Evidence map›Paper›PMID 40237505›Full record

ArticleAntimicrobial agents and chemotherapy2025

Population pharmacokinetics study on nebulized and intravenous administration of polymyxin B in patients with pneumonia caused by multidrug-resistant gram-negative bacteria.

Xueyong Li, Lili Zhou, Danjie Wang, Qiong Wu, Xuanxi Huang, Hui Zhang, Wenwei Wu, Maobai Liu, Xuemei Wu, Hongqiang Qiu and 1 more

Abstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Synergy Between the Auranofin Analogue PEtInternational journal of molecular sciences · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. 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

11 authors.

Xueyong Li *Department of Pharmacy, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.ORCID 0000-0002-4064-3735
Lili Zhou *Department of Critical Care Medicine, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.
Danjie WangDepartment of Critical Care Medicine, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.
Qiong WuDepartment of Critical Care Medicine, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.
Xuanxi HuangDepartment of Critical Care Medicine, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.
Hui ZhangDepartment of Critical Care Medicine, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.
Wenwei WuDepartment of Critical Care Medicine, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.
Maobai LiuDepartment of Pharmacy, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.
Xuemei WuDepartment of Pharmacy, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.
Hongqiang QiuDepartment of Pharmacy, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.ORCID 0000-0003-3285-8768
Yu ChengDepartment of Pharmacy, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.ORCID 0000-0001-8406-6098

Funding

Fujian Guiding Project of Sceince and Technology Grant No. 2021Y0019Fujian Science and Technology Plan Social Development Guidance Project Grant No.2022Y0020Funding for Top Hospital and Specialty Excellence, Fujian Province Grant No.2022(884)Joint Funds for the Innovation of Science and Technology, Fujian Province Grant No.2019Y9051Joint Funds for the Innovation of Science and Technology, Fujian Province Grant No. 2021Y9038Natural Science Foundation of Fujian Province (Fujian Natural Science Foundation) Grant No. 2021J01761
6 · The paper itself

Abstract

Polymyxin B (PMB) remains a last-line therapeutic agent for multidrug-resistant gram-negative bacteria (MDR-GNB) infections. However, reliable pharmacokinetic (PK) data to guide nebulized PMB dosing regimens in critically ill patients are limited. This study aimed to establish a population pharmacokinetic (PopPK) model for PMB in both epithelial lining fluid (ELF) and plasma of critically ill patients with MDR-GNB pneumonia and to optimize dosing regimens. A prospective PK study was conducted in 76 adult patients receiving nebulized PMB either as monotherapy or in combination with intravenous administration. PK data were analyzed using non-linear mixed-effect modeling, with PMB concentration-time profiles described by a coupled model integrating separate two-compartment models for plasma and ELF. The final model identified albumin levels and age as significant covariates influencing PK variability. Monte Carlo simulations demonstrated that nebulization therapy either alone or combined with intravenous administration significantly enhances ELF concentration and the probability of target attainment. Additionally,

Indexed as

Anti-Bacterial AgentsGram-Negative BacteriaGram-Negative Bacterial InfectionsPneumonia, BacterialPolymyxin BAcinetobacter baumanniiAdministration, InhalationAdministration, IntravenousAdultAgedCritical IllnessDrug Resistance, Multiple, BacterialFemaleHumansKlebsiella pneumoniaeMaleAnti-Bacterial AgentsPolymyxin Bmultidrug-resistantnebulizedpneumoniapolymyxin Bpopulation pharmacokinetic

Identifiers

PMID40237505
PMCPMC12057357

What OpenQuestion holds

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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.