Evidence map›Paper›PMID 25779556›Full record

ArticlePreventive veterinary medicine2015

The feasibility of testing whether Fasciola hepatica is associated with increased risk of verocytotoxin producing Escherichia coli O157 from an existing study protocol.

Graeme L Hickey, Peter J Diggle, Tom N McNeilly, Sue C Tongue, Margo E Chase-Topping, Diana J L Williams

Erratum issuedAbstract read
In one paragraph

Article in Preventive veterinary medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

6 authors.

Graeme L HickeyDepartment of Epidemiology and Population Health, Institute of Infection and Global Heath, University of Liverpool, The Farr Institute@HeRC, Waterhouse Building, 1-5 Brownlow Street, Liverpool L69 3GL, UK. Electronic address: graeme.hickey@liverpool.ac.uk.
Peter J DiggleDepartment of Epidemiology and Population Health, Institute of Infection and Global Heath, University of Liverpool, The Farr Institute@HeRC, Waterhouse Building, 1-5 Brownlow Street, Liverpool L69 3GL, UK.
Tom N McNeillyMoredun Research Institute, Pentlands, Science Park, Bush Loan, Penicuik, Midlothian EH26 0PZ, UK.
Sue C TongueSRUC (Scotland's Rural College), West Mains Road, Edinburgh, Scotland EH9 3JG, UK.
Margo E Chase-ToppingCentre for Immunity, Infection and Evolution, University of Edinburgh, Ashworth Laboratories, Charlotte Auerbach Road, Edinburgh, EH9 3FL, UK.
Diana J L WilliamsDepartment of Infection Biology, Institute of Infection and Global Heath, University of Liverpool, Liverpool L69 7ZJ, UK; School of Veterinary Science, University of Liverpool, Leahurst Campus, Chester High Road, Neston CH64 7TE, UK.

Funding

Wellcome Trust 095831
6 · The paper itself

Abstract

The parasite Fasciola hepatica is a major cause of economic loss to the agricultural community worldwide as a result of morbidity and mortality in livestock, including cattle. Cattle are the principle reservoir of verocytotoxigenic Escherichia coli O157 (VTEC O157), an important cause of disease in humans. To date there has been little empirical research on the interaction between F. hepatica and VTEC O157. It is hypothesised that F. hepatica, which is known to suppress type 1 immune responses and induce an anti-inflammatory or regulatory immune environment in the host, may promote colonisation of the bovine intestine with VTEC O157. Here we assess whether it is statistically feasible to augment a prospective study to quantify the prevalence of VTEC O157 in cattle in Great Britain with a pilot study to test this hypothesis. We simulate data under the framework of a mixed-effects logistic regression model in order to calculate the power to detect an association effect size (odds ratio) of 2. In order to reduce the resources required for such a study, we exploit the fact that the test results for VTEC O157 will be known in advance of testing for F. hepatica by restricting analysis to farms with a VTEC O157 sample prevalence of >0% and <100%. From a total of 270 farms (mean 27 cows per farm) that will be tested for VTEC O157, power of 87% can be achieved, whereby testing of F. hepatica would only be necessary for an expected 50 farms, thus considerably reducing costs. Pre-study sample size calculations are an important part of any study design. The framework developed here is applicable to the study of other co-infections.

Indexed as

Bacterial SheddingAnimalsCattleCattle DiseasesCoinfectionEnglandEscherichia coli InfectionsEscherichia coli O157Fasciola hepaticaFascioliasisFeasibility StudiesFemalePilot ProjectsPrevalenceProspective StudiesRisk AssessmentCo-infectionFasciola hepaticaMixed effects modelPowerSample sizeVerocytotoxigenic Escherichia coli O157

Identifiers

PMID25779556
PMCPMC4401447

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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.