Neonatal Group B Streptococcal Infection in Australia: A Case–control Study

Author:

Yanni Marianne12,Stark Michael23,Francis Laura4,Francis Joshua R.45,McMillan Mark26ORCID,Baird Rob7,Heath Paul T.8,Gordon Alex1,Riccardione James7,Wilson Angela7,Lee Rebecca4,Chooi Kathrina6,Quinn Olivia-Paris6,Marshall Helen S.126

Affiliation:

1. Department of Paediatrics, Women’s and Children’s Health Network, Adelaide, South Australia, Australia

2. Robinson Research Institute and Adelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia

3. Department of Neonatology, Women’s and Children’s Health Network, Adelaide, South Australia, Australia

4. Department of Paediatrics, Royal Darwin Hospital, Tiwi, Northern Territory, Australia

5. Global and Tropical Health Division, Menzies School of Health Research, Charles Darwin University, Casuarina, Northern Territory, Australia

6. Vaccinology and Immunology Research Trials Unit, Women’s and Children’s Health Network, Adelaide, South Australia, Australia

7. Territory Pathology, Royal Darwin Hospital, Tiwi, Northern Territory, Australia

8. Paediatric Infectious Diseases Research Group & Vaccine Institute St George’s, University of London, London, United Kingdom.

Abstract

Background: To determine maternal and neonatal risk factors for, and incidence of, neonatal early-onset group B streptococcus (EOGBS) and late-onset (LOGBS) infection in South Australia (SA) and the Northern Territory (NT). Methods: A case–control study with 2:1 matched controls to cases. The study included tertiary hospitals in South Australia and the Northern Territory, Australia. Retrospective data were collected from a 16-year epoch (2000–2015). Results: Of a total of 188 clinically suspected or confirmed cases, 139 were confirmed, of which 56.1% (n = 78) were EOGBS and 43.9% (n = 61) were LOGBS. The incidence of clinically suspected and confirmed cases of EOGBS was 0.26/1000 live births in SA and 0.73/1000 live births in the NT, and the incidence of confirmed cases was 0.19/1000 for SA and 0.36/1000 for the NT. The incidence of clinically suspected or confirmed LOGBS was 0.18/1000 live births in SA and 0.16/1000 for the NT. The majority of infants with GBS presented with sepsis, pneumonia, or meningitis. Developmental delay was the most commonly recorded long-term complication at 1 year old. Risk factors for EOGBS included maternal GBS carriage, previous fetal death, identifying as Aboriginal and/or Torres Strait Islander, and maternal fever in labor/chorioamnionitis. Conclusions: GBS remains a leading cause of neonatal morbidity and mortality. Adding previous fetal death to GBS screening guidelines would improve GBS prevention. The introduction of maternal GBS vaccination programs should be guided by country-specific disease epidemiology.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Infectious Diseases,Microbiology (medical),Pediatrics, Perinatology and Child Health

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