Evidence map›Paper›PMID 39269694›Full record

ArticleJAMA health forum2024

A Machine Learning Method for Allocating Scarce COVID-19 Monoclonal Antibodies.

Mengli Xiao, Kyle C Molina, Neil R Aggarwal, Laurel E Beaty, Tellen D Bennett, Nichole E Carlson, Lindsey E Fish, Mika K Hamer, Bethany M Kwan, David A Mayer and 3 more

Abstract readEvaluation Study
In one paragraph

Article in JAMA health forum, 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. Article
  2. Review
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

13 authors.

Mengli XiaoDepartment of Biostatistics and Informatics, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora.
Kyle C MolinaDepartment of Emergency Medicine, University of Colorado School of Medicine, Aurora.
Neil R AggarwalDivision of Pulmonary Sciences, Department of Medicine, University of Colorado School of Medicine, Aurora.
Laurel E BeatyDepartment of Biostatistics and Informatics, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora.
Tellen D BennettDepartment of Informatics and Data Science, University of Colorado School of Medicine, Aurora.
Nichole E CarlsonDepartment of Biostatistics and Informatics, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora.
Lindsey E FishDivision of General Internal Medicine, Denver Health, Denver, Colorado.
Mika K HamerCenter for Bioethics and Humanities, University of Colorado Anschutz Medical Campus, Aurora.
Bethany M KwanDepartment of Emergency Medicine, University of Colorado School of Medicine, Aurora.
David A MayerDepartment of Biostatistics and Informatics, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora.
Jennifer L PeersDepartment of Emergency Medicine, University of Colorado School of Medicine, Aurora.
Matthew K WyniaCenter for Bioethics and Humanities, University of Colorado Anschutz Medical Campus, Aurora.
Adit A GindeDepartment of Emergency Medicine, University of Colorado School of Medicine, Aurora.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: During the COVID-19 pandemic, the effective distribution of limited treatments became a crucial policy goal. Yet, limited research exists using electronic health record data and machine learning techniques, such as policy learning trees (PLTs), to optimize the distribution of scarce therapeutics. Objective: To evaluate whether a machine learning PLT-based method of scarce resource allocation optimizes the treatment benefit of COVID-19 neutralizing monoclonal antibodies (mAbs) during periods of resource constraint. Design, Setting, and Participants: This retrospective cohort study used electronic health record data from October 1, 2021, to December 11, 2021, for the training cohort and data from June 1, 2021, to October 1, 2021, for the testing cohort. The cohorts included patients who had positive test results for SARS-CoV-2 and qualified for COVID-19 mAb therapy based on the US Food and Drug Administration's emergency use authorization criteria, ascertained from the patient electronic health record. Only some of the qualifying candidates received treatment with mAbs. Data were analyzed between from January 2023 to May 2024. Main Outcomes and Measures: The primary outcome was overall expected hospitalization, assessed as the potential reduction in overall expected hospitalization if the PLT-based allocation system was used. This was compared to observed allocation using risk differences. Results: Among 9542 eligible patients in the training cohort (5418 female [56.8%]; age distribution: 18-44 years, 4151 [43.5%]; 45-64 years, 3146 [33.0%]; and ≥65 years, 2245 [23.5%]), a total of 3862 (40.5%) received mAbs. Among 6248 eligible patients in the testing cohort (3416 female [54.7%]; age distribution: 18-44 years, 2827 [45.2%]; 45-64 years, 1927 [30.8%]; and ≥65 years, 1494 [23.9%]), a total of 1329 (21.3%) received mAbs. Treatment allocation using the trained PLT model led to an estimated 1.6% reduction (95% CI, -2.0% to -1.2%) in overall expected hospitalization compared to observed treatment allocation in the testing cohort. The visual assessment showed that the PLT-based point system had a larger reduction in 28-day hospitalization compared with the Monoclonal Antibody Screening Score (maximum overall hospitalization difference, -1.0% [95% CI, -1.3% to -0.7%]) in the testing cohort. Conclusions and Relevance: This retrospective cohort study proposes and tests a PLT method, which can be linked to a electronic health record data platform to improve real-time allocation of scarce treatments. Use of this PLT-based allocation method would have likely resulted in fewer hospitalizations across a population than were observed in usual care, with greater expected reductions than a commonly used point system.

Indexed as

Antibodies, MonoclonalAntibodies, ViralCOVID-19COVID-19 Drug TreatmentHealth Care RationingMachine LearningAdolescentAdultAgedElectronic Health RecordsEmergency Use AuthorizationFemaleHealth PolicyHospitalizationHumansMaleAntibodies, MonoclonalAntibodies, Viral

Identifiers

PMID39269694
PMCPMC11400220

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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.