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Pregnancy and Neonatal Outcomes of Group B Streptococcus Infection in Preterm Births

Authors
Yae Heun LeeYoo Jung LeeSun Young JungSuk Young KimDong Woo Son서일혜
Issue Date
Dec-2018
Publisher
대한주산의학회
Keywords
Streptococcus agalactiae; Premature birth; Fetal membranes; Premature rupture
Citation
Perinatology, v.29, no.4, pp.147 - 152
Journal Title
Perinatology
Volume
29
Number
4
Start Page
147
End Page
152
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/4575
DOI
10.14734/PN.2018.29.4.147
ISSN
2508-4887
Abstract
Objective: This study examines whether maternal group B Streptococcus (Streptococcus agalactiae, GBS) infection was associated with preterm births and premature neonatal outcomes. Methods: Maternal and neonatal outcomes were examined among singleton pregnant women with preterm birth (from 24+0 weeks to 36+6 weeks) who were tested for GBS (n=203) during the pregnancy. Data were collected retrospectively from the medical records of women who delivered at our hospital from January 2015 to February 2017. We compared obstetrical factors (causes of preterm birth) and neonatal (gestational age at delivery, birth weight, Apgar score 1 min/5 min, hospitalization period, duration of mechanical ventilation, neonatal C-reactive protein within three days, and other complication [respiratory distress syndrome, neonatal deaths]) outcomes between GBS-infected and non-infected pregnant women. Results: There were 203 singleton pregnant women included in the study, 25 of whom were confirmed to have a GBS infection during the pregnancy. There was no difference in neonatal outcomes by GBS status. Preterm premature rupture of membranes (pPROM), as an obstetric factor, was associated with GBS infection (P=0.022). GBS infection raised the risk of pPROM by 3.6 times (odds ratio 3.648, 95% confidence interval 1.476-9.016, P=0.005). Conclusion: GBS infection in preterm birth was associated with pPROM but did not result in adverse neonatal outcomes. Continuous attention and evaluation of GBS infection, a major cause of neonatal sepsis and pneumonia, are needed.
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