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.
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
| Diagnosis | Key Features | Investigation |
|---|---|---|
| E. coli neonatal sepsis | Second most common cause of neonatal sepsis | Blood/CSF culture |
| Listeriosis | Maternal flu-like illness, preterm labour, meconium-stained liquor | Blood culture, placental histology |
| Transient tachypnoea of newborn | Respiratory distress at birth, resolves within 24-48h | CXR, clinical course |
| Respiratory distress syndrome | Preterm, ground glass CXR | CXR, surfactant |
| Congenital pneumonia | Respiratory distress, consolidation on CXR | CXR, 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)
| Indication | Action |
|---|---|
| Previous baby with invasive GBS disease | Offer IAP |
| GBS bacteriuria in current pregnancy | Offer IAP |
| Incidental GBS detection on vaginal/rectal swab | Offer IAP |
| Preterm labour (<37 weeks) | Offer IAP |
| Prolonged ROM >18 hours at term | Consider IAP |
| Intrapartum fever >38°C | Offer broad-spectrum antibiotics (include GBS cover) |
UK vs USA Screening Approach
| Feature | UK | USA |
|---|---|---|
| Screening | Risk-based (no routine) | Universal (35-37 weeks) |
| Guideline | RCOG GTG 36 | CDC/ACOG |
| Rationale | Cost, transient colonisation | Higher detection, lower EOGBS |