Evidence map›Paper›PMID 38302475›Full record

ArticleBMJ open gastroenterology2024

CD, or not CD, that is the question: a digital interobserver agreement study in coeliac disease.

James Denholm, Benjamin A Schreiber, Florian Jaeckle, Mike N Wicks, Emyr W Benbow, Tim S Bracey, James Y H Chan, Lorant Farkas, Eve Fryer, Kishore Gopalakrishnan and 13 more

Abstract read
In one paragraph

Article in BMJ open gastroenterology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

23 authors.

James DenholmDepartment of Pathology, University of Cambridge, Cambridge, UK.
Benjamin A SchreiberDepartment of Pathology, University of Cambridge, Cambridge, UK.
Florian JaeckleDepartment of Pathology, University of Cambridge, Cambridge, UK florian.jaeckle@gmail.com.ORCID 0009-0002-4607-6476
Mike N WicksDepartment of Pathology, The University of Edinburgh College of Medicine and Veterinary Medicine, Edinburgh, UK.
Emyr W BenbowDivision of Medical Education, The University of Manchester, Manchester, UK.
Tim S BraceyDepartment of Diagnostic and Molecular Pathology, Royal Cornwall Hospitals NHS Trust, Truro, UK.
James Y H ChanCambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Lorant FarkasDepartment of Pathology, Akershus University Hospital, Nordbyhagen, Norway.
Eve FryerDepartment of Cellular Pathology, Oxford University Hospitals NHS foundation Trust, Oxford, UK.
Kishore GopalakrishnanDepartment of Histopathology, University Hospitals Coventry and Warwickshire NHS Trust, Coventry, UK.
Caroline A HughesDepartment of Cellular Pathology, Oxford University Hospitals NHS foundation Trust, Oxford, UK.
Kathryn J KirkwoodDepartment of Pathology, Western General Hospital, Edinburgh, UK.
Gerald LangmanDepartment of Cellular Pathology, Heartlands Hospital, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Betania Mahler-AraujoCambridge University Hospitals NHS Foundation Trust, Cambridge, UK.ORCID 0000-0001-7952-0292
Raymond F T McMahonDivision of Medical Education, The University of Manchester, Manchester, UK.
Khun La Win MyintDepartment of Pathology, Queen Elizabeth University Hospital, Glasgow, UK.
Sonali NatuUniversity Hospital of North Tees, North Tees and Hartlepool NHS Foundation Trust, Stockton on Tees, UK.
Andrew RobinsonDepartment of Histopathology, University Hospitals Coventry and Warwickshire NHS Trust, Coventry, UK.
Ashraf SandukaCambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Katharine A SheppardDepartment of Cellular Pathology, Oxford University Hospitals NHS foundation Trust, Oxford, UK.
Yee Wah TsangDepartment of Histopathology, University Hospitals Coventry and Warwickshire NHS Trust, Coventry, UK.
Mark J ArendsDivision of Pathology, University of Edinburgh, Edinburgh, UK.
Elizabeth J SoilleuxDepartment of Pathology, University of Cambridge, Cambridge, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveCoeliac disease (CD) diagnosis generally depends on histological examination of duodenal biopsies. We present the first study analysing the concordance in examination of duodenal biopsies using digitised whole-slide images (WSIs). We further investigate whether the inclusion of immunoglobulin A tissue transglutaminase (IgA tTG) and haemoglobin (Hb) data improves the interobserver agreement of diagnosis.

designWe undertook a large study of the concordance in histological examination of duodenal biopsies using digitised WSIs in an entirely virtual reporting setting. Our study was organised in two phases: in phase 1, 13 pathologists independently classified 100 duodenal biopsies (40 normal; 40 CD; 20 indeterminate enteropathy) in the absence of any clinical or laboratory data. In phase 2, the same pathologists examined the (re-anonymised) WSIs with the inclusion of IgA tTG and Hb data.

resultsWe found the mean probability of two observers agreeing in the absence of additional data to be 0.73 (±0.08) with a corresponding Cohen's kappa of 0.59 (±0.11). We further showed that the inclusion of additional data increased the concordance to 0.80 (±0.06) with a Cohen's kappa coefficient of 0.67 (±0.09).

conclusionWe showed that the addition of serological data significantly improves the quality of CD diagnosis. However, the limited interobserver agreement in CD diagnosis using digitised WSIs, even after the inclusion of IgA tTG and Hb data, indicates the importance of interpreting duodenal biopsy in the appropriate clinical context. It further highlights the unmet need for an objective means of reproducible duodenal biopsy diagnosis, such as the automated analysis of WSIs using artificial intelligence.

Indexed as

Celiac DiseaseArtificial IntelligenceHumansImmunoglobulin AObserver VariationTransglutaminasesImmunoglobulin ATransglutaminasesCOELIAC DISEASEGLUTEN SENSITIVE ENTEROPATHYHISTOPATHOLOGYMEDICAL STATISTICSSMALL INTESTINAL BIOPSY

Identifiers

PMID38302475
PMCPMC10870791

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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.