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A common data model for the standardization of intensive care unit medication features.
Sikora, Andrea; Keats, Kelli; Murphy, David J; Devlin, John W; Smith, Susan E; Murray, Brian; Buckley, Mitchell S; Rowe, Sandra; Coppiano, Lindsey; Kamaleswaran, Rishikesan.
Afiliação
  • Sikora A; Department of Clinical and Administrative Pharmacy, University of Georgia College of Pharmacy, Augusta, GA 30912, United States.
  • Keats K; Department of Pharmacy, Augusta University Medical Center, Augusta, GA 30912, United States.
  • Murphy DJ; Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, Emory University, Atlanta, GA 30322, United States.
  • Devlin JW; Northeastern University School of Pharmacy, Boston, MA 02115, United States.
  • Smith SE; Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Boston, MA 02115, United States.
  • Murray B; Department of Clinical and Administrative Pharmacy, University of Georgia College of Pharmacy, Athens, GA 30601, United States.
  • Buckley MS; Department of Pharmacy, University of North Carolina Medical Center, Chapel Hill, NC 27514, United States.
  • Rowe S; Department of Pharmacy, Banner University Medical Center Phoenix, Phoenix, AZ 85032, United States.
  • Coppiano L; Department of Pharmacy, Oregon Health and Science University, Portland, OR 97239, United States.
  • Kamaleswaran R; Department of Biomedical Informatics, Emory University School of Medicine, Atlanta, GA 30322, United States.
JAMIA Open ; 7(2): ooae033, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38699649
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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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article