Author/Authors :
Barseem Naglaa Fathy نويسنده Pediatric Department, Faculty of Medicine, Menoufia
University, Egypt , Helwa Mohamed Ahmed نويسنده Clinical Pathology Department, Faculty of Medicine,
Menoufia University, Egypt
Abstract :
Objectives The aim of this study was to assess the presence of DNA
damage in full-term newborns with neonatal sepsis. Methods Sixty
neonates with early onset neonatal sepsis and 45 apparently healthy
controls were enrolled in the study. Screening of neonates was done
using a modified clinical sepsis score and hematological scoring system,
adjusted to the results of blood culture and screening tests. Complete
blood count, C-reactive protein (CRP), and DNA studies were done.
Results Sepsis was likely in 41 (68.3%) patients with scores of 3 or 4
and CRP levels of 12 - 48 mg/L. Sepsis was very likely in 19 (31.7%)
patients with scores of ≥ 5 and CRP of 48 - 96 mg/L. Sepsis was unlikely
in all controls with scores of ≤ 2. The mean neutrophil count was 9700 ±
4600/µL in patients and 4230 ± 1400/µL in controls. The higher the total
polymorphonuclear count and CRP level, the more severe was the sepsis.
Twenty-six of 60 (43.3%) sepsis patients and 5 of 45 controls (11%) had
DNA damage. There was a highly significant negative correlation between
DNA damage, blood culture results, and CRP levels. Conclusions DNA
damage, demonstrated by clinical and laboratory evidence with a
combination of blood cultures, CRP, and hematological scoring system
results, can be used as an indicator of both the immune status of the
neonate and the severity of the sepsis.