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A Murine Model of Group B Streptococcus Vaginal Colonization
Published on: November 16, 2016
Group B streptococcal disease in infants aged younger than 3 months: systematic review and meta-analysis
Karen M Edmond1, Christina Kortsalioudaki, Susana Scott
1London School of Hygiene and Tropical Medicine, London, UK. karen.edmond@lshtm.ac.uk
Insights
Group B Streptococcus (GBS) causes significant infant illness and death globally. A vaccine targeting five GBS serotypes could prevent the majority of invasive GBS disease cases.
Area of Science:
- Global Health
- Infectious Diseases
- Pediatrics
Background:
- Group B Streptococcus (GBS) is a major cause of infant morbidity and mortality worldwide.
- Intrapartum antibiotic prophylaxis is widely used but GBS disease burden estimates are lacking for many regions.
Purpose of the Study:
- To examine the current global burden of invasive GBS disease.
- To determine the serotype distribution of GBS isolates.
Main Methods:
- Searched Medline, Embase, and Wholis databases for studies on invasive GBS disease (early- and late-onset).
- Included studies reporting incidence, deaths, or serotypes; reviewed reference lists and contacted experts for unpublished data.
- Utilized random effects meta-analysis to pool data from 74 eligible studies.
Main Results:
- Mean incidence of GBS in infants (0-89 days) was 0.53 per 1000 livebirths, with a case fatality ratio of 9.6%.
- Early-onset GBS incidence and case fatality were double that of late-onset disease.
- Serotype III was most common (48.9%), followed by Ia (22.9%), V (9.1%), Ib (7.0%), and II (6.2%).
Conclusions:
- More high-quality studies are needed, particularly in low-income countries, to accurately estimate GBS burden.
- A conjugate vaccine targeting serotypes Ia, Ib, II, III, and V could prevent most global GBS disease.
Background:
Despite widespread use of intrapartum antibiotic prophylaxis, group B streptococcus remains a leading cause of morbidity and mortality in infants in Europe, the Americas, and Australia. However, estimates of disease burden in many countries outside of these regions is not available. We aimed to examine the current global burden of invasive disease and the serotype distribution of group B streptococcus isolates.
Methods:
We searched Medline, Embase, and Wholis databases for studies on invasive early-onset (day 0-6) and late-onset (day 7-89) group B streptococcal disease. Eligible studies were those that described incidence, deaths, or serotypes. We also reviewed reference lists and contacted experts to seek unpublished data and data missed by our search. Random effects meta-analysis was used to pool data.
Findings:
74 studies met the inclusion criteria; 56 studies reported incidence, 29 case fatality, and 19 serotype distribution. An additional search for studies that reported serotype distribution from Jan 1, 1980, yielded a total of 38 articles. Only five low-income countries were represented in the review and contributed 5% weight to the meta-analysis. 47 (69%) studies reported use of any intrapartum antibiotic prophylaxis. Substantial heterogeneity existed between studies. Mean incidence of group B streptococcus in infants aged 0-89 days was 0·53 per 1000 livebirths (95% CI 0·44-0·62) and the mean case fatality ratio was 9·6% (95% CI 7·5-11·8). Incidence of early-onset group B streptococcus (0·43 per 1000 livebirths [95% CI 0·37-0·49]) and case fatality (12·1%, [6·2-18·3]) were two-times higher than late-onset disease. Serotype III (48·9%) was the most frequently identified serotype in all regions with available data followed by serotypes Ia (22·9%), Ib (7·0%), II (6·2%), and V (9·1%). Studies that reported use of any intrapartum antibiotic prophylaxis were associated with lower incidence of early-onset group B streptococcus (0·23 per 1000 livebirths [95% CI 0·13-0·59]) than studies in which patients did not use prophylaxis (0·75 per 1000 livebirths [0·58-0·89]).
Interpretation:
More high-quality studies are needed to accurately estimate the global burden of group B streptococcus, especially in low-income countries. A conjugate vaccine incorporating five serotypes (Ia, Ib, II, III, V) could prevent most global group B streptococcal disease.
Funding:
Child Epidemiology Reference Group (CHERG), WHO.
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