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. 2019 Aug 6;19(1):695.
doi: 10.1186/s12879-019-4316-5.

Presepsin and fetuin-A dyad for the diagnosis of proven sepsis in preterm neonates

Affiliations

Presepsin and fetuin-A dyad for the diagnosis of proven sepsis in preterm neonates

Halil Değirmencioğlu et al. BMC Infect Dis. .

Abstract

Background: Diagnosis is the most strenuous step in the evaluation of neonatal sepsis. No gold standard diagnostic method is available except for blood culture. We aimed to investigate the role of positive and negative acute phase reactants, namely presepsin and fetuin-A, in the diagnosis of culture-proven late-onset sepsis.

Methods: A prospective, case-control study with the infants ≤32 weeks of age with a diagnosis of culture-proven late-onset sepsis was designed. Twenty-nine preterm infants with similar gestational and postnatal ages without sepsis constituted the control group. Serum values of presepsin, fetuin-A, C-reactive protein and interleukin-6 were evaluated at the enrollment, third and seventh days of the diagnosis in the infants with positive blood culture results.

Results: First-day presepsin values were significantly higher in the culture-positive infants than the control group [1583 ng/L (1023-1731) vs. 426 ng/L (287-589), p = < 0.0001]. Presepsin was found to have an 88.9% sensitivity and 88.9% specificity with a cut-off value of 823 ng/ml for culture-proven LOS in our study, and area under the receiver-operating curve was 0.939. Fetuin-A levels were similar between the study and control groups (p > 0.05).

Conclusion: Presepsin may be an accurate marker for both diagnosis and monitoring of treatment response for culture-proven late-onset sepsis in preterm infants. However, fetuin-A does not seem to be a useful tool for the diagnosis of sepsis.

Keywords: Diagnosis; Neonatal sepsis; Presepsin.

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Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
ROC curve of presepsin at enrollment in proven sepsis

References

    1. Greenberg RG, Kandefer S, Do BT, Smith PB, Stoll BJ, Bell EF, et al. Late-onset sepsis in extremely premature infants 2000–2011. Pediatr Infect Dis J. 2017;36(8):774–779. doi: 10.1097/INF.0000000000001570. - DOI - PMC - PubMed
    1. Dong Y, Speer CP. Late-onset neonatal sepsis: recent developments. Arch Dis Child Fetal Neonatal Ed. 2015;100(3):F257–F263. doi: 10.1136/archdischild-2014-306213. - DOI - PMC - PubMed
    1. Pammi M, Weisman LE. Late-onset sepsis in preterm infants: update on strategies for therapy and prevention. Expert Rev Anti-Infect Ther. 2015;13(4):487–504. - PubMed
    1. Markanday A. Acute phase reactants in infections: evidence-based review and a guide for clinicians. Open Forum Infect Dis. 2015;2(3):ofv098. doi: 10.1093/ofid/ofv098. - DOI - PMC - PubMed
    1. Cortese F, Scicchitano P, Gesualdo M, Filaninno A, De Giorgi E, Schettini F, et al. Early and late infections in newborns: where Do we stand? A review. Pediatr Neonatol. 2016;57(4):265–273. doi: 10.1016/j.pedneo.2015.09.007. - DOI - PubMed