Cefiderocol: early clinical experience for multi-drug resistant gram-negative infections

Author:

El Ghali Amer1ORCID,Kunz Coyne Ashlan J.1ORCID,Lucas Kristen1,Tieman Molly2,Xhemali Xhilda3,Lau Suet-ping4,Iturralde Gabriela5,Purdy Andrew2,Holger Dana J.56,Garcia Esther5,Veve Michael P.17,Rybak Michael J.189ORCID

Affiliation:

1. Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, Michigan, USA

2. Department of Pharmacy, Indiana University Health, Bloomington, Indiana, USA

3. Department of Pharmacy, Cleveland Clinic, Cleveland, Ohio, USA

4. Department of Pharmacy, Orlando Health, Orlando, Florida, USA

5. Department of Pharmacy, Memorial Hospital West, Pembroke Pines, Florida, USA

6. Department of Pharmacy Practice, Barry and Judy Silverman College of Pharmacy, Nova Southeastern University, Fort Lauderdale, Florida, USA

7. Department of Pharmacy, Henry Ford Hospital, Detroit, Michigan, USA

8. Department of Medicine, Division of Infectious Diseases, School of Medicine, Wayne State University, Detroit, Michigan, USA

9. Department of Pharmacy Services, Detroit Receiving Hospital, Detroit Medical Center, Detroit, Michigan, USA

Abstract

ABSTRACT Multi-drug resistant gram-negative bacteria present a significant global health threat. Cefiderocol (CFDC), a siderophore cephalosporin, has shown potential in combating this threat, but with the currently available data, its role in therapy remains poorly defined. This multi-center, retrospective cohort study evaluated the real-world application of CFDC across six U.S. medical centers from January 2018 to May 2023. Patients aged ≥18 years and who had received ≥72 hours of CFDC were included. The primary outcome was a composite of clinical success: survival at 30 days, absence of symptomatic microbiologic recurrence at 30 days following CFDC treatment initiation, and resolution of signs and symptoms. Secondary outcomes included time to CFDC therapy and on-treatment non-susceptibility to CFDC. A total of 112 patients were included, with median (interquartile range [IQR]) APACHE II scores of 15 (19–18). Clinical success was observed in 68.8% of patients, with a mortality rate of 16.1% and comparable success rates across patients infected with carbapenem-resistant gram-negative infections. The most common isolated organisms were Pseudomonas aeruginosa (61/112, 54.5%, of which 55/61 were carbapenem-resistant) and carbapenem-resistant Acinetobacter baumannii (32/112, 28.6%). Median (IQR) time to CFDC therapy was 77 (14–141) hours. Two patients experienced a non-anaphylactic rash as an adverse drug reaction. On-treatment non-susceptibility to CFDC was found in six patients, notably due to P. aeruginosa and A. baumannii . IMPORTANCE CFDC was safe and clinically effective as a monotherapy or in combination in treating a variety of carbapenem-resistant gram-negative infections. Further prospective studies are warranted to confirm these findings.

Publisher

American Society for Microbiology

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Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Use of Cefiderocol in Adult Patients: Descriptive Analysis from a Prospective, Multicenter, Cohort Study;Infectious Diseases and Therapy;2024-07-12

2. Cefiderocol;Reactions Weekly;2024-04-06

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