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Veröffentlicht in:Pediatric pulmonology 2017-01, Vol.52 (1), p.119-128
Hauptverfasser: İşgüder, Rana, Ceylan, Gökhan, Ağın, Hasan, Gülfidan, Gamze, Ayhan, Yüce, Devrim, İlker
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container_end_page 128
container_issue 1
container_start_page 119
container_title Pediatric pulmonology
container_volume 52
creator İşgüder, Rana
Ceylan, Gökhan
Ağın, Hasan
Gülfidan, Gamze
Ayhan, Yüce
Devrim, İlker
description Summary Purpose Our aim is to determine whether the presence of soluble triggering receptor expressed on myeloid cells‐1 (s‐TREM‐1) of bronchoalveolar lavage fluid (BALF), serum procalcitonin levels (PCT), and Clinical Pulmonary Infection Score (CPIS) have diagnostic value in children with VAP. Methods All children followed in pediatric intensive care unit (PICU) who were mechanically ventilated at least for 48 hr between January 2014 and December 2015 were enrolled into our study. BALF sample was obtained via non‐bronchoscopic method from the children with VAP suspicion (case group) and s‐TREM‐1 levels were measured. Furthermore we calculated CPIS and measured serum PCT levels. Same procedures were applied to the control group who were admitted to PICU without infectious problems and who were not under antimicrobial therapy. First we compared the case group with the control group and then we compared the quantitative culture confirmed and non‐confirmed VAP cases among themselves. Results Case group (n:58) had significant higher PCT and s‐TREM‐1 levels compared to control group (n:58). The VAP confirmed cases had higher s‐TREM‐1, PCT ve CPIS levels compared to non‐confirmed VAP cases. s‐TREM‐1, PCT ve CPIS variables were found to be independent risk factors for VAP. The cutoff values for s‐TREM‐1, CPIS, and PCT, are 281 pg/ml, 6, and 1.9 ng/ml, respectively. The patients whose s‐TREM‐1, CPIS, and PCT values above the cutoff levels were found to have higher cumulative VAP rate. Conclusions s‐TREM‐1 of BALF, serum PCT levels, and CPIS are useful predictors for ventilator‐associated pneumonia diagnosis in children. Pediatr Pulmonol. 2017;52:119–128. © 2016 Wiley Periodicals, Inc.
doi_str_mv 10.1002/ppul.23504
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Methods All children followed in pediatric intensive care unit (PICU) who were mechanically ventilated at least for 48 hr between January 2014 and December 2015 were enrolled into our study. BALF sample was obtained via non‐bronchoscopic method from the children with VAP suspicion (case group) and s‐TREM‐1 levels were measured. Furthermore we calculated CPIS and measured serum PCT levels. Same procedures were applied to the control group who were admitted to PICU without infectious problems and who were not under antimicrobial therapy. First we compared the case group with the control group and then we compared the quantitative culture confirmed and non‐confirmed VAP cases among themselves. Results Case group (n:58) had significant higher PCT and s‐TREM‐1 levels compared to control group (n:58). The VAP confirmed cases had higher s‐TREM‐1, PCT ve CPIS levels compared to non‐confirmed VAP cases. s‐TREM‐1, PCT ve CPIS variables were found to be independent risk factors for VAP. The cutoff values for s‐TREM‐1, CPIS, and PCT, are 281 pg/ml, 6, and 1.9 ng/ml, respectively. The patients whose s‐TREM‐1, CPIS, and PCT values above the cutoff levels were found to have higher cumulative VAP rate. Conclusions s‐TREM‐1 of BALF, serum PCT levels, and CPIS are useful predictors for ventilator‐associated pneumonia diagnosis in children. Pediatr Pulmonol. 2017;52:119–128. © 2016 Wiley Periodicals, Inc.</description><identifier>ISSN: 8755-6863</identifier><identifier>EISSN: 1099-0496</identifier><identifier>DOI: 10.1002/ppul.23504</identifier><identifier>PMID: 27280471</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adolescent ; biomarkers ; Bronchoalveolar Lavage Fluid ; Calcitonin - blood ; Child ; Child, Preschool ; Female ; Humans ; Infant ; Intensive Care Units, Pediatric ; Male ; mechanical ventilation ; Membrane Glycoproteins - blood ; pediatric critical care ; pneumonia ; Pneumonia, Ventilator-Associated - blood ; Pneumonia, Ventilator-Associated - diagnosis ; Prospective Studies ; Receptors, Immunologic - blood ; Triggering Receptor Expressed on Myeloid Cells-1</subject><ispartof>Pediatric pulmonology, 2017-01, Vol.52 (1), p.119-128</ispartof><rights>2016 Wiley Periodicals, Inc.</rights><rights>2017 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3574-8e0a344ece7db619655df4711cf24d9080183aaa354a746ed83fa5da213e13c63</citedby><cites>FETCH-LOGICAL-c3574-8e0a344ece7db619655df4711cf24d9080183aaa354a746ed83fa5da213e13c63</cites></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.23504$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fppul.23504$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27911,27912,45561,45562</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27280471$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>İşgüder, Rana</creatorcontrib><creatorcontrib>Ceylan, Gökhan</creatorcontrib><creatorcontrib>Ağın, Hasan</creatorcontrib><creatorcontrib>Gülfidan, Gamze</creatorcontrib><creatorcontrib>Ayhan, Yüce</creatorcontrib><creatorcontrib>Devrim, İlker</creatorcontrib><title>New parameters for childhood ventilator associated pneumonia diagnosis</title><title>Pediatric pulmonology</title><addtitle>Pediatr Pulmonol</addtitle><description>Summary Purpose Our aim is to determine whether the presence of soluble triggering receptor expressed on myeloid cells‐1 (s‐TREM‐1) of bronchoalveolar lavage fluid (BALF), serum procalcitonin levels (PCT), and Clinical Pulmonary Infection Score (CPIS) have diagnostic value in children with VAP. Methods All children followed in pediatric intensive care unit (PICU) who were mechanically ventilated at least for 48 hr between January 2014 and December 2015 were enrolled into our study. BALF sample was obtained via non‐bronchoscopic method from the children with VAP suspicion (case group) and s‐TREM‐1 levels were measured. Furthermore we calculated CPIS and measured serum PCT levels. Same procedures were applied to the control group who were admitted to PICU without infectious problems and who were not under antimicrobial therapy. First we compared the case group with the control group and then we compared the quantitative culture confirmed and non‐confirmed VAP cases among themselves. Results Case group (n:58) had significant higher PCT and s‐TREM‐1 levels compared to control group (n:58). The VAP confirmed cases had higher s‐TREM‐1, PCT ve CPIS levels compared to non‐confirmed VAP cases. s‐TREM‐1, PCT ve CPIS variables were found to be independent risk factors for VAP. The cutoff values for s‐TREM‐1, CPIS, and PCT, are 281 pg/ml, 6, and 1.9 ng/ml, respectively. The patients whose s‐TREM‐1, CPIS, and PCT values above the cutoff levels were found to have higher cumulative VAP rate. Conclusions s‐TREM‐1 of BALF, serum PCT levels, and CPIS are useful predictors for ventilator‐associated pneumonia diagnosis in children. Pediatr Pulmonol. 2017;52:119–128. © 2016 Wiley Periodicals, Inc.</description><subject>Adolescent</subject><subject>biomarkers</subject><subject>Bronchoalveolar Lavage Fluid</subject><subject>Calcitonin - blood</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Intensive Care Units, Pediatric</subject><subject>Male</subject><subject>mechanical ventilation</subject><subject>Membrane Glycoproteins - blood</subject><subject>pediatric critical care</subject><subject>pneumonia</subject><subject>Pneumonia, Ventilator-Associated - blood</subject><subject>Pneumonia, Ventilator-Associated - diagnosis</subject><subject>Prospective Studies</subject><subject>Receptors, Immunologic - blood</subject><subject>Triggering Receptor Expressed on Myeloid Cells-1</subject><issn>8755-6863</issn><issn>1099-0496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90E1LxDAQBuAgiq6rF3-AFLyI0DVpPpoeRfyCRT3oucw2UzfSNjVpFf-9WXf14MHTwMzDy_AScsTojFGanff92MwyLqnYIhNGiyKlolDbZKJzKVOlFd8j-yG8UhpvBdsle1meaSpyNiHX9_iR9OChxQF9SGrnk2ppG7N0ziTv2A22gSEuIQRXWRjQJH2HY-s6C4mx8NK5YMMB2amhCXi4mVPyfH31dHmbzh9u7i4v5mnFZS5SjRS4EFhhbhaKFUpKU8c_WFVnwhRUU6Y5AHApIBcKjeY1SAMZ48h4pfiUnK5ze-_eRgxD2dpQYdNAh24MJdOZUgVjvIj05A99daPv4ndRSap5ngsd1dlaVd6F4LEue29b8J8lo-Wq3XLVbvndbsTHm8hx0aL5pT91RsDW4MM2-PlPVPn4-Dxfh34BKGaEpQ</recordid><startdate>201701</startdate><enddate>201701</enddate><creator>İşgüder, Rana</creator><creator>Ceylan, Gökhan</creator><creator>Ağın, Hasan</creator><creator>Gülfidan, Gamze</creator><creator>Ayhan, Yüce</creator><creator>Devrim, İlker</creator><general>Wiley Subscription Services, Inc</general><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>7X8</scope></search><sort><creationdate>201701</creationdate><title>New parameters for childhood ventilator associated pneumonia diagnosis</title><author>İşgüder, Rana ; Ceylan, Gökhan ; Ağın, Hasan ; Gülfidan, Gamze ; Ayhan, Yüce ; Devrim, İlker</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3574-8e0a344ece7db619655df4711cf24d9080183aaa354a746ed83fa5da213e13c63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adolescent</topic><topic>biomarkers</topic><topic>Bronchoalveolar Lavage Fluid</topic><topic>Calcitonin - blood</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Intensive Care Units, Pediatric</topic><topic>Male</topic><topic>mechanical ventilation</topic><topic>Membrane Glycoproteins - blood</topic><topic>pediatric critical care</topic><topic>pneumonia</topic><topic>Pneumonia, Ventilator-Associated - blood</topic><topic>Pneumonia, Ventilator-Associated - diagnosis</topic><topic>Prospective Studies</topic><topic>Receptors, Immunologic - blood</topic><topic>Triggering Receptor Expressed on Myeloid Cells-1</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>İşgüder, Rana</creatorcontrib><creatorcontrib>Ceylan, Gökhan</creatorcontrib><creatorcontrib>Ağın, Hasan</creatorcontrib><creatorcontrib>Gülfidan, Gamze</creatorcontrib><creatorcontrib>Ayhan, Yüce</creatorcontrib><creatorcontrib>Devrim, İlker</creatorcontrib><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 &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric pulmonology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>İşgüder, Rana</au><au>Ceylan, Gökhan</au><au>Ağın, Hasan</au><au>Gülfidan, Gamze</au><au>Ayhan, Yüce</au><au>Devrim, İlker</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New parameters for childhood ventilator associated pneumonia diagnosis</atitle><jtitle>Pediatric pulmonology</jtitle><addtitle>Pediatr Pulmonol</addtitle><date>2017-01</date><risdate>2017</risdate><volume>52</volume><issue>1</issue><spage>119</spage><epage>128</epage><pages>119-128</pages><issn>8755-6863</issn><eissn>1099-0496</eissn><abstract>Summary Purpose Our aim is to determine whether the presence of soluble triggering receptor expressed on myeloid cells‐1 (s‐TREM‐1) of bronchoalveolar lavage fluid (BALF), serum procalcitonin levels (PCT), and Clinical Pulmonary Infection Score (CPIS) have diagnostic value in children with VAP. Methods All children followed in pediatric intensive care unit (PICU) who were mechanically ventilated at least for 48 hr between January 2014 and December 2015 were enrolled into our study. BALF sample was obtained via non‐bronchoscopic method from the children with VAP suspicion (case group) and s‐TREM‐1 levels were measured. Furthermore we calculated CPIS and measured serum PCT levels. Same procedures were applied to the control group who were admitted to PICU without infectious problems and who were not under antimicrobial therapy. First we compared the case group with the control group and then we compared the quantitative culture confirmed and non‐confirmed VAP cases among themselves. Results Case group (n:58) had significant higher PCT and s‐TREM‐1 levels compared to control group (n:58). The VAP confirmed cases had higher s‐TREM‐1, PCT ve CPIS levels compared to non‐confirmed VAP cases. s‐TREM‐1, PCT ve CPIS variables were found to be independent risk factors for VAP. The cutoff values for s‐TREM‐1, CPIS, and PCT, are 281 pg/ml, 6, and 1.9 ng/ml, respectively. The patients whose s‐TREM‐1, CPIS, and PCT values above the cutoff levels were found to have higher cumulative VAP rate. Conclusions s‐TREM‐1 of BALF, serum PCT levels, and CPIS are useful predictors for ventilator‐associated pneumonia diagnosis in children. Pediatr Pulmonol. 2017;52:119–128. © 2016 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>27280471</pmid><doi>10.1002/ppul.23504</doi><tpages>10</tpages></addata></record>
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subjects Adolescent
biomarkers
Bronchoalveolar Lavage Fluid
Calcitonin - blood
Child
Child, Preschool
Female
Humans
Infant
Intensive Care Units, Pediatric
Male
mechanical ventilation
Membrane Glycoproteins - blood
pediatric critical care
pneumonia
Pneumonia, Ventilator-Associated - blood
Pneumonia, Ventilator-Associated - diagnosis
Prospective Studies
Receptors, Immunologic - blood
Triggering Receptor Expressed on Myeloid Cells-1
title New parameters for childhood ventilator associated pneumonia diagnosis
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