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Updated: Jul 2, 2026

A Murine Model of Group B Streptococcus Vaginal Colonization
Published on: November 16, 2016
Update on group B streptococcal infections: perinatal and neonatal periods
1Oklahoma University Health Sciences Center, Oklahoma City, OK 73104, USA. Raja-Nandyal@ouhsc.edu
Insights
Universal screening for Group B Streptococcus (GBS) in pregnant women significantly reduced early-onset GBS disease in newborns. Guidelines recommend intrapartum antibiotic prophylaxis for GBS carriers to prevent neonatal sepsis.
Area of Science:
- Neonatal Medicine
- Infectious Diseases
- Public Health
Background:
- Group B Streptococcus (GBS) is a primary cause of neonatal sepsis in the US.
- Previous guidelines in 1996 aimed to prevent GBS disease through intrapartum antibiotic prophylaxis.
- Significant reductions in early-onset GBS disease have been observed since guideline implementation.
Purpose of the Study:
- To detail recommendations for screening, diagnosing, and treating Group B Streptococcus disease in newborns.
- To highlight the effectiveness of the screening-based strategy for GBS prevention.
- To provide an update on national guidelines for GBS management.
Main Methods:
- Universal screening of pregnant women (35-37 weeks gestation) for GBS colonization.
- Intrapartum antibiotic prophylaxis for identified GBS carriers.
- Specific antibiotic recommendations based on maternal allergy and GBS sensitivity.
Main Results:
- A 70% decrease in early-onset GBS disease rates following guideline implementation.
- Continued incidence decrease reported by the CDC in 2005.
- Screening-based strategy validated as superior for GBS prevention.
Conclusions:
- The screening-based strategy for GBS is highly effective in reducing neonatal sepsis.
- Current guidelines recommend universal screening and targeted intrapartum prophylaxis.
- Antibiotic resistance remains a theoretical concern, necessitating ongoing surveillance.
Abstract:
Group B Streptococcus (GBS), one of the beta-Hemolytic streptococci, remains a leading cause of neonatal sepsis in the United States. The first consensus guidelines for the prevention of neonatal GBS disease were published in 1996, recommending intrapartum antibiotic prophylaxis on the basis of screening-based or risk-based strategies. Since then, there has been a 70% decrease in the rate of early-onset GBS disease. On the basis of evidence-validating superiority of this screening-based strategy, new national guidelines were released in 2002. Data from the Centers for Disease Control and Prevention in 2005 showed a continued decrease in the annual incidence of early-onset GBS infection. The screening-based strategy involves universal screening of all pregnant women at 35 to 37 weeks' gestation for vaginal and rectal GBS colonization and recommends intrapartum antibiotic prophylaxis for all GBS carriers (unless delivered by planned cesarean section before the onset of labor in a woman with intact membranes) with penicillin-G (or ampicillin). For mothers with severe penicillin allergy, clindamycin or erythromycin is recommended, when GBS' sensitivity is known; otherwise, vancomycin is recommended. Cefazolin is recommended for individuals with mild penicillin allergy. Severe anaphylactic reactions to penicillin were extremely rare. Emergence of antibiotic resistance to penicillin is still a theoretical possibility. This article provides a detailed account of recommendations for screening, diagnosing, and treating GBS disease in newborns.
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