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Whitepaper
The content presented on this page is intended for informational and educational purposes. While it is available globally, it may reflect clinical practices or healthcare system considerations specific to a particular region.
Group B Streptococcus (GBS) is the leading cause of severe infections in newborns, including meningitis and sepsis. These infections can result in death or lifelong disability for affected babies and have a profound impact on families.1,2 Despite the availability of diagnostic technologies globally, the U.K. does not routinely test pregnant women for GBS carriage before birth, unlike countries such as the U.S., Germany, France, and Australia. This lack of routine testing, combined with inconsistent care and poor awareness, leads to preventable harm.3 Universal screening and intrapartum antibiotic prophylaxis (IAP) have been shown to decrease infection rates and improve outcomes for babies and families.4
The U.K. currently employs a risk-based strategy for GBS prevention. Only those with specific risk factors—such as having had a previous baby with GBS, GBS detected in urine, or preterm labour—are offered antibiotics during labour (IAP). Routine testing for GBS is not offered to all, and GBS is not a notifiable disease, meaning cases may be underreported and the true burden is not fully understood.
Each month, 43 babies in the U.K. develop early-onset GBS infection; three survive with long-term disabilities, and two die.5 The infection rate in infants under one year is significantly higher than in the general population.6 Families affected by GBS face psychological trauma, financial hardship, and long-term care costs.7 The NHS also bears substantial costs from clinical negligence claims and ongoing care.8
The U.K. National Screening Committee currently does not recommend universal screening, citing concerns about accuracy, unnecessary antibiotic use, and unclear benefit-to-harm ratio.1 However, new evidence is being collected through the GBS3 trial, which is comparing universal testing (enriched culture media and PCR) against the risk-based approach. Results are expected in the Spring of 2026 and may inform future policy decisions.9
There is currently no licensed vaccine for GBS. A maternal GBS vaccine could prevent hundreds of thousands of cases annually and reduce the need for antibiotics during labour. However, questions remain about the duration of protection and effectiveness across different groups.10
Cepheid and Group B Strep Support (GBSS) have partnered on a prospective paper to address the need for a new approach to Group B testing in the UK. The following are call to action addressed in the paper:
Access the full perspective paper here
References:
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