Evidence map›Paper›PMID 38989042›Full record

ArticleCardiovascular digital health journal2024

Feasibility of remote monitoring for fatal coronary heart disease using Apple Watch ECGs.

Liam Butler, Alexander Ivanov, Turgay Celik, Ibrahim Karabayir, Lokesh Chinthala, Melissa M Hudson, Kiri K Ness, Daniel A Mulrooney, Stephanie B Dixon, Mohammad S Tootooni and 6 more

Abstract read
In one paragraph

Article in Cardiovascular digital health journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. ECG Sex Index in children and adolescents.European heart journal. Digital health · 2026
    Article
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  4. Article
  5. Review
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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

16 authors.

Liam ButlerCardiovascular Section, Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
Alexander IvanovCardiovascular Section, Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
Turgay CelikCardiovascular Section, Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
Ibrahim KarabayirCardiovascular Section, Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
Lokesh ChinthalaCenter for Biomedical Informatics, University of Tennessee Health Sciences Center, Memphis, Tennessee.
Melissa M HudsonSt Jude Children's Research Hospital, Memphis, Tennessee.
Kiri K NessSt Jude Children's Research Hospital, Memphis, Tennessee.
Daniel A MulrooneySt Jude Children's Research Hospital, Memphis, Tennessee.
Stephanie B DixonSt Jude Children's Research Hospital, Memphis, Tennessee.
Mohammad S TootooniHealth Informatics and Data Science, Loyola University Chicago, Maywood, Illinois.
Adam J DoerrDepartment of Medicine, University of Massachusetts Chan Medical School, Massachusetts, Worcester, Massachusetts.
Byron C JaegerDivision of Public Health Science, Department of Biostatistics and Data Science, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
Robert L DavisCenter for Biomedical Informatics, University of Tennessee Health Sciences Center, Memphis, Tennessee.
David D McManusDepartment of Medicine, University of Massachusetts Chan Medical School, Massachusetts, Worcester, Massachusetts.
David HerringtonCardiovascular Section, Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
Oguz AkbilgicCardiovascular Section, Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina.

Funding

The St. Jude Lifetime CohortU01CA195547 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI HUDSON, MELISSA M, NESS, KIRSTEN KIMBERLIE · 2015 to 2024
$14.9M
Early Identification of Childhood Cancer Survivors at High Risk for Late Onset Cardiomyopathy: An Artificial Intelligence Approach utilizing ElectrocardiographyR01CA261834 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI AKBILGIC, OGUZ, HUDSON, MELISSA M · 2022 to 2025
$2.1M
NCI NIH HHS R01 CA261834NCI NIH HHS U01 CA195547
6 · The paper itself

Abstract

Background: Fatal coronary heart disease (FCHD) is often described as sudden cardiac death (affects >4 million people/year), where coronary artery disease is the only identified condition. Electrocardiographic artificial intelligence (ECG-AI) models for FCHD risk prediction using ECG data from wearable devices could enable wider screening/monitoring efforts. Objectives: To develop a single-lead ECG-based deep learning model for FCHD risk prediction and assess concordance between clinical and Apple Watch ECGs. Methods: An FCHD single-lead ("lead I" from 12-lead ECGs) ECG-AI model was developed using 167,662 ECGs (50,132 patients) from the University of Tennessee Health Sciences Center. Eighty percent of the data (5-fold cross-validation) was used for training and 20% as a holdout. Cox proportional hazards (CPH) models incorporating ECG-AI predictions with age, sex, and race were also developed. The models were tested on paired clinical single-lead and Apple Watch ECGs from 243 St. Jude Lifetime Cohort Study participants. The correlation and concordance of the predictions were assessed using Pearson correlation (R), Spearman correlation (ρ), and Cohen's kappa. Results: The ECG-AI and CPH models resulted in AUC = 0.76 and 0.79, respectively, on the 20% holdout and AUC = 0.85 and 0.87 on the Atrium Health Wake Forest Baptist external validation data. There was moderate-strong positive correlation between predictions (R = 0.74, ρ = 0.67, and κ = 0.58) when tested on the 243 paired ECGs. The clinical (lead I) and Apple Watch predictions led to the same low/high-risk FCHD classification for 99% of the participants. CPH prediction correlation resulted in an R = 0.81, ρ = 0.76, and κ = 0.78. Conclusion: Risk of FCHD can be predicted from single-lead ECGs obtained from wearable devices and are statistically concordant with lead I of a 12-lead ECG.

Indexed as

Apple WatchArtificial intelligenceConcordanceECG-AIFatal coronary heart diseaseRisk prediction

Identifiers

PMID38989042
PMCPMC11232422

What OpenQuestion holds

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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.