Clinical Outcomes of Third-Generation Cephalosporin Definitive Therapy for Bloodstream Infections Due to Enterobacterales with Potential AmpC Induction: A Single-Center Retrospective Study

Author:

Vossius Gilles1,Meex Cécile2,Moerman Filip3,Thys Marie4,Ernst Marie5ORCID,Bourgeois Marie-Eve6,Wagner Léa6ORCID,Delahaye Thibaut6,Darcis Gilles1ORCID

Affiliation:

1. Département des Maladies Infectieuses, Centre Hospitalier Universitaire de Liège, 4000 Liège, Belgium

2. Service de Microbiologie Clinique, Université de Liège, 4000 Liège, Belgium

3. Département des Maladies Infectieuses, Hôpital de la Citadelle, 4000 Liège, Belgium

4. Service des Informations Médico-Économiques, Centre Hospitalier Universitaire de Liège, 4000 Liège, Belgium

5. Biostatistics and Research Method Center (B-STAT), Centre Hospitalier Universitaire de Liège, 4000 Liège, Belgium

6. Faculté de Médecine, Université de Liège, 4000 Liège, Belgium

Abstract

The recommended therapy for severe infections caused by AmpC-inducible Enterobacterales (AmpC-E) typically involves cefepime or carbapenems. In an era of emerging resistance to these antimicrobials, we aim to assess the impact of third-generation cephalosporins (3GCs) vs. alternative antibiotics on clinical outcomes in bloodstream infections (BSIs) due to AmpC-E. We retrospectively included hospitalized adult patients with BSIs caused by 3GC-susceptible AmpC-E between 2012 and 2022, comparing the outcomes of 3GC and non-3GC definitive therapies. The primary outcome was overall treatment failure (OTF), encompassing 90-day all-cause mortality, 90-day reinfection, and 90-day readmission. Secondary outcomes comprised components of the OTF, in-hospital all-cause mortality, and length-of-stay. Within a total cohort of 353 patients, OTF occurred in 46.5% and 41.5% in the 3GC- and non-3GC-therapy groups, respectively (p = 0.36). The 3GC-therapy group exhibited a longer length-of-stay (38 vs. 21 days, p = 0.0003) and higher in-hospital mortality (23.3% vs. 13.4%, p = 0.019). However, the 90-day mortality, 90-day reinfection, and 90-day readmission were comparable between the therapy groups. Subgroup analyses involving high-risk AmpC-E and 3GC vs. standard-of-care yielded similar conclusions. Overall, our findings suggest that 3GC definitive therapy may not result in poorer clinical outcomes for the treatment of BSIs caused by AmpC-E.

Publisher

MDPI AG

Subject

Infectious Diseases,Microbiology (medical),General Immunology and Microbiology,Molecular Biology,Immunology and Allergy

Reference29 articles.

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