Evidence map›Paper›PMID 41398250›Full record

ArticleBMC medical informatics and decision making2025

Early prediction of vasopressor initiation in ICU sepsis patients using an interpretable EHR-based ML model.

Lucas Duval, Antoine Villié, Fei Zheng, Gabriel Terraz, Sophie Blein, Esther Duperchy, Martin Everett, Johan Frieling, Jean-François Llitjos, Maxime Bodinier

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Article in BMC medical informatics and decision making, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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5 · Who and what money

Authors and funding

10 authors.

Lucas Duval *Innovation and Partnerships (I&P) Department, bioMérieux S.A., Marcy L'Etoile, France.
Antoine Villié *AUROBAC Therapeutics S.A.S., Lyon, France.
Fei ZhengData Science Department, bioMérieux S.A., Marcy L'Etoile, France.
Gabriel TerrazEFOR, Champagne-au-Mont-d'Or, France.
Sophie BleinData Science Department, bioMérieux S.A., Marcy L'Etoile, France.
Esther DuperchyAUROBAC Therapeutics S.A.S., Lyon, France.
Martin EverettAUROBAC Therapeutics S.A.S., Lyon, France.
Johan FrielingAUROBAC Therapeutics S.A.S., Lyon, France.
Jean-François LlitjosInnovation and Partnerships (I&P) Department, bioMérieux S.A., Marcy L'Etoile, France.
Maxime BodinierInnovation and Partnerships (I&P) Department, bioMérieux S.A., Marcy L'Etoile, France. maxime.bodinier@biomerieux.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEarly identification of septic patients who will require vasopressor support could provide a critical window for hemodynamic optimisation, yet current bedside cues often appear only when shock is imminent.

objectiveWe aimed to develop and validate an interpretable electronic health record (EHR)-based machine-learning model that predicts vasopressor initiation several hours before therapy in intensive care unit (ICU) patients with sepsis.

methodsWe conducted a retrospective study using the MIMIC-IV v2.2 database (2008-2019). We screened adult Sepsis-3 ICU stays and labeled the patients who commenced continuous vasopressor infusions 6 to 48 hours after admission as cases; we defined controls as sepsis patients with ICU stays ≥48 hours and no vasopressor exposure. We performed one to one nearest neighbour matching on age, sex, Charlson index, SOFA score with the cardiovascular component removed, weight, and early lactate/hematocrit availability to minimise confounding. We engineered demographic, physiological, and laboratory features measured from -6 to -2 hours relative to vasopressor initiation (or a matched time point) under multiple parameter combinations. We trained seven algorithms with Monte Carlo cross validation and evaluated performance on an independent validation set. We assessed model interpretability with Shapley values.

resultsWe analyzed 1,539 cases and 1,431 controls; the independent validation set comprised 751 stays (~25%). A Random Forest classifier achieved an area under the receiver operating characteristic (AUROC) of 0.75 (95% CI, 0.72-0.79), a sensitivity of 0.74 (95% CI, 0.69-0.78), a specificity of 0.65 (95% CI, 0.60-0.70), a precision of 0.70 (95% CI, 0.66-0.74) and a F1 score of 0.72 (95% CI, 0.68-0.75) at the Youden's index threshold. The model outperformed simple surrogates-mean blood pressure (AUROC, 0.68; 95% CI, 0.64-0.72) and modified shock index (AUROC, 0.65; 95% CI, 0.62-0.69)-and a reproduced bidirectional LSTM (AUROC, 0.73; 95% CI, 0.70-0.77). Key predictors included declining mean blood pressure at - 2 to -4 hours, elevated lactate ( > 2.5 mmol/L), and hematocrit outside 30-37%. Model alerts would occur two to four hours before vasopressor initiation, providing actionable lead time for clinicians.

conclusionsThis proof-of-concept study shows that routinely collected ICU data can predict impending vasopressor initiation with clinically interpretable outputs. However, these findings reflect internal validation only and should be interpreted with caution. External validation on multi-center retrospective cohorts, followed by silent-mode prospective evaluation, is warranted to confirm generalisability and to assess the real-world impact on time-to-vasopressor, fluid balance, and patient outcomes.

Indexed as

Electronic Health RecordsIntensive Care UnitsMachine LearningSepsisVasoconstrictor AgentsAgedFemaleHumansMaleMiddle AgedRetrospective StudiesVasoconstrictor AgentsElectronic Health Records (EHR)Intensive care unit (ICU)Machine-learningSepsisVasopressor initiation

Identifiers

PMID41398250
PMCPMC12706921

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.