Evidence map›Paper›PMID 40724573›Full record

ArticleLife (Basel, Switzerland)2025

Which Classes of Antibiotics Are Associated with the Acquisition of Carbapenemase-Producing Enterobacterales?

Lisa Sadou, Benoît Pilmis, Rasha Eid, Pierre Moenne Locoz, Sophie Lefèvre, Françoise Jauréguy, Vanessa Rathouin, Jean-Ralph Zahar, Laura Foucault-Fruchard

Abstract read
In one paragraph

Article in Life (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Lisa SadouUnité de Prévention du Risque Infectieux, Department of Clinical Microbiology, AP-HP, Groupe Hospitalier Paris Seine Saint-Denis, 93000 Bobigny, France.
Benoît PilmisEquipe Mobile de Microbiologie Clinique, Hôpitaux Saint-Joseph et Marie-Lannelongue, 75014 Paris, France.
Rasha EidUnité de Prévention du Risque Infectieux, Department of Clinical Microbiology, AP-HP, Groupe Hospitalier Paris Seine Saint-Denis, 93000 Bobigny, France.
Pierre Moenne LocozUnité de Prévention du Risque Infectieux, Department of Clinical Microbiology, AP-HP, Groupe Hospitalier Paris Seine Saint-Denis, 93000 Bobigny, France.
Sophie LefèvreUnité de Prévention du Risque Infectieux, Department of Clinical Microbiology, AP-HP, Groupe Hospitalier Paris Seine Saint-Denis, 93000 Bobigny, France.ORCID 0000-0002-3065-6591
Françoise JauréguyDepartment of Clinical Microbiology, AP-HP, Groupe Hospitalier Paris Seine Saint-Denis, 93000 Bobigny, France.ORCID 0000-0001-6598-183X
Vanessa RathouinService de Pharmacie, AP-HP, Groupe Hospitalier Paris Seine Saint-Denis, 93000 Bobigny, France.
Jean-Ralph ZaharUnité de Prévention du Risque Infectieux, Department of Clinical Microbiology, AP-HP, Groupe Hospitalier Paris Seine Saint-Denis, 93000 Bobigny, France.
Laura Foucault-FruchardUnité de Prévention du Risque Infectieux, Department of Clinical Microbiology, AP-HP, Groupe Hospitalier Paris Seine Saint-Denis, 93000 Bobigny, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEnterobacterales are among the most frequent causes of healthcare-associated infections and are increasingly affected by antimicrobial resistance. Antibiotic use disrupts the gut microbiota, facilitating colonization by multidrug-resistant organisms, including carbapenemase-producing Enterobacterales (CPE). While animal studies have suggested that certain antibiotic classes may increase the risk of CPE acquisition, clinical data identifying which classes are most implicated remain limited.

methodsWe conducted a single-center, retrospective case-control study (2021-2024) comparing antibiotic prescriptions in patients who acquired CPE with those in controls hospitalized in the same unit and during the same risk period but who did not acquire CPE. The objective of this study was to identify which antibiotic classes or pharmacological properties are associated with the acquisition of carbapenemase-producing Enterobacterales (CPE) in hospitalized patients.

resultsDuring the study period, 35 cases and 70 controls were included. Most cases acquired NDM-type metalloenzymes. Before the risk period, 55 patients had received antibiotic therapy. Univariate analysis identified an association between CPE acquisition and the prescription of fluoroquinolones and antibiotics excreted in bile. During the risk period, only metronidazole prescription was significantly associated with CPE acquisition. Our study has several limitations, including the small sample size, the single-center retrospective design, and the lack of molecular typing (e.g., WGS) to confirm potential clonal transmission.

conclusionsIn this preliminary study, metronidazole use was associated with an increased risk of CPE acquisition during risk periods. However, these results should be interpreted cautiously and need to be confirmed in larger, multicenter studies. The high exposure of patients to multiple antibiotic classes highlights the importance of strict antibiotic stewardship policies in the current era of global CPE dissemination.

Indexed as

antibioticsantimicrobial stewardshipCPEfluoroquinolones

Identifiers

PMID40724573
PMCPMC12299048

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.