Ceftolozane/Tazobactam for the Treatment of Complicated Infections in Hospital Settings—A French Real-world Study

Author:

Timsit Jean-François1ORCID,Mootien Joy2,Akrich Brune3,Bourge Xavier3,Brassac Isabelle3,Castan Bernard4,Mackosso Carole3,Tavares Linsay Monteiro5,Ruiz Fabrice5,Boutoille David6ORCID,Ruimy Raymond7

Affiliation:

1. Réanimation Médicale et Infectieuse, AP-HP Bichat , Paris , France

2. Unité Fonctionnelle de Conseil en Antibiothérapie, CHU Mulhouse , Mulhouse , France

3. MSD France , Puteaux , France

4. Service de Médecine Interne et Maladies Infectieuses, CH Périgueux , Périgueux , France

5. ClinSearch , Malakoff , France

6. Service des Maladies Infectieuses, Nantes Université, CIC 1413, Inserm , Nantes , France

7. Laboratoire Médicale, CHU Nice , Nice

Abstract

Abstract Background This study describes the conditions of use of ceftolozane/tazobactam (C/T) and associated outcomes in French hospital settings. Methods This was a prospective, multicenter, French observational study. Patients who received at least 1 dose of C/T were included and followed up as per routine clinical practice, until stop of C/T. Results A total of 260 patients were enrolled between October 2018 and December 2019 in 30 centers across France. Of these, 177 (68.0%) received C/T as per indication of usage following the results of the antibiogram (documented cases). Among documented patients, the mean age was 61.8 years, 73.4% were males, and 93.8% presented with multidrug-resistant (MDR) bacteria at inclusion. C/T was most frequently prescribed for pneumonia (48.6%), bacteremia (14.7%), complicated intra-abdominal infections (13.0%), or complicated urinary tract infections (9.6%). Pseudomonas aeruginosa was the species most frequently isolated with 212 strains from 155 patients, and 96.2% of these strains were susceptible to C/T. The median duration of C/T treatment was 16.1 days (1–115, n = 176). Complete or partial cure was achieved in 71.7% of patients, C/T was discontinued upon adaptation to microbiology results in 11.3% of patients for the following reasons: treatment failure in 2.8%, death in 4.0%, adverse events in 1.7%, and other in 8.5%. Conclusions This is the first prospective observational study of C/T utilization in a health care setting enrolling many patients in France. C/T demonstrated a high rate of clinical effectiveness in MDR infections, confirming it as an effective treatment option for complicated infections in a high-risk population.

Funder

MSD, France

Merck & Co., Inc., Rahway, NJ, USA

Publisher

Oxford University Press (OUP)

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