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Elevated Red Cell Distribution Width as a Useful Marker in Neonatal Sepsis.
Ozgul Bulut1, Aysimin Akcakaya1, Nurgul Bulut2
1Department of Pediatrics, Division of Neonatology.
Journal of Pediatric Hematology/Oncology
|January 29, 2021
Summary
Red blood cell distribution width (RDW) is significantly elevated in neonatal sepsis cases. This readily available biomarker shows diagnostic potential for identifying sepsis in newborns within the neonatal intensive care unit.
Area of Science:
- Neonatal Medicine
- Hematology
- Clinical Diagnostics
Background:
- Neonatal sepsis is a critical cause of illness and death in neonatal intensive care units.
- Red blood cell distribution width (RDW) is a recognized prognostic indicator across various medical conditions.
Purpose of the Study:
- To assess the diagnostic utility of Red blood cell distribution width (RDW) in identifying neonatal sepsis.
- To determine if RDW can serve as an effective biomarker for neonatal sepsis.
Main Methods:
- An observational, retrospective cohort study was performed on newborns in a tertiary care university hospital from 2016 to 2019.
- Patients were categorized into sepsis and control groups, with demographic and laboratory data, including RDW, analyzed.
- Statistical analyses included ROC curve analysis and multivariable logistic regression.
Main Results:
- Red blood cell distribution width (RDW) levels were significantly higher in the neonatal sepsis group compared to the control group (P=0.001).
- The area under the ROC curve for RDW in diagnosing sepsis was 0.799.
- An RDW threshold of 17.4% demonstrated 60% sensitivity and 88.3% specificity for neonatal sepsis (P=0.001).
- Multivariable analysis indicated a positive association between RDW and sepsis (OR: 2.71; 95% CI: 2.19-3.36; P=0.001).
Conclusions:
- Elevated Red blood cell distribution width (RDW) is a significant finding in neonatal sepsis.
- RDW presents a valuable, easily accessible biomarker for the diagnosis of neonatal sepsis.
- RDW can be considered a useful alternative or adjunct to existing sepsis assessment tools in neonates.

