abstract
With improved obstetrical management and evidence-based use of
intrapartum antimicrobial therapy, early-onset neonatal sepsis is becoming
less frequent.
However, early-onset sepsis remains one of the
most common causes of neonatal morbidity and mortality in the preterm
population.
The identification of neonates at risk for early-onset
sepsis is frequently based on a constellation of perinatal risk factors
that are neither sensitive nor specific.
Furthermore, diagnostic tests for neonatal sepsis have a poor positive predictive accuracy.
As a result, clinicians often treat well-appearing infants for extended periods of time,
even when bacterial cultures are negative.
The optimal treatment of infants with suspected early-onset sepsis is broad-spectrum antimicrobial agents (ampicillin and an aminoglycoside).
Once a pathogen is identified, antimicrobial therapy should be narrowed (unless synergism is
needed).
Recent data suggest an association between prolonged empirical treatment of preterm infants (≥5 days) with broad-spectrum antibiotics and higher risks of late onset sepsis, necrotizing enterocolitis, and mortality.
To reduce these risks, antimicrobial therapy should be discontinued at 48 hours in clinical situations in which the probabilityof sepsis is low.
The purpose of this clinical report is to provide a practical and, when possible, evidence-based approach to the management of infants with suspected or proven early-onset sepsis. Pediatrics
2012;129:1006–1015