Group B streptococcal disease in UK and Irish infants younger than 90 days

Paul T Heath1, Gail Balfour, Abbie M Weisner

  • 1Vaccine Institute, St George's Hospital, London, UK. pheath@sghms.ac.uk

Lancet (London, England)
|January 31, 2004
PubMed

Insights

Group B Streptococcus (GBS) infections in infants are a significant concern. This study reveals a minimum incidence of 0.72 per 1000 live births in the UK and Ireland, with a 9.7% mortality rate.

Area of Science:

  • Neonatal Health
  • Infectious Diseases
  • Epidemiology

Background:

  • Group B streptococcal (GBS) disease poses a significant threat to infant health.
  • Data on GBS incidence, morbidity, and mortality in the UK and Republic of Ireland were previously limited.

Purpose of the Study:

  • To determine the incidence, morbidity, and mortality of invasive GBS disease in infants under 90 days old.
  • To establish the current burden of GBS disease in the UK and Irish infant population.
  • To provide data for the development of GBS prevention guidelines.

Main Methods:

  • A surveillance study was conducted between February 1, 2000, and February 28, 2001.
  • Invasive GBS cases in infants younger than 90 days were identified through a network of pediatricians, microbiologists, and parents.
  • Incidence rates for overall, early-onset, and late-onset GBS disease were calculated.

Main Results:

  • A total of 568 GBS cases were identified, equating to an overall incidence of 0.72 per 1000 live births.
  • Early-onset GBS disease incidence was 0.48 per 1000 live births (377 cases), and late-onset incidence was 0.24 per 1000 live births (191 cases).
  • The overall mortality rate was 9.7% (53 deaths), and identifiable risk factors were present in 58% of early-onset cases.

Conclusions:

  • The study established the minimum burden of invasive GBS disease in UK and Irish infants.
  • Findings highlight the substantial impact of GBS on neonatal health.
  • The data are crucial for informing and formulating effective prevention strategies for GBS disease.

Related Concept Videos

Development of Immunocompetence01:22

Development of Immunocompetence

The initiation of cell-mediated immunity can be observed as early as the third month of fetal growth, with active antibody-mediated immunity following approximately one month later.
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...
Bacterial Phylum Chlamydiae01:29

Bacterial Phylum Chlamydiae

The phylum Chlamydiae or Chlamydiota is composed of a single order, Chlamydiales. This phylum consists entirely of obligate intracellular parasites that infect eukaryotic hosts. While human pathogens within this group have been studied extensively, the phylum encompasses many species capable of interacting with various eukaryotic organisms. Members of Chlamydiae are typically small cocci, approximately 0.5 μm in diameter, and exhibit a distinctive developmental cycle. As is characteristic of...
Bacterial Phylum Spirochaetes01:30

Bacterial Phylum Spirochaetes

Spirochetes, unique bacteria in the phylum Spirochaetes, are gram-negative, motile, tightly coiled, slender, and flexible. They inhabit aquatic sediments and animals, with some causing diseases like syphilis. Spirochetes are classified into eight genera based on habitat, pathogenicity, phylogeny, and characteristics.Their distinctive motility arises from endoflagella, located within the cell’s periplasm. These endoflagella anchor at the cell poles and extend along the cell length, encased by a...
Development of Human Microbiota01:30

Development of Human Microbiota

The human microbiota begins developing at birth and undergoes continual change as we age. Infancy marks a critical period of microbial sensitivity, offering a “window of opportunity” during which beneficial microbes help mature the immune system. By age three, children typically develop a more stable and diverse microbial community. Newborns acquire microbes from their immediate environment; vaginal delivery favors maternal vaginal microbes, while cesarean births favor microbes from the skin...
Development of the Oral Microbiota01:28

Development of the Oral Microbiota

The establishment of the oral microbiome begins before birth, challenging the long-held belief that the fetal oral cavity is sterile. The presence of oral microbes such as Streptococcus and Fusobacterium in amniotic fluid suggests that microbial exposure may occur in utero, potentially through translocation from the maternal oral or gastrointestinal tract. This early colonization primes the neonatal immune system and sets the stage for subsequent microbial succession. Maternal health,...
Bacterial Gastroenteritis01:18

Bacterial Gastroenteritis

Bacterial gastroenteritis, characterized by diarrhea, abdominal cramps, and vomiting, is often caused by ingestion of contaminated food or water and is frequently associated with pathogenic Escherichia coli strains. These microbes exploit two principal mechanisms to inflict disease.Shiga toxin–producing E. coli, also referred to as STEC—notably O157:H7—release Shiga toxins that target ribosomes, blocking protein synthesis. The B subunit of the toxin binds the host glycolipid receptor...