Kraus, Ludwig; Kremmyda, Olympia; Brémovà-Ertl, Tatiana; Barceló, Sebastià; Feil, Katharina; Strupp, Michael (2019). An algorithm as a diagnostic tool for central ocular motor disorders, also to diagnose rare disorders. Orphanet journal of rare diseases, 14(1), p. 193. BioMed Central 10.1186/s13023-019-1164-8
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BACKGROUND
Recently an increasing number of digital tools to aid clinical work have been published. This study's aim was to create an algorithm which can assist physicians as a "digital expert" with the differential diagnosis of central ocular motor disorders, in particular in rare diseases.
RESULTS
The algorithm's input consists of a maximum of 60 neurological and oculomotor signs and symptoms. The output is a list of the most probable diagnoses out of 14 alternatives and the most likely topographical anatomical localizations out of eight alternatives. Positive points are given for disease-associated symptoms, negative points for symptoms unlikely to occur with a disease. The accuracy of the algorithm was evaluated using the two diagnoses and two brain zones with the highest scores. In a first step, a dataset of 102 patients (56 males, 48.0 ± 22 yrs) with various central ocular motor disorders and underlying diseases, with a particular focus on rare diseases, was used as the basis for developing the algorithm iteratively. In a second step, the algorithm was validated with a dataset of 104 patients (59 males, 46.0 ± 23 yrs). For 12/14 diseases, the algorithm showed a sensitivity of between 80 and 100% and the specificity of 9/14 diseases was between 82 and 95% (e.g., 100% sensitivity and 75.5% specificity for Niemann Pick type C, and 80% specificity and 91.5% sensitivity for Gaucher's disease). In terms of a topographic anatomical diagnosis, the sensitivity was between 77 and 100% for 4/8 brain zones, and the specificity of 5/8 zones ranged between 79 and 99%.
CONCLUSION
This algorithm using our knowledge of the functional anatomy of the ocular motor system and possible underlying diseases is a useful tool, in particular for the diagnosis of rare diseases associated with typical central ocular motor disorders, which are often overlooked.
Item Type: |
Journal Article (Original Article) |
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Division/Institute: |
04 Faculty of Medicine > Department of Head Organs and Neurology (DKNS) > Clinic of Neurology |
UniBE Contributor: |
Brémovà-Ertl, Tatiana |
Subjects: |
600 Technology > 610 Medicine & health |
ISSN: |
1750-1172 |
Publisher: |
BioMed Central |
Language: |
English |
Submitter: |
Chantal Kottler |
Date Deposited: |
15 Nov 2019 15:12 |
Last Modified: |
05 Dec 2022 15:32 |
Publisher DOI: |
10.1186/s13023-019-1164-8 |
PubMed ID: |
31395076 |
Uncontrolled Keywords: |
Algorithm Ataxia teleangiectasia Ataxia with oculomotor apraxia Gaucher’s disease type 3 Niemann pick type C Ocular motor disorder Progressive supranuclear palsy Wernicke encephalopathy |
BORIS DOI: |
10.7892/boris.134835 |
URI: |
https://boris.unibe.ch/id/eprint/134835 |