Evidence map›Paper›PMID 38109888›Full record

ArticleJournal of the American Medical Informatics Association : JAMIA2024

Data-driven automated classification algorithms for acute health conditions: applying PheNorm to COVID-19 disease.

Joshua C Smith, Brian D Williamson, David J Cronkite, Daniel Park, Jill M Whitaker, Michael F McLemore, Joshua T Osmanski, Robert Winter, Arvind Ramaprasan, Ann Kelley and 8 more

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Medical Informatics Association : JAMIA, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-weighted citation impact, top 12% of its field
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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. A general framework for developing computable clinical phenotype algorithms.Journal of the American Medical Informatics Association : JAMIA · 2024
    Article
  5. Article
  6. Celebrating Eta Berner and her influence on biomedical and health informatics.Journal of the American Medical Informatics Association : JAMIA · 2024
    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

18 authors at 6 institutions in 1 country.

Joshua C SmithDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN 37203, United States.
Brian D WilliamsonKaiser Permanente Washington Health Research Institute, Seattle, WA 98101, United States.
David J CronkiteKaiser Permanente Washington Health Research Institute, Seattle, WA 98101, United States.
Daniel ParkDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN 37203, United States.
Jill M WhitakerDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN 37203, United States.
Michael F McLemoreDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN 37203, United States.
Joshua T OsmanskiDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN 37203, United States.
Robert WinterDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN 37203, United States.
Arvind RamaprasanKaiser Permanente Washington Health Research Institute, Seattle, WA 98101, United States.
Ann KelleyKaiser Permanente Washington Health Research Institute, Seattle, WA 98101, United States.
Mary SheaKaiser Permanente Washington Health Research Institute, Seattle, WA 98101, United States.
Saranrat WittayanukornCenter for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, MD 20903, United States.
Danijela StojanovicCenter for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, MD 20903, United States.
Yueqin ZhaoCenter for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, MD 20903, United States.
Sengwee TohHarvard Pilgrim Health Care Institute, Boston, MA 02215, United States.
Kevin B JohnsonDepartment of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia, PA 19104, United States.
David M AronoffDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN 46202, United States.
David S CarrellKaiser Permanente Washington Health Research Institute, Seattle, WA 98101, United States.ORCID 0000-0002-8471-0928
Kaiser Permanente Washington Health Research Institute · USVanderbilt University Medical Center · USUnited States Food and Drug Administration · USHarvard Pilgrim Health Care · USIndiana University School of MedicineUniversity of Pennsylvania · US

Funding

Vanderbilt Institute for Clinical and Translational Research (VICTR) -Identifying correlates of functional immunity in SARS-CoV-2 convalescent plasmaUL1TR002243 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Paul A. Harris, Wesley H Self · 2017 to 2026
$130.7M
FDA HHSNCATS NIH HHS UL1 TR002243NIH HHS
6 · The paper itself

Abstract

objectivesAutomated phenotyping algorithms can reduce development time and operator dependence compared to manually developed algorithms. One such approach, PheNorm, has performed well for identifying chronic health conditions, but its performance for acute conditions is largely unknown. Herein, we implement and evaluate PheNorm applied to symptomatic COVID-19 disease to investigate its potential feasibility for rapid phenotyping of acute health conditions. MATERIALS AND

methodsPheNorm is a general-purpose automated approach to creating computable phenotype algorithms based on natural language processing, machine learning, and (low cost) silver-standard training labels. We applied PheNorm to cohorts of potential COVID-19 patients from 2 institutions and used gold-standard manual chart review data to investigate the impact on performance of alternative feature engineering options and implementing externally trained models without local retraining.

resultsModels at each institution achieved AUC, sensitivity, and positive predictive value of 0.853, 0.879, 0.851 and 0.804, 0.976, and 0.885, respectively, at quantiles of model-predicted risk that maximize F1. We report performance metrics for all combinations of silver labels, feature engineering options, and models trained internally versus externally. DISCUSSION: Phenotyping algorithms developed using PheNorm performed well at both institutions. Performance varied with different silver-standard labels and feature engineering options. Models developed locally at one site also worked well when implemented externally at the other site.

conclusionPheNorm models successfully identified an acute health condition, symptomatic COVID-19. The simplicity of the PheNorm approach allows it to be applied at multiple study sites with substantially reduced overhead compared to traditional approaches.

Indexed as

AlgorithmsCOVID-19Electronic Health RecordsHumansMachine LearningNatural Language ProcessingCOVID-19electronic health recordsmachine learningnatural language processingphenotyping

Identifiers

PMID38109888
PMCPMC10873852
OpenAlexW4389903773

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.