Empirical therapy of newborns at risk for or with suspected early-onset sepsis (EOS) represents the main contributor to the use of antibiotics in early life.
1 The reported number of newborns receiving antibiotic therapy for 1 episode of culture-proven EOS ranges from 18 to 118 in high-risk infants, and up to 1400 in well-appearing newborns born to mothers with chorioamnionitis.
2-4 Thus, for each case of culture-proven EOS many newborns are exposed to potential harms related to empirical antibiotic therapy. Use of antibiotics in newborns is associated with early adverse consequences such as increased risk of necrotizing enterocolitis, fungal infections, and death in preterm infants.
5,6 Moreover, antibiotics increase antibiotic resistance, mother-child separation, and health care costs.
7,8 Antibiotic-induced microbiome alterations early in life, with downstream effects on the developing immune system,
9,10 are also associated with increased risks of allergic diseases, obesity, and autoimmune diseases later in life.
6,11,12