Evidence map›Paper›PMID 41808272›Full record

ArticleCytopathology : official journal of the British Society for Clinical Cytology2026

Validation of Digital Cytology for Primary Diagnosis Across a Range of Specimen Types.

Talisa Mistry, Harriet Hunter, Dahmane Oukrif, Sabine Pomplun, Reena Khiroya, Mary Falzon, Tanya Alan, Manuel Rodriguez-Justo, Adam P Levine

Abstract read
In one paragraph

Article in Cytopathology : official journal of the British Society for Clinical Cytology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Talisa MistryResearch Department of Pathology, UCL Cancer Institute, University College London, London, UK.ORCID 0000-0001-8637-6815
Harriet HunterDepartment of Cellular Pathology, University College London Hospitals NHS Foundation Trust, London, UK.
Dahmane OukrifResearch Department of Pathology, UCL Cancer Institute, University College London, London, UK.
Sabine PomplunDepartment of Cellular Pathology, University College London Hospitals NHS Foundation Trust, London, UK.
Reena KhiroyaDepartment of Cellular Pathology, University College London Hospitals NHS Foundation Trust, London, UK.
Mary FalzonDepartment of Cellular Pathology, University College London Hospitals NHS Foundation Trust, London, UK.
Tanya AlanDepartment of Cellular Pathology, University College London Hospitals NHS Foundation Trust, London, UK.
Manuel Rodriguez-JustoResearch Department of Pathology, UCL Cancer Institute, University College London, London, UK.ORCID 0000-0001-5007-1761
Adam P LevineResearch Department of Pathology, UCL Cancer Institute, University College London, London, UK.ORCID 0000-0003-1333-9938

Funding

Hamamatsu Photonics K.K.The Jean Shanks Foundation and The Pathological Society of Great Britain & Ireland.
6 · The paper itself

Abstract

objectiveThis study evaluated the diagnostic performance of high-resolution whole slide imaging (WSI) for primary cytological diagnosis across a broad range of specimen types and preparations.

methodsIn a single-centre, retrospective validation study, 88 archived cytology cases representative of routine clinical practice were scanned at 40× equivalent magnification (0.23 μm/pixel) using the Hamamatsu NanoZoomer S360MD Slide scanner system. Specimens included gynaecological and non-gynaecological exfoliative and fine needle aspirate samples, prepared as smears, ThinPreps, cytospins or cell blocks. WSI were each reviewed independently by two expert cytopathologists with minimal prior digital cytology reporting experience, blinded to original light microscopy (LM) diagnoses. Discordant cases underwent LM review. Diagnostic concordance and agreement were assessed using percentage concordance and Cohen's κ (unweighted and weighted, for non-gynaecological cases only). A post-study questionnaire captured qualitative feedback.

resultsOf the 88 cases, 65 showed concordance between digital and LM diagnoses. Amongst the remaining 23 cases, 15 demonstrated diagnostic discrepancy by LM. Excluding these, the digital-LM concordance rate was 95.1%. When all cases were included, concordance ranged from 89.5% for within-observer analysis to 89.8% when compared with a majority LM diagnosis. Agreement analysis demonstrated substantial to near-perfect digital-LM agreement (unweighted κ = 0.86; weighted κ = 0.83-0.95), improving further following exclusion of diagnostically discrepant cases (κ = 0.89-0.97). Inter-observer agreement was lower than intra-observer agreement for both digital and LM comparisons. Feedback indicated that image quality was generally good. Challenges included visualising thick smear preparations, three-dimensional cell clusters, sparse atypical cells and screening gynaecological (cervical) cytology cases. All participants expressed openness to adopting digital cytology.

conclusionHigh-resolution WSI demonstrated strong diagnostic concordance with traditional LM across a wide range of cytological specimen types and preparations. Despite limited prior experience, digital cytology was considered acceptable and feasible, supporting its integration into routine clinical practice, with appropriate training and quality assurance.

Indexed as

CytodiagnosisImage Processing, Computer-AssistedBiopsy, Fine-NeedleFemaleHumansMicroscopyRetrospective StudiesVaginal Smearscytologydigitalscannervalidationwhole‐slide image

Identifiers

PMID41808272
PMCPMC13059545

What Socratic holds

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LicenceCC BY
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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 Socratic graph.