TY - JOUR
T1 - Intravenous fosfomycin for treatment of severe infections caused by carbapenem-resistant Acinetobacter baumannii: A multi-centre clinical experience
AU - Russo, Alessandro
AU - Gullì, Sara Palma
AU - D'Avino, Alessandro
AU - Borrazzo, Cristian
AU - Carannante, Novella
AU - Dezza, Francesco Cogliati
AU - Covino, Sara
AU - Polistina, Giorgio
AU - Fiorentino, Giuseppe
AU - Trecarichi, Enrico Maria
AU - Mastroianni, Claudio Maria
AU - Torti, Carlo
AU - Oliva, Alessandra
PY - 2024
Y1 - 2024
N2 - Background: Severe infections caused by carbapenem-resistant Acinetobacter baumannii (CRAB) have been reported increasingly over the past few years. Many in-vivo and in-vitro studies have suggested a possible role of intravenous fosfomycin for the treatment of CRAB infections. Methods: This multi-centre, retrospective study included patients treated with intravenous fosfomycin for severe infections caused by CRAB admitted consecutively to four hospitals in Italy from December 2017 to December 2022. The primary goal of the study was to evaluate the risk factors associated with 30-day mortality in the study population. A propensity score matched analysis was added to the model. Results: One hundred and two patients with severe infections caused by CRAB treated with an intravenous fosfomycin-containing regimen were enrolled in this study. Ventilator-associated pneumonia (VAP) was diagnosed in 59% of patients, primary bacteraemia in 22% of patients, and central-venous-catheter-related infection in 16% of patients. All patients were treated with a regimen containing intravenous fosfomycin, mainly in combination with cefiderocol (n=54), colistin (n=48) or ampicillin/sulbactam (n=18). Forty-eight (47%) patients died within 30 days. Fifty-eight (57%) patients experienced clinical therapeutic failure. Cox regression analysis showed that diabetes, primary bacteraemia and a colistin-containing regimen were independently associated with 30-day mortality, whereas adequate source control of infection, early 24-h active in-vitro therapy, and a cefiderocol-containing regimen were associated with survival. A colistin-based regimen, A. baumannii colonization and primary bacteraemia were independently associated with clinical failure. Conversely, adequate source control of infection, a cefiderocol-containing regimen, and early 24-h active in-vitro therapy were associated with clinical success. Conclusions: Different antibiotic regimens containing fosfomycin in combination can be used for treatment of severe infections caused by CRAB.
AB - Background: Severe infections caused by carbapenem-resistant Acinetobacter baumannii (CRAB) have been reported increasingly over the past few years. Many in-vivo and in-vitro studies have suggested a possible role of intravenous fosfomycin for the treatment of CRAB infections. Methods: This multi-centre, retrospective study included patients treated with intravenous fosfomycin for severe infections caused by CRAB admitted consecutively to four hospitals in Italy from December 2017 to December 2022. The primary goal of the study was to evaluate the risk factors associated with 30-day mortality in the study population. A propensity score matched analysis was added to the model. Results: One hundred and two patients with severe infections caused by CRAB treated with an intravenous fosfomycin-containing regimen were enrolled in this study. Ventilator-associated pneumonia (VAP) was diagnosed in 59% of patients, primary bacteraemia in 22% of patients, and central-venous-catheter-related infection in 16% of patients. All patients were treated with a regimen containing intravenous fosfomycin, mainly in combination with cefiderocol (n=54), colistin (n=48) or ampicillin/sulbactam (n=18). Forty-eight (47%) patients died within 30 days. Fifty-eight (57%) patients experienced clinical therapeutic failure. Cox regression analysis showed that diabetes, primary bacteraemia and a colistin-containing regimen were independently associated with 30-day mortality, whereas adequate source control of infection, early 24-h active in-vitro therapy, and a cefiderocol-containing regimen were associated with survival. A colistin-based regimen, A. baumannii colonization and primary bacteraemia were independently associated with clinical failure. Conversely, adequate source control of infection, a cefiderocol-containing regimen, and early 24-h active in-vitro therapy were associated with clinical success. Conclusions: Different antibiotic regimens containing fosfomycin in combination can be used for treatment of severe infections caused by CRAB.
KW - Bacteraemia
KW - Carbapenem-resistant Acinetobacter baumannii
KW - Source control of infection
KW - Colistin
KW - Fosfomycin
KW - Cefiderocol
KW - Bacteraemia
KW - Carbapenem-resistant Acinetobacter baumannii
KW - Source control of infection
KW - Colistin
KW - Fosfomycin
KW - Cefiderocol
UR - http://hdl.handle.net/10807/303358
U2 - 10.1016/j.ijantimicag.2024.107190
DO - 10.1016/j.ijantimicag.2024.107190
M3 - Article
SN - 0924-8579
VL - 64
SP - N/A-N/A
JO - International Journal of Antimicrobial Agents
JF - International Journal of Antimicrobial Agents
ER -