Cefiderocol for the Treatment of Infections by VIM-Type-Producing Gram-Negative Bacteria

Author:

Kirkegaard-Biosca Cristina12ORCID,del Barrio-Tofiño Ester3,Villamarín Miguel1,Larrosa Nieves234,Campany David5ORCID,González-López Juan José234ORCID,Ferrer Ricard267ORCID,Viñado Belén3,Doménech Laura5ORCID,Sellarès-Nadal Julia12,Escolà-Vergé Laura248ORCID,Fernández-Hidalgo Nuria124ORCID,Los-Arcos Ibai124ORCID

Affiliation:

1. Infectious Diseases Department, Hospital Universitari Vall d’Hebron, 08035 Barcelona, Spain

2. Department of Medicine, Universitat Autònoma de Barcelona, 08035 Barcelona, Spain

3. Microbiology Department, Hospital Universitari Vall d’Hebron, 08035 Barcelona, Spain

4. CIBERINFEC, ISCIII—CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III, 28029 Madrid, Spain

5. Pharmacy Department, Hospital Universitari Vall d’Hebron, 08035 Barcelona, Spain

6. Critical Care Department, Hospital Universitari Vall d’Hebron, 08035 Barcelona, Spain

7. Sepsis Organ Dysfunction and Resuscitation (SODIR) Research Group, Vall d’Hebron Institut de Recerca (VHIR), 08035 Barcelona, Spain

8. Infectious Diseases Unit, Internal Medicine Department, Hospital de la Santa Creu i Sant Pau, 08025 Barcelona, Spain

Abstract

VIM-type-producing Gram-negative bacteria (GNB) infections are difficult to treat. This is a retrospective single-center study of 34 patients who received cefiderocol for the treatment of VIM-type-producing GNB infections, including 25 Pseudomonas spp., 7 Enterobacterales, and 5 Achromobacter sp. 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. The median age was 59 years (IQR 53.7–73.4), and the median Charlson comorbidity index was 3.5 (IQR 2–5). The main infections were respiratory tract infections (n = 9, 27%) and skin and soft tissue infections (n = 9, 27%). Eight patients exhibited bacteremia. In 9/17 patients with a drainable focus, drainage was performed. The median cefiderocol treatment duration was 13 days (IQR 8–24). Five patients (15%) experienced clinical failure on day 14, and the thirty-day mortality rate was 9/34 (27%); two cases occurred because of an uncontrolled infection source, and one was due to a new infection caused by the same bacteria. The other six deaths were unrelated to the index infection. Five patients experienced microbiological recurrence within three months. Susceptibility testing revealed the development of cefiderocol resistance in 1/7 cases with persistent or recurrent positive cultures. Cefiderocol, even in monotherapy, could be considered for the treatment of VIM-type-producing GNB infections.

Publisher

MDPI AG

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