Please use this identifier to cite or link to this item:
http://hdl.handle.net/11452/22647
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.date.accessioned | 2021-11-15T07:44:45Z | - |
dc.date.available | 2021-11-15T07:44:45Z | - |
dc.date.issued | 2009-03 | - |
dc.identifier.citation | Çetinkaya, 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.issn | 0743-8346 | - |
dc.identifier.uri | https://doi.org/10.1038/jp.2008.207 | - |
dc.identifier.uri | https://www.nature.com/articles/jp2008207 | - |
dc.identifier.uri | http://hdl.handle.net/11452/22647 | - |
dc.description.abstract | Objective: 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.iso | en | en_US |
dc.publisher | Springernature | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.rights | Atıf Gayri Ticari Türetilemez 4.0 Uluslararası | tr_TR |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject | Serum amyloid A | en_US |
dc.subject | C-reactive protein | en_US |
dc.subject | Procalcitonin | en_US |
dc.subject | Neonatal sepsis | en_US |
dc.subject | Newborn | en_US |
dc.subject | Late-onset sepsis | en_US |
dc.subject | Bacterial sepsis | en_US |
dc.subject | Markers | en_US |
dc.subject | Infection | en_US |
dc.subject | Increase | en_US |
dc.subject | Values | en_US |
dc.subject | Obstetrics & gynecology | en_US |
dc.subject | Pediatrics | en_US |
dc.subject.mesh | Biological markers | en_US |
dc.subject.mesh | C-reactive protein | en_US |
dc.subject.mesh | Calcitonin | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Infant, newborn | en_US |
dc.subject.mesh | Infant, premature | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Prospective studies | en_US |
dc.subject.mesh | Protein precursors | en_US |
dc.subject.mesh | ROC curve | en_US |
dc.subject.mesh | Sepsis | en_US |
dc.subject.mesh | Serum amyloid a protein | en_US |
dc.subject.mesh | Severity of illness index | en_US |
dc.title | 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 | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000263893500009 | tr_TR |
dc.identifier.scopus | 2-s2.0-61849135704 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Bölümü/Neonatoloji Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Bölümü/Çocuk Enfeksiyon Hastalıkları Anabilim Dalı. | tr_TR |
dc.identifier.startpage | 225 | tr_TR |
dc.identifier.endpage | 231 | tr_TR |
dc.identifier.volume | 29 | tr_TR |
dc.identifier.issue | 3 | tr_TR |
dc.relation.journal | Journal of Perinatology | en_US |
dc.contributor.buuauthor | Çetinkaya, Merih | - |
dc.contributor.buuauthor | Özkan, Hilal Burcu | - |
dc.contributor.buuauthor | Köksal, Nirgül | - |
dc.contributor.buuauthor | Çelebi, Solmaz | - |
dc.contributor.buuauthor | Hacımustafaoğlu, Mustafa | - |
dc.identifier.pubmed | 19078972 | tr_TR |
dc.subject.wos | Obstetrics & gynecology | en_US |
dc.subject.wos | Pediatrics | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | Pubmed | en_US |
dc.wos.quartile | Q3 (Obstetrics & gynecology) | en_US |
dc.wos.quartile | Q2 (Pediatrics) | en_US |
dc.contributor.scopusid | 23994946300 | tr_TR |
dc.contributor.scopusid | 16679325400 | tr_TR |
dc.contributor.scopusid | 7003323615 | tr_TR |
dc.contributor.scopusid | 7006095295 | tr_TR |
dc.contributor.scopusid | 6602154166 | tr_TR |
dc.subject.scopus | Newborn Sepsis; Procalcitonin; C Reactive Protein | en_US |
dc.subject.emtree | Amyloid A protein | en_US |
dc.subject.emtree | Antibiotic agent | en_US |
dc.subject.emtree | Procalcitonin | en_US |
dc.subject.emtree | C reactive protein | en_US |
dc.subject.emtree | Antibiotic therapy | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Blood cell count | en_US |
dc.subject.emtree | Blood culture | en_US |
dc.subject.emtree | Blood examination | en_US |
dc.subject.emtree | Clinical evaluation | en_US |
dc.subject.emtree | Clinical trial | en_US |
dc.subject.emtree | Controlled clinical trial | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Diagnostic accuracy | en_US |
dc.subject.emtree | Diagnostic value | en_US |
dc.subject.emtree | Disease marker | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Follow up | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Infant | en_US |
dc.subject.emtree | Intermethod comparison | en_US |
dc.subject.emtree | Major clinical study | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Newborn sepsis | en_US |
dc.subject.emtree | Prematurity | en_US |
dc.subject.emtree | Protein blood level | en_US |
dc.subject.emtree | Sensitivity analysis | en_US |
Appears in Collections: | Scopus Web of Science |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
Çetinkaya_vd_2009.pdf | 145.42 kB | Adobe PDF | View/Open |
This item is licensed under a Creative Commons License