Ciprofloxacin for the Treatment of Infections Caused by Carbapenemase-Producing Gram-Negative Bacteria
- PMID: 39766528
- PMCID: PMC11672814
- DOI: 10.3390/antibiotics13121138
Ciprofloxacin for the Treatment of Infections Caused by Carbapenemase-Producing Gram-Negative Bacteria
Abstract
Background: There is no experience with ciprofloxacin for the treatment of carbapenemase-producing Gram-negative bacteria (CP-GNB) infections. Methods: This is a retrospective single-centre study where we describe the clinical evolution of all consecutive adult patients who received ciprofloxacin monotherapy for the treatment of CP-GNB infections. Primary outcomes were clinical failure (defined as death, lack of clinical improvement or a switch to another drug) at day 14 and 30-day all-cause mortality. Results: Nineteen patients were included. Fifteen (79%) were men, the median age was 74 years (IQR 66-79) and the median Charlson comorbidity index was five (IQR 3-6.5). The most frequent infections were: nine complicated urinary tract infections, three soft tissue infections and three intra-abdominal infections. Twenty CP-GNBs were isolated (one patient had a coinfection): nine VIM-type-producing Enterobacterales, nine OXA-48-type-producing Enterobacterales and two VIM-type-producing Pseudomonas aeruginosa. Six (32%) patients had positive blood cultures, and one presented with septic shock. The median duration of ciprofloxacin treatment was 14 days (IQR 10-15). One patient presented with clinical failure at day 14. There was no 30-day mortality. Two patients exhibited microbiological recurrence at day 90. There were no reported adverse effects. Conclusions: Monotherapy with ciprofloxacin may be an alternative treatment for selected, clinically stable patients with ciprofloxacin-susceptible CP-GNB infections.
Keywords: OXA; VIM; carbapenem-resistant; fluoroquinolones; multidrug-resistant.
Conflict of interest statement
D. Campany has received honoraria for speaking at educational events from Shionogi. D. Rodriguez-Pardo declares no conflicts of interest in relation to this work. Regarding other activities outside this study, D. Rodriguez-Pardo declares having received honoraria from Pfizer, Angellini, MSD, Tillots and Astellas as payment for lectures, consultancy tasks and travel/accommodation for scientific purposes. X. Nuvials has received honoraria from MSD, Pfizer, Gilead and Shionogi as payment for speaking at educational events and consultancy tasks. L. Escolà-Vergé declares no conflicts of interest in relation to this work. Regarding other activities, L. Escolà-Vergé has received travel/accommodation support from Pfizer, Menarini and MSD for scientific purposes. I. Los-Arcos has received honoraria for speaking at educational events from MSD, Pfizer and Shionogi and has received travel support from Gilead, MSD, Shionogi and Menarini for scientific purposes. J.J. González-López has received honoraria for participating at educational events from Shionogi and MSD. The rest of the authors declare no conflicts of interests.
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