Evidence map›Paper›PMID 38886694›Full record

ArticleAnnals of clinical microbiology and antimicrobials2024

Cefiderocol susceptibility of Achromobacter spp.: study of an accurately identified collection of 230 strains.

Vincent Jean-Pierre, Pauline Sorlin, Alix Pantel, Raphaël Chiron, Jean-Philippe Lavigne, Katy Jeannot, Hélène Marchandin, Collaborative study group on antimicrobial resistance of Achromobacter spp.

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In one paragraph

Article in Annals of clinical microbiology and antimicrobials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Early and matureBiofilm · 2026
    Article
  2. Biomedical reports · 2026
    Review
  3. JAC-antimicrobial resistance · 2026
    Article
  4. Article
  5. Cefiderocol treatment for patients infected by Stenotrophomonas maltophilia, Burkholderia cepacia complex and Achromobacter spp.: subgroup analysis from the PERSEUS study.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2025
    Observational
  6. Article
  7. Review
  8. 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

8 authors.

Vincent Jean-PierreHydroSciences Montpellier, Univ. Montpellier, CNRS, IRD, Service de Microbiologie et Hygiène Hospitalière, CHU de Nîmes, 34093, Montpellier, France.
Pauline SorlinHydroSciences Montpellier, Univ. Montpellier, CNRS, IRD, Service de Microbiologie et Hygiène Hospitalière, CHU de Nîmes, 34093, Montpellier, France.
Alix PantelVBIC, INSERM U1047, Univ. Montpellier, Service de Microbiologie et Hygiène Hospitalière, CHU de Nîmes, 30029, Nîmes Cedex 9, France.
Raphaël ChironHydroSciences Montpellier, Univ. Montpellier, CNRS, IRD, Centre de Ressources et de Compétences de la Mucoviscidose, CHU de Montpellier, 34093, Montpellier, France.
Jean-Philippe LavigneVBIC, INSERM U1047, Univ. Montpellier, Service de Microbiologie et Hygiène Hospitalière, CHU de Nîmes, 30029, Nîmes Cedex 9, France.
Katy JeannotLaboratoire Associé Au Centre National de Référence de La Résistance Aux Antibiotiques, CHU de Besançon, 25000, Besançon, France.
Hélène MarchandinHydroSciences Montpellier, Univ. Montpellier, CNRS, IRD, Service de Microbiologie et Hygiène Hospitalière, CHU de Nîmes, 34093, Montpellier, France. helene.marchandin@umontpellier.fr.
Collaborative study group on antimicrobial resistance of Achromobacter spp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAchromobacter spp. are opportunistic pathogens, mostly infecting immunocompromised patients and patients with cystic fibrosis (CF) and considered as difficult-to-treat pathogens due to both intrinsic resistance and the possibility of acquired antimicrobial resistance. Species identification remains challenging leading to imprecise descriptions of resistance in each taxon. Cefiderocol is a broad-spectrum siderophore cephalosporin increasingly used in the management of Achromobacter infections for which susceptibility data remain scarce. We aimed to describe the susceptibility to cefiderocol of a collection of Achromobacter strains encompassing different species and isolation sources from CF or non-CF (NCF) patients.

methodsWe studied 230 Achromobacter strains (67 from CF, 163 from NCF patients) identified by nrdA gene-based analysis, with available susceptibility data for piperacillin-tazobactam, meropenem and trimethoprim-sulfamethoxazole. Minimal inhibitory concentrations (MICs) of cefiderocol were determined using the broth microdilution reference method according to EUCAST guidelines.

resultsStrains belonged to 15 species. A. xylosoxidans represented the main species (71.3%). MICs ranged from ≤ 0.015 to 16 mg/L with MIC

conclusionsCefiderocol exhibited excellent in vitro activity against a large collection of accurately identified Achromobacter strains, irrespective of species and origin.

Indexed as

AchromobacterAnti-Bacterial AgentsCefiderocolCephalosporinsCystic FibrosisGram-Negative Bacterial InfectionsMicrobial Sensitivity TestsHumansAnti-Bacterial AgentsCefiderocolCephalosporinsAchromobacterCefiderocolCystic fibrosisOpportunistic pathogenSusceptibility

Identifiers

PMID38886694
PMCPMC11184864

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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.