ArticleJAMIA open2024
A common data model for the standardization of intensive care unit medication features.
Article in JAMIA open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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The trial behind it
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Who cites it
5 citing papers in PubMed.
- Beyond Human Error: Building Intelligent Resilience for Medication Safety in the ICU.Healthcare (Basel, Switzerland) · 2026Review
- Big multiple sclerosis data network: novel modelling approaches for real-world data analysis.Journal of neurology · 2025Review
- Article
- A common longitudinal intensive care unit data format (CLIF) for critical illness research.Intensive care medicine · 2025Article
- Unsupervised machine learning analysis to identify patterns of ICU medication use for fluid overload prediction.Pharmacotherapy · 2025Article
Corrections and comments
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Authors and funding
10 authors.
Funding
Abstract
Objective: Common data models provide a standard means of describing data for artificial intelligence (AI) applications, but this process has never been undertaken for medications used in the intensive care unit (ICU). We sought to develop a common data model (CDM) for ICU medications to standardize the medication features needed to support future ICU AI efforts. Materials and Methods: A 9-member, multi-professional team of ICU clinicians and AI experts conducted a 5-round modified Delphi process employing conference calls, web-based communication, and electronic surveys to define the most important medication features for AI efforts. Candidate ICU medication features were generated through group discussion and then independently scored by each team member based on relevance to ICU clinical decision-making and feasibility for collection and coding. A key consideration was to ensure the final ontology both distinguished unique medications and met Findable, Accessible, Interoperable, and Reusable (FAIR) guiding principles. Results: Using a list of 889 ICU medications, the team initially generated 106 different medication features, and 71 were ranked as being core features for the CDM. Through this process, 106 medication features were assigned to 2 key feature domains: drug product-related (n = 43) and clinical practice-related (n = 63). Each feature included a standardized definition and suggested response values housed in the electronic data library. This CDM for ICU medications is available online. Conclusion: The CDM for ICU medications represents an important first step for the research community focused on exploring how AI can improve patient outcomes and will require ongoing engagement and refinement.
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Registered trials
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