4.6 Article

Cefiderocol-Based Combination Therapy for Difficult-to-Treat Gram-Negative Severe Infections: Real-Life Case Series and Future Perspectives

Journal

ANTIBIOTICS-BASEL
Volume 10, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/antibiotics10060652

Keywords

cefiderocol; multidrug resistant gram-negative bacteria; novel antimicrobial strategies; Pseudomonas aeruginosa; Acinetobacter baumannii; Klebsiella pneumoniae; immunocompromised hosts; critically ill patients

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This study investigated the efficacy of cefiderocol-based combination therapies as rescue treatments for eradicating severe infections caused by multidrug-resistant bacteria. Most patients were immunocompromised or critically ill, and showed good treatment outcomes during the course of therapy, with some deaths attributed to other causes.
Cefiderocol is a new cephalosporin displaying against extensively resistant (XDR) Gram-negative bacteria. We report our experience with cefiderocol-based combination therapies as rescue treatments in immunocompromised or critically ill patients or in patients with post-surgical infections who had failed previous regimens. A total of 13 patients were treated from 1 September 2020 to 31 March 2021. In total, 5/13 (38%) patients were classified as critically ill, due to severe COVID-19 lung failure; 4/13 (31%) patients had post-surgical infections and 4/13 (31%) had severe infections in immunocompromised subjects due to solid organ transplantation (2/4) or hematological malignancy (2/4). Overall, 10/13 infections were caused by carbapenem-resistant Acinetobacter baumannii, one by KPC-positive ceftazidime/avibactam-resistant Klebsiella pneumonia and two by Pseudomonas aeruginosa XDR. Based on clinical, microbiological and hematobiochemical evaluation, cefiderocol was associated with different companion drugs, particularly with fosfomycin, high-dose tigecycline and/or colistin. Microbiological eradication was achieved in all cases and the 30-day survival rate was 10/13; two patients died due to SARS-CoV-2 lung failure, whereas one death was attributed to subsequent infections. No recurrent infections within 30 days were reported. Finally, we hereby discuss the therapeutic potential of cefiderocol and the possible place in the therapy of this novel drug.

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