Role of presepsin in the diagnosis of late-onset neonatal sepsis in preterm infants

J Matern Fetal Neonatal Med. 2016;29(11):1834-9. doi: 10.3109/14767058.2015.1064885. Epub 2015 Jul 30.

Abstract

Objective: One of the most challenging aspects in the management of neonates with late-onset neonatal sepsis (LOS) is to make the diagnosis. Presepsin is a novel and promising marker of sepsis. The aim of this study was to assess the role of presepsin in the diagnosis of LOS in preterm infants.

Methods: Forty-two premature newborns ≤32 weeks gestational age with a diagnosis of LOS were prospectively involved in the study. Forty gestational and postnatal age-matched infants without sepsis served as controls. Levels of presepsin, C-reactive protein, and procalcitonin were measured at enrollment and on the third and seventh days of sepsis.

Results: Initial presepsin levels in the LOS group were significantly higher than in the control group (1024 pg/mL, min-max: 295-8202; versus 530 pg/mL, min-max: 190-782; p < 0.0001). The area under the receiver-operating curve for presepsin was 0.864. A presepsin value of 800.5 pg/mL was established as a cut-off value, with 67% sensitivity and 100% specificity. Presepsin levels gradually decreased during treatment.

Conclusion: Presepsin can be used as a reliable biomarker for LOS and treatment response in preterm infants. However, we could not demonstrate the efficacy of presepsin for the detection of disease severity or prognosis.

Keywords: Late-onset sepsis; newborn; premature; presepsin.

Publication types

  • Clinical Trial

MeSH terms

  • Biomarkers / blood
  • Case-Control Studies
  • Female
  • Humans
  • Infant, Newborn
  • Infant, Premature
  • Lipopolysaccharide Receptors / blood*
  • Male
  • Peptide Fragments / blood*
  • Prospective Studies
  • Sepsis / blood*

Substances

  • Biomarkers
  • Lipopolysaccharide Receptors
  • Peptide Fragments
  • presepsin protein, human