Evidence map›Paper›PMID 40916049›Full record

ReviewDiagnostic and prognostic research2025

Predicting venous thromboembolism among hospitalized adults: a protocol for development and validation of an implementable real-time prognostic model.

Henry J Domenico, Benjamin F Tillman, Shari L Just, Yeji Ko, Amanda S Mixon, Asli Weitkamp, Jonathan S Schildcrout, Colin Walsh, Thomas Ortel, Benjamin French

Abstract readReview
In one paragraph

Review 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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Henry J DomenicoDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, USA. henry.domenico@vumc.org.
Benjamin F TillmanDivision of Hematology and Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Shari L JustKnowledge Engineering, Health IT, Vanderbilt University Medical Center, Nashville, TN, USA.
Yeji KoDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, USA.
Amanda S MixonGeriatric Research, Education and Clinical Center, VA Tennessee Valley Healthcare System, Nashville, TN, USA.
Asli WeitkampDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, United States.
Jonathan S SchildcroutDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, USA.
Colin WalshDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, United States.
Thomas OrtelDepartment of Medicine, Duke University School of Medicine, Durham, NC, USA.
Benjamin FrenchDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, USA.

Funding

Optimizing the implementation of personalized risk-prediction models for venous thromboembolism among hospitalized adultsR01HL164482 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BENJAMIN FRENCH, Amanda Salanitro Mixon · 2023 to 2026
$2.8M
NHLBI NIH HHS R01 HL164482NHLBI NIH HHS R01-HL164482
6 · The paper itself

Abstract

backgroundHospital-acquired venous thromboembolism (HA-VTE) is a leading cause of morbidity and mortality among hospitalized adults. Numerous prognostic models have been developed to identify those patients with elevated risk of HA-VTE. None, however, has met the necessary criteria to guide clinical decision-making. This study outlines a protocol for refining and validating a general-purpose prognostic model for HA-VTE, designed for real-time automation within the electronic health record (EHR) system.

methodsA retrospective cohort of 132,561 inpatient encounters (89,586 individual patients) at a large academic medical center will be collected, along with clinical and demographic data available as part of routine care. Data for temporal, geographic, and domain external validation cohorts will also be collected. Logistic regression will be used to predict occurrence of HA-VTE during an inpatient encounter. Variables considered for model inclusion will be based on prior demonstrated association with HA-VTE and their availability in both retrospective EHR data and routine clinical care. Least absolute shrinkage and selection operator (LASSO) with tenfold cross-validation will be used for initial variable selection. Variables selected by the LASSO procedure, along with those deemed necessary by clinicians, will be used in an unpenalized multivariable logistic regression model. Discrimination and calibration will be reported for the derivation and validation cohorts. Discrimination will be measured using Harrell's C statistic. Calibration will be measured using calibration intercept, calibration slope, Brier score, integrated calibration index, and visual examination of non-linear calibration curve. Model reporting will adhere to the Transparent Reporting of a multivariable prediction model for Individual Prognosis Or Diagnosis guidelines for clinical prediction models using machine learning methods (TRIPOD + AI). DISCUSSION: We describe methods for developing, evaluating, and validating a prognostic model for HA-VTE using routinely collected EHR data. By combining best practices in statistical development and validation, knowledge engineering, and clinical domain knowledge, the resulting model should be well suited for real-time clinical implementation. Although this protocol describes our development of a model for HA-VTE, the general approach can be applied to other clinical outcomes.

Indexed as

Clinical prediction modelElectronic health recordExternal validationModel developmentVenous thromboembolism

Identifiers

PMID40916049
PMCPMC12416065

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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.