Abstract
Early diagnosis is crucial for well-being and life quality of the rare disease patient. Access to the most complete knowledge about diseases through intelligent user interfaces can play an important role in supporting the physician reaching the correct diagnosis. Case reports may offer information about heterogeneous phenotypes which often further complicate rare disease diagnosis. The rare disease search engine FindZebra.com is extended to also access case report abstracts extracted from PubMed for several diseases. A search index for each disease is built in Apache Solr adding age, sex and clinical features extracted using text segmentation to enhance the specificity of search. Clinical experts performed retrospective validation of the search engine, utilising real-world Outcomes Survey data on Gaucher and Fabry patients. Medical experts evaluated the search results as being clinically relevant for the Fabry patients and less clinically relevant for the Gaucher patients. The shortcomings for Gaucher patients mainly reflect a mismatch between the current understanding and treatment of the disease and how it is reported in PubMed, notably in the older case reports. In response to this observation, a filter for the publication date was added in the final version of the tool available from deep.findzebra.com/<disease> with <disease> = gaucher, fabry, hae (Hereditary angioedema).
Funder
Takeda Pharmaceuticals U.S.A.
Novo Nordisk Fonden
Google
Publisher
Public Library of Science (PLoS)
Reference30 articles.
1. Rare diseases. (n.d.). Retrieved April 4, 2022, from https://ec.europa.eu/health/non-communicable-diseases/steering-group/rare-diseases_en.
2. The patient journey of patients with Fabry disease, Gaucher disease and Mucopolysaccharidosis type II: A German-wide telephone survey;E Mengel;PLoS One,2020
3. Internet Use by Parents of Children With Rare Conditions: Findings From a Study on Parents’ Web Information Needs;H Nicholl;J Med Internet Res,2017
4. Wake Forest Baptist Medical Center. "Internet can be valuable tool for people with undiagnosed rare disorders." ScienceDaily 2019 Aug 7. .
5. Fabry Disease: Molecular Basis, Pathophysiology, Diagnostics and Potential Therapeutic Directions;K Kok;Biomolecules,2021
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献