Group B Streptococcus

Group B Streptococcus (GBS) is a leading cause of early-onset neonatal sepsis in the UK, managed with intrapartum antibiotic prophylaxis (IAP) in high-risk women.

DRCOGPLAB 1UKMLA0 questions

Key Facts

GBS (Streptococcus agalactiae) colonises the vagina/rectum of approximately 20-30% of pregnant women in the UK Leading cause of early-onset neonatal sepsis (<7 days) in the UK, with incidence of 0.5 per 1,000 live births The UK does not have a universal screening programme (unlike USA); instead uses a risk-based approach (RCOG GTG 36) Intrapartum antibiotic prophylaxis (IAP): benzylpenicillin 3g IV loading then 1.5g IV 4-hourly until delivery Risk factors for IAP: previous baby with GBS disease, GBS bacteriuria in current pregnancy, incidental GBS detection, preterm labour <37 weeks, prolonged ROM >18 hours, intrapartum fever >38°C If penicillin allergic: clindamycin 900mg IV 8-hourly (if GBS sensitive) or vancomycin 1g IV 12-hourly Early-onset GBS disease mortality: approximately 5-10% in term neonates; higher in preterm Neonatal signs: respiratory distress, temperature instability, poor feeding within 12-24 hours of birth

Overview

Key Facts

Group B Streptococcus (GBS, Streptococcus agalactiae) is a Gram-positive coccus that commonly colonises the gastrointestinal and genital tracts. It is the most frequent cause of early-onset neonatal sepsis, meningitis, and pneumonia in the UK.

Epidemiology

  • Vaginal/rectal colonisation in 20-30% of pregnant women (transient, intermittent, or chronic)
  • Early-onset GBS disease (EOGBS): 0.5 per 1,000 live births in the UK
  • Late-onset GBS disease (7-90 days): 0.3 per 1,000 live births
  • Vertical transmission rate: 50% of babies born to colonised mothers become colonised; 1-2% of these develop invasive disease

Aetiology

  • Ascending infection from the maternal genital tract during labour
  • Risk increases with prolonged rupture of membranes, preterm delivery, intrapartum fever
  • Previous GBS disease in a sibling is the strongest risk factor

Pathophysiology

  • GBS ascends through ruptured or intact membranes to the amniotic fluid
  • Aspiration of infected amniotic fluid causes neonatal pneumonia
  • Haematogenous spread leads to septicaemia and meningitis
  • GBS capsular polysaccharide is the major virulence factor (serotype III most commonly causes meningitis)

Clinical Presentation

Maternal Presentation

  • Usually asymptomatic carrier
  • May present with GBS urinary tract infection (bacteriuria)
  • Rarely: chorioamnionitis, endometritis, wound infection

Neonatal Early-Onset Disease (<7 days, usually <24 hours)

  • Respiratory distress (tachypnoea, grunting, nasal flaring)
  • Temperature instability (hypothermia or fever)
  • Poor feeding, lethargy
  • Apnoea, cyanosis
  • Signs of sepsis: tachycardia, poor perfusion, hypotension

Neonatal Late-Onset Disease (7-90 days)

  • Meningitis (most common presentation)
  • Fever, irritability, poor feeding
  • Bulging fontanelle, seizures

Red Flags

  • Respiratory distress within 6 hours of birth
  • Temperature instability in first 24 hours
  • Maternal fever in labour (>38°C)
  • Prolonged ROM >18 hours with known GBS colonisation

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
E. coli neonatal sepsisSecond most common cause of neonatal sepsisBlood/CSF culture
ListeriosisMaternal flu-like illness, preterm labour, meconium-stained liquorBlood culture, placental histology
Transient tachypnoea of newbornRespiratory distress at birth, resolves within 24-48hCXR, clinical course
Respiratory distress syndromePreterm, ground glass CXRCXR, surfactant
Congenital pneumoniaRespiratory distress, consolidation on CXRCXR, cultures

Diagnosis / Investigation

Bedside

  • Maternal observations (temperature, HR, BP)
  • CTG if in labour
  • Neonatal observations: HR, RR, temperature, SpO2

Bloods

  • Maternal: midstream urine culture (GBS bacteriuria), vaginal/rectal swab if requested (not routine in UK)
  • Neonatal: blood culture (before antibiotics), FBC, CRP
  • Blood gas if respiratory distress

Imaging

  • Neonatal CXR if respiratory distress
  • Cranial USS if meningitis suspected

Special Tests

  • Lumbar puncture: if neonatal meningitis suspected (CSF culture, protein, glucose)
  • Surface swabs (ear, throat) of neonate for GBS
  • Rapid antigen detection tests (limited sensitivity)

Management

Non-pharmacological

  • Awareness of risk factors and indications for IAP
  • Patient information for GBS-positive women about signs of neonatal infection
  • Neonatal observation: all babies born to GBS-positive mothers should have enhanced monitoring for ≥12 hours

Pharmacological

  • Intrapartum antibiotic prophylaxis (IAP):
    • Benzylpenicillin: 3g IV loading dose, then 1.5g IV every 4 hours until delivery
    • Penicillin allergy (not anaphylaxis): cephalosporin (cefuroxime 1.5g IV 8-hourly)
    • Severe penicillin allergy: clindamycin 900mg IV 8-hourly (if GBS sensitive) or vancomycin 1g IV 12-hourly
  • IAP should ideally be given ≥4 hours before delivery for maximum effectiveness
  • Neonatal treatment: benzylpenicillin + gentamicin IV for suspected/confirmed EOGBS disease

Surgical/Interventional

  • No specific surgical management
  • Delivery should not be delayed to complete a course of IAP

Referral Criteria

  • All neonates with suspected GBS infection require paediatric assessment
  • Neonatal unit admission if symptomatic
  • Follow-up hearing assessment for neonates with GBS meningitis

Prognosis

  • EOGBS disease mortality: 5-10% overall; higher in preterm infants (up to 20%)
  • EOGBS meningitis mortality: 10%; 25-50% of survivors have long-term neurological sequelae
  • Late-onset GBS meningitis mortality: 2-6%
  • IAP reduces EOGBS disease by approximately 86% (NNT approximately 200 for colonised women)
  • With appropriate IAP, risk of neonatal disease is <0.5%

Other Relevant Information

Indications for Intrapartum Antibiotic Prophylaxis (RCOG GTG 36)

IndicationAction
Previous baby with invasive GBS diseaseOffer IAP
GBS bacteriuria in current pregnancyOffer IAP
Incidental GBS detection on vaginal/rectal swabOffer IAP
Preterm labour (<37 weeks)Offer IAP
Prolonged ROM >18 hours at termConsider IAP
Intrapartum fever >38°COffer broad-spectrum antibiotics (include GBS cover)

UK vs USA Screening Approach

FeatureUKUSA
ScreeningRisk-based (no routine)Universal (35-37 weeks)
GuidelineRCOG GTG 36CDC/ACOG
RationaleCost, transient colonisationHigher detection, lower EOGBS