Autor: |
Rudi Agius, Anders C. Riis-Jensen, Bettina Wimmer, Caspar da Cunha-Bang, Daniel Dawson Murray, Christian Bjorn Poulsen, Marianne B. Bertelsen, Berit Schwartz, Jens Dilling Lundgren, Henning Langberg, Carsten Utoft Niemann |
Jazyk: |
angličtina |
Rok vydání: |
2024 |
Předmět: |
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Zdroj: |
npj Digital Medicine, Vol 7, Iss 1, Pp 1-12 (2024) |
Druh dokumentu: |
article |
ISSN: |
2398-6352 |
DOI: |
10.1038/s41746-024-01132-6 |
Popis: |
Abstract Research algorithms are seldom externally validated or integrated into clinical practice, leaving unknown challenges in deployment. In such efforts, one needs to address challenges related to data harmonization, the performance of an algorithm in unforeseen missingness, automation and monitoring of predictions, and legal frameworks. We here describe the deployment of a high-dimensional data-driven decision support model into an EHR and derive practical guidelines informed by this deployment that includes the necessary processes, stakeholders and design requirements for a successful deployment. For this, we describe our deployment of the chronic lymphocytic leukemia (CLL) treatment infection model (CLL-TIM) as a stand-alone platform adjoined to an EPIC-based Danish Electronic Health Record (EHR), with the presentation of personalized predictions in a clinical context. CLL-TIM is an 84-variable data-driven prognostic model utilizing 7-year medical patient records and predicts the 2-year risk composite outcome of infection and/or treatment post-CLL diagnosis. As an independent validation cohort for this deployment, we used a retrospective population-based cohort of patients diagnosed with CLL from 2018 onwards (n = 1480). Unexpectedly high levels of missingness for key CLL-TIM variables were exhibited upon deployment. High dimensionality, with the handling of missingness, and predictive confidence were critical design elements that enabled trustworthy predictions and thus serves as a priority for prognostic models seeking deployment in new EHRs. Our setup for deployment, including automation and monitoring into EHR that meets Medical Device Regulations, may be used as step-by-step guidelines for others aiming at designing and deploying research algorithms into clinical practice. |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
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