The Effect of Perinatal GBS Screening and IAP on Maternal and Infant Prognosis

Authors: Choi Ka Wai; Ieong Weng San; Chan Iok Mui
DIN
IJOER-MAY-2024-1
Abstract

Objective: To investigate the effect of perinatal Group B Streptococcus (GBS) infection and intrapartum antibiotic prophylaxis (IAP) regimen on maternal and infant clinical outcome.

Methods: From January to December 2023, 626 GBS-positive and 2565 GBS-negative, gestation 35-37 weeks pregnant women were included in the observation and the control groups respectively. We compared the outcomes of the maternal and infant between the two groups. 

Results: The preterm birth rate and postpartum hemorrhage rate in the observation group were significantly lower than that in the control group. However the incidence of preterm rupture of membranes, the incidence for "placenta pathological examination" critically evaluated by "after- However the incidence of preterm rupture of membranes, the incidence for "placenta pathological examination" critically evaluated by "after- delivery check protocol" and neonatal clinical sepsis in the observation group was significantly higher than that of the control group. There was no statistically significant difference in terms of delivery methods, the incidence of macrosomia, the incidence of neonatal 1'Apgar score. There was no statistically significant difference in terms of delivery methods, the incidence of macrosomia, the incidence of neonatal 1'Apgar score ≤7 and neonatal pneumonia between the two groups. 

Conclusions: The standardized maternal GBS screening and intrapartum antibiotic prophylaxis (IAP) programme adopted at our hospital was effective in reducing adverse maternal and neonatal outcomes.

Keywords
Group B Streptococcus (GBS) Neonatal pneumonia neonatal clinical sepsis Intrapartum antibiotic prophylaxis(IAP).
Introduction

GBS, also known as Streptococcus lactis, is the leading cause of infection during pregnancy, premature birth and neonatal infections. It is also a common species found in the vagina and rectum of women. Its presence is intermittent, temporary and persistent [1]. However, reproduction in the female vagina is a high-risk indicator for neonatal diseases and premature birth [2] . Normally, there is a balance between the microflora in the vagina and the host's environment. However, if the level of oestrogen rises in the pregnant woman's body, advantageous bacteria such as vaginal glycogen and lactobacilli will proliferate, resulting in a disturbance of the originally balanced microflora in the organism, which is most obvious in the late stage of pregnancy. The edema of the vaginal mucosa and other factors can easily induce GBS infection in the genital tract, leading to adverse pregnancy outcomes and threatening the safety of the newborn.[3] GBS infection is often associated with sepsis, urinary tract infections, endometritis, and fetal infections in pregnant women. Failure to detect GBS in the antenatal period may increase the risk of infection in both the mother and the newborn[4]-[6] . The most common type of GBS infection is early-onset group B streptococcus (EOGBS) in newborns, which manifests itself as an infection within 7 days of birth and is characterized by respiratory symptoms and pneumonia[7] . The incidence of vaginal/rectal GBS in pregnant women is 10-30% [8] . The prevalence of GBS in low-income countries, Africa, and black women is higher, and the incidence of neonatal disease is higher, too [9]-[10] .

Conclusion

GBS is a rare infection in immunocompetent adults but carries a high risk in newborns with immature immune systems. 40- 70% of mothers carrying GBS will infect their newborns, and 1-2% of these newborns will become infected. When GBS comes into contact with the amniotic cavity or placenta, amnionitis or chorioamnionitis may occur, leading to preterm labour and stillbirth[24] . A study on how GBS crosses the placenta barrier to cause chorioamnionitis when it infects the chorionic villus found that GBS can adhere to and invade chorionic villus and amniotic epithelial cells[25] . Chorioamnionitis can cause direct fetal lung damage[26 ] , without the need for bacterial invasion of the lungs.

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