Evidence map›Paper›PMID 28158441›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2017

Contribution to Clostridium Difficile Transmission of Symptomatic Patients With Toxigenic Strains Who Are Fecal Toxin Negative.

Damian P C Mawer, David W Eyre, David Griffiths, Warren N Fawley, Jessica S H Martin, T Phuong Quan, Timothy E A Peto, Derrick W Crook, A Sarah Walker, Mark H Wilcox

Open access · bronzeAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

32 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. ImprovingAntibiotics (Basel, Switzerland) · 2024
    Article
  3. Comparative Genomics of Clostridioides difficile.Advances in experimental medicine and biology · 2024
    Article
  4. Article
  5. Strategies to preventInfection control and hospital epidemiology · 2023
    Article
  6. Prevalence of diagnostically-discrepantFrontiers in medicine · 2023
    Article
  7. Prevalence and risk factors of toxigenicFrontiers in medicine · 2023
    Article
  8. Low-toxinEmerging microbes & infections · 2022
    Article
  9. Review
  10. Article
  11. Article
  12. High Prevalence of Genetically RelatedFrontiers in microbiology · 2020
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Enterotoxic Clostridia:Microbiology spectrum · 2019
    Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 2 countries.

Damian P C MawerDepartment of Microbiology, Leeds Teaching Hospitals NHS Trust, UK.
David W EyreNuffield Department of Medicine, University of Oxford, UK.
David GriffithsNuffield Department of Medicine, University of Oxford, UK.
Warren N FawleyDepartment of Microbiology, Leeds Teaching Hospitals NHS Trust, UK.
Jessica S H MartinLeeds Institute of Biomedical and Clinical Sciences, University of Leeds, UK.
T Phuong QuanNuffield Department of Medicine, University of Oxford, UK.
Timothy E A PetoNuffield Department of Medicine, University of Oxford, UK.
Derrick W CrookNuffield Department of Medicine, University of Oxford, UK.
A Sarah WalkerNuffield Department of Medicine, University of Oxford, UK.
Mark H WilcoxDepartment of Microbiology, Leeds Teaching Hospitals NHS Trust, UK.
National Institute for Health Research · GBOxford Biomedical Research · USUniversity of Leeds · GBLeeds Teaching Hospitals NHS Trust · GBPublic Health England · GBUniversity of Oxford · GB

Funding

Department of Health DRF-2010-03-40Medical Research Council G0800778Wellcome Trust
6 · The paper itself

Abstract

Background: The role of symptomatic patients who are toxigenic strain positive (TS+) but fecal toxin negative (FT-) in transmission of Clostridium difficile is currently unknown. Methods: We investigated the contribution of symptomatic TS+/FT- and TS+/FT+ patients in C. difficile transmission in 2 UK regions. From 2-step testing, all glutamate dehydrogenase (GDH)-positive specimens, regardless of fecal toxin result, from Oxford (April 2012 through April 2013) and Leeds (July 2012 through April 2013) microbiology laboratories underwent culture and whole-genome sequencing (WGS), using WGS to identify toxigenic strains. Plausible sources for each TS+/FT+ case, including TS+/FT- and TS+/FT+ patients, were determined using WGS, with and without hospital admission data. Results: A total of 1447 of 12772 (11%) fecal samples were GDH positive, 866 of 1447 (60%) contained toxigenic C. difficile, and fecal toxin was detected in 511 of 866 (59%), representing 235 Leeds and 191 Oxford TS+/FT+ cases. TS+/FT+ cases were 3 times more likely to be plausibly acquired from a previous TS+/FT+ case than a TS+/FT- patient. Fifty-one of 265 (19%) TS+/FT+ cases diagnosed >3 months into the study were genetically related (≤2 single-nucleotide polymorphisms) to ≥1 previous TS+/FT+ case or TS+/FT- patient: 27 (10%) to only TS+/FT+ cases, 9 (3%) to only TS+/FT- patients, and 15 (6%) to both. Only 10 of 265 (4%) were genetically related to a previous TS+/FT+ or TS+/FT- patient and shared the same ward simultaneously or within 28 days. Conclusions: Symptomatic TS+/FT- patients were a source of C. difficile transmission, although they accounted for less onward transmission than TS+/FT+ cases. Although transmission from symptomatic patients with either fecal toxin status accounted for a low overall proportion of new cases, both groups should be infection control targets.

Indexed as

Disease Transmission, InfectiousAgedAged, 80 and overBacterial ToxinsBacteriological TechniquesClostridioides difficileClostridium InfectionsFecesFemaleGenotypeHumansMaleMiddle AgedMolecular EpidemiologyMolecular TypingSequence Analysis, DNABacterial ToxinsClostridium difficilefecal toxininfectiontransmission

Identifiers

PMID28158441
PMCPMC5850559
OpenAlexW2584801492

What OpenQuestion holds

Textmetadata
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.