Iskrov, Georgi; Raycheva, Ralitsa; Kostadinov, Kostadin; Gillner, Sandra; Blankart, Carl Rudolf; Gross, Edith Sky; Gumus, Gulcin; Mitova, Elena; Stefanov, Stefan; Stefanov, Georgi; Stefanov, Rumen (2024). Are the European reference networks for rare diseases ready to embrace machine learning? A mixed-methods study. Orphanet journal of rare diseases, 19(1) BioMed Central 10.1186/s13023-024-03047-7
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BACKGROUND
The delay in diagnosis for rare disease (RD) patients is often longer than for patients with common diseases. Machine learning (ML) technologies have the potential to speed up and increase the precision of diagnosis in this population group. We aim to explore the expectations and experiences of the members of the European Reference Networks (ERNs) for RDs with those technologies and their potential for application.
METHODS
We used a mixed-methods approach with an online survey followed by a focus group discussion. Our study targeted primarily medical professionals but also other individuals affiliated with any of the 24 ERNs.
RESULTS
The online survey yielded 423 responses from ERN members. Participants reported a limited degree of knowledge of and experience with ML technologies. They considered improved diagnostic accuracy the most important potential benefit, closely followed by the synthesis of clinical information, and indicated the lack of training in these new technologies, which hinders adoption and implementation in routine care. Most respondents supported the option that ML should be an optional but recommended part of the diagnostic process for RDs. Most ERN members saw the use of ML limited to specialised units only in the next 5 years, where those technologies should be funded by public sources. Focus group discussions concluded that the potential of ML technologies is substantial and confirmed that the technologies will have an important impact on healthcare and RDs in particular. As ML technologies are not the core competency of health care professionals, participants deemed a close collaboration with developers necessary to ensure that results are valid and reliable. However, based on our results, we call for more research to understand other stakeholders' opinions and expectations, including the views of patient organisations.
CONCLUSIONS
We found enthusiasm to implement and apply ML technologies, especially diagnostic tools in the field of RDs, despite the perceived lack of experience. Early dialogue and collaboration between health care professionals, developers, industry, policymakers, and patient associations seem to be crucial to building trust, improving performance, and ultimately increasing the willingness to accept diagnostics based on ML technologies.
Item Type: |
Journal Article (Original Article) |
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Division/Institute: |
04 Faculty of Medicine > Faculty Institutions > sitem Center for Translational Medicine and Biomedical Entrepreneurship 11 Centers of Competence > KPM Center for Public Management |
UniBE Contributor: |
Gillner, Sandra, Blankart, Rudolf |
Subjects: |
300 Social sciences, sociology & anthropology > 350 Public administration & military science |
ISSN: |
1750-1172 |
Publisher: |
BioMed Central |
Language: |
English |
Submitter: |
Pubmed Import |
Date Deposited: |
26 Jan 2024 14:46 |
Last Modified: |
26 Jan 2024 14:55 |
Publisher DOI: |
10.1186/s13023-024-03047-7 |
PubMed ID: |
38273306 |
Uncontrolled Keywords: |
Artificial intelligence Diagnosis Diagnostic delay European reference networks Machine learning Rare diseases |
BORIS DOI: |
10.48350/192146 |
URI: |
https://boris.unibe.ch/id/eprint/192146 |