Journal
LANCET CHILD & ADOLESCENT HEALTH
Volume 5, Issue 6, Pages 398-407Publisher
ELSEVIER SCI LTD
DOI: 10.1016/S2352-4642(21)00022-5
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- Bill & Melinda Gates Foundation
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This study evaluated the long-term effects of infant invasive Group B Streptococcus (GBS) disease on mortality, neurodevelopmental impairments, and economic outcomes up to adolescence in Denmark and the Netherlands. The findings showed that meningitis was associated with increased mortality at age 5, any iGBS disease increased the risk of NDI at age 10, and children with a history of iGBS disease required more frequent outpatient clinic visits and hospital admissions by age 5.
Background Group B Streptococcus (GBS) disease is a leading cause of neonatal death, but its long-term effects have not been studied after early childhood. The aim of this study was to assess long-term mortality, neurodevelopmental impairments (NDIs), and economic outcomes after infant invasive GBS (iGBS) disease up to adolescence in Denmark and the Netherlands. Methods For this cohort study, children with iGBS disease were identified in Denmark and the Netherlands using national medical and administrative databases and culture results that confirmed their diagnoses. Exposed children were defined as having a history of iGBS disease (sepsis, meningitis, or pneumonia) by the age of 89 days. For each exposed child, ten unexposed children were randomly selected and matched by sex, year and month of birth, and gestational age. Mortality data were analysed with the use of Cox proportional hazards models. NDI data up to adolescence were captured from discharge diagnoses in the National Patient Registry (Denmark) and special educational support records (the Netherlands). Health care use and household income were also compared between the exposed and unexposed cohorts. Findings 2258 children-1561 in Denmark (born from Jan 1, 1997 to Dec 31, 2017) and 697 in the Netherlands (born from Jan 1, 2000 to Dec 31, 2017)-were identified to have iGBS disease and followed up for a median of 14 years (IQR 7-18) in Denmark and 9 years (6-11) in the Netherlands. 366 children had meningitis, 1763 had sepsis, and 129 had pneumonia (in Denmark only). These children were matched with 22 462 children with no history of iGBS disease. iGBS meningitis was associated with an increased mortality at age 5 years (adjusted hazard ratio 4.08 [95% CI 1.78-9.35] for Denmark and 6.73 [3.76-12.06] for the Netherlands). Any iGBS disease was associated with an increased risk of NDI at 10 years of age, both in Denmark (risk ratio 1.77 [95% CI 1.44-2.18]) and the Netherlands (2.28 [1.64-3.17]). A history of iGBS disease was associated with more frequent outpatient clinic visits (incidence rate ratio 1.93 [95% CI 1.79-2.09], p<0.0001) and hospital admissions (1.33 [1.27-1.38], p<0.0001) in children 5 years or younger. No differences in household income were observed between the exposed and unexposed cohorts. Interpretation iGBS disease, especially meningitis, was associated with increased mortality and a higher risk of NDIs in later childhood. This previously unquantified burden underlines the case for a maternal GBS vaccine, and the need to track and provide care for affected survivors of iGBS disease.
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