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

Author:

Rodríguez-Núñez Olga1,Periañez-Parraga Leonor2,Oliver Antonio3,Munita Jose M45,Boté Anna6,Gasch Oriol6,Nuvials Xavier7,Dinh Aurélien8,Shaw Robert9,Lomas Jose M910,Torres Vicente11,Castón Juanjo12,Araos Rafael5,Abbo Lilian M13,Rakita Robert14,Pérez Federico15,Aitken Samuel L16,Arias Cesar A45,Martín-Pena M Luisa17,Colomar Asun18,Núñez M Belén19,Mensa Josep1,Martínez José Antonio1,Soriano Alex1

Affiliation:

1. Servicio de Enfermedades Infecciosas, Hospital Clínic, Barcelona, Spain

2. Servicio de Farmacia Hospitalaria, Hospital Universitari Son Espases, Palma de Mallorca-IdISBa, Spain

3. Servicio de Microbiología, Hospital Universitari Son Espases, Palma de Mallorca-IdISBa, Spain

4. Center for Antimicrobial Resistance and Microbial Genomics and Division of Infectious Diseases, UTHealth McGovern Medical School, Houston, Texas, USA

5. Genomics & Resistant Microbes (GeRM), Instituto de Ciencias e Innovación en Medicina, Clínica Alemana, Universidad del Desarrollo and Millenium Initiative for Collaborative Research Bacterial Resistance (MICROB-R), Iniciativa Científica Milenio, Chile

6. Servicio de Enfermedades Infecciosas, Hospital Universitari Parc Taulí, Sabadell, Spain

7. Unidad de Cuidados Intensivos, Hospital Vall d’Hebron, Barcelona, Spain

8. Department of Infectious Diseases, Hospital Raymond-Poincaré, Paris Ile-de-France, France

9. Department of Infectious Diseases, John Radcliffe Hospital, Oxford, UK

10. Unidad de Enfermedades Infecciosas, Hospitales Juan Ramón Jiménez-Infanta Elena, Huelva

11. Unidad de Cuidados Intensivos, Hospital Son Espases, Palma de Mallorca, Spain

12. Unidad Clínica de Enfermedades Infecciosas, Hospital Universitario Reina Sofía-IMIBIC, Córdoba, Spain

13. Department of Medicine, Jackson Memorial Hospital and Division of Infectious Diseases, University of Miami Miller School of Medicine, Florida, USA

14. Division of Allergy and Infectious Diseases, University of Washington, Seattle, USA

15. Cleveland Veterans Affairs Medical Center, Case Western Reserve University, Cleveland, Ohio, USA

16. Division of Pharmacy, University of Texas MD Anderson Cancer Center, Houston, Texas, USA

17. Servicio de Medicina Interna, Hospital Universitari Son Espases, Palma de Mallorca-IdISBa, Spain

18. Unidad de Cuidados Intensivos, Hospital Universitari Son Espases, Palma de Mallorca-IdISBa, Spain

19. Servicio de Neumología, Hospital Universitari Son Espases, Palma de Mallorca-IdISBa, Spain

Abstract

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% ƒT > 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.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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