What is the recommended dosing and administration protocol for vancomycin (Vancomycin) in pediatric patients?

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Last updated: November 21, 2025View editorial policy

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Vancomycin Dosing in Pediatric Patients

For children with serious or invasive infections, administer vancomycin 15 mg/kg IV every 6 hours, targeting trough concentrations of 15-20 μg/mL for severe infections such as bacteremia, meningitis, osteomyelitis, or pneumonia. 1

Standard Dosing Protocol

Initial Dosing by Infection Severity

For serious/invasive infections (MRSA bacteremia, meningitis, osteomyelitis, pneumonia, severe SSTI):

  • Dose: 15 mg/kg IV every 6 hours 1
  • Target trough: 15-20 μg/mL 1
  • Target AUC/MIC: >400 1

For moderate infections (community-acquired pneumonia, less severe SSTI):

  • Dose: 40-60 mg/kg/day divided every 6-8 hours 1
  • This translates to approximately 10-15 mg/kg every 6 hours or 13-20 mg/kg every 8 hours 1

Neonatal Dosing (≤1 month old)

  • Initial loading dose: 15 mg/kg 2
  • Maintenance dosing:
    • First week of life: 10 mg/kg every 12 hours 2
    • After first week to 1 month: 10 mg/kg every 8 hours 2
  • Premature infants: Require longer dosing intervals due to decreased vancomycin clearance as postconceptional age decreases 2
  • Critical: Close monitoring of serum concentrations is mandatory in neonates 2

Administration Guidelines

Infusion Parameters

  • Infusion time: Minimum 60 minutes per dose 3, 2
  • Maximum rate: 10 mg/min 3, 2
  • Maximum concentration: 5 mg/mL (up to 10 mg/mL only in fluid-restricted patients, though this increases infusion reaction risk) 3, 2
  • Each dose must be infused over at least 60 minutes OR at ≤10 mg/min, whichever is longer 2

Loading Dose Considerations

For critically ill children with suspected MRSA sepsis, meningitis, or necrotizing infections:

  • Consider loading dose of 25-30 mg/kg (actual body weight) 1, 3
  • Prolong infusion to 2 hours for loading doses 1, 3
  • Premedicate with antihistamine to reduce red man syndrome risk 1, 3
  • Loading dose is NOT adjusted for renal dysfunction—only maintenance doses require adjustment 3

Therapeutic Drug Monitoring

When to Monitor

  • Mandatory monitoring: Serious infections, renal dysfunction, obesity, fluctuating volumes of distribution 1, 3
  • Obtain trough levels: Before 4th or 5th dose at steady state 1
  • Peak monitoring is NOT recommended 1

Target Levels

  • Serious infections: Trough 15-20 μg/mL 1, 3
  • Moderate infections: Trough 10-15 μg/mL (though specific pediatric data limited) 1
  • Predictive value: Trough >5 μg/mL is 81% predictive of peak >20 μg/mL 4

Dosing Adjustments

Renal Impairment

  • Initial dose remains 15 mg/kg regardless of renal function 2
  • Maintenance dosing: Adjust interval based on creatinine clearance 2
  • Children on ECMO with renal impairment: May require significantly lower doses (median 22.5 mg/kg/day vs 42.1 mg/kg/day in non-ECMO patients with renal impairment) 5
  • Early therapeutic drug monitoring recommended, even before steady state, in ECMO patients 5

Obesity

  • Use actual body weight for dosing calculations 1, 3, 2
  • Obese children may require doses up to 60-70 mg/kg/day to achieve target AUC/MIC ≥400 6, 7
  • Weight-based dosing is critical—fixed dosing leads to underdosing in most patients 3

Evidence-Based Dosing Recommendations

Recent pharmacokinetic studies demonstrate that traditional dosing (40-45 mg/kg/day) is inadequate for most children 4, 7. Current evidence supports:

  • Children <12 years: 70 mg/kg/day (approximately 17.5 mg/kg every 6 hours) achieves target AUC/MIC ≥400 in ~75% of patients 7
  • Children ≥12 years: 60 mg/kg/day (15 mg/kg every 6 hours) achieves target AUC/MIC ≥400 in ~75% of patients 7
  • PICU patients with normal renal function: Required mean final dose of 60 mg/kg/day to achieve conventional peak/trough targets 4

Critical Pitfalls to Avoid

Never use fixed 1 g doses without weight-based calculation—this results in underdosing in the majority of pediatric patients 3

Do not target high trough levels (15-20 μg/mL) for non-severe infections, as this unnecessarily increases nephrotoxicity risk without proven benefit 3

If vancomycin MIC ≥2 μg/mL, switch to alternative therapy (linezolid, daptomycin, clindamycin if susceptible) as target AUC/MIC ratios are not achievable 1, 3

The correlation between trough levels and AUC/MIC is imperfect: an AUC/MIC of 400 corresponds to trough concentration of only 8-9 μg/mL, not 15-20 μg/mL 7. This suggests that targeting AUC/MIC rather than trough concentrations is more appropriate 7.

For organisms with MIC ≤1 mg/L, higher trough levels (15-20 μg/mL) may not be necessary 8

Always determine the MIC of the organism being treated, as this guides appropriate trough level targets 8

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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