Evidence map›Paper›PMID 24218500›Full record

Trial reportThe Journal of infectious diseases2014

Whole-genome sequencing demonstrates that fidaxomicin is superior to vancomycin for preventing reinfection and relapse of infection with Clostridium difficile.

David W Eyre, Farah Babakhani, David Griffiths, Jaime Seddon, Carlos Del Ojo Elias, Sherwood L Gorbach, Tim E A Peto, Derrick W Crook, A Sarah Walker

Abstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in The Journal of infectious diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Emergence and Spread of Clostridioides difficile Isolates With Reduced Fidaxomicin Susceptibility in an Acute Care Hospital.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2025
    Article
  2. Comparative Genomics of Clostridioides difficile.Advances in experimental medicine and biology · 2024
    Article
  3. Genomic epidemiology and transmission dynamics of recurrent Clostridioides difficile infection in Western Australia.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2023
    Article
  4. Article
  5. Fidaxomicin for the Treatment ofAntibiotics (Basel, Switzerland) · 2022
    Review
  6. High Prevalence of Genetically RelatedFrontiers in microbiology · 2020
    Article
  7. Article
  8. Genomics of the Pathogenic Clostridia.Microbiology spectrum · 2019
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Clostridium difficile Infection.Microbiology spectrum · 2016
    Review
  14. Genome-Based Infection Tracking Reveals Dynamics of Clostridium difficile Transmission and Disease Recurrence.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2016
    Article
  15. Article
  16. Within-host evolution of bacterial pathogens.Nature reviews. Microbiology · 2016
    Review
  17. Review
  18. Article
  19. Article
  20. Review
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.

David W EyreNIHR Oxford Biomedical Research Centre, University of Oxford, United Kingdom.
Farah Babakhani
David Griffiths
Jaime Seddon
Carlos Del Ojo Elias
Sherwood L Gorbach
Tim E A Peto
Derrick W Crook
A Sarah Walker

Funding

Biotechnology and Biological Sciences Research CouncilDepartment of Health DRF-2010-03-40Medical Research Council G0800778Wellcome Trust
6 · The paper itself

Abstract

Whole-genome sequencing was used to determine whether the reductions in recurrence of Clostridium difficile infection observed with fidaxomicin in pivotal phase 3 trials occurred by preventing relapse of the same infection, by preventing reinfection with a new strain, or by preventing both outcomes. Paired isolates of C. difficile were available from 93 of 199 participants with recurrences (28 were treated with fidaxomicin, and 65 were treated with vancomycin). Given C. difficile evolutionary rates, paired samples ≤2 single-nucleotide variants (SNVs) apart were considered relapses, paired samples >10 SNVs apart were considered reinfection, and those 3-10 SNVs apart (or without whole-genome sequences) were considered indeterminate in a competing risks survival analysis. Fidaxomicin reduced the risk of both relapse (competing risks hazard ratio [HR], 0.40 [95% confidence interval {CI}, .25-.66]; P = .0003) and reinfection (competing risks HR, 0.33 [95% CI, 0.11-1.01]; P = .05).

Indexed as

AminoglycosidesAnti-Bacterial AgentsClostridioides difficileClostridium InfectionsDNA, BacterialDouble-Blind MethodDrug Resistance, BacterialFidaxomicinGenome, BacterialHumansPolymorphism, Single NucleotideSecondary PreventionSequence Analysis, DNAVancomycinAminoglycosidesAnti-Bacterial AgentsDNA, BacterialFidaxomicinVancomycinClostridium difficilefidaxomicinrecurrencewhole genome sequencing

Identifiers

PMID24218500
PMCPMC3982846

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.