Higher MICs (>2 mg/L) Predict 30-Day Mortality in Patients with Lower Respiratory Tract Infections Caused by Multidrug- And Extensively Drug-Resistant Pseudomonas aeruginosa Treated with Ceftolozane/Tazobactam

  • Olga Rodríguez-Núñez*
  • , Leonor Periañez-Parraga
  • , Antonio Oliver
  • , Jose M. Munita
  • , Anna Boté
  • , Oriol Gasch
  • , Xavier Nuvials
  • , Aurélien Dinh
  • , Robert Shaw
  • , Jose M. Lomas
  • , Vicente Torres
  • , Juanjo Castón
  • , Rafael Araos
  • , Lilian M. Abbo
  • , Robert Rakita
  • , Federico Pérez
  • , Samuel L. Aitken
  • , Cesar A. Arias
  • , M. Luisa Martín-Pena
  • , Asun Colomar
  • M. Belén Núñez, Josep Mensa, José Antonio Martínez, Alex Soriano
*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

24 Citations (Scopus)

Abstract

Background: Ceftolozane/tazobactam (C/T) efficacy and safety in ventilator-associated pneumonia (VAP) is being evaluated at a double dose by several trials. This dosing is based on a pharmacokinetic (PK) model that demonstrated that 3 g q8h achieved ≥90% probability of target attainment (50%T > minimal inhibitory concentration [MIC]) in plasma and epithelial lining fluid against C/T-susceptible P. aeruginosa. The aim of this study was to evaluate the efficacy of different C/T doses in patients with lower respiratory infection (LRI) due to MDR- or XDR-P. aeruginosa considering the C/T MIC. Methods: This was a multicenter retrospective study of 90 patients with LRI caused by resistant P. aeruginosa who received a standard or high dose (HDo) of C/T. Univariable and multivariable analyses were performed to identify independent predictors of 30-day mortality. Results: The median age (interquartile range) was 65 (51-74) years. Sixty-three (70%) patients had pneumonia, and 27 (30%) had tracheobronchitis. Thirty-three (36.7%) were ventilator-associated respiratory infections. The median C/T MIC (range) was 2 (0.5-4) mg/L. Fifty-four (60%) patients received HDo. Thirty-day mortality was 27.8% (25/90). Mortality was significantly lower in patients with P. aeruginosa strains with MIC ≤2 mg/L and receiving HDo compared with the groups with the same or higher MIC and dosage (16.2% vs 35.8%; P =. 041). Multivariate analysis identified septic shock (P <. 001), C/T MIC >2 mg/L (P =. 045), and increasing Charlson Comorbidity Index (P =. 019) as independent predictors of mortality. Conclusions: The effectiveness of C/T in P. aeruginosa LRI was associated with an MIC ≤2 mg/L, and the lowest mortality was observed when HDo was administered for strains with C/T MIC ≤2 mg/L. HDo was not statistically associated with a better outcome.

Original languageEnglish
Article numberofz416
JournalOpen Forum Infectious Diseases
Volume6
Issue number10
DOIs
Publication statusPublished - 1 Oct 2019
Externally publishedYes

Keywords

  • Pseudomonas aeruginosa
  • ceftolozane/tazobactam
  • multidrug-resistant
  • pneumonia
  • tracheobronchitis

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