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. 2024 Nov 26;13(12):1138.
doi: 10.3390/antibiotics13121138.

Ciprofloxacin for the Treatment of Infections Caused by Carbapenemase-Producing Gram-Negative Bacteria

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Ciprofloxacin for the Treatment of Infections Caused by Carbapenemase-Producing Gram-Negative Bacteria

Pablo Rubiñan et al. Antibiotics (Basel). .

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.

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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.

Figures

Figure 1
Figure 1
Flow diagram of the patients included in this study.

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References

    1. The World Health Organization Global Antimicrobial Resistance and Use Surveillance System (GLASS) Report 2022. [(accessed on 7 November 2024)]. Available online: https://iris.who.int/bitstream/handle/10665/364996/9789240062702-eng.pdf....
    1. Logan L.K., Weinstein R.A. The Epidemiology of Carbapenem-Resistant Enterobacteriaceae: The Impact and Evolution of a Global Menace. J. Infect. Dis. 2017;215((Suppl. 1)):S28–S36. doi: 10.1093/infdis/jiw282. - DOI - PMC - PubMed
    1. Bonomo R.A., Burd E.M., Conly J., Limbago B.M., Poirel L., A Segre J., Westblade L.F. Carbapenemase-Producing Organisms: A Global Scourge. Clin. Infect. Dis. 2018;66:1290–1297. doi: 10.1093/cid/cix893. - DOI - PMC - PubMed
    1. Martin A., Fahrbach K., Zhao Q., Lodise T. Association Between Carbapenem Resistance and Mortality Among Adult, Hospitalized Patients with Serious Infections Due to Enterobacteriaceae: Results of a Systematic Literature Review and Meta-analysis. Open Forum Infect. Dis. 2018;5:ofy150. doi: 10.1093/ofid/ofy150. - DOI - PMC - PubMed
    1. Palacios-Baena Z.R., Giannella M., Manissero D., Rodríguez-Baño J., Viale P., Lopes S., Wilson K., McCool R., Longshaw C. Risk factors for carbapenem-resistant Gram-negative bacterial infections: A systematic review. Clin. Microbiol. Infect. 2021;27:228–235. doi: 10.1016/j.cmi.2020.10.016. - DOI - PubMed

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