Antimicrobial pharmacokinetics in pediatric patients on kidney replacement therapy: a comprehensive narrative review

Shannon Reinert1, Sonya Tang Girdwood2,3, H Rhodes Hambrick4,5

  • 1Division of Nephrology and Hypertension, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. Shannon.reinert@cchmc.org.

Insights

Pediatric patients on dialysis need adjusted antimicrobial doses due to altered pharmacokinetics (PK). More research is crucial for safe and effective antimicrobial drug dosing in children undergoing kidney replacement therapy (KRT).

Area of Science:

  • Pharmacology
  • Nephrology
  • Pediatrics

Background:

  • Patients on dialysis often require antimicrobial therapy, particularly for sepsis.
  • Altered pharmacokinetics (PK) in dialysis patients necessitate antimicrobial dose adjustments, as established in adult studies.
  • Existing pediatric studies on antimicrobial PK during kidney replacement therapy (KRT) are limited, leading to reliance on extrapolated adult data.

Purpose of the Study:

  • To review existing literature on antimicrobial PK in pediatric patients undergoing dialysis.
  • To identify knowledge gaps in pediatric antimicrobial dosing for patients on KRT.
  • To guide future research priorities in this vulnerable population.

Main Methods:

  • A comprehensive literature review was performed.
  • Searched for original studies evaluating antimicrobial PK in pediatric patients on hemodialysis, peritoneal dialysis, or continuous KRT.
  • Synthesized findings to describe current knowledge and identify research needs.

Main Results:

  • Identified 56 original studies on the PK of twelve different antimicrobials in pediatric dialysis patients.
  • Demonstrated a significant under-study of antimicrobial PK in pediatric patients on dialysis.
  • Highlighted the reliance on adult data for pediatric dosing recommendations.

Conclusions:

  • Antimicrobial PK in pediatric patients on dialysis is an understudied area.
  • This population is at high risk for infections and drug toxicity.
  • Future research should prioritize commonly used antimicrobials and those with known toxicity risks at higher concentrations.

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