Evidence map›Paper›PMID 27795380›Full record

ArticleAntimicrobial agents and chemotherapy2017

Pharmacodynamics of Aerosolized Fosfomycin and Amikacin against Resistant Clinical Isolates of Pseudomonas aeruginosa and Klebsiella pneumoniae in a Hollow-Fiber Infection Model: Experimental Basis for Combination Therapy.

Fekade Bruck Sime, Adam Johnson, Sarah Whalley, Anahi Santoyo-Castelazo, A Bruce Montgomery, Kathie Ann Walters, Jeffrey Lipman, William W Hope, Jason A Roberts

Open access · hybridAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Amikacin: Uses, Resistance, and Prospects for Inhibition.Molecules (Basel, Switzerland) · 2017
    Review
  12. Review
  13. Frontiers in cellular and infection microbiology · 2017
    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

9 authors at 2 institutions in 2 countries.

Fekade Bruck SimeCentre for Translational Anti-infective Pharmacodynamics, School of Pharmacy, The University of Queensland, Brisbane, Queensland, Australia.
Adam JohnsonDepartment of Molecular and Clinical Pharmacology, The University of Liverpool, Liverpool, United Kingdom.
Sarah WhalleyDepartment of Molecular and Clinical Pharmacology, The University of Liverpool, Liverpool, United Kingdom.
Anahi Santoyo-CastelazoDepartment of Molecular and Clinical Pharmacology, The University of Liverpool, Liverpool, United Kingdom.
A Bruce MontgomeryCardeas Pharma Corporation, Seattle, Washington, USA.
Kathie Ann WaltersCardeas Pharma Corporation, Seattle, Washington, USA.
Jeffrey LipmanBurns, Trauma and Critical Care Research Centre, The University of Queensland, Brisbane, Queensland, Australia.
William W HopeDepartment of Molecular and Clinical Pharmacology, The University of Liverpool, Liverpool, United Kingdom.
Jason A RobertsCentre for Translational Anti-infective Pharmacodynamics, School of Pharmacy, The University of Queensland, Brisbane, Queensland, Australia j.roberts2@uq.edu.au.
University of Liverpool · GBUniversity of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There has been a resurgence of interest in aerosolization of antibiotics for treatment of patients with severe pneumonia caused by multidrug-resistant pathogens. A combination formulation of amikacin-fosfomycin is currently undergoing clinical testing although the exposure-response relationships of these drugs have not been fully characterized. The aim of this study was to describe the individual and combined antibacterial effects of simulated epithelial lining fluid exposures of aerosolized amikacin and fosfomycin against resistant clinical isolates of Pseudomonas aeruginosa (MICs of 16 mg/liter and 64 mg/liter) and Klebsiella pneumoniae (MICs of 2 mg/liter and 64 mg/liter) using a dynamic hollow-fiber infection model over 7 days. Targeted peak concentrations of 300 mg/liter amikacin and/or 1,200 mg/liter fosfomycin as a 12-hourly dosing regimens were used. Quantitative cultures were performed to describe changes in concentrations of the total and resistant bacterial populations. The targeted starting inoculum was 10

Indexed as

Drug Resistance, Multiple, BacterialAerosolsAmikacinAnti-Bacterial AgentsColony Count, MicrobialDrug Administration ScheduleDrug SynergismDrug Therapy, CombinationFosfomycinHumansKlebsiella pneumoniaeMicrobial Sensitivity TestsModels, BiologicalPseudomonas aeruginosaRespiratory MucosaAerosolsAmikacinAnti-Bacterial AgentsFosfomycinmultidrug resistancenebulizedpharmacodynamicspharmacokinetics

Identifiers

PMID27795380
PMCPMC5192115
OpenAlexW2538195174

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.