ArticleScientific reports2023
Cluster analysis driven by unsupervised latent feature learning of medications to identify novel pharmacophenotypes of critically ill patients.
Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 8 citations in OpenAlex.
- A Data-Driven Medication Regimen Complexity Score for Critically Ill Patients: MRC-ICU 2.0.Pharmacotherapy · 2026Observational
- Data-driven endocrine-metabolic phenotypes in young women with polycystic ovary syndrome and associations with cardiometabolic risk markers.Journal of endocrinological investigation · 2026Article
- Artificial intelligence-based clustering to identify functional risk phenotypes in heart failure.Open heart · 2026Article
- Prediction of pharmacist medication interventions using medication regimen complexity.JAMIA open · 2025Article
- PharmacyGPT: exploration of artificial intelligence for medication management in the intensive care unit.BMC medical informatics and decision making · 2025Article
- Unsupervised machine learning analysis to identify patterns of ICU medication use for fluid overload prediction.Pharmacotherapy · 2025Article
- Does artificial intelligence close gaps in clinical pharmacology in the ICU?Intensive care medicine · 2025Article
- A common data model for the standardization of intensive care unit medication features.JAMIA open · 2024Article
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Authors and funding
6 authors at 4 institutions in 1 country.
Funding
Abstract
Unsupervised clustering of intensive care unit (ICU) medications may identify unique medication clusters (i.e., pharmacophenotypes) in critically ill adults. We performed an unsupervised analysis with Restricted Boltzmann Machine of 991 medications profiles of patients managed in the ICU to explore pharmacophenotypes that correlated with ICU complications (e.g., mechanical ventilation) and patient-centered outcomes (e.g., length of stay, mortality). Six unique pharmacophenotypes were observed, with unique medication profiles and clinically relevant differences in ICU complications and patient-centered outcomes. While pharmacophenotypes 2 and 4 had no statistically significant difference in ICU length of stay, duration of mechanical ventilation, or duration of vasopressor use, their mortality differed significantly (9.0% vs. 21.9%, p < 0.0001). Pharmacophenotype 4 had a mortality rate of 21.9%, compared with the rest of the pharmacophenotypes ranging from 2.5 to 9%. Phenotyping approaches have shown promise in classifying the heterogenous syndromes of critical illness to predict treatment response and guide clinical decision support systems but have never included comprehensive medication information. This first-ever machine learning approach revealed differences among empirically-derived subgroups of ICU patients that are not typically revealed by traditional classifiers. Identification of pharmacophenotypes may enable enhanced decision making to optimize treatment decisions.
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