What is the recommended dose of ceftriaxone (Ceftriaxone) per kilogram (kg) of body weight in pediatric patients?

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Ceftriaxone Pediatric Dosing

For most pediatric infections, ceftriaxone should be dosed at 50-75 mg/kg/day given once daily, with bacterial meningitis requiring 100 mg/kg/day (maximum 4 g daily), divided every 12-24 hours. 1

Age-Specific Dosing Considerations

Neonates

  • Postnatal age ≤7 days: 50 mg/kg/day given every 24 hours 1
  • Postnatal age >7 days and weight ≤2000 g: 50 mg/kg/day given every 24 hours 1
  • Postnatal age >7 days and weight >2000 g: 50-75 mg/kg/day given every 24 hours 1
  • Critical contraindication: Do not use ceftriaxone in hyperbilirubinemic neonates due to risk of bilirubin displacement 1

Infants and Children

The dosing varies significantly based on infection severity and pathogen:

Indication-Specific Dosing

Bacterial Meningitis (Highest Priority)

  • 100 mg/kg/day divided every 12-24 hours (maximum 4 g daily) 1
  • This higher dose is essential for adequate CSF penetration, which averages only 4.8% of plasma concentrations 2
  • Recent pharmacokinetic modeling demonstrates that once-daily dosing (100 mg/kg) achieves superior CSF target attainment (88% PTA at 24h) compared to twice-daily dosing (50 mg/kg BD, 53% PTA) for pathogens with MIC ≤1 mg/L 3

Severe Infections (Pneumonia, Sepsis, Complicated Intra-abdominal Infections)

  • 50-100 mg/kg/day given once daily or divided every 12-24 hours 1
  • For pneumococcal pneumonia with penicillin resistance: 100 mg/kg/day every 12-24 hours 1, 4

Less Severe Infections

  • 50-75 mg/kg/day given once daily or divided every 12-24 hours 1

Pathogen-Specific Considerations

Penicillin-Resistant Streptococcus pneumoniae

  • MIC ≥4.0 μg/mL: 100 mg/kg/day every 12-24 hours 4
  • MIC <2.0 μg/mL: 50-100 mg/kg/day every 12-24 hours 4

HACEK Organisms (Endocarditis)

  • 100 mg/kg/day IV/IM once daily for 4 weeks (native valve) or 6 weeks (prosthetic valve) 5

Gram-Negative Enteric Bacilli

  • 100 mg/kg/day divided every 12 hours or 80 mg/kg/day every 24 hours (maximum 4 g daily) 1

Group A Streptococcus and β-lactamase Producing Haemophilus influenzae

  • 50-100 mg/kg/day every 12-24 hours 4

Critical Dosing Nuances

Once-Daily vs. Twice-Daily Debate

The evidence strongly supports once-daily dosing for most indications:

  • Pharmacokinetic advantage: Ceftriaxone has a prolonged elimination half-life of 4.2-4.6 hours in pediatric patients 2, 6
  • Clinical efficacy: Studies demonstrate 94-98% cure rates with once-daily dosing at 50-100 mg/kg 7, 8
  • Exception for critically ill: In patients with estimated GFR >80 mL/min/1.73 m² or areas with less-susceptible pathogens (MIC ≥0.5 mg/L), consider 50 mg/kg twice daily to improve target attainment (93.4% vs 60.8% PTA) 9

Maximum Dose Limitations

  • Pediatric doses should not exceed adult doses (maximum 4 g daily) 5, 1

Administration Considerations

  • IV infusion should occur over 30 minutes 6
  • IM injection is painful and patients should be counseled accordingly 5

Common Pitfalls to Avoid

  1. Underdosing meningitis: Using 50 mg/kg instead of 100 mg/kg for CNS infections results in inadequate CSF concentrations 3
  2. Using ceftriaxone in jaundiced neonates: Risk of kernicterus from bilirubin displacement 1
  3. Assuming twice-daily is always better: Once-daily dosing achieves superior early target attainment for meningitis 3
  4. Inadequate dosing for resistant organisms: Staphylococcus aureus meningitis (MIC 4 mg/L) requires alternative therapy as neither standard regimen achieves adequate CSF levels 3

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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