Evidence map›Paper›PMID 41324735›Full record

ArticleAnnals of biomedical engineering2026

Machine Learning Localization of Early Right Ventricular Activation Sites Using QRS Integral Features.

Avery Seagren, Daniel Lancini, Zixuan Ni, John L Sapp, Amir AbdelWahab, Shijie Zhou

Abstract read
PubMed Publisher
In one paragraph

Article in Annals of biomedical engineering, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Avery SeagrenThe Department of Chemical, Paper, and Biomedical Engineering, Miami University, Oxford, OH, 45056, USA.
Daniel LanciniSt Vincent's Private Hospital Northside, Chermside, QLD, Australia.
Zixuan NiThe Department of Chemical, Paper, and Biomedical Engineering, Miami University, Oxford, OH, 45056, USA.
John L SappCardiology Division, Department of Medicine, Queen Elizabeth II Health Sciences Centre, Halifax, Canada.
Amir AbdelWahabCardiology Division, Department of Medicine, Queen Elizabeth II Health Sciences Centre, Halifax, Canada.
Shijie ZhouThe Department of Chemical, Paper, and Biomedical Engineering, Miami University, Oxford, OH, 45056, USA. szhou12@wpi.edu.ORCID http://orcid.org/0000-0002-6082-8921

Funding

Development of an automatic real-time personalized non-invasive localization of the site of origin of the earliest ventricular activationR15HL167222 · NHLBI · WORCESTER POLYTECHNIC INSTITUTE · PI ZHOU, SHIJIE · 2023 to 2025
$496k
American Heart Association 25CDA1436927NHLBI NIH HHS R15HL167222
6 · The paper itself

Abstract

backgroundAccurate non-invasive localization of right ventricular (RV) arrhythmia origins remains a challenge in electrophysiology. This study investigates the feasibility of using machine learning models based on 12-lead ECG QRS integrals to localize early RV activation sites.

methodsA generic RV mesh was constructed from a CT scan, consisting of 277 triangular elements. Two cohorts were used: a development cohort with 8 patients and 227 known pacing sites, and a validation cohort with 3 patients and 34 pacing sites. Each pacing site was assigned to the centroid of a mesh element. QRS integrals (∫QRS) were computed from eight ECG leads and used as input features for support vector regression (SVR) models with radial basis function (RBF) and linear kernels. ∫QRS values were trimmed over varying durations (30-160 ms in 10 ms increments) to identify the optimal QRS integration window through bootstrapped cross-validation. Localization accuracy was assessed using Euclidean distance, RMSE, and R2 across both cohorts.

resultsThe RBF SVR trained on the initial 60 ms QRS interval yielded the lowest mean localization error - 9.5 mm in the development set and 14.4 mm in the independent test set. In contrast, the linear SVR yielded a mean localization error of 16.6 mm on the development set and 17.0 mm on the independent test set, with more stable performance across QRS durations. Axis-specific analysis revealed superior predictive accuracy along the y- and z-axes, while the x-axis-corresponding to the septal-free wall direction-showed reduced performance. In a validation cohort (n = 34), the mean localization errors were similar between kernels, and the difference was not statistically significant (p = 0.31).

conclusionQRS-integral-based SVR models enable millimeter-scale localization of RV pacing sites from surface ECGs. While nonlinear models provide greater accuracy in anatomically complex regions, linear models offer robustness and simplicity. These findings support the clinical potential of ECG-driven machine learning for guiding RV arrhythmia localization and complementing traditional mapping approaches.

Indexed as

Arrhythmias, CardiacElectrocardiographyHeart VentriclesMachine LearningAgedFemaleHumansMaleMiddle AgedSupport Vector MachineCatheter ablationPace-mappingQRS integralRight ventricleSupport vector machine regressionVA origin localization

Identifiers

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.