What is the recommended dose of Meropenem (generic name) for a 1-month-old infant weighing 2.6 kg?

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Meropenem Dosing for a 1-Month-Old Infant Weighing 2.6 kg

For this 1-month-old infant weighing 2.6 kg, administer meropenem 20 mg every 12 hours (40 mg/kg/day divided every 12 hours), given as an intravenous infusion over 30 minutes. 1

Dosing Calculation and Rationale

  • This infant falls into the category: 32 weeks or older gestational age (GA) with postnatal age (PNA) less than 2 weeks, which requires 20 mg/kg every 8 hours for complicated intra-abdominal infections 1
  • However, if the infant is 32 weeks or older GA with PNA of 2 weeks or older, the dose increases to 30 mg/kg every 8 hours 1
  • For this 2.6 kg infant:
    • If PNA <2 weeks: 20 mg/kg = 52 mg per dose every 8 hours
    • If PNA ≥2 weeks: 30 mg/kg = 78 mg per dose every 8 hours 1

Critical Age-Specific Considerations

  • The FDA labeling specifically addresses infants less than 3 months of age, stratifying dosing by both gestational age and postnatal age, which is essential for proper dosing in this vulnerable population 1
  • Infants less than 32 weeks GA with PNA less than 2 weeks receive 20 mg/kg every 12 hours (longer dosing interval due to immature renal function) 1
  • Infants less than 32 weeks GA with PNA 2 weeks and older receive 20 mg/kg every 8 hours 1
  • There is no clinical experience with meropenem in pediatric patients with renal impairment, so careful monitoring is essential if renal dysfunction is suspected 1

Administration Guidelines

  • Administer as an intravenous infusion over 30 minutes for all infants less than 3 months of age 1
  • Do not administer as a bolus injection in this age group, as the safety data for bolus dosing is limited even in older pediatric patients 1
  • Reconstitute vials with Sterile Water for Injection: for a 500 mg vial, add 10 mL to achieve approximately 50 mg/mL concentration 1

Pharmacokinetic Considerations in Neonates

  • Meropenem has an elimination half-life of approximately 1 hour in adults, but this may be prolonged in neonates due to immature renal function 2
  • Up to 70% of meropenem is recovered unchanged in urine, making renal function the primary determinant of drug clearance 2
  • The volume of distribution is approximately 21L in adults (predominantly extracellular), but neonates may have different distribution characteristics 2

Important Clinical Pitfalls

  • Do not use adult or older pediatric dosing regimens for infants under 3 months, as they require specific age-stratified dosing 1
  • Verify both gestational age and postnatal age before calculating the dose, as both parameters affect the dosing interval 1
  • Freshly prepared solutions should be used, and reconstituted solutions should not be frozen 1
  • Do not mix meropenem with other drugs in the same solution, as compatibility has not been established 1
  • Unlike imipenem, meropenem does not require coadministration with cilastatin because it is stable against renal dehydropeptidase-I 3, 4

Monitoring Recommendations

  • Monitor for therapeutic response and consider therapeutic drug monitoring in critically ill neonates, as inadequate levels can lead to treatment failure 5
  • Assess renal function if available, though specific dosing adjustments for neonatal renal impairment are not established 1
  • Meropenem appears to have a lower risk of seizures compared to imipenem, which is particularly relevant in the neonatal population 4, 6

References

Research

Meropenem clinical pharmacokinetics.

Clinical pharmacokinetics, 1995

Research

Update on the efficacy and tolerability of meropenem in the treatment of serious bacterial infections.

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2008

Research

Meropenem, a new carbapenem antibiotic.

Pharmacotherapy, 1997

Research

Meropenem: evaluation of a new generation carbapenem.

International journal of antimicrobial agents, 1997

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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