What is the recommended dose of Monocef (ceftriaxone) for pediatric patients?

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Monocef (Ceftriaxone) Pediatric Dosing

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

Age-Specific Dosing for Neonates

  • Neonates ≤7 days old: 50 mg/kg/day given every 24 hours 1
  • Neonates >7 days and ≤2000 g: 50 mg/kg/day given every 24 hours 1
  • Neonates >7 days and >2000 g: 50-75 mg/kg/day given every 24 hours 1
  • Critical contraindication: Never use ceftriaxone in hyperbilirubinemic neonates due to risk of bilirubin displacement 1

Weight-Based Dosing Algorithm

Children <45 kg

Uncomplicated infections (urethritis, cervicitis, pharyngitis, proctitis):

  • Single dose of 125 mg IM 2

Bacteremia or arthritis:

  • 50 mg/kg IM or IV once daily for 7 days (maximum 1 g) 2, 1

Meningitis:

  • 50 mg/kg IM or IV once daily for 10-14 days (maximum 2 g) 2
  • Alternative dosing: 100 mg/kg/day divided every 12-24 hours (maximum 4 g daily) 1

Children ≥45 kg

  • Use adult dosing regimens 2

Indication-Specific Dosing

Severe Infections (Pneumonia, Sepsis)

  • Standard dose: 50-100 mg/kg/day given once daily or divided every 12-24 hours 1
  • For critically ill children: Current evidence supports 100 mg/kg once daily as adequate for most patients 3
  • For augmented renal clearance or less-susceptible pathogens: Consider 50 mg/kg twice daily to improve target attainment 3

Bacterial Meningitis

  • Recommended dose: 100 mg/kg/day divided every 12-24 hours (maximum 4 g daily) 1
  • CSF penetration: Achieves concentrations 480-5,600 times above the MIC of causative bacteria 4
  • Duration: 10-14 days depending on pathogen and clinical response 1

Community-Acquired Pneumonia

  • 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

Complicated Intra-Abdominal Infections

  • 50-75 mg/kg/day given every 12-24 hours 1

Gonococcal Infections

Conjunctivitis (children ≤45 kg):

  • 25-50 mg/kg IV or IM single dose (maximum 250 mg) 1

Uncomplicated infections:

  • 125 mg IM single dose 2

Bacteremia, arthritis, or meningitis:

  • 50 mg/kg/day (maximum 1 g) for 7 days 2
  • Extend to 10-14 days for meningitis 2

Pharmacokinetic Considerations

  • Half-life in pediatric patients: 4.2-4.6 hours in children with meningitis 4, but can range from 6.6-16.8 hours in neonates 5
  • Peak concentrations: 216 mcg/mL after 50 mg/kg IV dose, 275 mcg/mL after 75 mg/kg IV dose 6
  • Protein binding: 95% at low concentrations, decreasing to 85% at higher concentrations 6
  • Once-daily dosing is effective for most serious pediatric infections due to the long half-life 7, 8

Critical Dosing Pitfalls to Avoid

  1. Never exceed adult maximum doses: Pediatric doses should not exceed 4 g daily even when weight-based calculations suggest higher amounts 1

  2. Do not use lower dosing ranges for severe sepsis: Use 80-100 mg/kg/day rather than 50 mg/kg/day for critically ill patients 1

  3. Avoid ceftriaxone in hyperbilirubinemic neonates: Risk of kernicterus from bilirubin displacement 1

  4. Consider twice-daily dosing for:

    • Patients with estimated GFR >80 mL/min/1.73 m² 3
    • Areas with high prevalence of less-susceptible pathogens (MIC ≥0.5 mg/L) 3
    • Meningitis cases requiring sustained CSF concentrations 1
  5. Adjust for specific pathogens:

    • If staphylococcal infection suspected: Add flucloxacillin 50 mg/kg every 6 hours plus gentamicin 7.5 mg/kg daily 1
    • If Listeria concern: Add ampicillin 50 mg/kg every 6 hours 1

Administration Routes

  • Both IM and IV routes are acceptable 2, 6
  • IM injection is painful; counsel patients accordingly 1
  • IV doses should be infused over 30 minutes for optimal pharmacokinetics 6

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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