Evidence map›Paper›PMID 36978184›Full record

ArticleOrphanet journal of rare diseases2023

A diagnostic support system based on pain drawings: binary and k-disease classification of EDS, GBS, FSHD, PROMM, and a control group with Pain2D.

D Emmert, N Szczypien, Tim T A Bender, L Grigull, A Gass, C Link, F Klawonn, R Conrad, M Mücke, J Sellin

Abstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

10 authors.

D Emmert *Center for Rare Diseases Bonn (ZSEB), University Hospital Bonn, Bonn, Germany.
N Szczypien *Institute for Information Engineering, Ostfalia University of Applied Sciences, Wolfenbüttel, Germany.
Tim T A BenderCenter for Rare Diseases Bonn (ZSEB), University Hospital Bonn, Bonn, Germany.
L GrigullCenter for Rare Diseases Bonn (ZSEB), University Hospital Bonn, Bonn, Germany.
A GassClinic for Anesthesiology and Operative Intensive Care Medicine, Department of Pain Medicine, University Hospital Bonn, Bonn, Germany.
C LinkClinic for Anesthesiology and Operative Intensive Care Medicine, Department of Pain Medicine, University Hospital Bonn, Bonn, Germany.
F KlawonnInstitute for Information Engineering, Ostfalia University of Applied Sciences, Wolfenbüttel, Germany.
R ConradDepartment of Psychosomatic Medicine and Psychotherapy, University Hospital Muenster, Muenster, Germany. rupert.conrad@ukmuenster.de.
M MückeInstitute for Digitalization and General Medicine, University Hospital RWTH Aachen, Aachen, Germany. mamuecke@ukaachen.de.
J SellinInstitute for Digitalization and General Medicine, University Hospital RWTH Aachen, Aachen, Germany. jsellin@ukaachen.de.ORCID 0000-0001-5354-2872

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveThe diagnosis of rare diseases (RDs) is often challenging due to their rarity, variability and the high number of individual RDs, resulting in a delay in diagnosis with adverse effects for patients and healthcare systems. The development of computer assisted diagnostic decision support systems could help to improve these problems by supporting differential diagnosis and by prompting physicians to initiate the right diagnostic tests. Towards this end, we developed, trained and tested a machine learning model implemented as part of the software called Pain2D to classify four rare diseases (EDS, GBS, FSHD and PROMM), as well as a control group of unspecific chronic pain, from pen-and-paper pain drawings filled in by patients.

methodsPain drawings (PDs) were collected from patients suffering from one of the four RDs, or from unspecific chronic pain. The latter PDs were used as an outgroup in order to test how Pain2D handles more common pain causes. A total of 262 (59 EDS, 29 GBS, 35 FSHD, 89 PROMM, 50 unspecific chronic pain) PDs were collected and used to generate disease specific pain profiles. PDs were then classified by Pain2D in a leave-one-out-cross-validation approach.

resultsPain2D was able to classify the four rare diseases with an accuracy of 61-77% with its binary classifier. EDS, GBS and FSHD were classified correctly by the Pain2D k-disease classifier with sensitivities between 63 and 86% and specificities between 81 and 89%. For PROMM, the k-disease classifier achieved a sensitivity of 51% and specificity of 90%.

conclusionsPain2D is a scalable, open-source tool that could potentially be trained for all diseases presenting with pain.

Indexed as

Chronic PainMuscular Dystrophy, FacioscapulohumeralControl GroupsHumansRare DiseasesSoftwareAIDiagnostic supportk-disease classificationMachine learningORPHA: 2103ORPHA: 269ORPHA: 287ORPHA: 606Pain drawingsRare diseases

Identifiers

PMID36978184
PMCPMC10053427

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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.