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Patient handout

Neonatal sepsis — early-onset (< 72 h) + late-onset (72 h - 28 d)

PRODUCTION

1. Your condition

This handout is for neonatal sepsis — early-onset (< 72 h) + late-onset (72 h - 28 d). Your care team identified this based on: neonate (≤ 28 d) with temperature instability (t < 36 °c or ≥ 38 °c rectal), poor feeding, lethargy, apnoea, hypoglycaemia, jaundice progression, or respiratory distress (aap puopolo 2018).

Other reasons your team may use this plan: maternal risk factor: gbs-positive without intrapartum prophylaxis or chorioamnionitis or prom > 18 h or preterm < 37 wk or intrapartum maternal temperature ≥ 38 °c (cdc verani 2010 pmid 21088663; aap puopolo 2018); preterm neonate < 32 wk gestation in nicu with new-onset clinical deterioration — late-onset sepsis high-pretest cohort (stoll nichd 2011 pmid 21873694); neonate ≤ 28 d with vesicles / seizures / hypothermia / unexplained transaminitis / encephalopathy / maternal genital hsv — empiric acyclovir until hsv excluded (kimberlin pediatrics 2013).

2. Your medications

Take these medications exactly as prescribed. Do not stop or change a dose without talking to your provider.

MedicationStarting doseHowWhenWhat it does
ampicillin200 mg/kg/day divided q8h (DOL 0-7) or q6h (DOL > 7); meningitis dose: 300 mg/kg/day divided q6-8hIVq6-8hCovers Listeria (cephalosporins do not) + GBS + sensitive E. coli (AAP Puopolo 2018)
gentamicinTerm ≥ 35 wk: 4 mg/kg q24h; late-preterm 30-34 wk: 4.5 mg/kg q36h; preterm < 30 wk: 5 mg/kg q48h (extended interval per gestational age)IVq24-48h extended intervalGram-negative synergy with ampicillin; extended-interval dosing per Neofax + AAP Puopolo 2018; trough monitoring before 3rd dose
cefotaxime50 mg/kg/dose IV q8-12h (gestational + chronological-age dependent); meningitis: 50 mg/kg q6-8hIVq6-12hCNS penetration superior to gentamicin; use INSTEAD OF gentamicin if meningitis suspected. AVOID ceftriaxone in neonates < 28 d (bilirubin displacement + calcium-IVF interaction) (AAP Puopolo 2018; FDA 2009)
acyclovir60 mg/kg/day divided q8h IV (20 mg/kg/dose) for ≥ 35 wk; reduced interval q12h if preterm < 35 wkIVq8h (q12h preterm)Cover neonatal HSV until excluded; high mortality if missed (Kimberlin Pediatrics 2013 AAP Red Book 2024). Duration: 14-21 d SEM; 21 d CNS/disseminated; suppressive PO acyclovir × 6 mo post-treatment for CNS disease (Kimberlin NEJM 2011)
vancomycin15 mg/kg/dose IV; interval per gestational + chronological age (q6h-q18h)IVper nomogramAdd-on for MRSA / CoNS / severe SSTI source; AUC target 400-600 (Rybak IDSA 2020) with caveat — limited neonatal data

Plan: Neonatal sepsis empiric antibiotics — by onset (early < 72 h vs late 72 h - 28 d) + comorbidity

3. When to call your provider

Contact your care team if any of the following happen:

  • New fever > 38 °C OR recurrent symptoms within 4 weeks of discharge → return to ED, blood culture, source-directed workup
  • New focal neurological signs OR seizures → urgent neuro + neuroimaging
  • Feeding intolerance + weight loss + bilious emesis → urgent peds + GI evaluation for late NEC / post-NEC stricture
  • Hearing loss confirmed on audiology → ENT + audiology + speech + early intervention
  • Family caregiver PHQ-9 ≥ 15 OR EPDS elevated → mental-health urgent referral
  • Suspected immunodeficiency (≥ 2 serious infections in 12 mo OR unusual pathogen recurrence) → clinical immunology referral

4. When to seek emergency care

Call 911 or go to the nearest emergency room right away if you have:

  • Neonate < 72 h of life with sepsis features (temperature instability, poor feeding, lethargy, apnoea, hypoglycaemia, respiratory distress, hypotension) OR culture-positive blood / CSF — life-threatening early-onset sepsis per AAP Puopolo 2018(life-threatening)
  • Neonate ≤ 28 d with vesicles / seizures / hypothermia / unexplained transaminitis (ALT/AST > 100) / encephalopathy / maternal genital HSV — neonatal HSV until excluded (Kimberlin Pediatrics 2013 AAP Red Book 2024)(life-threatening)
  • Neonate 72 h - 28 d with sepsis features (new-onset apnoea, lethargy, poor feeding, hypotension, thrombocytopenia, line-associated source) — life-threatening late-onset sepsis per AAP late-onset clinical-report series(life-threatening)
  • Preterm neonate with abdominal distention + bloody stools + thrombocytopenia + pneumatosis intestinalis on KUB (bell stage II) OR pneumoperitoneum / portal venous gas (bell stage III) — life-threatening NEC + sepsis coinfection (Walsh & Kliegman 1986 modified Bell staging)(life-threatening)
  • Neonate with empiric antibiotics × 48-72 h + cultures negative + normal clinical course + normalising labs (CRP trending down, CBC normal) — antimicrobial stewardship "rule-out" course per Cantey 2018
  • GBS-positive antepartum screen + inadequate intrapartum prophylaxis (no IAP OR < 4 h before delivery OR penicillin-allergic with non-GBS-targeted abx) — newborn risk-stratification per Kaiser EOS calculator (Escobar 2014 PMID 24379228) OR AAP categorical pathway
  • Preterm neonate (< 32 wk OR < 1500 g) with > 5-7 d empiric antibiotic exposure + negative cultures — increases NEC + late-onset sepsis + mortality (Cantey 2016 + Cantey 2018)
  • Preterm (< 32 wk OR < 1500 g) + TPN + broad-abx + thrombocytopenia + persistent fever despite antibacterial cover OR positive Candida blood culture — life-threatening neonatal candidemia (IDSA candidiasis 2016 Pappas)(life-threatening)
  • CSF pleocytosis ≥ 20 WBC/µL + protein ≥ 100 mg/dL + glucose ratio < 0.5 OR positive CSF Gram stain / culture in neonate ≤ 28 d — life-threatening neonatal bacterial meningitis (IDSA bacterial meningitis 2024)(life-threatening)

5. Follow-up

Outpatient peds visit within 24-48 h of discharge for high-risk; 1-week visit for all; growth + feeding tracking + developmental milestones; immunization catch-up per cause (PCV / Hib not yet age-eligible at < 28 d but tracked for first dose); hearing screen if meningitis (AABR + audiology referral); developmental peds referral at 6-12 mo if functional decline / neurological sequelae; family education on return precautions; vaccination of family contacts (Tdap, influenza, COVID-19 per ACIP); breastfeeding support; PT/OT if neurological sequelae; PICS-p / PICU-Family syndrome screening at 1-3 months for caregivers + child.

6. Sources

Guideline: AAP Clinical Report — Puopolo et al, Management of Neonates ≥35 wk With Suspected/Proven Early-Onset Sepsis, Pediatrics 2018 (PMID 30455342) + CDC Verani 2010 GBS prophylaxis (PMID 21088663) + Phoenix pediatric sepsis criteria JAMA 2024 (PMID 38245890) + FEAST fluid-bolus trial NEJM 2011 (PMID 21615299). Neonatal HSV (Kimberlin), candidiasis (IDSA), and AAP Red Book cited by name.

  1. pubmed.ncbi.nlm.nih.gov/30455342
  2. pubmed.ncbi.nlm.nih.gov/21088663
  3. pubmed.ncbi.nlm.nih.gov/24379228