## Clinical Recognition of Early-Onset Neonatal Sepsis **Key Point:** This neonate meets criteria for suspected early-onset sepsis (EOS) and requires immediate empiric antibiotic therapy without delay for culture results. ### Risk Factors Present - Maternal PROM ≥12 hours (major risk factor for GBS and gram-negative colonization) - Maternal fever or chorioamnionitis signs (implied by PROM duration) - Signs of systemic infection: lethargy, poor feeding, temperature instability, tachypnea, poor perfusion ### Laboratory Findings Supporting Sepsis - Leukopenia (WBC 3,200/μL) — actually more ominous than leukocytosis in neonatal sepsis - Left shift: 12% bands (immature forms) - Elevated CRP (18 mg/L; normal <5 mg/L) ### Why Empiric Therapy Now? **High-Yield:** Early-onset sepsis (first 72 hours) has mortality rates of 5–10% if antibiotics are delayed. The combination of maternal risk factors (PROM) + clinical signs (poor perfusion, lethargy, tachypnea) + laboratory abnormalities (leukopenia, left shift, elevated CRP) mandates **immediate** broad-spectrum coverage. ### Empiric Regimen for EOS | Drug | Spectrum | Rationale | | --- | --- | --- | | **Ampicillin** | GBS, Listeria, gram-positive | Essential for Listeria coverage (cephalosporins do not cover) | | **Gentamicin** | Gram-negative (E. coli, Klebsiella) | Synergy with ampicillin; covers most neonatal gram-negatives | **Clinical Pearl:** Do NOT wait for culture results or repeat CRP before starting antibiotics in a clinically septic neonate. Culture is obtained *before* antibiotics, but therapy initiation is not contingent on culture growth. ### Supportive Care Adjuncts - IV fluids, glucose monitoring, thermal support - Consider vasopressors if shock persists (dopamine 5–10 μg/kg/min) - Reassess at 48 hours; if cultures negative and clinical improvement, consider stopping antibiotics [cite:Nelson Textbook of Pediatrics 21e Ch 108]
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