Evidence map›Paper›PMID 41169969›Full record

ArticleHeart rhythm O22025

Leveraging artificial intelligence for risk stratification of inherited cardiomyopathies in under-resourced settings.

Salah H Alahwany, Omnia Kamel, Amir Abdelghany, Ahmed Ammar

Abstract read
In one paragraph

Article in Heart rhythm O2, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

4 authors.

Salah H AlahwanyArrhythmogenic Cardiomyopathy Program, Vanderbilt Heart and Vascular Institute, Nashville, Tennessee.
Omnia KamelCardiology Department, Aswan Heart Center, Aswan, Egypt.
Amir AbdelghanyCardiology Department, King Abdullah Medical Complex, Jeddah, Saudi Arabia.
Ahmed AmmarCardiology Department, Ain Shams University, Cairo, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inherited cardiomyopathies are a significant global cause of sudden cardiac death, particularly among younger individuals and those in under-resourced regions. Despite progress in diagnostics and therapeutics, screening and risk stratification remain challenging due to genetic complexity, variable clinical presentation, and the interpretive limitations of current electrophysiological and imaging tools. Artificial intelligence (AI)-particularly machine learning, deep learning, and natural language processing offers transformative potential by enabling large-scale analysis of complex data and detecting subtle disease patterns which could potentially improve diagnostic accuracy and cost-effectiveness, particularly in low-resource environments. This review evaluates the limitations of existing risk models, synthesizes disease-specific AI applications within a unified framework, and explores the role of AI in advancing personalized care and risk prediction in underserved populations.

Indexed as

Artificial intelligenceDeep learningDeveloping countriesInherited cardiomyopathyMachine learningRisk stratificationSudden cardiac deathUnder-resourced settingsVentricular arrhythmias

Identifiers

PMID41169969
PMCPMC12570201

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.