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"The use of extended intermittent infusion (EII) or continuous infusion (CI) of meropenem is recommended in ICU patients, but few data comparing these two options are available" Tournayre et al (2023).
Meropenem extended intermittent infusion or continuous infusion

Abstract:

The use of extended intermittent infusion (EII) or continuous infusion (CI) of meropenem is recommended in ICU patients, but few data comparing these two options are available. We conducted a retrospective cohort study, between 01/01/2019 and 31/03/2020, in a teaching hospital ICU which aimed to determine the meropenem plasma concentrations achieved with CI and EII. We included septic patients treated with meropenem who had ≥1 meropenem plasma trough (Cmin) or steady-state concentration (Css) measurement, as appropriate. Then, we assessed the factors independently associated with attainment of the target concentration (Cmin or Css ≥10 mg/L) and the toxicity threshold (Cmin or Css ≥50 mg/L) using logistic regression models. Among the 70 patients analysed, the characteristics of those treated with EII (N= 33) and CI (N= 37) were balanced with the exception of eGFR: median 30 mL/min/m2 (interquartile range: 30, 84) versus 79 mL/min/m2 (IQR: 30, 124). Of the patients treated with EII, 21 (64%) achieved the target concentration, whereas 31 (97%) of those treated with CI achieved it (P <0.001). Factors associated with target attainment were: CI (odd ratio= 16.28, 95% confidence interval [2.05-407.5]), daily dose ≥40 mg/kg (OR= 12.23, 95%CI [1.76-197.0], P= 0.03) and eGFR (OR= 0.98, 95%CI [0.97-0.99], P= 0.02). Attainment of toxicity threshold was associated with daily dose >70 mg/kg (OR= 35.5, 95%CI [5.61-410.3], P <0.001). In conclusion, our results suggest the use of meropenem CI, at 40-70 mg/kg/day, particularly in septic ICU patients with normal or augmented renal clearance.

Reference:

Tournayre S, Mathieu O, Villiet M, Besnard N, Brunot V, Daubin D, Platon L, Corne P, Klouche K, Larcher R. Factors associated with meropenem pharmacokinetic/pharmacodynamic target attainment in septic critically ill patients treated with extended intermittent infusion or continuous infusion. Int J Antimicrob Agents. 2023 May 25:106868. doi: 10.1016/j.ijantimicag.2023.106868. Epub ahead of print. PMID: 37244425.