Evidence map›Paper›PMID 30994430›Full record

ArticleJournal of medical microbiology2019

The potential of fosfomycin for multi-drug resistant sepsis: an analysis of in vitro activity against invasive paediatric Gram-negative bacteria.

Phoebe C M Williams, Joseph Waichungo, N Claire Gordon, Mike Sharland, Sheila Murunga, Alice Kamau, James A Berkley

Open access · hybridAbstract read
In one paragraph

Article in Journal of medical microbiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 42% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

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  8. Frontiers in cellular and infection microbiology · 2021
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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 at 2 institutions in 2 countries.

Phoebe C M WilliamsThe University of Oxford, Nuffield Department of Clinical Medicine, Headington, Oxford, UK.
Joseph WaichungoKEMRI-Wellcome Trust Research Programme, Kilifi 80108, Kenya.
N Claire GordonKEMRI-Wellcome Trust Research Programme, Kilifi 80108, Kenya.
Mike SharlandSt. Georges University Hospital, London, UK.
Sheila MurungaKEMRI-Wellcome Trust Research Programme, Kilifi 80108, Kenya.
Alice KamauKEMRI-Wellcome Trust Research Programme, Kilifi 80108, Kenya.
James A BerkleyThe University of Oxford, Nuffield Department of Clinical Medicine, Headington, Oxford, UK.
Kenya Medical Research Institute · KEUniversity of Oxford · GB

Funding

Medical Research Council MR/M007367/1Wellcome Trust
6 · The paper itself

Abstract

purposeAntimicrobial resistance (AMR) is of increasing global concern, threatening to undermine recent progress in reducing child and neonatal mortality. Repurposing older antimicrobials is a prominent strategy to combat multidrug-resistant sepsis. A potential agent is fosfomycin, however, there is scarce data regarding its in vitro activity and pharmacokinetics in the paediatric population. METHODOLOGY: We analysed a contemporary, systematically collected archive of community-acquired (CA) and hospital-acquired (HA) paediatric Gram-negative bacteraemia isolates for their susceptibility to fosfomcyin. MICs were determined using agar serial dilution methods and validated by disk diffusion testing where breakpoints are available. Disk diffusion antimicrobial susceptibility testing was also conducted for current empirical therapies (ampicillin, gentamicin, ceftriaxone) and amikacin (proposed in the literature as a new combination empirical therapeutic option).

resultsFosfomycin was highly active against invasive Gram-negative isolates, including 90  % (202/224) of Enterobacteriaceae and 96  % (22/23) of Pseudomonas spp. Fosfomycin showed high sensitivity against both CA isolates (94 %, 142/151) and HA isolates (81 %, 78/96; P =0.0015). CA isolates were significantly more likely to be susceptible to fosfomycin than the current first-line empirical therapy (96  % vs 59  %, P <0.0001). Extended spectrum β-lactamases (ESBL) production was detected in 34  % (85/247) of isolates with no significant difference in fosfomycin susceptibility between ESBL-positive or -negative isolates [73/85 (86  %) vs 147/162 (91  %) respectively, P =0.245]. All isolates were susceptible to a fosfomycin-amikacin combination.

conclusionGram-negative paediatric bacteraemia isolates are highly susceptible to fosfomycin, which could be combined with aminoglycosides as a new, carbapenem-sparing regimen to achieve excellent coverage to treat antimicrobial-resistant neonatal and paediatric sepsis.

Indexed as

Anti-Bacterial AgentsBacteremiaChild, PreschoolCommunity-Acquired InfectionsCross InfectionEnterobacteriaceaeEnterobacteriaceae InfectionsEscherichia coli InfectionsFemaleFosfomycinGram-Negative BacteriaHumansInfantInfant, NewbornKlebsiella pneumoniaeMaleAnti-Bacterial AgentsFosfomycinantibiotic resistanceAntimicrobial resistanceESBLfosfomycinGram-negative sepsisneonatal sepsis

Identifiers

PMID30994430
PMCPMC7116424
OpenAlexW2939057367

What OpenQuestion holds

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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.