Publication:
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

dc.contributor.buuauthorÇetinkaya, Merih
dc.contributor.buuauthorÖzkan, Hilal Burcu
dc.contributor.buuauthorKöksal, Nirgül
dc.contributor.buuauthorÇelebi, Solmaz
dc.contributor.buuauthorHacımustafaoğlu, Mustafa
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları Bölümü
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları Bölümü
dc.contributor.departmentNeonatoloji Ana Bilim Dalı
dc.contributor.departmentÇocuk Enfeksiyon Hastalıkları Ana Bilim Dalı
dc.contributor.scopusid23994946300
dc.contributor.scopusid16679325400
dc.contributor.scopusid7003323615
dc.contributor.scopusid7006095295
dc.contributor.scopusid6602154166
dc.date.accessioned2021-11-15T07:44:45Z
dc.date.available2021-11-15T07:44:45Z
dc.date.issued2009-03
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.
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.
dc.identifier.endpage231
dc.identifier.issn0743-8346
dc.identifier.issue3
dc.identifier.pubmed19078972
dc.identifier.scopus2-s2.0-61849135704
dc.identifier.startpage225
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.identifier.volume29
dc.identifier.wos000263893500009
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherSpringernature
dc.relation.journalJournal of Perinatology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectSerum amyloid A
dc.subjectC-reactive protein
dc.subjectProcalcitonin
dc.subjectNeonatal sepsis
dc.subjectNewborn
dc.subjectLate-onset sepsis
dc.subjectBacterial sepsis
dc.subjectMarkers
dc.subjectInfection
dc.subjectIncrease
dc.subjectValues
dc.subjectObstetrics & gynecology
dc.subjectPediatrics
dc.subject.emtreeAmyloid A protein
dc.subject.emtreeAntibiotic agent
dc.subject.emtreeProcalcitonin
dc.subject.emtreeC reactive protein
dc.subject.emtreeAntibiotic therapy
dc.subject.emtreeArticle
dc.subject.emtreeBlood cell count
dc.subject.emtreeBlood culture
dc.subject.emtreeBlood examination
dc.subject.emtreeClinical evaluation
dc.subject.emtreeClinical trial
dc.subject.emtreeControlled clinical trial
dc.subject.emtreeControlled study
dc.subject.emtreeDiagnostic accuracy
dc.subject.emtreeDiagnostic value
dc.subject.emtreeDisease marker
dc.subject.emtreeFemale
dc.subject.emtreeFollow up
dc.subject.emtreeHuman
dc.subject.emtreeInfant
dc.subject.emtreeIntermethod comparison
dc.subject.emtreeMajor clinical study
dc.subject.emtreeMale
dc.subject.emtreeNewborn sepsis
dc.subject.emtreePrematurity
dc.subject.emtreeProtein blood level
dc.subject.emtreeSensitivity analysis
dc.subject.meshBiological markers
dc.subject.meshC-reactive protein
dc.subject.meshCalcitonin
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshInfant, newborn
dc.subject.meshInfant, premature
dc.subject.meshMale
dc.subject.meshProspective studies
dc.subject.meshProtein precursors
dc.subject.meshROC curve
dc.subject.meshSepsis
dc.subject.meshSerum amyloid a protein
dc.subject.meshSeverity of illness index
dc.subject.scopusNewborn Sepsis; Procalcitonin; C Reactive Protein
dc.subject.wosObstetrics & gynecology
dc.subject.wosPediatrics
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 infants
dc.typeArticle
dc.wos.quartileQ3 (Obstetrics & gynecology)
dc.wos.quartileQ2 (Pediatrics)
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Bölümü/Neonatoloji Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Bölümü/Çocuk Enfeksiyon Hastalıkları Ana Bilim Dalı
local.indexed.atPubMed
local.indexed.atWOS

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