What are the recommended doses of intraperitoneal (IP) ceftazidime and gentamicin for pediatric peritonitis?

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Intraperitoneal Antibiotic Dosing for Pediatric Peritoneal Dialysis Peritonitis

For pediatric PD peritonitis, administer intraperitoneal ceftazidime at 125 mg/L in each dialysate exchange and gentamicin at 0.6 mg/kg body weight per exchange (loading dose 8 mg/L, maintenance 4 mg/L), based on established pediatric dosing protocols that achieve therapeutic serum and dialysate concentrations. 1

Ceftazidime Dosing

  • Continuous maintenance dosing of 125 mg/L in each dialysate bag achieves therapeutic levels without requiring a loading dose 1
  • This concentration produces serum levels of approximately 29 mcg/mL after short cycles and 24 mcg/mL at 24 hours, with dialysate concentrations of 87 mcg/mL and 32 mcg/mL respectively 1
  • Therapeutic concentrations exceeding the mean inhibitory concentration (MIC) for sensitive organisms are achieved within 4 hours and persist for 24 hours 1
  • Serum bioavailability reaches 74% at 24 hours with this regimen 1

Gentamicin Dosing

  • Administer 0.6 mg/kg body weight per exchange for pediatric patients (based on extrapolation from adult dosing adjusted for pediatric pharmacokinetics) 2
  • Alternative approach: Loading dose of 8 mg/L in one exchange, followed by maintenance dose of 4 mg/L in subsequent exchanges 3
  • Once-daily dosing at 40 mg per 2L in the overnight/long-dwell bag is effective and reduces toxicity risk 4, 5
  • Monitor serum gentamicin levels and renal function, targeting trough levels <2 mcg/mL to minimize ototoxicity and nephrotoxicity 2

Critical Dosing Considerations

  • Weight-based dosing for gentamicin (3-7.5 mg/kg/day) should be calculated on total body weight 2
  • For continuous cycling peritoneal dialysis (CCPD) patients, the continuous maintenance approach without loading dose is validated and effective 1
  • Once-daily gentamicin administration achieves treatment success rates of 74-80% for gram-negative organisms (excluding pseudomonas) 4
  • Antibiotic serum concentrations and renal function must be monitored throughout therapy 2

Treatment Duration and Monitoring

  • Continue therapy until dialysate clears (typically 14-21 days for most organisms) 1, 3
  • Adjust antibiotics based on culture results when available 3, 6
  • Treatment success rates with ceftazidime-gentamicin combinations range from 75-80% 3, 6
  • Relapse rates are approximately 9-18% within 4 weeks of completing therapy 3, 5

Important Caveats

  • These doses assume normal residual renal function; adjust for anuric patients or those with significant residual function 2
  • For Pseudomonas peritonitis, higher ceftazidime doses or alternative agents may be required 4
  • The once-daily gentamicin approach produces lower trough levels (0.75 mg/L vs 1.5 mg/L with multiple dosing), potentially reducing toxicity while maintaining efficacy 5
  • Vancomycin (15-30 mg/kg loading dose, then 1-2 g per week maintenance) should be added for gram-positive coverage until cultures exclude these organisms 3, 6

References

Research

Disposition of ceftazidime after intraperitoneal administration in adolescent patients receiving continuous cycling peritoneal dialysis.

American journal of kidney diseases : the official journal of the National Kidney Foundation, 2006

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Initial treatment of peritoneal dialysis peritonitis without vancomycin with a once-daily cefazolin-based regimen.

American journal of kidney diseases : the official journal of the National Kidney Foundation, 2001

Research

Once-daily intraperitoneal gentamicin is effective therapy for gram-negative CAPD peritonitis.

Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis, 1999

Research

A prospective randomized comparison of single versus multidose gentamicin in the treatment of CAPD peritonitis.

Advances in peritoneal dialysis. Conference on Peritoneal Dialysis, 1995

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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