What are the recommended doses of ampicillin and gentamicin for a 920gm preterm baby?

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Ampicillin and Gentamicin Dosing for a 920g Preterm Neonate

For a 920g preterm infant, administer ampicillin 50 mg/kg/day divided every 12 hours (25 mg/kg/dose IV q12h) and gentamicin 3.5 mg/kg IV every 24 hours.

Ampicillin Dosing

The dosing for this extremely low birth weight infant depends critically on postnatal age:

If ≤7 Days Postnatal Age:

  • 50 mg/kg/day divided every 12 hours (25 mg/kg/dose IV q12h) 1
  • This applies to neonates ≤2000g during the first week of life 1

If >7 Days Postnatal Age:

  • 50 mg/kg/day divided every 12 hours (25 mg/kg/dose IV q12h) 1
  • For infants <1200g beyond the first week, this lower dose frequency is maintained due to immature renal clearance 1

Key Point: At 920g, this infant falls into the <1200g weight category, which requires the most conservative dosing regardless of postnatal age 1. The 2022 guidelines confirm gestational age <34 weeks with weight considerations: for infants >34 weeks gestation but <1200g, the same 50 mg/kg/day q12h regimen applies 1.

Gentamicin Dosing

For premature neonates <1000g: 3.5 mg/kg IV every 24 hours 1

This once-daily extended-interval dosing is specifically designed for extremely premature infants with:

  • Larger volume of distribution
  • Reduced renal clearance
  • Need for concentration-dependent bacterial killing 2

Alternative Dosing from 2022 Guidelines:

The more recent guidelines suggest for gestational age <30 weeks 1:

  • If postnatal age <14 days: 5 mg/kg/dose IV every 48 hours
  • If postnatal age >14 days: 5 mg/kg/dose IV every 36 hours

However, the 3.5 mg/kg every 24 hours regimen from the 2009 IDSA guidelines remains the most widely validated approach for infants <1000g 1, with extensive safety data showing 100% achievement of non-toxic trough levels 2.

Critical Monitoring Requirements

Gentamicin Levels:

  • Obtain trough level before the 3rd or 4th dose (target <2 mcg/mL) 2
  • Obtain peak level 30 minutes after infusion (target 6-12 mcg/mL) 2
  • Adjust dosing interval if trough >2 mcg/mL to prevent nephrotoxicity and ototoxicity 1, 2

Renal Function:

  • Monitor serum creatinine on days 1 and 3 of therapy 3
  • Assess for signs of nephrotoxicity throughout treatment 3

Ototoxicity Screening:

  • Perform hearing assessment if prolonged therapy (>72 hours) 3

Common Pitfalls to Avoid

  1. Do not use weight-based dosing intended for larger neonates - the 2.5 mg/kg q12h or q18-24h regimens are for infants 1200-2000g, not <1000g 1

  2. Do not use higher ampicillin doses (75-100 mg/kg/day) - these are reserved for larger or older neonates and risk toxicity in extremely low birth weight infants 1

  3. Avoid checking levels too early - gentamicin requires at least 48-72 hours to reach steady state in premature neonates 2

  4. Do not assume gestational age alone determines dosing - actual birth weight is equally critical, particularly for small-for-gestational-age infants who may have lower drug levels 4

Practical Administration

  • Ampicillin: For a 920g infant, each dose = 23 mg IV q12h (50 mg/kg/day ÷ 2 doses)
  • Gentamicin: For a 920g infant, dose = 3.2 mg IV q24h (3.5 mg/kg × 0.92 kg)

Both medications should be administered as slow IV infusions over 30 minutes to minimize adverse effects 1.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Once-daily gentamicin dosing for the preterm and term newborn: proposal for a simple regimen that achieves target levels.

Journal of perinatology : official journal of the California Perinatal Association, 2003

Research

Once-daily gentamicin dosing of 4 Mg/Kg/dose in neonates.

Journal of the Medical Association of Thailand = Chotmaihet thangphaet, 2005

Research

Gentamicin dosage in preterm and term neonates.

Archives of disease in childhood, 1977

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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