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Updated: Jan 11, 2026
A Controlled Mouse Model for Neonatal Polymicrobial Sepsis
Published on: January 27, 2019
Diagnostic and prognostic utility of D-dimer and heparin-binding protein in neonatal sepsis: A prospective
Hosam-Eldin M Basiouny1, Soha S Allam1,2, Alif A Allam1
1Department of Pediatric Hepatology, Gastroenterology and Nutrition, National Liver Institute, Menoufia University, Shebin El-Koom 32511, Menoufia, Egypt.
Background:
Neonatal sepsis is a serious health problem, with high morbidity and mortality during the first 28 days of life. Clinical diagnosis at presentation is challenging due to the nonspecific signs and symptoms. Although blood culture is the gold standard for diagnosis, it is not always positive.
Aim:
To evaluate the diagnostic and prognostic utility of D-dimer and heparin-binding protein (HBP) in neonatal sepsis.
Methods:
This prospective case-control study included 90 neonates in two groups: A sepsis group (n = 45) and a control group (n = 45) without sepsis. Sepsis group was further subdivided based on blood culture results into proven sepsis (n = 28 culture-positive sepsis) and suspected sepsis (n = 17 culture-negative sepsis). All neonates underwent complete history taking, thorough clinical examination and investigations [complete blood count, C-reactive protein (CRP), liver and kidney function tests, plasma D-dimer and HBP].
Results:
Levels of CRP, D-dimer and HBP were significantly higher in the sepsis group compared to the controls. At a cutoff value above 517.9 ng/mL, D-dimer outperformed CRP and HBP in distinguishing sepsis group from controls with 95.6% sensitivity and 97.8% specificity. D-dimer was also a better prognostic marker than the neonatal sequential organ failure assessment (nSOFA) for predicting mortality, with 100% sensitivity and 92.5% specificity vs 80% sensitivity and 82.5% specificity. There was a significant positive correlation between CRP, D-dimer and HBP.
Conclusion:
D-dimer demonstrated superior diagnostic accuracy compared to CRP and HBP in predicting sepsis, and demonstrated superior prognostic accuracy compared to nSOFA in predicting the outcome of neonatal sepsis.
