Evidence map›Paper›PMID 38448469›Full record

ArticleScientific reports2024

Visual acuity prediction on real-life patient data using a machine learning based multistage system.

Tobias Schlosser, Frederik Beuth, Trixy Meyer, Arunodhayan Sampath Kumar, Gabriel Stolze, Olga Furashova, Katrin Engelmann, Danny Kowerko

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
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  3. Review
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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

8 authors.

Tobias SchlosserJunior Professorship of Media Computing, Chemnitz University of Technology, 09107, Chemnitz, Germany. tobias.schlosser@cs.tu-chemnitz.de.ORCID 0000-0002-0682-4284
Frederik BeuthJunior Professorship of Media Computing, Chemnitz University of Technology, 09107, Chemnitz, Germany.ORCID 0000-0001-5482-9787
Trixy MeyerJunior Professorship of Media Computing, Chemnitz University of Technology, 09107, Chemnitz, Germany.ORCID 0000-0002-3372-1619
Arunodhayan Sampath KumarJunior Professorship of Media Computing, Chemnitz University of Technology, 09107, Chemnitz, Germany.ORCID 0000-0002-2654-7050
Gabriel StolzeDepartment of Ophthalmology, Klinikum Chemnitz gGmbH, 09116, Chemnitz, Germany.
Olga FurashovaDepartment of Ophthalmology, Klinikum Chemnitz gGmbH, 09116, Chemnitz, Germany.ORCID 0000-0002-1273-7005
Katrin EngelmannDepartment of Ophthalmology, Klinikum Chemnitz gGmbH, 09116, Chemnitz, Germany.
Danny KowerkoJunior Professorship of Media Computing, Chemnitz University of Technology, 09107, Chemnitz, Germany. danny.kowerko@cs.tu-chemnitz.de.ORCID 0000-0002-4538-7814

Funding

Federal Ministry of Education and Research 01ZZ2101CFederal Ministry of Education and Research 01ZZ2101E
6 · The paper itself

Abstract

In ophthalmology, intravitreal operative medication therapy (IVOM) is a widespread treatment for diseases related to the age-related macular degeneration (AMD), the diabetic macular edema, as well as the retinal vein occlusion. However, in real-world settings, patients often suffer from loss of vision on time scales of years despite therapy, whereas the prediction of the visual acuity (VA) and the earliest possible detection of deterioration under real-life conditions is challenging due to heterogeneous and incomplete data. In this contribution, we present a workflow for the development of a research-compatible data corpus fusing different IT systems of the department of ophthalmology of a German maximum care hospital. The extensive data corpus allows predictive statements of the expected progression of a patient and his or her VA in each of the three diseases. For the disease AMD, we found out a significant deterioration of the visual acuity over time. Within our proposed multistage system, we subsequently classify the VA progression into the three groups of therapy "winners", "stabilizers", and "losers" (WSL classification scheme). Our OCT biomarker classification using an ensemble of deep neural networks results in a classification accuracy (F1-score) of over 98%, enabling us to complete incomplete OCT documentations while allowing us to exploit them for a more precise VA modelling process. Our VA prediction requires at least four VA examinations and optionally OCT biomarkers from the same time period to predict the VA progression within a forecasted time frame, whereas our prediction is currently restricted to IVOM/no therapy. We achieve a final prediction accuracy of 69% in macro average F1-score, while being in the same range as the ophthalmologists with 57.8 and

Indexed as

Diabetic RetinopathyMacular DegenerationMacular EdemaDocumentationFemaleHumansMachine LearningMaleVisual AcuityComputer vision and pattern recognitionDeep learningMachine learningOCT biomarkersOphthalmologyOphthalmology diseasesPredictive statisticsTreatment progression

Identifiers

PMID38448469
PMCPMC10917755

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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.