Evidence map›Paper›PMID 41573238›Full record

ArticleJAC-antimicrobial resistance2026

Activity of cefepime/enmetazobactam against highly multidrug-resistant bacterial isolates recovered from war-associated wounds in Ukraine.

Jale Boral, Nora Toft, Alp Eren Baybes, Chaitanya Tellapragada, Oleksandr Nazarchuk, Celine Fernandez, Christian Giske, Kristian Riesbeck

Abstract read
In one paragraph

Article in JAC-antimicrobial resistance, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

8 authors.

Jale BoralClinical Microbiology, Department of Translational Medicine, Lund University, Malmö, Sweden.ORCID https://orcid.org/0000-0002-7910-5301
Nora ToftClinical Microbiology, Department of Translational Medicine, Lund University, Malmö, Sweden.
Alp Eren BaybesClinical Microbiology, Department of Translational Medicine, Lund University, Malmö, Sweden.
Chaitanya TellapragadaDivision of Clinical Microbiology, Department of Laboratory Medicine, Karolinska Institute, Stockholm, Sweden.ORCID https://orcid.org/0000-0002-0117-5369
Oleksandr NazarchukCenter for Thermal Injury and Plastic Surgery, Vinnytsya Regional Clinical Hospital Named After Pirogov, Vinnytsya, Ukraine.
Celine FernandezMedical Department, ADVANZ Pharma, Helsingborg, Sweden.
Christian GiskeDivision of Clinical Microbiology, Department of Laboratory Medicine, Karolinska Institute, Stockholm, Sweden.
Kristian RiesbeckClinical Microbiology, Department of Translational Medicine, Lund University, Malmö, Sweden.ORCID https://orcid.org/0000-0001-6274-6965

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Escalating resistance among Gram-negative pathogens limits β-lactam options. Cefepime/enmetazobactam combines a fourth-generation cephalosporin with a class A β-lactamase inhibitor. We evaluated its activity against multidrug, extensive and pandrug-resistant war-wound isolates from Ukraine. Materials and methods: We tested 215 clinical samples (2022-2023) isolated from wounded patients in Ukraine by broth microdilution. Paired comparisons of cefepime monotherapy versus cefepime/enmetazobactam was done to evaluate enmetazobactam. Whole-genome sequencing ( Results: Across Enterobacterales, resistance decreased from 60.5% (26/43) with cefepime to 27.9% (12/43) with the cefepime/enmetazobactam combination. In Conclusions: Cefepime/enmetazobactam improved susceptibility relative to cefepime, most notably in Enterobacterales, but activity was constrained by permeability defects and non-target β-lactamases. Combination therapy with agents that does not get hydrolysed by MBLs and integrated β-lactamase detection with practical permeability indicators may optimize the clinical use of this combination in high-resistance settings.

Identifiers

PMID41573238
PMCPMC12820527

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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.