Evidence map›Paper›PMID 42095743›Full record

SynthesisEmerging microbes & infections2026

Clinical outcomes of carbapenem therapy in OXA-48-producing Enterobacterales infections: a French multicentre cohort, systematic review, and meta-analysis.

Laurent Dortet, Charlotte Moreau, Aurélien Dinh, Rémy A Bonnin, Lélia Escaut, Manon Seguret, Laura Weber, Samy Figueiredo, Benoît Pilmis

Abstract readSystematic ReviewMeta-AnalysisMulticenter Study
In one paragraph

Synthesis in Emerging microbes & infections, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Article
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.

Laurent DortetTeam "Resist" UMR1184 "Immunology of Viral, Auto-Immune, Hematological, and Bacterial diseases (IMVA-HB)." INSERM, CEA, Faculty of Medicine, Université Paris-Saclay, Le Kremlin-Bicêtre, France.
Charlotte MoreauDepartment of Infectious Diseases and Tropical Diseases, Assistance Publique-Hôpitaux de Paris, Raymond Poincaré Hospital, Paris-Saclay University, Boulogne Billancourt, France.
Aurélien DinhDepartment of Infectious Diseases and Tropical Diseases, Assistance Publique-Hôpitaux de Paris, Raymond Poincaré Hospital, Paris-Saclay University, Boulogne Billancourt, France.
Rémy A BonninTeam "Resist" UMR1184 "Immunology of Viral, Auto-Immune, Hematological, and Bacterial diseases (IMVA-HB)." INSERM, CEA, Faculty of Medicine, Université Paris-Saclay, Le Kremlin-Bicêtre, France.
Lélia EscautTeam "Resist" UMR1184 "Immunology of Viral, Auto-Immune, Hematological, and Bacterial diseases (IMVA-HB)." INSERM, CEA, Faculty of Medicine, Université Paris-Saclay, Le Kremlin-Bicêtre, France.
Manon SeguretDepartment of Anesthesia and Surgical Intensive Care, Bicêtre Hospital, Assistance Publique-Hôpitaux de Paris, Paris-Saclay University, Paris, France.
Laura WeberDepartment of Anesthesia and Surgical Intensive Care, Bicêtre Hospital, Assistance Publique-Hôpitaux de Paris, Paris-Saclay University, Paris, France.
Samy FigueiredoDepartment of Anesthesia and Surgical Intensive Care, Bicêtre Hospital, Assistance Publique-Hôpitaux de Paris, Paris-Saclay University, Paris, France.
Benoît PilmisTeam "Resist" UMR1184 "Immunology of Viral, Auto-Immune, Hematological, and Bacterial diseases (IMVA-HB)." INSERM, CEA, Faculty of Medicine, Université Paris-Saclay, Le Kremlin-Bicêtre, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

OXA-48-producing Enterobacterales (OXA-48-PE) represent a growing global health threat. Most of OXA-48-PE remain categorized susceptible to carbapenems, which might encourage their use despite uncertain clinical efficacy. This study evaluated clinical outcomes of infections caused by OXA-48-PE treated with carbapenem compared with alternative active therapies. The analyses were performed at three levels: a descriptive analysis of the French cohort, a comparative descriptive analysis of all published studies, and a meta-analysis restricted to studies providing direct comparisons between carbapenem-based and alternative active regimens. Between September 2021 and March 2023, 59 patients with monomicrobial OXA-48-PE infections were included in a French multicenter retrospective cohort. In parallel, a systematic review was conducted to identify clinical studies published through 31 December 2024, reporting outcomes of OXA-48-PE infections. In the French cohort, the overall 30-day mortality was 49.1%. Clinical failure occurred in 57.1% of patients receiving meropenem monotherapy, including patients infected with isolates exhibiting meropenem MICs within the susceptible range. Across 12 clinical studies (817 patients), carbapenem therapy was associated with high and variable crude mortality (52%), whereas newer agents active against OXA-48-PE, particularly ceftazidime-avibactam, were associated with lower and more consistent crude mortality (30.7%). In the primary meta-analysis of 6 human comparative studies, carbapenem therapy was associated with an increased risk of clinical failure compared with alternative active regimens (OR = 2.02; 95% CI = 1.05-3.88). Despite apparent

Indexed as

Anti-Bacterial Agentsbeta-LactamasesCarbapenemsEnterobacteriaceaeEnterobacteriaceae InfectionsCeftazidimeFranceHumansMicrobial Sensitivity TestsRetrospective StudiesTreatment OutcomeAnti-Bacterial Agentsbeta-LactamasesCarbapenemsCeftazidimeantimicrobial resistancecarbapenemase-producing Enterobacteralescarbapenem therapyceftazidime-avibactammeta-analysisOXA-48

Identifiers

PMID42095743
PMCPMC13188539

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Registered trials

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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.