TY - JOUR
T1 - Dementia Care Research and Psychosocial Factors
AU - Sannemann, Lena
AU - Rhodius-Meester, Hanneke F.M.
AU - Ekelund, Mats
AU - van der Flier, Wiesje M.
AU - Frederiksen, Kristian Steen
AU - Georges, Jean
AU - Hartmanis, Maris
AU - Kivipelto, Miia
AU - Knapskog, Anne Brita
AU - Kramberger, Milica G.
AU - Lindgren, Peter
AU - Gispert, Juan Domingo
AU - Lötjönen, Jyrki
AU - Pla, Sandra
AU - Solomon, Alina
AU - Jönsson, Linus
AU - Jessen, Frank
AU - PROMINENT consortium
N1 - Publisher Copyright:
© 2025 The Alzheimer's Association. Alzheimer's & Dementia published by Wiley Periodicals LLC on behalf of Alzheimer's Association.
PY - 2025/12/1
Y1 - 2025/12/1
N2 - BACKGROUND: Research advances in diagnostics, therapies and prevention strategies for Alzheimer's disease necessitate a paradigm shift towards timely precision diagnostics and early treatment in routine care. Clinical decision support systems (CDSS) based on artificial intelligence technology have the potential to assist clinicians in the interpretation of complex diagnostic data and facilitate patient management. The PROMINENT study is part of the Innovative Health Initiative (IHI) program and aims to evaluate and validate the use of a CDSS in memory clinics. The tool combines key patient data and uses decision models to provide a probability for the diagnosis and underlying pathology. METHOD: The PROMINENT evaluation and validation studies will be carried out at seven European memory clinics. To evaluate the perspectives of different stakeholders on the use of a CDSS, two clinicians, 25 patients and 25 care partners per site will be surveyed, and a subsample will be invited to in-depth qualitative interviews. A multi-reader multi-case design will be applied in the validation study to analyze if the CDSS affects patients' diagnostic pathways and clinicians' diagnostic confidence. Two clinicians will retrospectively evaluate the data of 50 patients per site and mimic the real-world stepwise diagnostic process, with each patient case being assessed once with and without access to the CDSS. RESULT: We present the rationale and design of the PROMINENT evaluation and validation studies. The primary endpoint of the evaluation study is the opinion of clinicians on the usefulness of the CDSS and CDSS-generated reports and the perspective of patients and care partners on the comprehensibility and usefulness of patient-centered reports. The primary outcome of the validation study is the difference in diagnostic resources required to reach a final diagnosis and the associated diagnostic confidence of clinicians depending on access to the CDSS. In addition, the validation study will assess the performance of the CDSS. CONCLUSION: The results of these studies will address the potential of a CDSS to improve diagnostic pathways and clinicians' diagnostic confidence in memory clinics. Feedback from clinicians, patients, and care partners will inform the tool's integration into routine care, potentially improving decision-making, quality of care and communication.
AB - BACKGROUND: Research advances in diagnostics, therapies and prevention strategies for Alzheimer's disease necessitate a paradigm shift towards timely precision diagnostics and early treatment in routine care. Clinical decision support systems (CDSS) based on artificial intelligence technology have the potential to assist clinicians in the interpretation of complex diagnostic data and facilitate patient management. The PROMINENT study is part of the Innovative Health Initiative (IHI) program and aims to evaluate and validate the use of a CDSS in memory clinics. The tool combines key patient data and uses decision models to provide a probability for the diagnosis and underlying pathology. METHOD: The PROMINENT evaluation and validation studies will be carried out at seven European memory clinics. To evaluate the perspectives of different stakeholders on the use of a CDSS, two clinicians, 25 patients and 25 care partners per site will be surveyed, and a subsample will be invited to in-depth qualitative interviews. A multi-reader multi-case design will be applied in the validation study to analyze if the CDSS affects patients' diagnostic pathways and clinicians' diagnostic confidence. Two clinicians will retrospectively evaluate the data of 50 patients per site and mimic the real-world stepwise diagnostic process, with each patient case being assessed once with and without access to the CDSS. RESULT: We present the rationale and design of the PROMINENT evaluation and validation studies. The primary endpoint of the evaluation study is the opinion of clinicians on the usefulness of the CDSS and CDSS-generated reports and the perspective of patients and care partners on the comprehensibility and usefulness of patient-centered reports. The primary outcome of the validation study is the difference in diagnostic resources required to reach a final diagnosis and the associated diagnostic confidence of clinicians depending on access to the CDSS. In addition, the validation study will assess the performance of the CDSS. CONCLUSION: The results of these studies will address the potential of a CDSS to improve diagnostic pathways and clinicians' diagnostic confidence in memory clinics. Feedback from clinicians, patients, and care partners will inform the tool's integration into routine care, potentially improving decision-making, quality of care and communication.
UR - http://www.scopus.com/inward/record.url?scp=105025826935&partnerID=8YFLogxK
U2 - 10.1002/alz70858_105478
DO - 10.1002/alz70858_105478
M3 - Journal article
C2 - 41449725
AN - SCOPUS:105025826935
SN - 1552-5260
VL - 21
JO - Alzheimer's & dementia : the journal of the Alzheimer's Association
JF - Alzheimer's & dementia : the journal of the Alzheimer's Association
M1 - e105478
ER -