Evidence map›Paper›PMID 37269570›Full record

ArticleEBioMedicine2023

A Bayesian approach to predictive uncertainty in chemotherapy patients at risk of acute care utilization.

Claudio Fanconi, Anne de Hond, Dylan Peterson, Angelo Capodici, Tina Hernandez-Boussard

Abstract read
In one paragraph

Article in EBioMedicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Claudio FanconiDepartment of Information Technology and Electrical Engineering, ETH Zürich, Zürich, Switzerland; Department of Medicine (Biomedical Informatics), Stanford University, Stanford, USA. Electronic address: fanconic@ethz.ch.
Anne de HondDepartment of Medicine (Biomedical Informatics), Stanford University, Stanford, USA; Clinical AI Implementation and Research Lab, Leiden University Medical Centre, Leiden, the Netherlands. Electronic address: a.a.h.de_hond@lumc.nl.
Dylan PetersonDepartment of Medicine (Biomedical Informatics), Stanford University, Stanford, USA. Electronic address: dpeters9@stanford.edu.
Angelo CapodiciDepartment of Medicine (Biomedical Informatics), Stanford University, Stanford, USA; Department of Biomedical and Neuromotor Science, University of Bologna, Bologna, Italy. Electronic address: angelo.capodici@studio.unibo.it.
Tina Hernandez-BoussardDepartment of Medicine (Biomedical Informatics), Stanford University, Stanford, USA. Electronic address: https://twitter.com/Boussard.

Funding

Advancing Knowledge Discovery for Postoperative Pain ManagementR01LM013362 · NLM · STANFORD UNIVERSITY · PI HERNANDEZ-BOUSSARD, TINA · 2019 to 2023
$3.2M
NLM NIH HHS R01 LM013362
6 · The paper itself

Abstract

backgroundMachine learning (ML) predictions are becoming increasingly integrated into medical practice. One commonly used method, ℓ

methodsThis study evaluates the predictive performance of different BLLRs compared to standard logistic LASSO regression, using real-world, high-dimensional, structured electronic health record (EHR) data from cancer patients initiating chemotherapy at a comprehensive cancer centre. Multiple BLLR models were compared against a LASSO model using an 80-20 random split using 10-fold cross-validation to predict the risk of acute care utilization (ACU) after starting chemotherapy.

findingsThis study included 8439 patients. The LASSO model predicted ACU with an area under the receiver operating characteristic curve (AUROC) of 0.806 (95% CI: 0.775-0.834). BLLR with a Horseshoe+ prior and a posterior approximated by Metropolis-Hastings sampling showed similar performance: 0.807 (95% CI: 0.780-0.834) and offers the advantage of uncertainty estimation for each prediction. In addition, BLLR could identify predictions too uncertain to be automatically classified. BLLR uncertainties were stratified by different patient subgroups, demonstrating that predictive uncertainties significantly differ across race, cancer type, and stage.

interpretationBLLRs are a promising yet underutilised tool that increases explainability by providing risk estimates while offering a similar level of performance to standard LASSO-based models. Additionally, these models can identify patient subgroups with higher uncertainty, which can augment clinical decision-making.

fundingThis work was supported in part by the National Library Of Medicine of the National Institutes of Health under Award Number R01LM013362. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Indexed as

Clinical Decision-MakingBayes TheoremHumansLogistic ModelsUncertaintyAcute care utilizationBayesian logistic LASSO regressionChemotherapyPredictive uncertainty

Identifiers

PMID37269570
PMCPMC10250586

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.