Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/123614
Campo DC Valoridioma
dc.contributor.authorSantana Reyes, Candelariaen_US
dc.contributor.authorGarcía-Muñoz, F.en_US
dc.contributor.authorReyes, D.en_US
dc.contributor.authorGonzález Azpeitia, Gloriaen_US
dc.contributor.authorDomínguez, C.en_US
dc.contributor.authorDomenech, E.en_US
dc.date.accessioned2023-06-20T07:03:02Z-
dc.date.available2023-06-20T07:03:02Z-
dc.date.issued2003en_US
dc.identifier.issn0803-5253en_US
dc.identifier.urihttp://hdl.handle.net/10553/123614-
dc.description.abstractAim: To investigate whether the serum levels of interleukin-1β, 6, 8, tumour necrosis factor-α and the soluble receptor of IL-2 are useful in the diagnosis of neonatal sepsis, and whether their diagnostic power is increased when in combination with classical markers such as C-reactive protein and white blood cell count. Methods: Blood samples were collected at admission from 40 neonates with suspected infection. Patients were included in different groups according to the bacteriological and laboratory results: Group I consisted of 20 newborns with positive blood cultures and other biological tests suggestive of infection. Group II included 20 neonates with negative blood cultures and biological tests not suggestive of infection. The control group included 20 healthy neonates with no clinical or biological data of infection. Results: Mean values of C-reactive protein were significantly higher in Group I. No differences were found between the groups for white blood cell count, with the exception of the presence of leucocytosis in Group II. Levels of interleukin-1β, 6, 8, tumour necrosis factor-α, soluble receptor of interleukin-2, and C-reactive protein were significantly higher in infected neonates than in the control groups. Detection sensitivity and specificity were 80 and 92% for C-reactive protein, 60 and 87% for interleukin-1β, 61 and 80% for interleukin-6, 62 and 96% for interleukin-8, 54 and 92% for tumour necrosis factor-α and 63 and 94% for soluble receptor of interleukin-2. The discriminant analysis showed that the best combination for sepsis diagnosis was C-reactive protein + interleukin-8 + soluble receptor of interleukin-2, with a sensitivity of 85% and a specificity of 97.1%. Conclusion: Our study suggests that no individual test can on its own identify infected neonates, and that although the combination of C-reactive protein, interleukin-8 and the soluble receptor of interleukin-2 exhibits a high specificity, its sensitivity is limited.en_US
dc.languageengen_US
dc.relation.ispartofActa Paediatrica, International Journal of Paediatricsen_US
dc.sourceActa Paediatrica, International Journal of Paediatrics [ISSN 0803-5253], v. 92 (2), p. 221-227, (Febrero 2003)en_US
dc.subject32 Ciencias médicasen_US
dc.subject320110 Pediatríaen_US
dc.subject.otherC-reactive proteinen_US
dc.subject.otherCytokinesen_US
dc.subject.otherInterleukinsen_US
dc.subject.otherNeonatal sepsisen_US
dc.subject.otherTumour necrosis factor-alphaen_US
dc.titleRole of cytokines (interleukin-1 beta, 6, 8, tumour necrosis factor-alpha, and soluble receptor of interleukin-2) and C-reactive protein in the diagnosis of neonatal sepsisen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1111/j.1651-2227.2003.tb00530.xen_US
dc.identifier.pmid12710650-
dc.identifier.scopus2-s2.0-0037238655-
dc.identifier.isiWOS:000182015500016-
dc.contributor.orcid#NODATA#-
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dc.contributor.orcid#NODATA#-
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dc.description.lastpage227en_US
dc.identifier.issue2-
dc.description.firstpage221en_US
dc.relation.volume92en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.description.numberofpages7en_US
dc.utils.revisionen_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.jcr1,128
dc.description.jcrqQ2
dc.description.scieSCIE
item.grantfulltextopen-
item.fulltextCon texto completo-
crisitem.author.deptGIR IUIBS: Nutrición-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Clínicas-
crisitem.author.orcid0009-0004-2207-9095-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameGonzález Azpeitia, Gloria-
Colección:Artículos
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