Evidence map›Paper›PMID 42127953›Full record

ArticleThe Lancet. Microbe2026

Emergence of carbapenemase-producing Escherichia coli in acute care hospitals in 32 European countries (the CCRE survey): a prospective, multicentre, cross-sectional, epidemiological, microbiological, and genomic surveillance study.

Sophia David, Anke Kohlenberg, Corin Yeats, Khalil Abu-Dahab, Barbara Albiger, Nabil-Fareed Alikhan, Erik Alm, Sara Byfors, Natacha Couto, Julio Diaz Caballero and 14 more

Abstract readMulticenter Study
In one paragraph

Article in The Lancet. Microbe, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

24 authors.

Sophia DavidCentre for Genomic Pathogen Surveillance, Pandemic Sciences Institute, University of Oxford, Oxford, UK.
Anke KohlenbergEuropean Centre for Disease Prevention and Control, Solna, Sweden. Electronic address: anke.kohlenberg@ecdc.europa.eu.
Corin YeatsCentre for Genomic Pathogen Surveillance, Pandemic Sciences Institute, University of Oxford, Oxford, UK.
Khalil Abu-DahabCentre for Genomic Pathogen Surveillance, Pandemic Sciences Institute, University of Oxford, Oxford, UK.
Barbara AlbigerEuropean Centre for Disease Prevention and Control, Solna, Sweden.
Nabil-Fareed AlikhanCentre for Genomic Pathogen Surveillance, Pandemic Sciences Institute, University of Oxford, Oxford, UK.
Erik AlmEuropean Centre for Disease Prevention and Control, Solna, Sweden.
Sara ByforsPublic Health Agency of Sweden, Solna, Sweden.
Natacha CoutoCentre for Genomic Pathogen Surveillance, Pandemic Sciences Institute, University of Oxford, Oxford, UK.
Julio Diaz CaballeroCentre for Genomic Pathogen Surveillance, Pandemic Sciences Institute, University of Oxford, Oxford, UK.
Christian G GiskeDepartment of Laboratory Medicine, Division of Clinical Microbiology, Karolinska Institute, Stockholm, Sweden; Department of Clinical Microbiology, Karolinska University Hospital, Stockholm, Sweden.
Corinna GlasnerUniversity of Groningen, Groningen, Netherlands.
Marius LinkeviciusEuropean Centre for Disease Prevention and Control, Solna, Sweden.
Erika MatuschekEuropean Committee on Antimicrobial Susceptibility Testing Development Laboratory, Växjö, Sweden.
Daniel PalmEuropean Centre for Disease Prevention and Control, Solna, Sweden.
Olov SvartströmEuropean Centre for Disease Prevention and Control, Solna, Sweden.
Hajo GrundmannInstitute for Infection Prevention and Hospital Epidemiology, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Marc J StruelensFaculty of Medicine, Université Libre de Bruxelles, Brussels, Belgium.
Karin Tegmark WisellPublic Health Agency of Sweden, Solna, Sweden.
Dominique L MonnetEuropean Centre for Disease Prevention and Control, Solna, Sweden.
Inga FrödingPublic Health Agency of Sweden, Solna, Sweden; Department of Laboratory Medicine, Division of Clinical Microbiology, Karolinska Institute, Stockholm, Sweden.
David M AanensenCentre for Genomic Pathogen Surveillance, Pandemic Sciences Institute, University of Oxford, Oxford, UK.
Alma BrolundPublic Health Agency of Sweden, Solna, Sweden.
EURGen-Net CCRE Survey Working Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe emergence of carbapenem resistance in Escherichia coli is of major concern due to the high propensity of spread of this species and scarce treatment options. Herein, we examined the occurrence and spread of carbapenem-resistant E coli based on the carbapenem-resistant and/or colistin-resistant Enterobacterales (CCRE) survey performed across European countries in 2019.

methodsWe analysed epidemiological, microbiological, and whole-genome sequencing data of 548 E coli isolates from individual patients from 156 hospitals in 32 European countries over 6 months in 2019. These hospitals collected the first ten successive isolates of carbapenem-resistant or carbapenem-susceptible increased exposure (carbapenem-R/I) Klebsiella pneumoniae species complex or E coli, and carbapenem-susceptible (carbapenem-S) comparator isolates of the same species. Antimicrobial susceptibility testing was performed for 19 antimicrobial agents. Whole-genome sequencing was performed centrally using Illumina technology. Isolates from the CCRE survey were compared with those from the European Survey of Carbapenemase-Producing Enterobacteriaceae (EuSCAPE) study.

findingsOf the 548 E coli isolates, 211 (38·5%) were carbapenem-resistant or susceptible, increased exposure (carbapenem-R/I), and 337 (61·5%) were carbapenem-susceptible (carbapenem-S). Five sequence types (STs) accounted for 96 (45·5%) of 211 carbapenem-R/I isolates: ST131 (27), ST410 (20), ST38 (19), ST167 (16), and ST648 (14). Carbapenemase genes were identified in 182 (86·3%) carbapenem-R/I isolates, a pronounced increase from the 2013-14 EuSCAPE study (36 of 99, 36·4%). The most common genes were bla

interpretationHigh-risk STs of E coli carrying carbapenemase genes are rapidly spreading globally, although our results indicate that, in 2019, most cases in Europe were sporadic. We urge vigilant monitoring, including genomic surveillance, and strengthening of control efforts, to reduce mortality and morbidity associated with the impending rise in carbapenem-R/I E coli cases.

fundingEuropean Centre for Disease Prevention and Control and the Centre for Genomic Pathogen Surveillance.

Indexed as

Bacterial Proteinsbeta-LactamasesEscherichia coliEscherichia coli InfectionsAnti-Bacterial AgentsCarbapenem-Resistant EnterobacteriaceaeCarbapenemsCross-Sectional StudiesEuropeHospitalsHumansMicrobial Sensitivity TestsProspective StudiesWhole Genome SequencingAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasescarbapenemaseCarbapenems

Identifiers

PMID42127953
PMCPMC13259978

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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.