Timeframe for Group B Streptococcus (GBS) Infection Development
Group B Streptococcus infections in newborns typically develop within the first 24-48 hours of life for early-onset disease, while late-onset disease occurs between 7 days and 3 months of age. 1
Early-Onset GBS Disease (0-6 days)
Early-onset GBS disease is characterized by:
- Presentation primarily within the first 24-48 hours of life 1
- Most cases manifest with respiratory distress, apnea, or other signs of sepsis 1
- Common clinical syndromes include sepsis and pneumonia; less frequently meningitis 1
- Vertical transmission occurs when:
- GBS ascends from the vagina to amniotic fluid after labor onset or membrane rupture
- GBS invades through intact membranes (less common)
- Infants are exposed during passage through the birth canal 1
Risk Factors for Early-Onset Disease
- Maternal GBS colonization (primary risk factor) - colonized mothers are >25 times more likely to deliver infants with early-onset disease 1
- Gestational age <37 weeks 2
- Prolonged rupture of membranes (>18 hours) 2
- Intrapartum fever (>38°C) 2
- GBS bacteriuria during current pregnancy 2
- Previous delivery of infant with invasive GBS disease 2
- Young maternal age (<20 years) 2
- Black race 2
- Low maternal levels of GBS-specific anticapsular antibody 2
Late-Onset GBS Disease (7-89 days)
Late-onset disease:
- Occurs in infants aged >1 week, with most infections evident during the first 3 months of life 1
- Presents more commonly as meningitis compared to early-onset disease 1
- Transmission routes are less understood but may include breast milk, household contacts, nosocomial, or community sources 3
- Not preventable through current intrapartum antibiotic prophylaxis strategies 4
Disease Progression and Outcomes
Without intervention, approximately 1-2% of infants born to GBS-colonized mothers develop early-onset disease 1, 5. The case-fatality ratio has declined from as high as 50% in the 1970s to 4-6% in recent years due to advances in neonatal care 1.
Mortality is significantly higher among preterm infants:
- 20% case-fatality rate overall for preterm infants
- Up to 30% for those ≤33 weeks' gestation
- 2-3% for full-term infants 1
Clinical Implications
For clinicians managing potential GBS cases:
- Rapid onset: Be vigilant for signs of infection within the first 24-48 hours after birth
- Prompt intervention: Early recognition is critical given the rapid progression of disease
- Risk stratification: Identify high-risk situations requiring intrapartum antibiotic prophylaxis
- Prevention strategies: Universal screening at 36-37 weeks gestation and appropriate intrapartum antibiotic prophylaxis remain the cornerstone of prevention 5
Common Pitfalls
- Failing to recognize that early-onset disease can manifest at or shortly after birth
- Assuming that negative maternal GBS cultures eliminate risk (transient colonization can occur)
- Delaying necessary obstetric interventions solely to provide 4 hours of antibiotic prophylaxis 5
- Overlooking the possibility of late-onset disease, which is not prevented by current intrapartum strategies 4
The rapid progression of GBS disease underscores the importance of timely identification of at-risk infants and prompt initiation of appropriate treatment to reduce morbidity and mortality.