Evidence map›Paper›PMID 40691852›Full record

ArticleDiagnostic and prognostic research2025

A comparison of modeling approaches for static and dynamic prediction of central line-associated bloodstream infections using electronic health records (part 2): random forest models.

Elena Albu, Shan Gao, Pieter Stijnen, Frank E Rademakers, Christel Janssens, Veerle Cossey, Yves Debaveye, Laure Wynants, Ben Van Calster

Abstract read
In one paragraph

Article in Diagnostic and prognostic research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Elena AlbuDepartment of Development & Regeneration, KU Leuven, Leuven, Belgium.
Shan GaoDepartment of Development & Regeneration, KU Leuven, Leuven, Belgium.
Pieter StijnenManagement Information Reporting Department, University Hospitals Leuven, Leuven, Belgium.
Frank E RademakersFaculty of Medicine, KU Leuven, Leuven, Belgium.
Christel JanssensVascular Access Specialty Team, University Hospitals Leuven, Leuven, Belgium.
Veerle CosseyDepartment of Development & Regeneration, KU Leuven, Leuven, Belgium.
Yves DebaveyeDepartment of Cellular and Molecular Medicine, University Hospitals Leuven, Leuven, Belgium.
Laure WynantsDepartment of Development & Regeneration, KU Leuven, Leuven, Belgium.
Ben Van CalsterDepartment of Development & Regeneration, KU Leuven, Leuven, Belgium. ben.vancalster@kuleuven.be.

Funding

KU Leuven C24M/20/064
6 · The paper itself

Abstract

objectivePrognostic outcomes related to hospital admissions typically do not suffer from censoring, and can be modeled either categorically or as time-to-event. Competing events are common but often ignored. We compared the performance of static and dynamic random forest (RF) models to predict the risk of central line-associated bloodstream infections (CLABSI) using different outcome operationalizations.

methodsWe included data from 27,478 admissions to the University Hospitals Leuven, covering 30,862 catheter episodes (970 CLABSI, 1466 deaths and 28,426 discharges) to build static and dynamic RF models for binary (CLABSI vs no CLABSI), multinomial (CLABSI, discharge, death or no event), survival (time to CLABSI) and competing risks (time to CLABSI, discharge or death) outcomes to predict the 7-day CLABSI risk. Static models used information at the onset of the catheter episode, while dynamic models updated predictions daily for 30 days (landmark 0-30). We evaluated model performance across 100 train/test splits.

resultsPerformance of binary, multinomial and competing risks models was similar: AUROC was 0.74 for predictions at catheter onset, rose to 0.77 for predictions at landmark 5, and decreased thereafter. Survival models overestimated the risk of CLABSI (E:O ratios between 1.2 and 1.6), and had AUROCs about 0.01 lower than other models. Binary and multinomial models had lowest computation times. Models including multiple outcome events (multinomial and competing risks) display a different internal structure compared to binary and survival models, choosing different variables for early splits in trees. DISCUSSION AND

conclusionIn the absence of censoring, complex modelling choices do not considerably improve the predictive performance compared to a binary model for CLABSI prediction in our studied settings. Survival models censoring the competing events at their time of occurrence should be avoided.

Indexed as

CLABSICompeting risksDynamic predictionEHRRandom forestsSurvival

Identifiers

PMID40691852
PMCPMC12278561

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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.