Evidence map›Paper›PMID 42232899›Full record

ArticleFrontiers in microbiology2026

Comparative study on the wound healing effects of local versus systemic application of Polymyxin B in mice infected with multidrug-resistant

Chenhu Ma, Dan Wang, Bingjie Zhang, Jianshe Xu, Miaomiao Lin, Yishan Zheng, Yuxin Guo

Abstract read
In one paragraph

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

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0cells of the map it votes in
0citing papers in PubMed
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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

7 authors.

Chenhu Ma *Department of Intensive Care Unit, The Second Hospital of Nanjing, Affiliated to Nanjing University of Chinese Medicine, Nanjing, China.
Dan Wang *Department of Intensive Care Unit, The Second Hospital of Nanjing, Affiliated to Nanjing University of Chinese Medicine, Nanjing, China.
Bingjie ZhangDepartment of Intensive Care Unit, The Second Hospital of Nanjing, Affiliated to Nanjing University of Chinese Medicine, Nanjing, China.
Jianshe XuSchool of Public Health, Nanjing Medical University, Nanjing, China.
Miaomiao LinDepartment of Intensive Care Unit, Peking University Shenzhen Hospital, Shenzhen, China.
Yishan ZhengDepartment of Intensive Care Unit, The Second Hospital of Nanjing, Affiliated to Nanjing University of Chinese Medicine, Nanjing, China.
Yuxin GuoDepartment of Intensive Care Unit, The Second Hospital of Nanjing, Affiliated to Nanjing University of Chinese Medicine, Nanjing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Wound infections caused by extensively drug-resistant Objective: This study aimed to investigate the efficacy differences of different PMB administration routes (topical, intravenous, and combined therapy) in treating XDR-PA wound infections in mice, providing experimental evidence for optimizing clinical treatment regimens. Methods: One hundred and twenty Kunming mice were randomly assigned to five groups ( Results: Compared to the untreated infected group, all administered treatment groups demonstrated therapeutic efficacy. The topical administration group exhibited the most pronounced wound healing promotion, it achieved the highest wound closure rate, fastest resolution of erythema and oedema, and optimal bacterial clearance efficiency. Additionally, it showed effective regulation of inflammatory response, and minimal histopathological damage. The intravenous administration group exhibited the next highest efficacy. The combination therapy group did not demonstrate synergistic effects superior to local monotherapy. Mice in the untreated infection group exhibited the slowest weight gain and delayed wound healing. Mice in the untreated infection group exhibited the slowest weight loss and delayed wound healing. Discussion Conclusion: Under the experimental conditions employed, topical application of PMB demonstrated superior efficacy to intravenous administration and combined therapy in treating wound infections in XDR-PA mice. Due to the equal total daily dose design (5 mg/kg for all treatment groups), the combination therapy group received a lower dose per route (2.5 mg/kg each) compared to the monotherapy groups (5 mg/kg via a single route). Therefore, no definitive conclusion can be drawn regarding potential synergistic or antagonistic effects of combination therapy based on this study design. This suggests that targeted local administration may represent a more effective and cost-efficient strategy for localized infections caused by resistant bacteria, which warrants further clinical translational research.

Indexed as

extensively drug-resistantmouse modelPolymyxin BPseudomonas aeruginosawound infection

Identifiers

PMID42232899
PMCPMC13223157

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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.