Evidence map›Paper›PMID 42505870›Full record

ArticleJournal of cardiovascular development and disease2026

From Minor Monitoring to Major Insight: Predicting AF Development in the Congenital Heart Disease Population.

Can Zhang, Lixia Dai, Annemien E van den Bosch, Vehpi Yildirim, Mathijs S van Schie, Yannick J H J Taverne, Natasja M S de Groot

Abstract read
In one paragraph

Article in Journal of cardiovascular development and disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

7 authors.

Can ZhangDepartment of Cardiology, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.ORCID 0000-0001-9638-5344
Lixia DaiDepartment of Cardiology, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.ORCID 0009-0000-3132-9376
Annemien E van den BoschDepartment of Cardiology, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.ORCID 0000-0002-0422-9860
Vehpi YildirimDepartment of Cardiology, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.ORCID 0000-0003-3837-4756
Mathijs S van SchieDepartment of Cardiology, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.ORCID 0000-0001-6695-5465
Yannick J H J TaverneDepartment of Cardiothoracic Surgery, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.
Natasja M S de GrootDepartment of Cardiology, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.ORCID 0000-0002-0259-6691

Funding

CIRCULAR NWA.1389.20.157Dutch Heart Foundation 0-005-2025-0146
6 · The paper itself

Abstract

backgroundThe prognostic value of electrocardiography (ECG)- and continuous rhythm monitoring (CRM)-derived markers for predicting atrial fibrillation (AF) onset and progression remains unclear in patients with congenital heart disease (CHD).

methodsWe retrospectively analyzed 573 CHD patients who underwent 24 h Holter monitoring between 2003 and 2015. Baseline ECG and CRM parameters were assessed. Cox regression identified predictors of new-onset AF and AF progression, and interaction analyses explored effect modification by left atrial (LA) dilatation.

resultsDuring 13 ± 5 years of follow-up, AF occurred in 107 patients (18.7%), of whom 32 (29.9%) progressed to persistent/permanent AF (PeAF). Patients with AF more frequently had prolonged PR and QTc intervals and higher atrial ectopy (AE) and ventricular ectopy burdens. Independent predictors of new-onset AF were older age, LA dilatation, higher AE burden, atrial tachycardia, and pacemaker implantation. AF progression was independently associated with older age, LA dilatation, higher AE burden, and prolonged PR interval. AE burden showed a stronger association with AF risk in patients without LA dilatation.

conclusionsIn CHD patients, baseline ECG PR-intervals and CRM-derived AE burden independently predict AF onset and/or progression. These noninvasive markers may improve risk stratification and support earlier personalized rhythm management.

Indexed as

atrial fibrillationcongenital heart diseaseectopic beatselectrocardiographyHolter monitoringPR intervalQTc interval

Identifiers

PMID42505870
PMCPMC13409886

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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.