Evidence map›Paper›PMID 39831110›Full record

ArticleJCO clinical cancer informatics2024

Bias in Prediction Models to Identify Patients With Colorectal Cancer at High Risk for Readmission After Resection.

Mary M Lucas, Mario Schootman, Jonathan A Laryea, Sonia T Orcutt, Chenghui Li, Jun Ying, Jennifer A Rumpel, Christopher C Yang

Abstract read
In one paragraph

Article in JCO clinical cancer informatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

8 authors.

Mary M LucasCollege of Computing and Informatics, Drexel University, Philadelphia, PA.
Mario SchootmanDivision of Community Health and Research, Department of Internal Medicine, College of Medicine, the University of Arkansas for Medical Sciences, Springdale, AR.
Jonathan A LaryeaWinthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, AR.
Sonia T OrcuttWinthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, AR.
Chenghui LiWinthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, AR.
Jun YingDepartment of Biostatistics, Fay W. Boozman College of Public Health, University of Arkansas for Medical Sciences, Little Rock, AR.
Jennifer A RumpelDepartment of Pediatrics, College of Medicine, the University of Arkansas for Medical Sciences, Little Rock, AR.
Christopher C YangCollege of Computing and Informatics, Drexel University, Philadelphia, PA.

Funding

Expanding Translational Research in ArkansasUL1TR003107 · NCATS · UNIV OF ARKANSAS FOR MED SCIS · PI JAMES, LAURA P · 2019 to 2023
$21.6M
NCATS NIH HHS UL1 TR003107
6 · The paper itself

Abstract

purposeMachine learning algorithms are used for predictive modeling in medicine, but studies often do not evaluate or report on the potential biases of the models. Our purpose was to develop clinical prediction models for readmission after surgery in colorectal cancer (CRC) patients and to examine their potential for racial bias.

methodsWe used the 2012-2020 American College of Surgeons' National Surgical Quality Improvement Program (ACS-NSQIP) Participant Use File and Targeted Colectomy File. Patients were categorized into four race groups - White, Black or African American, Other, and Unknown/Not Reported. Potential predictive features were identified from studies of risk factors of 30-day readmission in CRC patients. We compared four machine learning-based methods - logistic regression (LR), multilayer perceptron (MLP), random forest (RF), and XGBoost (XGB). Model bias was assessed using false negative rate (FNR) difference, false positive rate (FPR) difference, and disparate impact.

resultsIn all, 112,077 patients were included, 67.2% of whom were White, 9.2% Black, 5.6% Other race, and 18% with race not recorded. There were significant differences in the AUROC, FPR and FNR between race groups across all models. Notably, patients in the 'Other' race category had higher FNR compared to Black patients in all but the XGB model, while Black patients had higher FPR than White patients in some models. Patients in the 'Other' category consistently had the lowest FPR. Applying the 80% rule for disparate impact, the models consistently met the threshold for unfairness for the 'Other' race category.

conclusionPredictive models for 30-day readmission after colorectal surgery may perform unequally for different race groups, potentially propagating to inequalities in delivery of care and patient outcomes if the predictions from these models are used to direct care.

Indexed as

Black or African AmericanColectomyColorectal NeoplasmsPatient ReadmissionWhiteAgedBiasFemaleHumansMachine LearningMaleMiddle AgedRisk AssessmentRisk Factors

Identifiers

PMID39831110
PMCPMC11741203

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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.