Computer-assisted diagnosis of rare diseases

被引:0
|
作者
Mueller, T. [1 ]
Jerrentrup, A. [1 ]
Schaefer, J. R. [1 ]
机构
[1] Univ Klinikum Giessen & Marburg UKGM, Zentrum Unerkannte & Seltene Erkrankungen ZusE, Baldingerstr 1, D-35043 Marburg, Germany
来源
INTERNIST | 2018年 / 59卷 / 04期
关键词
Diagnosis; differential; Search engine; Diagnostic decision support; Rare diseases; Diagnostic errors; HEALTH INFORMATION-SYSTEMS; HUMAN PHENOTYPE ONTOLOGY; SEARCH ENGINE; ORPHANET; SUPPORT;
D O I
10.1007/s00108-017-0218-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To establish a comprehensive diagnosis is by far the most challenging task in a physician's daily routine. Especially rare diseases place high demands on differential diagnosis, caused by the high number of around 8000 diseases and their clinical variability. No clinician can be aware of all the different entities and memorizing them all is impossible and inefficient. Specific diagnostic decision-supported systemsprovide better results than standard search engines in this context. The systems FindZebra, Phenomizer, Orphanet, and Isabel are presented here concisely with their advantages and limitations. An outlook is given to social media usage and big data technologies. Due to the high number of initial misdiagnoses and long periods of time until a confirmatory diagnosis is reached, these tools might be promising in practice to improve the diagnosis of rare diseases.
引用
收藏
页码:391 / 400
页数:10
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