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 |
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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 |
format | Article |
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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><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 & 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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