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What are the primary capsular polysaccharide types of Group B streptococci that account for most cases in infants?
What are the primary capsular polysaccharide types of Group B streptococci that account for most cases in infants?
Types Ia, Ib, II, III, and V account for approximately 95% of cases in infants.
What is the relevance of type III capsular polysaccharide in Group B streptococci infections in infants?
What is the relevance of type III capsular polysaccharide in Group B streptococci infections in infants?
Type III is the predominant cause of early- and late-onset meningitis in infants.
What was the incidence rate of early-onset Group B streptococcal disease before the introduction of maternal intrapartum antimicrobial prophylaxis?
What was the incidence rate of early-onset Group B streptococcal disease before the introduction of maternal intrapartum antimicrobial prophylaxis?
The incidence was 1 to 4 cases per 1000 live births.
How has the incidence of early-onset Group B streptococcal disease changed since the implementation of maternal prophylaxis?
How has the incidence of early-onset Group B streptococcal disease changed since the implementation of maternal prophylaxis?
What factors contribute to higher case-fatality ratios in infants with Group B streptococcal infection?
What factors contribute to higher case-fatality ratios in infants with Group B streptococcal infection?
What are the transmission routes for Group B streptococci from mother to infant?
What are the transmission routes for Group B streptococci from mother to infant?
What percentage of pregnant women are typically colonized by Group B streptococci?
What percentage of pregnant women are typically colonized by Group B streptococci?
What challenges exist concerning the incidence of late-onset Group B streptococcal disease?
What challenges exist concerning the incidence of late-onset Group B streptococcal disease?
Which populations are at an increased risk for sporadic, invasive GAS disease?
Which populations are at an increased risk for sporadic, invasive GAS disease?
Why is targeted chemoprophylaxis recommended for certain high-risk populations?
Why is targeted chemoprophylaxis recommended for certain high-risk populations?
What is the rationale for not recommending chemoprophylaxis in schools or childcare facilities?
What is the rationale for not recommending chemoprophylaxis in schools or childcare facilities?
Identify two specific medical conditions considered as risk factors for invasive GAS disease.
Identify two specific medical conditions considered as risk factors for invasive GAS disease.
In relation to GAS disease, what age group is particularly highlighted for targeted interventions?
In relation to GAS disease, what age group is particularly highlighted for targeted interventions?
What are the key virulence factors associated with Group B Streptococcus (GBS) infections?
What are the key virulence factors associated with Group B Streptococcus (GBS) infections?
How does the epidemiology of GBS differ between pregnant women and non-pregnant populations?
How does the epidemiology of GBS differ between pregnant women and non-pregnant populations?
What role does maternal intrapartum prophylaxis play in preventing GBS infections in newborns?
What role does maternal intrapartum prophylaxis play in preventing GBS infections in newborns?
Identify the main risk factors for GBS infection among pregnant women.
Identify the main risk factors for GBS infection among pregnant women.
Explain the transmission routes of Group B Streptococcus in a healthcare setting.
Explain the transmission routes of Group B Streptococcus in a healthcare setting.
Flashcards
GAS disease risk in certain populations
GAS disease risk in certain populations
Increased risk of invasive GAS disease exists in high-risk groups like people with HIV, those aged 65 and older, and others with specific illnesses (e.g., varicella, diabetes mellitus).
Chemoprophylaxis in household contacts
Chemoprophylaxis in household contacts
Doctors might recommend preventive medicine (chemoprophylaxis) to household contacts of high-risk individuals (e.g., age 65+) to reduce GAS infection risk.
Chemoprophylaxis for children
Chemoprophylaxis for children
Chemoprophylaxis isn't usually recommended in schools or childcare settings due to low risk in children.
High-risk Populations (GAS)
High-risk Populations (GAS)
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Secondary cases of GAS
Secondary cases of GAS
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Household contact risk
Household contact risk
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Routine GAS testing for contacts?
Routine GAS testing for contacts?
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Chemoprophylaxis for contacts
Chemoprophylaxis for contacts
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Severe invasive GAS risk
Severe invasive GAS risk
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STSS
STSS
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Group B Strep Types
Group B Strep Types
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Virulence Factors in Group B Strep
Virulence Factors in Group B Strep
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Where is Group B Strep Found?
Where is Group B Strep Found?
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Group B Strep Colonization in Pregnant Women
Group B Strep Colonization in Pregnant Women
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Early-Onset GBS Disease
Early-Onset GBS Disease
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Late-Onset GBS Disease
Late-Onset GBS Disease
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GBS Disease Transmission
GBS Disease Transmission
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Group B Strep Control Measures
Group B Strep Control Measures
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Study Notes
Group B Streptococcal Infections
- Group B streptococci (GBS) are a major cause of perinatal infections, including bacteremia, endometritis, intra-amniotic infection, and urinary tract infections in women during pregnancy and postpartum, and systemic/focal infections in neonates and infants.
Clinical Manifestations
- Early-onset disease: typically within 24 hours of life, characterized by systemic infection, respiratory distress, apnea, shock, pneumonia, and sometimes meningitis.
- Late-onset disease: typically at 3-4 weeks of age, often manifests as occult bacteremia or meningitis, also osteomyelitis, septic arthritis, necrotizing fasciitis, pneumonia, adenitis, and cellulitis.
Etiology
- Gram-positive, aerobic diplococci, producing beta hemolysis on 5% sheep blood agar.
- Classified into 10 types (Ia, Ib, and II-IX); types Ia, Ib, II, III, and V account for ~95% of infant cases in the US.
- Capsular polysaccharides and pilus-like structures are important virulence factors.
Epidemiology
- Common inhabitants of the human gastrointestinal and genitourinary tracts.
- Colonization rate in pregnant women ranges from 15-35%.
- Early-onset incidence was 1-4 cases per 1000 live births, reduced to ~0.25 cases per 1000 live births post-intrapartum antimicrobial prophylaxis.
- Increased risk for preterm infants, infants with ruptured membranes (>18 hours), mothers with high genital GBS inoculum, intrapartum fever, previous infant with invasive GBS disease, and low/undetectable maternal antibody levels.
- Black infants have higher incidence of both early- and late-onset disease than white infants.
Diagnosis
- Gram stain of body fluids shows gram-positive cocci in pairs or short chains.
- Culture of blood, CSF, or affected sites is necessary for confirmation.
- Multiplex polymerase chain reaction assay can directly detect GBS in CSF.
- Culture screening at 35-37 weeks gestation in pregnant women is recommended to identify GBS colonization.
Treatment
- For early-onset GBS infection in newborns, ampicillin plus an aminoglycoside is the initial treatment of choice.
- Late-onset meningitis: ampicillin/aminoglycoside, cefotaxime, or vancomycin/ceftriaxone for infants >2 months.
- For infants with meningitis, the recommended dose of penicillin G or ampicillin is adjusted for age (<7 days vs >7 days).
- Intrapartum chemoprophylaxis is recommended for certain high-risk pregnant women to prevent neonatal GBS disease.
Control Measures
- Pregnant women should undergo GBS culture screening.
- Intrapartum antibiotic prophylaxis is recommended in certain high-risk scenarios.
- Chemoprophylaxis is not recommended in schools or child care settings due to low risk of secondary cases and minimal risk of invasive GBS infections in children.
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Description
Explore the clinical manifestations and etiology of Group B Streptococcal infections, particularly in perinatal contexts. This quiz covers early and late-onset diseases, their symptoms, and the types of bacteria involved. Test your understanding of this critical area of infectious disease in obstetrics and pediatrics.