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Updated: Jan 18, 2026

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A Neonatal Imaging Model of Gram-Negative Bacterial Sepsis
Published on: August 12, 2020
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Neonatal leucocyte cell population data: reference intervals and relevance for detecting sepsis and necrotizing
Flavia Ferraro1, Laura Fillistorf2, Varvara Dimopoulou2
1Clinic of Neonatology, Department Mother-Woman-Child, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland. flavia.ferraro@hug.ch.
Pediatric Research
|June 6, 2025
Summary
This study establishes reference intervals for neonatal Cell Population Data (CPD) and finds neutrophil fluorescence intensity (NE-SFL) to be a promising biomarker for early sepsis detection in newborns. NE-SFL shows higher accuracy than traditional tests.
Area of Science:
- Neonatal immunology
- Clinical diagnostics
- Biomarker discovery
Background:
- Timely diagnosis of neonatal sepsis is critical but challenging.
- Cell Population Data (CPD) offer high-resolution leukocyte phenotyping for potential sepsis detection.
- This study aimed to establish neonatal CPD reference intervals and assess their utility for detecting sepsis and necrotizing enterocolitis (NEC).
Purpose of the Study:
- Establish reference intervals for neonatal leukocyte Cell Population Data (CPD).
- Evaluate the diagnostic performance of CPD, particularly NE-SFL, for neonatal sepsis and NEC.
- Compare CPD accuracy against traditional biomarkers like CBC and CRP.
Main Methods:
- Analyzed CPD from neutrophils, monocytes, and lymphocytes in hospitalized newborns.
- Derived reference intervals (5-95th percentiles) from a healthy reference group.
- Assessed CPD performance in detecting sepsis/NEC against CBC and CRP.
Main Results:
- Established reference intervals for neonatal CPD, showing distinct trajectories and decreasing distribution width with age.
- CPD in sepsis/NEC cases differed significantly from the reference group, especially neutrophil fluorescence intensity (NE-SFL).
- NE-SFL demonstrated superior accuracy (90% sensitivity, 76% specificity) compared to other CPD, CBC, and CRP.
Conclusions:
- Established neonatal CPD reference intervals, aiding interpretation of these preclinical parameters.
- Identified NE-SFL as a potential sepsis biomarker with superior diagnostic accuracy.
- CPD, particularly NE-SFL, offer a cost-effective, real-time tool for improving neonatal sepsis detection.
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