ArticleNew microbes and new infections2026
The emergence of pan-drug-resistant
Article in New microbes and new infections, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Methods: From April 2023 to January 2025, 364 non-duplicate Results: Antimicrobial susceptibility testing revealed high resistance to fluoroquinolones (65.9%) and carbapenems (47.2%), while colistin remained most effective (95.6% susceptibility). Among the isolates, 41% were MDR, 25% XDR, and 4.4% PDR. Phenotypic assays showed that 73.8% of carbapenem-resistant isolates produced metallo-β-lactamase (MBL), and 85.2% were biofilm producers, with a significant association between biofilm formation and MDR phenotype (p < 0.05). Efflux pump activity, detected in 28.9% of ciprofloxacin-resistant isolates, was prominent in all PDR strains. Genotypic analysis identified Conclusion: This study underscores the critical convergence of multiple resistance mechanisms (enzymatic degradation, efflux overexpression, porin loss, and biofilm formation) driving the emergence of PDR
Indexed as
Identifiers
What Socratic holds
Registered trials
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 Socratic graph.