Evidence map›Paper›PMID 27266773›Full record

ArticleBMJ open2016

Clinical outcomes at 12 months and risk of inflammatory bowel disease in patients with an intermediate raised fecal calprotectin: a 'real-world' view.

Michael McFarlane, Samantha Chambers, Ahmad Malik, Bee Lee, Edmond Sung, Chuka Nwokolo, Norman Waugh, Ramesh Arasaradnam

Open access · goldAbstract read
In one paragraph

Article in BMJ open, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
1.2field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Trial
  4. Review
  5. Review
  6. Biomarkers in inflammatory bowel disease: a practical guide.Therapeutic advances in gastroenterology · 2024
    Review
  7. Article
  8. 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

8 authors at 4 institutions in 1 country.

Michael McFarlaneDepartment of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, UK.ORCID 0000-0002-8156-8014
Samantha ChambersDepartment of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, UK.
Ahmad MalikDepartment of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, UK.
Bee LeeDepartment of Gastroenterology, Warwick Hospital, Warwick, UK.
Edmond SungDepartment of Gastroenterology, George Eliot Hospital, Nuneaton, UK.
Chuka NwokoloDepartment of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, UK.
Norman WaughDepartment of Warwick Evidence, University of Warwick, Coventry, UK.ORCID 0000-0003-0934-4961
Ramesh ArasaradnamDepartment of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, UK Clinical Sciences Research Institute, University of Warwick, Coventry, UK.
University Hospital Coventry · GBGeorge Eliot Hospital · GBUniversity of Warwick · GBWarwick Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesA recent systematic review confirmed the usefulness of fecal calprotectin (FC) in distinguishing organic (inflammatory bowel disease (IBD)) from non-organic gastrointestinal disease (irritable bowel syndrome (IBS)). FC levels <50 μg/g have a negative predictive value >92% to exclude organic gastrointestinal (GI) disease. Levels >250 μg/g correlate with endoscopic IBD disease activity; sensitivity 90%. We aimed to determine clinical outcomes in intermediate raised FC results (50-250 μg/g).

settingPrimary care general practices in Coventry and Warwickshire, and 3 secondary care hospitals.

participants443 FC results in adults (>16 years old) were reviewed from July 2012 to October 2013. Clinical data was collected from hospital databases and general practitioners. Long-term clinical data was available in 41 patients (out of 48). PRIMARY AND SECONDARY OUTCOME MEASURES: The number of new diagnoses of IBD, IBS and other diagnoses for the intermediate group. The number referred and discharged from secondary care.

resultsA new IBD diagnosis was made in 19% (n=8) of intermediate results (1% of normal and 38% of raised results). 5% (n=2) of intermediate results had known IBD in remission. A new IBS diagnosis was made in 27% (n=11) of intermediate results, while 34% (n=14) remained undiagnosed, although 8 of these were not referred to secondary care.

conclusionsFC testing remains useful in aiding diagnosis of organic GI conditions. However, unlike negative and strongly positive FC results, intermediate FC results lead to a mixture of diagnoses. The OR of a new diagnosis of IBD for an intermediate result compared to normal FC result was 26.6, while an intermediate FC result gave an OR of 0.54 for a new IBS diagnosis compared to normal FC. For intermediate FC results, 1 in 3 patients remained in secondary care after 12 months with an OR of 3.6 compared to a normal FC result.

Indexed as

AdolescentAdultBiomarkersColonoscopyDatabases, FactualFecesFemaleHumansInflammatory Bowel DiseasesLeukocyte L1 Antigen ComplexMaleMiddle AgedPredictive Value of TestsUnited KingdomYoung AdultBiomarkersLeukocyte L1 Antigen ComplexFaecal CalprotectinIntermediateOutcomes

Identifiers

PMID27266773
PMCPMC4908885
OpenAlexW2413783028

What OpenQuestion holds

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LicenceCC BY-NC
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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.