[Obtain best usage of meropenem dose in severe infections. Results of an observational multicenter study]

B Alvarez-Sánchez1, F Alvarez-Lerma, Jl Romero

  • 1Servicio de Medicina Intensiva, Hospital General Universitario, Alicante. alvarez_ber@gva.es

Abstract

Insights

Reducing meropenem dosage to 0.5 g every 8 hours effectively treats severe nosocomial infections in critically-ill patients. This dose adjustment is safe and beneficial, except when non-fermenting Gram-negative bacteria are the cause.

Area of Science:

  • Infectious Diseases
  • Critical Care Medicine
  • Pharmacology

Background:

  • Nosocomial infections pose a significant threat to critically-ill patients in intensive care units.
  • Empirical antibiotic treatment, including meropenem, is crucial but requires careful dose optimization.
  • Understanding the effectiveness and tolerability of meropenem dose adjustments is vital for improving patient outcomes.

Purpose of the Study:

  • To evaluate the effectiveness and tolerability of adjusting meropenem dosage in critically-ill patients with nosocomial infections.
  • To assess the clinical and microbiological outcomes following meropenem dose reduction.
  • To identify specific pathogens or conditions where meropenem dose adjustment may be less effective.

Main Methods:

  • A prospective, observational, multicenter study involving 17 intensive care units.
  • Patients initially treated with meropenem (1 g every 8 hours) for nosocomial infections were included.
  • Dose was adjusted to 0.5 g every 8 hours based on favorable clinical course and susceptible pathogens or absence of pathogens.

Main Results:

  • Ninety-two patients had their meropenem dose adjusted; ventilator-associated pneumonia and bacteremia were common infections.
  • A high clinical success rate of 90.5% was observed in evaluable patients (74), with 54 cured and 13 improved.
  • Microbiological eradication was achieved in 50 out of 53 cases; adverse events were rare (4%) and not severe.

Conclusions:

  • Meropenem dose adjustment to 0.5 g every 8 hours is a valuable strategy for treating severe nosocomial infections in intensive care settings.
  • This dose reduction demonstrates good tolerability and effectiveness, leading to favorable clinical outcomes.
  • The strategy should be used cautiously in cases involving non-fermenting Gram-negative bacteria, as they may persist or new resistant pathogens may emerge.

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