Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/22647
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dc.date.accessioned2021-11-15T07:44:45Z-
dc.date.available2021-11-15T07:44:45Z-
dc.date.issued2009-03-
dc.identifier.citationÇetinkaya, M. vd. (2009). "Comparison of serum amyloid A concentrations with those of C-reactive protein and procalcitonin in diagnosis and follow-up of neonatal sepsis in premature infants". Journal of Perinatology, 29(3), 225-231.en_US
dc.identifier.issn0743-8346-
dc.identifier.urihttps://doi.org/10.1038/jp.2008.207-
dc.identifier.urihttps://www.nature.com/articles/jp2008207-
dc.identifier.urihttp://hdl.handle.net/11452/22647-
dc.description.abstractObjective: The purpose of this study was to determine the role of serum amyloid A (SAA) in diagnosis of neonatal sepsis and evaluation of clinical response to antibiotic therapy. We also aimed to compare the efficiency of SAA with that of C-reactive protein (CRP) and procalcitonin (PCT) in diagnosis and follow-up of neonatal sepsis in preterm infants. Study Design: A total of 163 infants were enrolled in this prospective study. The infants were classified into four groups: group 1 (high probable sepsis), group 2 (probable sepsis), group 3 (possible sepsis) and group 4 (no sepsis, control group). Blood samples for whole blood count, CRP, PCT, SAA and culture were obtained before initiating antibiotic treatment. This procedure was repeated three times at 48 h, 7 and 10 days. Result: Initial CRP, PCT and SAA levels were found to be positive in 73.2, 75.6 and 77.2% of all infants, respectively. Sensitivities of CRP, PCT and SAA at 0 h were 72.3, 74.8 and 76.4%, respectively. Although it was not statistically significant, SAA was found to be more sensitive than CRP and PCT in diagnosis of neonatal sepsis. The area under the curve (AUC) for CRP, PCT and SAA at 0 h were 0.870, 0.870 and 0.875, respectively. Although the AUC for SAA at 0 h was higher than PCT and CRP, the difference was not statistically significant. Conclusion: SAA is an accurate and reliable marker for diagnosis and follow-up of neonatal sepsis. It is especially useful at the onset of inflammation for rapid diagnosis of neonatal sepsis and can be safely and accurately used in combination with other sepsis markers such as CRP and PCT in diagnosis and follow-up of neonatal sepsis in preterm infants.en_US
dc.language.isoenen_US
dc.publisherSpringernatureen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectSerum amyloid Aen_US
dc.subjectC-reactive proteinen_US
dc.subjectProcalcitoninen_US
dc.subjectNeonatal sepsisen_US
dc.subjectNewbornen_US
dc.subjectLate-onset sepsisen_US
dc.subjectBacterial sepsisen_US
dc.subjectMarkersen_US
dc.subjectInfectionen_US
dc.subjectIncreaseen_US
dc.subjectValuesen_US
dc.subjectObstetrics & gynecologyen_US
dc.subjectPediatricsen_US
dc.subject.meshBiological markersen_US
dc.subject.meshC-reactive proteinen_US
dc.subject.meshCalcitoninen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshInfant, newbornen_US
dc.subject.meshInfant, prematureen_US
dc.subject.meshMaleen_US
dc.subject.meshProspective studiesen_US
dc.subject.meshProtein precursorsen_US
dc.subject.meshROC curveen_US
dc.subject.meshSepsisen_US
dc.subject.meshSerum amyloid a proteinen_US
dc.subject.meshSeverity of illness indexen_US
dc.titleComparison of serum amyloid A concentrations with those of C-reactive protein and procalcitonin in diagnosis and follow-up of neonatal sepsis in premature infantsen_US
dc.typeArticleen_US
dc.identifier.wos000263893500009tr_TR
dc.identifier.scopus2-s2.0-61849135704tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Bölümü/Neonatoloji Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Bölümü/Çocuk Enfeksiyon Hastalıkları Anabilim Dalı.tr_TR
dc.identifier.startpage225tr_TR
dc.identifier.endpage231tr_TR
dc.identifier.volume29tr_TR
dc.identifier.issue3tr_TR
dc.relation.journalJournal of Perinatologyen_US
dc.contributor.buuauthorÇetinkaya, Merih-
dc.contributor.buuauthorÖzkan, Hilal Burcu-
dc.contributor.buuauthorKöksal, Nirgül-
dc.contributor.buuauthorÇelebi, Solmaz-
dc.contributor.buuauthorHacımustafaoğlu, Mustafa-
dc.identifier.pubmed19078972tr_TR
dc.subject.wosObstetrics & gynecologyen_US
dc.subject.wosPediatricsen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ3 (Obstetrics & gynecology)en_US
dc.wos.quartileQ2 (Pediatrics)en_US
dc.contributor.scopusid23994946300tr_TR
dc.contributor.scopusid16679325400tr_TR
dc.contributor.scopusid7003323615tr_TR
dc.contributor.scopusid7006095295tr_TR
dc.contributor.scopusid6602154166tr_TR
dc.subject.scopusNewborn Sepsis; Procalcitonin; C Reactive Proteinen_US
dc.subject.emtreeAmyloid A proteinen_US
dc.subject.emtreeAntibiotic agenten_US
dc.subject.emtreeProcalcitoninen_US
dc.subject.emtreeC reactive proteinen_US
dc.subject.emtreeAntibiotic therapyen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBlood cell counten_US
dc.subject.emtreeBlood cultureen_US
dc.subject.emtreeBlood examinationen_US
dc.subject.emtreeClinical evaluationen_US
dc.subject.emtreeClinical trialen_US
dc.subject.emtreeControlled clinical trialen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDiagnostic accuracyen_US
dc.subject.emtreeDiagnostic valueen_US
dc.subject.emtreeDisease markeren_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeFollow upen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeInfanten_US
dc.subject.emtreeIntermethod comparisonen_US
dc.subject.emtreeMajor clinical studyen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeNewborn sepsisen_US
dc.subject.emtreePrematurityen_US
dc.subject.emtreeProtein blood levelen_US
dc.subject.emtreeSensitivity analysisen_US
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