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Loading Dose of Ceftazidime Needs to Be Increased in Critically Ill Patients: A Retrospective Study to Evaluate Recommended Loading Dose with Pharmacokinetic Modelling.
Launay, Manon; Ollier, Edouard; Kably, Benjamin; Le Louedec, Félicien; Thiery, Guillaume; Lanoiselée, Julien; Perinel-Ragey, Sophie.
Afiliación
  • Launay M; Medical Intensive Care Unit, University Hospital of Saint-Etienne, 42000 Saint Etienne, France.
  • Ollier E; Pharmacovigilance Department, University Hospital of Saint-Etienne, 42000 Saint Etienne, France.
  • Kably B; Mines Saint-Étienne, Université Jean Monnet, INSERM, U1059, SAINBIOSE, 42000 Saint Etienne, France.
  • Le Louedec F; Clinical Pharmacology Unit, University Hospital of Saint-Etienne, 42000 Saint Etienne, France.
  • Thiery G; Pharmacology Unit DMU BioPhyGen, European Hospital Georges-Pompidou, APHP, 75015 Paris, France.
  • Lanoiselée J; Cancer Research Center of Toulouse (CRCT), Team 14, INSERM UMR1037, University of Toulouse, CS 53717, 31037 Toulouse, France.
  • Perinel-Ragey S; Medical Intensive Care Unit, University Hospital of Saint-Etienne, 42000 Saint Etienne, France.
Antibiotics (Basel) ; 13(8)2024 Aug 11.
Article en En | MEDLINE | ID: mdl-39200056
ABSTRACT
To rapidly achieve ceftazidime target concentrations, a 2 g loading dose (LD) is recommended before continuous infusion, but its adequacy in critically ill patients, given their unique pharmacokinetics, needs investigation. This study included patients from six ICUs in Saint-Etienne and Paris, France, who received continuous ceftazidime infusion with plasma concentration measurements. Using MONOLIX and R, a pharmacokinetic (PK) model was developed, and the literature on ICU patient PK models was reviewed. Simulations calculated the LD needed to reach a 60 mg/L target concentration and assessed ceftazidime exposure for various regimens. Among 86 patients with 223 samples, ceftazidime PK was best described by a one-compartment model with glomerular filtration rate explaining clearance variability. Typical clearance and volume of distribution were 4.45 L/h and 88 L, respectively. The literature median volume of distribution was 37.2 L. Simulations indicated that an LD higher than 2 g was needed to achieve 60 mg/L in 80% of patients, with a median LD of 4.9 g. Our model showed a 4 g LD followed by 6 g/day infusion reached effective concentrations within 1 h, while a 2 g LD caused an 18 h delay in achieving target steady state.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Antibiotics (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Antibiotics (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Francia
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