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Therapeutic drug monitoring of liposomal amphotericin B in children. Are we there yet? A systematic review.
Lai, Tony; Yeo, Chin-Yen; Rockliff, Bradley; Stokes, Michael; Kim, Hannah Yejin; Marais, Ben J; McLachlan, Andrew J; Alffenaar, Jan-Willem C.
Affiliation
  • Lai T; Pharmacy Department, The Children's Hospital at Westmead, Sydney, NSW, Australia.
  • Yeo CY; The University of Sydney Infectious Diseases Institute (Sydney ID), Sydney, NSW, Australia.
  • Rockliff B; Sydney Pharmacy School, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.
  • Stokes M; Pharmacy Department, Concord Hospital, Sydney, Australia.
  • Kim HY; Pharmacy Department, The Children's Hospital at Westmead, Sydney, NSW, Australia.
  • Marais BJ; Pharmacy Department, The Children's Hospital at Westmead, Sydney, NSW, Australia.
  • McLachlan AJ; The University of Sydney Infectious Diseases Institute (Sydney ID), Sydney, NSW, Australia.
  • Alffenaar JC; Sydney Pharmacy School, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.
J Antimicrob Chemother ; 79(4): 703-711, 2024 Apr 02.
Article in En | MEDLINE | ID: mdl-38252921
ABSTRACT

INTRODUCTION:

Therapeutic drug monitoring (TDM) is a tool that supports personalized dosing, but its role for liposomal amphotericin B (L-amb) is unclear. This systematic review assessed the evidence for L-amb TDM in children.

OBJECTIVES:

To evaluate the concentration-efficacy relationship, concentration-toxicity relationship and pharmacokinetic/pharmacodynamic (PK/PD) variability of L-amb in children.

METHODS:

We systematically reviewed PubMed and Embase databases following PRISMA guidelines. Eligible studies included L-amb PK/PD studies in children aged 0-18 years. Review articles, case series of patients, editorials and animal studies were excluded. Quality assessment was performed using the Critical Appraisal of Clinical Pharmacokinetics tool. The concentration-efficacy and concentration-toxicity relationships and PK/PD variability were analysed.

RESULTS:

In total, 4220 studies were screened; 6 were included, presenting data on 195 children. Invasive candidiasis and aspergillosis were the two most common infections treated with L-amb. Studies showed significant PK variability due to age (mean age ranged from 14 days to 17 years), body weight, non-linear PK and changes in the volume of distribution. Limited evidence supported a peak concentration/MIC (Cmax/MIC) of 25-50 for optimal efficacy and an AUC24 of >600 mg·h/L for nephrotoxicity. L-amb doses of 2.5-10 mg/kg/day were reported to achieve Cmax/MIC > 25 using an MIC of 1 mg/L.

CONCLUSIONS:

While significant PK variability was observed in children, evidence to support routine L-amb TDM was limited. Further studies on efficacy and toxicity benefits are required before routine TDM of L-amb can be recommended.

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Guideline / Systematic_reviews Language: En Journal: J Antimicrob Chemother Year: 2024 Document type: Article Affiliation country: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Guideline / Systematic_reviews Language: En Journal: J Antimicrob Chemother Year: 2024 Document type: Article Affiliation country: Australia