Understanding Factors in Group B Streptococcus Late-Onset Disease.
Alberto BerardiViola TrevisaniAntonella Di CaprioJenny BuaMariachiara ChinaBarbara PerroneRossella PaganoLaura LucaccioniSilvia FanaroLorenzo IughettiLicia LugliRoberta CretiPublished in: Infection and drug resistance (2021)
Group B streptococcus (GBS) infection remains a leading cause of sepsis, pneumonia, and meningitis in infants. Rates of GBS early onset disease have declined following the widcespread use of intrapartum antibiotic prophylaxis; hence, late-onset infections (LOGBS) are currently a common presentation of neonatal GBS dicsease. The pathogenesis, mode of transmission, and risk factors associated with LOGBS are unclear, which interfere with effective prevention efforts. GBS may be transmitted from the mother to the infant at the time of delivery or during the postpartum period via contaminated breast milk, or as nosocomial or community-acquired infection. Maternal GBS colonization, prematurity, young maternal age, HIV exposure, and ethnicity (Black) are identified as risk factors for LOGBS disease; however, further studies are necessary to confirm additional risk factors, if any, for the implementation of effective prevention strategies. This narrative review discusses current and previous studies that have reported LOGBS. Few well-designed studies have described this condition; therefore, reliable assessment of maternal GBS colonization, breastfeeding, and twin delivery as risk factors for LOGBS remains limited.
Keyphrases
- late onset
- early onset
- risk factors
- birth weight
- case control
- pregnancy outcomes
- candida albicans
- hepatitis c virus
- mental health
- hiv infected
- biofilm formation
- primary care
- antiretroviral therapy
- intensive care unit
- human immunodeficiency virus
- acute kidney injury
- hiv positive
- pregnant women
- drinking water
- quality improvement
- hiv testing
- escherichia coli
- weight loss
- case report
- staphylococcus aureus
- weight gain
- cystic fibrosis
- south africa
- acute respiratory distress syndrome
- mechanical ventilation
- community acquired pneumonia