Case Report: Therapeutic Drug Monitoring of Polymyxin B During Continuous Renal Replacement Therapy in Two Pediatric

Caifang Xu1, Xiaofen Liu2,3, Yun Cui1

  • 1Department of Critical Care Medicine, Shanghai Children's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Insights

Polymyxin B dosing requires adjustment in critically ill children on continuous renal replacement therapy (CRRT). High drug clearance during CRRT necessitates increased polymyxin B doses for effective infection control.

Area of Science:

  • Pharmacology
  • Nephrology
  • Critical Care Medicine

Background:

  • Polymyxin B is a last-resort antibiotic for carbapenem-resistant bacterial infections.
  • Optimal dosing strategies for polymyxin B in pediatric patients undergoing continuous renal replacement therapy (CRRT) are not well-established.
  • Carbapenem-resistant organism bloodstream infections pose a significant challenge in critically ill pediatric populations.

Observation:

  • Two pediatric cases with acute kidney injury requiring CRRT were treated with polymyxin B for carbapenem-resistant infections.
  • Therapeutic drug monitoring (TDM) using LC-MS/MS guided dose adjustments.
  • Initial doses of 1 mg/kg every 12 hours resulted in sub-target plasma concentrations.

Findings:

  • Escalating doses to 2 mg/kg every 12 hours achieved target average steady-state concentrations (2.60 and 1.73 mg/L) and controlled infections.
  • Polymyxin B demonstrated high clearance during CRRT (45-51%), with significantly lower concentrations compared to post-CRRT periods.
  • Individual patient responses and drug exposure varied between CRRT and non-CRRT phases.

Implications:

  • CRRT significantly increases polymyxin B clearance in pediatric patients.
  • Adjusted or 'supplanted' dosing regimens are crucial for achieving therapeutic polymyxin B levels during CRRT.
  • TDM is essential for optimizing polymyxin B therapy in critically ill children with renal replacement therapy.

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