Literature DB >> 23462700

FindZebra: a search engine for rare diseases.

Radu Dragusin1, Paula Petcu, Christina Lioma, Birger Larsen, Henrik L Jørgensen, Ingemar J Cox, Lars Kai Hansen, Peter Ingwersen, Ole Winther.   

Abstract

BACKGROUND: The web has become a primary information resource about illnesses and treatments for both medical and non-medical users. Standard web search is by far the most common interface to this information. It is therefore of interest to find out how well web search engines work for diagnostic queries and what factors contribute to successes and failures. Among diseases, rare (or orphan) diseases represent an especially challenging and thus interesting class to diagnose as each is rare, diverse in symptoms and usually has scattered resources associated with it.
METHODS: We design an evaluation approach for web search engines for rare disease diagnosis which includes 56 real life diagnostic cases, performance measures, information resources and guidelines for customising Google Search to this task. In addition, we introduce FindZebra, a specialized (vertical) rare disease search engine. FindZebra is powered by open source search technology and uses curated freely available online medical information.
RESULTS: FindZebra outperforms Google Search in both default set-up and customised to the resources used by FindZebra. We extend FindZebra with specialized functionalities exploiting medical ontological information and UMLS medical concepts to demonstrate different ways of displaying the retrieved results to medical experts.
CONCLUSIONS: Our results indicate that a specialized search engine can improve the diagnostic quality without compromising the ease of use of the currently widely popular standard web search. The proposed evaluation approach can be valuable for future development and benchmarking. The FindZebra search engine is available at http://www.findzebra.com/.
Copyright © 2013 Elsevier Ireland Ltd. All rights reserved.

Mesh:

Year:  2013        PMID: 23462700     DOI: 10.1016/j.ijmedinf.2013.01.005

Source DB:  PubMed          Journal:  Int J Med Inform        ISSN: 1386-5056            Impact factor:   4.046


  21 in total

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2.  [Computer-assisted diagnosis of rare diseases].

Authors:  T Müller; A Jerrentrup; J R Schäfer
Journal:  Internist (Berl)       Date:  2018-04       Impact factor: 0.743

3.  The Clinical Genome and Ancestry Report: An interactive web application for prioritizing clinically implicated variants from genome sequencing data with ancestry composition.

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Journal:  Hum Mutat       Date:  2019-11-15       Impact factor: 4.878

4.  A quick reference guide for rare disease: supporting rare disease management in general practice.

Authors:  Ashleen Crowe; Helen McAneney; Patrick J Morrison; Margaret E Cupples; Amy Jayne McKnight
Journal:  Br J Gen Pract       Date:  2020-04-30       Impact factor: 5.386

Review 5.  The utility of phenomics in diagnosis of inherited metabolic disorders.

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Journal:  Clin Med (Lond)       Date:  2019-01       Impact factor: 2.659

Review 6.  Clinical Decision Support Systems.

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Journal:  Visc Med       Date:  2021-09-28

Review 7.  [Digital diagnostic support in rheumatology].

Authors:  J Knitza; M Krusche; J Leipe
Journal:  Z Rheumatol       Date:  2021-10-04       Impact factor: 1.372

8.  How to build personalized multi-omics comorbidity profiles.

Authors:  Mohammad Ali Moni; Pietro Liò
Journal:  Front Cell Dev Biol       Date:  2015-06-24

Review 9.  Rare disease diagnosis: A review of web search, social media and large-scale data-mining approaches.

Authors:  Dan Svenstrup; Henrik L Jørgensen; Ole Winther
Journal:  Rare Dis       Date:  2015-09-16

Review 10.  The patient is in: patient involvement strategies for diagnostic error mitigation.

Authors:  Kathryn M McDonald; Cindy L Bryce; Mark L Graber
Journal:  BMJ Qual Saf       Date:  2013-07-26       Impact factor: 7.035

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