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. Author manuscript; available in PMC: 2024 Mar 22.
Published in final edited form as: Semin Perinatol. 2022 Jun 10;46(7):151637. doi: 10.1016/j.semperi.2022.151637

Table 5.

Laboratory infection research

Reference Study Population Years Key Points
Hertz, et al. J Perinatol 199945 1700 blood cultures Not provided
  • DNA probe not sufficiently sensitive to be clinically useful

  • Automated blood culture systems are sufficiently sensitive to aid in clinical decision-making regarding discontinuation of antibiotics after 48 hours

Carlo, et al. J Pediatr 201146 1,067 ELBW infants 1999–2002
  • Infants with cerebral palsy had altered cytokine profiles early in life, suggesting the condition may have late perinatal and/or early neonatal inflammatory origin

Schelonka, et al. Cytokine 201147 996 ELBW infants 2000–2001 (secondary analysis)
  • Infants with bacteremia had lower levels of IL-17, and higher levels of IL-6 and IL-10

  • Ratio of immune regulatory cytokines to inflammatory cytokines was associated with development of bacteremia

Sood, et al. Pediatr Res 201148 1,066 ELBW infants 1999–2002 (secondary analysis)
  • Significant differences between infants with fungal sepsis, bacterial sepsis, or no sepsis for interferon-γ, IL-10 and IL-18, transforming growth factor-β, and tumor necrosis factor-α

Morrow, et al. J Pediatr 201149 410 infants ≤32wks GA 2000–2004
  • 15% of 135 infants with low secretor phenotype died, compared with 2% of 248 infants with high secretor phenotype

  • Low secretor phenotype was associated with NEC, and non-secretor genotype was associated with gram negative sepsis

Srinvasan, et al. Arch Dis Child Fetal Neonatal Ed 201750 757 ELBW infants Not provided
  • No SNPs reached genome-wide significance levels

  • Areas of potential association and pathways meriting further study were identified

Footnotes: Studies listed in order of publication. DNA (deoxyribonucleic acid); ELBW (extremely low birth weight); GA (gestational age); IL (interleukin); NEC (necrotizing enterocolitis); SNP (single-nucleotide polymorphism)

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