Evidence map›Paper›PMID 40001398›Full record

ArticleAntibiotics (Basel, Switzerland)2025

Characterization of

Branka Bedenić, Josefa Luxner, Gernot Zarfel, Ana Benčić, Sanda Sardelić, Maja Anušić, Jasmina Vraneš, Verena Dobretzberger, Ivan Barišić, Andrea Grisold

Abstract read
In one paragraph

Article in Antibiotics (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

10 authors.

Branka BedenićBiomedical Research Center-BIMIS, University of Zagreb School of Medicine, 10000 Zagreb, Croatia.
Josefa LuxnerDiagnostic and Research Institute of Hygiene, Microbiology and Environmental Medicine, Medical University of Graz, 8036 Graz, Austria.ORCID 0009-0002-6579-5089
Gernot ZarfelDiagnostic and Research Institute of Hygiene, Microbiology and Environmental Medicine, Medical University of Graz, 8036 Graz, Austria.ORCID 0000-0003-1592-4559
Ana BenčićDepartment of Gynecology and Obstetrics, University Hospital Centre Sestre Milosrdnice, 10000 Zagreb, Croatia.
Sanda SardelićDepartment of Microbiology and Parasitology, University Hospital of Split, 21000 Split, Croatia.
Maja AnušićDepartment of Clinical Microbiology, Dr. Andrija Štampar Teaching Institute of Public Health Zagreb, 10000 Zagreb, Croatia.
Jasmina VranešDepartment of Clinical Microbiology, Dr. Andrija Štampar Teaching Institute of Public Health Zagreb, 10000 Zagreb, Croatia.ORCID 0000-0002-3282-0973
Verena DobretzbergerDepartment of Molecular Diagnostics, Austrian Institute for Technology, 1210 Vienna, Austria.ORCID 0000-0003-2365-8975
Ivan BarišićDepartment of Molecular Diagnostics, Austrian Institute for Technology, 1210 Vienna, Austria.ORCID 0000-0002-1301-6197
Andrea GrisoldDiagnostic and Research Institute of Hygiene, Microbiology and Environmental Medicine, Medical University of Graz, 8036 Graz, Austria.ORCID 0000-0002-6937-521X

Funding

The University of Zagreb School of Medicine (extend-ed-spectrum β-lactamases, plasmid-mediated β-lactamases, and carbapenemases in Proteus mira-bilis). 10106-24-1294
6 · The paper itself

Abstract

BACKGROUND/

objectivesWe conducted this study to evaluate the genotypic and phenotypic profiles of carbapenem-resistant

methodsSusceptibility to a wide range of antibiotics was determined by the disk diffusion and broth microdilution method. Carbapenemases were screened by a modified Hodge test while carbapenem hydrolysis was investigated using mCIM and eCIM tests. The screening for β-lactamase and fluoroquinolone cluster resistance genes was carried out by PCR. Plasmids were characterized by PCR-based replicon typing (PBRT). An inter-array genotyping CarbaResist test and whole genome sequencing (WGS) were applied on selected isolates.

resultsAll of the 31 isolates studied exhibited high-level resistance to amoxicillin-clavulanate, piperacillin-tazobactam, cefuroxime, expanded-spectrum cephalosporins (ESC), cefepime, ceftolozan-tazobactam and ciprofloxacin and the majority to gentamicin, and amikacin. Colistin and ceftazidime-avibactam preserved activity against 71% and 87% of the isolates, respectively. The combined disk method with clavulanic acid was positive in all but one isolate, indicating the production of an ESBL. Twenty-eight isolates carried one single carbapenemase-encoding gene, whereas three harbored double

conclusionTo our knowledge, this is the first study on FDC resistance in Croatia. The diffusion of FDC-resistant isolates was detected in both hospital and outpatient settings, emphasizing the need for a "One Health" approach.

Indexed as

cefiderocolKlebsiella pneumoniaeKPCmetallo-β-lactamaseOXA-48

Identifiers

PMID40001398
PMCPMC11851357

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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.