Related Experiment Video
Updated: Aug 11, 2026

A Murine Model of Group B Streptococcus Vaginal Colonization
Published on: November 16, 2016
Efficacy of a strategy to prevent neonatal early-onset group B streptococcal (GBS) sepsis
Regina M Renner1, A Renner, Seraina Schmid
1Department of Obstetrics and Gynecology, University Hospital, Basel, Switzerland.
Insights
Our new strategy for preventing early-onset Group B Streptococcus (GBS) sepsis in newborns, involving GBS screening and targeted intrapartum antibiotic prophylaxis (IAP), significantly reduced sepsis incidence. This approach is effective and cost-efficient compared to broader strategies.
Area of Science:
- Neonatal Health
- Infectious Disease Prevention
- Obstetrics
Background:
- Existing guidelines for preventing early-onset neonatal Group B Streptococcus (GBS) sepsis vary.
- A new prevention strategy was developed in 1997, incorporating GBS screening at 36 weeks' gestation.
- This strategy includes intrapartum antibiotic prophylaxis (IAP) for women with positive or unknown GBS colonization and at least one risk factor.
Purpose of the Study:
- To evaluate the efficacy of the new prevention strategy for early-onset neonatal GBS sepsis.
- To compare the incidence of GBS sepsis before and after the implementation of the new strategy.
Main Methods:
- Retrospective study of early-onset GBS sepsis incidence among live births from 1997-2002.
- Analysis of risk factors, GBS screening, and IAP in GBS sepsis cases.
- Comparison with a historical cohort (1984-1993) that did not utilize GBS screening or routine IAP.
Main Results:
- The incidence of early-onset GBS sepsis decreased from 1/1000 live births (G1) to 0.53/1000 live births (G2).
- A significant reduction in overall intrapartum risk factors was observed in GBS sepsis cases.
- The new strategy demonstrated a notable decrease in neonatal GBS sepsis rates.
Conclusions:
- The implemented prevention strategy effectively reduces early-onset GBS sepsis in neonates.
- The strategy is more cost-effective and has fewer associated complications than broader approaches like the CDC's strategy.
- Targeted screening and IAP offer a beneficial approach to neonatal GBS sepsis prevention.
Background:
Existing guidelines recommend different strategies to prevent early-onset neonatal GBS sepsis. In 1997, using our own data on incidence and risk factors, we established a new prevention strategy which includes GBS screening at 36 weeks' gestation and intrapartum antibiotic prophylaxis (IAP) in women with positive or unknown GBS colonization with at least one risk factor. The present study evaluates the efficacy of the new prevention strategy.
Methods:
Retrospective study of the incidence of early-onset GBS sepsis among all live births at the University Women's Hospital Basel between 1997 and 2002. Additional analysis of delivery and post partum period of all GBS sepsis cases, including GBS screening, risk factors during labor (prematurity, rupture of membranes (ROM) <12 h, intrapartum signs of infection), and IAP. Comparison of this group's characteristics G2 (9,385 live births, using the new strategy) with the previous group, G1 (1984-1993, 16,126 live births, without GBS screening or routine IAP) was performed.
Results:
The incidence of early-onset GBS sepsis was reduced from 1/1000 (G1) to 0.53/1000 (G2). We observed a significant reduction of overall intrapartum risk factors in cases of GBS sepsis.
Conclusion:
This study suggests that our new prevention strategy is effective in reducing the incidence of early-onset GBS sepsis in neonates. In comparison, implementation of the CDC's prevention strategy might have prevented 2 additional cases in 9385 live births. However, this would have required treating a much larger number of pregnant women with IAP with consequential increasing costs, side effects and complications.
Related Concept Videos
Healthcare Associated Infections II: Preventive Measures
The best practices for preventing healthcare-associated infections include hand hygiene, patient risk...
Streptococcal Pharyngitis
Respiratory Syncytial Virus Disease
