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Assessing the added value of group B Streptococcus maternal immunisation in preventing maternal infection and fetal harm: population surveillance study.

Lamagni, T; Wloch, C; Broughton, K; Collin, SM; Chalker, V; Coelho, J; Ladhani, SN; Brown, CS; Shetty, N; Johnson, AP (2021) Assessing the added value of group B Streptococcus maternal immunisation in preventing maternal infection and fetal harm: population surveillance study. BJOG, 129 (2). pp. 233-240. ISSN 1471-0528 https://doi.org/10.1111/1471-0528.16852
SGUL Authors: Ladhani, Shamez Nizarali

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Abstract

OBJECTIVE: To assess the incidence of maternal group B Streptococcus (GBS) infection in England. DESIGN: Population surveillance augmented through data linkage. SETTING: England. POPULATION: All pregnant women accessing the National Health Service (NHS) in England. METHODS: Invasive GBS (iGBS) infections during pregnancy or within 6 weeks of childbirth were identified by linking Public Health England (PHE) national microbiology surveillance data for 2014 to NHS hospital admission records. Capsular serotypes of GBS were determined by reference laboratory typing of clinical isolates from women aged 15-44 years. Post-caesarean section surgical site infection (SSI) caused by GBS was identified in 21 hospitals participating in PHE SSI surveillance (2009-2015). MAIN OUTCOME MEASURES: iGBS rate per 1000 maternities; risk of GBS SSI per 1000 caesarean sections. RESULTS: Of 1601 patients diagnosed with iGBS infections in England in 2014, 185 (12%) were identified as maternal infections, a rate of 0.29 (95% CI 0.25-0.33) per 1000 maternities and representing 83% of all iGBS cases in women aged 18-44 years. Seven (3.8%) were associated with miscarriage. Fetal outcome identified excess rates of stillbirth (3.4 versus 0.5%) and extreme prematurity (<28 weeks of gestation, 3.7 versus 0.5%) compared with national averages (P < 0.001). Caesarean section surveillance in 27 860 women (21 hospitals) identified 47 cases of GBS SSI, with an estimated 4.24 (3.51-5.07) per 1000 caesarean sections, a median time-to-onset of 10 days (IQR 7-13 days) and ten infections that required readmission. Capsular serotype analysis identified a diverse array of strains with serotype III as the most common (43%). CONCLUSIONS: Our assessment of maternal GBS infection in England indicates the potential additional benefit of GBS vaccination in preventing adverse maternal and fetal outcomes.

Item Type: Article
Additional Information: © 2021 Crown copyright. BJOG: An International Journal of Obstetrics and Gynaecology published by John Wiley & Sons Ltd. This article is published with the permission of the Controller of HMSO and the Queen's Printer for Scotland. This is an open access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Keywords: Streptococcus agalactiae, England, ethnic groups, infectious, population surveillance, pregnancy complications, surgical wound infection, Adolescent, Adult, England, Female, Hospitalization, Humans, Infant, Newborn, Infant, Newborn, Diseases, Medical Records, Population Surveillance, Pregnancy, Pregnancy Complications, Infectious, Prenatal Care, State Medicine, Streptococcal Infections, Streptococcus agalactiae, Vaccination, Young Adult, Humans, Streptococcus agalactiae, Streptococcal Infections, Pregnancy Complications, Infectious, Infant, Newborn, Diseases, Vaccination, Hospitalization, Prenatal Care, Population Surveillance, Medical Records, Pregnancy, Adolescent, Adult, Infant, Newborn, State Medicine, England, Female, Young Adult, 11 Medical and Health Sciences, Obstetrics & Reproductive Medicine
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: BJOG
ISSN: 1471-0528
Language: eng
Dates:
DateEvent
17 December 2021Published
17 August 2021Published Online
20 July 2021Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
UNSPECIFIEDPHEUNSPECIFIED
PubMed ID: 34324252
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/116679
Publisher's version: https://doi.org/10.1111/1471-0528.16852

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