Безопасность и риск фармакотерапии (Jul 2022)

Experience of Using Therapeutic Drug Monitoring to Control the Safety of Vancomycin in Intensive Care Unit Patients with Sepsis

  • A. B. Prokofiev,
  • S. A. Belkov,
  • R. E. Kazakov,
  • N. G. Berdnikova,
  • T. A. Rodina,
  • E. S. Melnikov,
  • A. A. Danko,
  • N. E. Voronova,
  • R. Z. Vafina,
  • A. V. Zavtoniev,
  • D. V. Tsyganko,
  • E. Yu. Demchenkova

DOI
https://doi.org/10.30895/2312-7821-2022-10-2-139-150
Journal volume & issue
Vol. 10, no. 2
pp. 139 – 150

Abstract

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Vancomycin is prescribed to patients in serious condition with infections caused by Gram-positive microorganisms; however, if the therapeutic plasma concentration of the medicinal product is exceeded, it can have a nephrotoxic effect.The aim of the study was to demonstrate the possibility of using therapeutic drug monitoring (TDM) to reduce the risk of developing nephropathy in intensive care unit patients with sepsis.Materials and methods: the study comprised a retrospective analysis of four clinical cases of patients with sepsis admitted to intensive care units of I.V. Davydovsky City Clinical Hospital in 2021 and treated with vancomycin. TDM of vancomycin plasma levels was performed by reverse-phase high-performance liquid chromatography with mass spectrometric detection.Results: using the four cases of septic patients, the study demonstrated that vancomycin at adequate case-specific doses may result in plasma concentrations beyond the therapeutic range. TDM of vancomycin concentrations helped to prevent further deterioration of renal dysfunction in one septic patient having developed acute kidney injury and to control the achievement of therapeutic vancomycin concentrations or timely adjust the dose to that effect in the other three cases.Conclusions: a timely correction of vancomycin dosing with plasma TDM allows for achieving high antimicrobial efficacy in patients with sepsis and minimising the nephrotoxic effect of the medicinal product. Studies of the feasibility of using TDM as a treatment personalisation tool for patients in serious condition will continue in the future.

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