Introduction: Cefiderocol is a siderophore cephalosporin showing activity against various carbapenem-resistant Gram-negative bacteria (CR-GNB). No data currently exist about real-world use of cefiderocol in terms of types of therapy (e.g., empirical or targeted, monotherapy or combined regimens), indications, and patient characteristics. Methods: In this multicenter, prospective study, we aimed at describing the use of cefiderocol in terms of types of therapy, indications, and patient characteristics. Results: Cefiderocol was administered as empirical and targeted therapy in 27.5% (55/200) and 72.5% (145/200) of cases, respectively. Overall, it was administered as monotherapy in 101/200 cases (50.5%) and as part of a combined regimen for CR-GNB infections in the remaining 99/200 cases (49.5%). In multivariable analysis, previous isolation of carbapenem-resistant Acinetobacter baumannii odds ratio (OR) 2.56, with 95% confidence interval (95% CI) 1.01–6.46, p = 0.047] and previous hematopoietic stem cell transplantation (OR 8.73, 95% CI 1.05–72.54, p = 0.045) were associated with administration of cefiderocol as part of a combined regimen, whereas chronic kidney disease was associated with cefiderocol monotherapy (OR 0.38 for combined regimen, 95% CI 0.16–0.91, p = 0.029). Cumulative 30-day mortality was 19.8%, 45.0%, 20.7%, and 22.7% in patients receiving targeted cefiderocol for infections by Enterobacterales, A. baumannii, Pseudomonas aeruginosa, and any metallo-β-lactamase producers, respectively. Conclusions: Cefiderocol is mainly used for targeted treatment, although empirical therapies account for more than 25% of prescriptions, thus requiring dedicated standardization and guidance. The almost equal distribution of cefiderocol monotherapy and cefiderocol-based combination therapies underlines the need for further study to ascertain possible differences in efficacy between the two approaches.

Use of Cefiderocol in Adult Patients: Descriptive Analysis from a Prospective, Multicenter, Cohort Study / Giacobbe, D. R.; Labate, L.; Russo Artimagnella, C.; Marelli, C.; Signori, A.; Di Pilato, V.; Aldieri, C.; Bandera, A.; Briano, F.; Cacopardo, B.; Calabresi, A.; Capra Marzani, F.; Carretta, A.; Cattelan, A.; Ceccarelli, L.; Cenderello, G.; Corcione, S.; Cortegiani, A.; Cultrera, R.; De Rosa, F. G.; Del Bono, V.; Del Puente, F.; Fanelli, C.; Fava, F.; Francisci, D.; Geremia, N.; Graziani, L.; Lombardi, A.; Losito, A. R.; Maida, I.; Marino, A.; Mazzitelli, M.; Merli, M.; Monardo, R.; Mularoni, A.; Oltolini, C.; Pallotto, C.; Pontali, E.; Raffaelli, F.; Rinaldi, M.; Ripa, M.; Santantonio, T. A.; Serino, F. S.; Spinicci, M.; Torti, C.; Trecarichi, E. M.; Tumbarello, M.; Mikulska, M.; Giacomini, M.; Marchese, A.; Vena, A.; Bassetti, M.; Maci, C.; Castagna, A.. - In: INFECTIOUS DISEASES AND THERAPY. - ISSN 2193-6382. - 13:9(2024), pp. 1929-1948. [10.1007/s40121-024-01016-y]

Use of Cefiderocol in Adult Patients: Descriptive Analysis from a Prospective, Multicenter, Cohort Study

Merli M.;Monardo R.;Ripa M.;Maci C.
Membro del Collaboration Group
;
Castagna A.
Membro del Collaboration Group
2024-01-01

Abstract

Introduction: Cefiderocol is a siderophore cephalosporin showing activity against various carbapenem-resistant Gram-negative bacteria (CR-GNB). No data currently exist about real-world use of cefiderocol in terms of types of therapy (e.g., empirical or targeted, monotherapy or combined regimens), indications, and patient characteristics. Methods: In this multicenter, prospective study, we aimed at describing the use of cefiderocol in terms of types of therapy, indications, and patient characteristics. Results: Cefiderocol was administered as empirical and targeted therapy in 27.5% (55/200) and 72.5% (145/200) of cases, respectively. Overall, it was administered as monotherapy in 101/200 cases (50.5%) and as part of a combined regimen for CR-GNB infections in the remaining 99/200 cases (49.5%). In multivariable analysis, previous isolation of carbapenem-resistant Acinetobacter baumannii odds ratio (OR) 2.56, with 95% confidence interval (95% CI) 1.01–6.46, p = 0.047] and previous hematopoietic stem cell transplantation (OR 8.73, 95% CI 1.05–72.54, p = 0.045) were associated with administration of cefiderocol as part of a combined regimen, whereas chronic kidney disease was associated with cefiderocol monotherapy (OR 0.38 for combined regimen, 95% CI 0.16–0.91, p = 0.029). Cumulative 30-day mortality was 19.8%, 45.0%, 20.7%, and 22.7% in patients receiving targeted cefiderocol for infections by Enterobacterales, A. baumannii, Pseudomonas aeruginosa, and any metallo-β-lactamase producers, respectively. Conclusions: Cefiderocol is mainly used for targeted treatment, although empirical therapies account for more than 25% of prescriptions, thus requiring dedicated standardization and guidance. The almost equal distribution of cefiderocol monotherapy and cefiderocol-based combination therapies underlines the need for further study to ascertain possible differences in efficacy between the two approaches.
2024
Inglese
Adis
13
9
1929
1948
20
Pubblicato
https://link.springer.com/article/10.1007/s40121-024-01016-y
Esperti anonimi
Internazionale
Goal 3: Good health and well-being
Antimicrobial resistance
Carbapenem resistance
Carbapenemases
Cefiderocol
Clinical practice
Use of Cefiderocol in Adult Patients: Descriptive Analysis from a Prospective, Multicenter, Cohort Study / Giacobbe, D. R.; Labate, L.; Russo Artimagnella, C.; Marelli, C.; Signori, A.; Di Pilato, V.; Aldieri, C.; Bandera, A.; Briano, F.; Cacopardo, B.; Calabresi, A.; Capra Marzani, F.; Carretta, A.; Cattelan, A.; Ceccarelli, L.; Cenderello, G.; Corcione, S.; Cortegiani, A.; Cultrera, R.; De Rosa, F. G.; Del Bono, V.; Del Puente, F.; Fanelli, C.; Fava, F.; Francisci, D.; Geremia, N.; Graziani, L.; Lombardi, A.; Losito, A. R.; Maida, I.; Marino, A.; Mazzitelli, M.; Merli, M.; Monardo, R.; Mularoni, A.; Oltolini, C.; Pallotto, C.; Pontali, E.; Raffaelli, F.; Rinaldi, M.; Ripa, M.; Santantonio, T. A.; Serino, F. S.; Spinicci, M.; Torti, C.; Trecarichi, E. M.; Tumbarello, M.; Mikulska, M.; Giacomini, M.; Marchese, A.; Vena, A.; Bassetti, M.; Maci, C.; Castagna, A.. - In: INFECTIOUS DISEASES AND THERAPY. - ISSN 2193-6382. - 13:9(2024), pp. 1929-1948. [10.1007/s40121-024-01016-y]
open
54
info:eu-repo/semantics/article
262
Giacobbe, D. R.; Labate, L.; Russo Artimagnella, C.; Marelli, C.; Signori, A.; Di Pilato, V.; Aldieri, C.; Bandera, A.; Briano, F.; Cacopardo, B.; Cal...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/172302
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