Clinical features analysis for complications in infants with late-onset Group B streptococcal sepsis: a retrospective

Haifeng Geng1, Wenqiang Sun1, Qiuping Shen1

  • 1Department of Neonatology, Children's Hospital of Soochow University, Suzhou, China.

Frontiers in Medicine
|December 1, 2025
PubMed

Insights

High PELOD-2 and pSOFA scores, elevated creatinine, and hypoalbuminemia are key risk factors for complications in late-onset Group B Streptococcal (GBS) sepsis infants. Early identification aids in risk stratification and tailored interventions for better outcomes.

Area of Science:

  • Neonatal Medicine
  • Infectious Diseases
  • Pediatric Critical Care

Background:

  • Late-onset Group B Streptococcal (GBS) sepsis poses a significant threat to infants, often leading to severe complications.
  • Identifying early risk factors is crucial for timely intervention and improved patient outcomes.

Purpose of the Study:

  • To investigate risk factors associated with complications in infants diagnosed with late-onset GBS sepsis.
  • To provide evidence-based insights for clinical intervention strategies.

Main Methods:

  • Retrospective case-control study analyzing clinical data of 101 infants with late-onset GBS sepsis.
  • Infants were categorized into complication and non-complication groups for comparative analysis.
  • Univariate, multivariate analyses, and ROC curves were employed to identify risk factors and assess predictive efficacy.

Main Results:

  • Infants with complications had lower gestational age, higher incidence of seizures, fever, and bulging fontanelle.
  • Laboratory findings indicated hypoalbuminemia, elevated creatinine and BUN, and lower pH in the complication group.
  • High PELOD-2 and pSOFA scores, elevated creatinine, and hypoalbuminemia were identified as significant risk factors (AUC=0.858).

Conclusions:

  • High PELOD-2 score, high pSOFA score, elevated creatinine levels, and hypoalbuminemia are independent predictors of complications in late-onset GBS sepsis.
  • These findings enable early risk stratification and personalized treatment approaches for affected infants.
Abstract

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