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Meta-Analysis
.2022 Sep 30;75(7):1255-1264.
doi: 10.1093/cid/ciac206.

Clinical Risk Factors Associated With Late-Onset Invasive Group B Streptococcal Disease: Systematic Review and Meta-Analyses

Affiliations
Meta-Analysis

Clinical Risk Factors Associated With Late-Onset Invasive Group B Streptococcal Disease: Systematic Review and Meta-Analyses

Konstantinos Karampatsas et al. Clin Infect Dis..

Abstract

Background: Group B streptococcal (GBS) infection remains one of the most significant causes of late-onset sepsis and meningitis (LOGBS) among young infants. However, transmission routes and risk factors for LOGBS are not yet fully understood.

Methods: We conducted systematic reviews on clinical risk factors previously reported in the literature (prematurity, low birth weight [<2500 g], antenatal colonization, multiple-gestation pregnancy, maternal age <20 years, male infant sex, intrapartum fever, prolonged rupture of membranes) and meta-analyses to determine pooled estimates of risk.

Results: We included 27 articles, reporting 5315 cases. Prematurity (odds ratio [OR] 5.66; 95% confidence interval [CI]: 4.43-7.22), low birth weight (OR 6.73; 95% CI: 4.68-9.67), maternal colonization (2.67; [2.07-3.45]), and multiple-gestation pregnancies (OR 8.01; 95% CI: 5.19-12.38) were associated with an increased risk of LOGBS.

Conclusions: Prematurity/low birth weight and maternal colonization are major risk factors for LOGBS. Future GBS vaccine studies should try to establish the optimal time for vaccination during pregnancy to protect preterm infants.

Keywords: Streptococcus agalactiae; Group B Streptococcus; neonatal sepsis; risk.

© The Author(s) 2022. Published by Oxford University Press for the Infectious Diseases Society of America.

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Conflict of interest statement

Potential conflicts of interest. K. L. D. is supported by Future Leaders Fellowships by UK Research and Innovation (UKRI) Future Leaders Fellowship (MR/S016570/1). P. T. H. reports research grants to the institution from Pfizer and Minervax outside of the submitted work. All other authors report no potential conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

Figures

Figure 1.
Figure 1.
Data search and included studies for risk factor for LOGBS. Abbreviation: LOGBS, late-onset group B streptococcal disease.
Figure 2.
Figure 2.
Forest plot of meta-analysis of risk of LOGBS for prematurity. Abbreviations: CI, confidence interval; LOGBS, late-onset group B streptococcal disease.
Figure 3.
Figure 3.
Forest plot of meta-analysis of risk of LOGBS for LBW. Abbreviations: CI, confidence interval; LBW, low birth weight; LOGBS, late-onset Group B streptococcal disease.
Figure 4.
Figure 4.
Forest plot of meta-analysis of risk of LOGBS for antenatal GBS colonization. Abbreviations: CI, confidence interval; GBS, Group BStreptococcus; LOGBS, late-onset group B streptococcal disease.
Figure 5.
Figure 5.
Forest plot of meta-analysis of risk of LOGBS for multiple gestation pregnancies. Abbreviations: CI, confidence interval; LOGBS, late-onset group B streptococcal disease.
See this image and copyright information in PMC

References

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