1183 Comparison of Urinary Neutrophil Gelatinase-Associated Lipocalin, C-Reactive Protein and Procalcitonin in Diagnosis of Late Onset Sepsis in Preterm Newborns
Objective Urinary neutrophil gelatinase-associated lipocalin (uNGAL) has been suggested as a useful marker in limited recent studies for diagnosis of sepsis in pediatric and adult patients. We aimed to determine the value of uNGAL levels in early diagnosis of late-onset sepsis in preterms, and to co...
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Veröffentlicht in: | Archives of disease in childhood 2012-10, Vol.97 (Suppl 2), p.A339-A339 |
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description | Objective Urinary neutrophil gelatinase-associated lipocalin (uNGAL) has been suggested as a useful marker in limited recent studies for diagnosis of sepsis in pediatric and adult patients. We aimed to determine the value of uNGAL levels in early diagnosis of late-onset sepsis in preterms, and to compare CRP and PCT. Materials and Methods Between February - May 2011, preterm infants admitted to NICU between the ages of 7 to 28 days divided into two groups: 24 cases with clinical sepsis (gestational age 32.88±1.45w) and 20 cases as control group (gestational age 33±1.49w). Results There is no difference in two groups in terms of demographic features of babies. At 1. and 7. days of treatment in sepsis group, CRP (median:25.09mg/Lvs8.63mg/L), PCT (median; 17.11ng/mlvs1.39ng/ml)and uNGAL levels were found 45.69±18.37ng/ml, 7.89±4.19ng/ml respectively. In control group, uNGAL levels were found 5.78±1.6ng/ml. We found significant differences CRP, PCT and uNGAL levels between groups. On the seventh day of treatment, CRP, PCT and uNGAL levels significantly decreased. We found that the sensitivity, specificity, positive and negative predictive values, respectively: for CRP; 58.3%, 80%, 77.8% and 61.5%, for PCT; 91.7%, 75%, 81.5% and 88.2%, for uNGAL; 91.7%, 100%, 100% and 90.9%. Conclusion Urinary NGAL seems to be more sensitive and spesific, reliable biomarker than serum CRP and PCT. We believe that uNGAL unlike other biomarkers that does not require a blood sample, non-invasive and non-sterile conditions, with small amounts of urine collection in newborn sepsis might be an ideal biomarker. |
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We aimed to determine the value of uNGAL levels in early diagnosis of late-onset sepsis in preterms, and to compare CRP and PCT. Materials and Methods Between February - May 2011, preterm infants admitted to NICU between the ages of 7 to 28 days divided into two groups: 24 cases with clinical sepsis (gestational age 32.88±1.45w) and 20 cases as control group (gestational age 33±1.49w). Results There is no difference in two groups in terms of demographic features of babies. At 1. and 7. days of treatment in sepsis group, CRP (median:25.09mg/Lvs8.63mg/L), PCT (median; 17.11ng/mlvs1.39ng/ml)and uNGAL levels were found 45.69±18.37ng/ml, 7.89±4.19ng/ml respectively. In control group, uNGAL levels were found 5.78±1.6ng/ml. We found significant differences CRP, PCT and uNGAL levels between groups. On the seventh day of treatment, CRP, PCT and uNGAL levels significantly decreased. We found that the sensitivity, specificity, positive and negative predictive values, respectively: for CRP; 58.3%, 80%, 77.8% and 61.5%, for PCT; 91.7%, 75%, 81.5% and 88.2%, for uNGAL; 91.7%, 100%, 100% and 90.9%. Conclusion Urinary NGAL seems to be more sensitive and spesific, reliable biomarker than serum CRP and PCT. We believe that uNGAL unlike other biomarkers that does not require a blood sample, non-invasive and non-sterile conditions, with small amounts of urine collection in newborn sepsis might be an ideal biomarker.</description><identifier>ISSN: 0003-9888</identifier><identifier>EISSN: 1468-2044</identifier><identifier>DOI: 10.1136/archdischild-2012-302724.1183</identifier><identifier>CODEN: ADCHAK</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</publisher><subject>Control Groups ; Neonates</subject><ispartof>Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A339-A339</ispartof><rights>2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><rights>Copyright: 2012 (c) 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://adc.bmj.com/content/97/Suppl_2/A339.1.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://adc.bmj.com/content/97/Suppl_2/A339.1.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,776,780,3183,23550,27901,27902,77343,77374</link.rule.ids></links><search><creatorcontrib>Ertuğrul, S</creatorcontrib><creatorcontrib>Örs, R</creatorcontrib><creatorcontrib>Kurban, S</creatorcontrib><title>1183 Comparison of Urinary Neutrophil Gelatinase-Associated Lipocalin, C-Reactive Protein and Procalcitonin in Diagnosis of Late Onset Sepsis in Preterm Newborns</title><title>Archives of disease in childhood</title><addtitle>Arch Dis Child</addtitle><description>Objective Urinary neutrophil gelatinase-associated lipocalin (uNGAL) has been suggested as a useful marker in limited recent studies for diagnosis of sepsis in pediatric and adult patients. We aimed to determine the value of uNGAL levels in early diagnosis of late-onset sepsis in preterms, and to compare CRP and PCT. Materials and Methods Between February - May 2011, preterm infants admitted to NICU between the ages of 7 to 28 days divided into two groups: 24 cases with clinical sepsis (gestational age 32.88±1.45w) and 20 cases as control group (gestational age 33±1.49w). Results There is no difference in two groups in terms of demographic features of babies. At 1. and 7. days of treatment in sepsis group, CRP (median:25.09mg/Lvs8.63mg/L), PCT (median; 17.11ng/mlvs1.39ng/ml)and uNGAL levels were found 45.69±18.37ng/ml, 7.89±4.19ng/ml respectively. In control group, uNGAL levels were found 5.78±1.6ng/ml. We found significant differences CRP, PCT and uNGAL levels between groups. On the seventh day of treatment, CRP, PCT and uNGAL levels significantly decreased. We found that the sensitivity, specificity, positive and negative predictive values, respectively: for CRP; 58.3%, 80%, 77.8% and 61.5%, for PCT; 91.7%, 75%, 81.5% and 88.2%, for uNGAL; 91.7%, 100%, 100% and 90.9%. Conclusion Urinary NGAL seems to be more sensitive and spesific, reliable biomarker than serum CRP and PCT. We believe that uNGAL unlike other biomarkers that does not require a blood sample, non-invasive and non-sterile conditions, with small amounts of urine collection in newborn sepsis might be an ideal biomarker.</description><subject>Control Groups</subject><subject>Neonates</subject><issn>0003-9888</issn><issn>1468-2044</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNqVkVFvFCEUhYmxiWvrfyAxvokywMwwDz40o64mm-1GrQ99IQzcsay7MAXW6s_xn8pkTOOrCQnk8N1zknsQelHRV1XFm9c6mlvrkrl1B0sYrRjhlLVMlF_JH6FVJRpZdCEeoxWllJNOSvkEPU1pTwstJV-h3zOL-3CcdHQpeBxGfB2d1_EX3sIpxzAVe7yGg85FTUAuUwrG6QwWb9wUjD44_xL35BNok90PwLsYMjiPtbfzuwDG5eCLUs5bp7_5kFyagzbFBV_5BBl_hmkWC7GLkCEeS_r9EKJPF-hs1IcEz_7e5-j6_bsv_QeyuVp_7C83ZGBMcGJGbXlj644bamshZNd00ArWiVHqrh41a0cLtoGBDqZqNBOjsCANHaisWsP4OXq--E4x3J0gZbUPp-hLpKpkWVYtmagL9WahTAwpRRjVFN2xbEtVVM2tqH9bUXMramlFzZsu82SZdynDz4dhHb-rpuVtrbZfe7UV6932ht4oWXi58MNx_59RfwB2lqgI</recordid><startdate>201210</startdate><enddate>201210</enddate><creator>Ertuğrul, S</creator><creator>Örs, R</creator><creator>Kurban, S</creator><general>BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>0-V</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88B</scope><scope>88E</scope><scope>88I</scope><scope>8A4</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>CJNVE</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0P</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEDU</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>201210</creationdate><title>1183 Comparison of Urinary Neutrophil Gelatinase-Associated Lipocalin, C-Reactive Protein and Procalcitonin in Diagnosis of Late Onset Sepsis in Preterm Newborns</title><author>Ertuğrul, S ; Örs, R ; Kurban, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b2243-cfad36d593c0d5448969e74294f8a95fa27fded6eb0bc16a24f4de8c0b0817c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Control Groups</topic><topic>Neonates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ertuğrul, S</creatorcontrib><creatorcontrib>Örs, R</creatorcontrib><creatorcontrib>Kurban, S</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>ProQuest Social Sciences Premium Collection【Remote access available】</collection><collection>ProQuest Central (Corporate)</collection><collection>Health Medical collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Education Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>Education Periodicals</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Social Science Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Education Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Education Database</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</collection><collection>ProQuest One Education</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><jtitle>Archives of disease in childhood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ertuğrul, S</au><au>Örs, R</au><au>Kurban, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>1183 Comparison of Urinary Neutrophil Gelatinase-Associated Lipocalin, C-Reactive Protein and Procalcitonin in Diagnosis of Late Onset Sepsis in Preterm Newborns</atitle><jtitle>Archives of disease in childhood</jtitle><addtitle>Arch Dis Child</addtitle><date>2012-10</date><risdate>2012</risdate><volume>97</volume><issue>Suppl 2</issue><spage>A339</spage><epage>A339</epage><pages>A339-A339</pages><issn>0003-9888</issn><eissn>1468-2044</eissn><coden>ADCHAK</coden><abstract>Objective Urinary neutrophil gelatinase-associated lipocalin (uNGAL) has been suggested as a useful marker in limited recent studies for diagnosis of sepsis in pediatric and adult patients. We aimed to determine the value of uNGAL levels in early diagnosis of late-onset sepsis in preterms, and to compare CRP and PCT. Materials and Methods Between February - May 2011, preterm infants admitted to NICU between the ages of 7 to 28 days divided into two groups: 24 cases with clinical sepsis (gestational age 32.88±1.45w) and 20 cases as control group (gestational age 33±1.49w). Results There is no difference in two groups in terms of demographic features of babies. At 1. and 7. days of treatment in sepsis group, CRP (median:25.09mg/Lvs8.63mg/L), PCT (median; 17.11ng/mlvs1.39ng/ml)and uNGAL levels were found 45.69±18.37ng/ml, 7.89±4.19ng/ml respectively. In control group, uNGAL levels were found 5.78±1.6ng/ml. We found significant differences CRP, PCT and uNGAL levels between groups. On the seventh day of treatment, CRP, PCT and uNGAL levels significantly decreased. We found that the sensitivity, specificity, positive and negative predictive values, respectively: for CRP; 58.3%, 80%, 77.8% and 61.5%, for PCT; 91.7%, 75%, 81.5% and 88.2%, for uNGAL; 91.7%, 100%, 100% and 90.9%. Conclusion Urinary NGAL seems to be more sensitive and spesific, reliable biomarker than serum CRP and PCT. We believe that uNGAL unlike other biomarkers that does not require a blood sample, non-invasive and non-sterile conditions, with small amounts of urine collection in newborn sepsis might be an ideal biomarker.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</pub><doi>10.1136/archdischild-2012-302724.1183</doi><oa>free_for_read</oa></addata></record> |
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title | 1183 Comparison of Urinary Neutrophil Gelatinase-Associated Lipocalin, C-Reactive Protein and Procalcitonin in Diagnosis of Late Onset Sepsis in Preterm Newborns |
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