Evidence map›Paper›PMID 42774611›Full record

ArticleHeart rhythm O22026

Automatic measurement of short-term variability of repolarization on human intracardiac electrograms predicts VT/VF events.

Alfonso Aranda Hernández, Mathias Meine, Marc Vos

Abstract read
In one paragraph

Article in Heart rhythm O2, 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

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Alfonso Aranda HernándezCardiac Rhythm Management, Medtronic, Mounds View, Minnesota.
Mathias MeineDepartment of Cardiology, University Medical Center Utrecht, Utrecht, The Netherlands.
Marc VosDepartment of Medical Physiology, University Medical Center Utrecht, Utrecht, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Implantable cardioverter-defibrillators (ICDs) have proven highly effective in reducing sudden cardiac death by terminating life-threatening arrhythmias. However, their reactive nature underscores the need for preventive strategies to further improve patient outcomes. Short-term variability (STV) of repolarization has emerged as a promising predictive marker for ventricular arrhythmias. Despite its potential, the feasibility of implementing STV monitoring in real-world ICD settings remains uncertain owing to challenges such as noise, abnormal depolarizations, and device-specific constraints. Objective: This study aimed to evaluate the feasibility of STV monitoring in clinical practice using anonymized electrogram recordings from Medtronic Cobalt/Crome ICD and cardiac resynchronization therapy defibrillator devices. Methods: The dataset includes 636 monomorphic ventricular tachycardia episodes, 107 ventricular fibrillation events, and 6000 baseline recordings. Cardiac beats with abnormal repolarization patterns or noise were excluded to ensure reliable STV estimation. STV values were then compared within individuals (baseline vs arrhythmic events) and across groups (patients with and without arrhythmic events). Results: STV values were significantly elevated before arrhythmic events compared with baseline 5.8 ms (interquartile range, 3.3-7.6) vs 4.3 ms (interquartile range, 2.8-7.6) ( Conclusion: This study supports the role of STV as a marker for arrhythmic risk, evidenced by significant elevations in STV preceding arrhythmic events. It also emphasizes the importance of signal preprocessing to mitigate confounding factors and enhance the predictive accuracy of the STV parameter.

Indexed as

ElectrogramImplantable cardioverter-defibrillatorRepolarizationShort-term variabilityVentricular arrhythmia

Identifiers

PMID42774611
PMCPMC13594440

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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.