Evidence map›Paper›PMID 38446176›Full record

ArticlePathologie (Heidelberg, Germany)2024

[Fluorescence confocal microscopy-complete digitization of pathology].

Andreas G Loth, Anne Fassl, Felix K H Chun, Jens Köllermann, Sylvia Hartmann, Steffen Gretser, Paul K Ziegler, Nadine Flinner, Falko Schulze, Peter J Wild and 1 more

Open access · hybridAbstract readEnglish Abstract
In one paragraph

Article in Pathologie (Heidelberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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

11 authors at 1 institution in 1 country.

Andreas G LothUniversitätsklinikum Frankfurt, Klinik für Hals‑, Nasen- und Ohrenheilkunde, Goethe-Universität Frankfurt, Frankfurt am Main, Deutschland.
Anne FasslUniversitätsklinikum Frankfurt, Klinik für Urologie, Goethe-Universität Frankfurt, Frankfurt am Main, Deutschland.
Felix K H ChunUniversitätsklinikum Frankfurt, Klinik für Urologie, Goethe-Universität Frankfurt, Frankfurt am Main, Deutschland.
Jens KöllermannUniversitätsklinikum Frankfurt, Dr. Senckenbergisches Institut für Pathologie, Goethe-Universität Frankfurt, Frankfurt am Main, Deutschland.
Sylvia HartmannUniversitätsklinikum Frankfurt, Dr. Senckenbergisches Institut für Pathologie, Goethe-Universität Frankfurt, Frankfurt am Main, Deutschland.
Steffen GretserUniversitätsklinikum Frankfurt, Dr. Senckenbergisches Institut für Pathologie, Goethe-Universität Frankfurt, Frankfurt am Main, Deutschland.
Paul K ZieglerUniversitätsklinikum Frankfurt, Dr. Senckenbergisches Institut für Pathologie, Goethe-Universität Frankfurt, Frankfurt am Main, Deutschland.
Nadine FlinnerUniversitätsklinikum Frankfurt, Dr. Senckenbergisches Institut für Pathologie, Goethe-Universität Frankfurt, Frankfurt am Main, Deutschland.
Falko SchulzeUniversitätsklinikum Frankfurt, Dr. Senckenbergisches Institut für Pathologie, Goethe-Universität Frankfurt, Frankfurt am Main, Deutschland.
Peter J WildUniversitätsklinikum Frankfurt, Dr. Senckenbergisches Institut für Pathologie, Goethe-Universität Frankfurt, Frankfurt am Main, Deutschland.
Maximilian N KinzlerUniversitätsklinikum Frankfurt, Medizinische Klinik 1, Goethe-Universität Frankfurt, Frankfurt am Main, Deutschland. kinzler@med.uni-frankfurt.de.ORCID http://orcid.org/0000-0003-2378-1455
Goethe University Frankfurt · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFluorescence-based confocal microscopy (FCM) can be used to create virtual H&E sections in real time. So far, FCM has been used in dermato-, uro-, and gynecopathology. FCM allows the creation of a completely digitized frozen section, which could potentially replace conventional frozen sections in the future.

objectiveThe aim of the current work is to implement FCM technology as a component of fully digitized processes in the pathological workflow. For this purpose, the current use of FCM in liver transplant pathology will be extended to other disciplines such as urology and otorhinolaryngology. MATERIALS AND

methodsThe FCM technique continues to be used prospectively on native tissue samples from potential donor livers. Conventional frozen sections are used comparatively to virtual FCM scans.

resultsThe data show a nearly perfect agreement for the detection of cholangitis, fibrosis, and malignancy, and a high level of agreement for, e.g., macrovesicular steatosis, inflammation, steatohepatitis, and necrosis between virtual FCM scans and conventional routine diagnostic frozen sections.

conclusionSince the availability of time- and cost-intensive frozen section diagnostics in the context of transplant pathology in continuous operation (24/7) is now only established at very few university centers in Germany due to an increasing shortage of specialists, the use of FCM could be an important building block in the current process leading towards a fully digitized pathology workflow and should thus be extended to various disciplines.

Indexed as

Microscopy, ConfocalFrozen SectionsHumansLiverLiver TransplantationMicroscopy, FluorescenceDigital HE scanDigital pathologyFrozen sectionLiver transplantationTransplantation pathology

Identifiers

PMID38446176
PMCPMC11045597
OpenAlexW4392499992

What OpenQuestion holds

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LicenceCC BY
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.