Literature DB >> 33602191

Evaluation of a clinical decision support system for rare diseases: a qualitative study.

Jannik Schaaf1, Martin Sedlmayr2, Brita Sedlmayr2, Hans-Ulrich Prokosch3, Holger Storf4.   

Abstract

BACKGROUND: Rare Diseases (RDs) are difficult to diagnose. Clinical Decision Support Systems (CDSS) could support the diagnosis for RDs. The Medical Informatics in Research and Medicine (MIRACUM) consortium developed a CDSS for RDs based on distributed clinical data from eight German university hospitals. To support the diagnosis for difficult patient cases, the CDSS uses data from the different hospitals to perform a patient similarity analysis to obtain an indication of a diagnosis. To optimize our CDSS, we conducted a qualitative study to investigate usability and functionality of our designed CDSS.
METHODS: We performed a Thinking Aloud Test (TA-Test) with RDs experts working in Rare Diseases Centers (RDCs) at MIRACUM locations which are specialized in diagnosis and treatment of RDs. An instruction sheet with tasks was prepared that the participants should perform with the CDSS during the study. The TA-Test was recorded on audio and video, whereas the resulting transcripts were analysed with a qualitative content analysis, as a ruled-guided fixed procedure to analyse text-based data. Furthermore, a questionnaire was handed out at the end of the study including the System Usability Scale (SUS).
RESULTS: A total of eight experts from eight MIRACUM locations with an established RDC were included in the study. Results indicate that more detailed information about patients, such as descriptive attributes or findings, can help the system perform better. The system was rated positively in terms of functionality, such as functions that enable the user to obtain an overview of similar patients or medical history of a patient. However, there is a lack of transparency in the results of the CDSS patient similarity analysis. The study participants often stated that the system should present the user with an overview of exact symptoms, diagnosis, and other characteristics that define two patients as similar. In the usability section, the CDSS received a score of 73.21 points, which is ranked as good usability.
CONCLUSIONS: This qualitative study investigated the usability and functionality of a CDSS of RDs. Despite positive feedback about functionality of system, the CDSS still requires some revisions and improvement in transparency of the patient similarity analysis.

Entities:  

Keywords:  Clinical decision support systems; Computer-assisted diagnosis; Rare diseases; Usability

Year:  2021        PMID: 33602191      PMCID: PMC7890997          DOI: 10.1186/s12911-021-01435-8

Source DB:  PubMed          Journal:  BMC Med Inform Decis Mak        ISSN: 1472-6947            Impact factor:   2.796


  27 in total

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2.  Rare diseases and now rare data?

Authors:  Deborah Mascalzoni; Bartha Maria Knoppers; Ségolène Aymé; Matteo Macilotti; Hugh Dawkins; Simon Woods; Mats G Hansson
Journal:  Nat Rev Genet       Date:  2013-06       Impact factor: 53.242

3.  Rare diseases in general practice: recognising the zebras among the horses.

Authors:  William Rh Evans; Imran Rafi
Journal:  Br J Gen Pract       Date:  2016-11       Impact factor: 5.386

4.  [Registries for rare diseases : OSSE - An open-source framework for technical implementation].

Authors:  Holger Storf; Jannik Schaaf; Dennis Kadioglu; Jens Göbel; Thomas O F Wagner; Frank Ückert
Journal:  Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz       Date:  2017-05       Impact factor: 1.513

5.  Finding the Needle in the Hay Stack: An Open Architecture to Support Diagnosis of Undiagnosed Patients.

Authors:  Jannik Schaaf; Martin Boeker; Thomas Ganslandt; Christian Haverkamp; Tim Hermann; Dennis Kadioglu; Hans-Ulrich Prokosch; Thomas O F Wagner; Michael von Wagner; Johanna Schaefer; Martin Sedlmayr; Holger Storf
Journal:  Stud Health Technol Inform       Date:  2019-08-21

6.  Undiagnosed Diseases: Italy-US Collaboration and International Efforts to Tackle Rare and Common Diseases Lacking a Diagnosis.

Authors:  Domenica Taruscio; Giovanna Floridia; Marco Salvatore; Stephen C Groft; William A Gahl
Journal:  Adv Exp Med Biol       Date:  2017       Impact factor: 2.622

Review 7.  A review of user-centered design for diabetes-related consumer health informatics technologies.

Authors:  Cynthia LeRouge; Nilmini Wickramasinghe
Journal:  J Diabetes Sci Technol       Date:  2013-07-01

8.  Searching for rare diseases in PubMed: a blind comparison of Orphanet expert query and query based on terminological knowledge.

Authors:  N Griffon; M Schuers; F Dhombres; T Merabti; G Kerdelhué; L Rollin; S J Darmoni
Journal:  BMC Med Inform Decis Mak       Date:  2016-08-02       Impact factor: 2.796

9.  Utilization of Electronic Medical Records and Biomedical Literature to Support the Diagnosis of Rare Diseases Using Data Fusion and Collaborative Filtering Approaches.

Authors:  Feichen Shen; Sijia Liu; Yanshan Wang; Andrew Wen; Liwei Wang; Hongfang Liu
Journal:  JMIR Med Inform       Date:  2018-10-10

Review 10.  An overview of clinical decision support systems: benefits, risks, and strategies for success.

Authors:  Reed T Sutton; David Pincock; Daniel C Baumgart; Daniel C Sadowski; Richard N Fedorak; Karen I Kroeker
Journal:  NPJ Digit Med       Date:  2020-02-06
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1.  Participatory Design of a Medication Module in an Electronic Medical Record for Paediatric Palliative Care: A Think-Aloud Approach with Nurses and Physicians.

Authors:  Sven Kernebeck; Chantal Jux; Theresa Sophie Busse; Dorothee Meyer; Larissa Alice Dreier; Daniel Zenz; Boris Zernikow; Jan Peter Ehlers
Journal:  Children (Basel)       Date:  2022-01-06

2.  Evaluation of an Electronic Medical Record Module for Nursing Documentation in Paediatric Palliative Care: Involvement of Nurses with a Think-Aloud Approach.

Authors:  Sven Kernebeck; Theresa Sophie Busse; Chantal Jux; Larissa Alice Dreier; Dorothee Meyer; Daniel Zenz; Boris Zernikow; Jan Peter Ehlers
Journal:  Int J Environ Res Public Health       Date:  2022-03-18       Impact factor: 3.390

Review 3.  [se-atlas.de-Medical care atlas for people with rare diseases].

Authors:  Michaela Neff; Jannik Schaaf; Niels Tegtbauer; Johanna Schäfer; Manuela Till; Thomas O F Wagner; Holm Graeßner; Christine Mundlos; Holger Storf
Journal:  Internist (Berl)       Date:  2021-07-20       Impact factor: 0.743

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