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Lung penetration, bronchopulmonary pharmacokinetic/pharmacodynamic profile and safety of 3 g of ceftolozane/tazobactam administered to ventilated, critically ill patients with pneumonia.
Caro, Luzelena; Nicolau, David P; De Waele, Jan J; Kuti, Joseph L; Larson, Kajal B; Gadzicki, Elaine; Yu, Brian; Zeng, Zhen; Adedoyin, Adedayo; Rhee, Elizabeth G.
Afiliação
  • Caro L; Merck & Co., Inc., Kenilworth, NJ, USA.
  • Nicolau DP; Center for Anti-Infective Research and Development, Hartford Hospital, Hartford, CT, USA.
  • De Waele JJ; Department of Critical Care Medicine, Ghent University Hospital, Ghent, Belgium.
  • Kuti JL; Center for Anti-Infective Research and Development, Hartford Hospital, Hartford, CT, USA.
  • Larson KB; Merck & Co., Inc., Kenilworth, NJ, USA.
  • Gadzicki E; Merck & Co., Inc., Kenilworth, NJ, USA.
  • Yu B; Merck & Co., Inc., Kenilworth, NJ, USA.
  • Zeng Z; Merck & Co., Inc., Kenilworth, NJ, USA.
  • Adedoyin A; Merck & Co., Inc., Kenilworth, NJ, USA.
  • Rhee EG; Merck & Co., Inc., Kenilworth, NJ, USA.
J Antimicrob Chemother ; 75(6): 1546-1553, 2020 06 01.
Article em En | MEDLINE | ID: mdl-32211756
ABSTRACT

OBJECTIVES:

Ceftolozane/tazobactam is approved for hospital-acquired/ventilator-associated bacterial pneumonia at double the dose (i.e. 2 g/1 g) recommended for other indications. We evaluated the bronchopulmonary pharmacokinetic/pharmacodynamic profile of this 3 g ceftolozane/tazobactam regimen in ventilated pneumonia patients.

METHODS:

This was an open-label, multicentre, Phase 1 trial (clinicaltrials.gov NCT02387372). Mechanically ventilated patients with proven/suspected pneumonia received four to six doses of 3 g of ceftolozane/tazobactam (adjusted for renal function) q8h. Serial plasma samples were collected after the first and last doses. One bronchoalveolar lavage sample per patient was collected at 1, 2, 4, 6 or 8 h after the last dose and epithelial lining fluid (ELF) drug concentrations were determined. Pharmacokinetic parameters were estimated by non-compartmental analysis and pharmacodynamic analyses were conducted to graphically evaluate achievement of target exposures (plasma and ELF ceftolozane concentrations >4 mg/L and tazobactam concentrations >1 mg/L; target in plasma ≥30% and ≥20% of the dosing interval, respectively).

RESULTS:

Twenty-six patients received four to six doses of study drug; 22 were included in the ELF analyses. Ceftolozane and tazobactam Tmax (6 and 2 h, respectively) were delayed in ELF compared with plasma (1 h). Lung penetration, expressed as the ratio of mean drug exposure (AUC) in ELF to plasma, was 50% (ceftolozane) and 62% (tazobactam). Mean ceftolozane and tazobactam ELF concentrations remained >4 mg/L and >1 mg/L, respectively, for 100% of the dosing interval. There were no deaths or adverse event-related study discontinuations.

CONCLUSIONS:

In ventilated pneumonia patients, 3 g of ceftolozane/tazobactam q8h yielded ELF exposures considered adequate to cover ceftolozane/tazobactam-susceptible respiratory pathogens.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pneumonia / Estado Terminal Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pneumonia / Estado Terminal Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article