Evidence map›Paper›PMID 37042261›Full record

ArticleJournal of the American Heart Association2023

Ventricular Conduction Stability Noninvasively Identifies an Arrhythmic Substrate in Survivors of Idiopathic Ventricular Fibrillation.

Ji-Jian Chow, Kevin M W Leong, Matthew J Shun-Shin, Julian O M Ormerod, Michael Koa-Wing, David C Lefroy, Phang Boon Lim, Nicholas W F Linton, Fu Siong Ng, Norman A Qureshi and 5 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2023. 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, top 91% of its field
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, 0 citations in OpenAlex.

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

15 authors at 2 institutions in 1 country.

Ji-Jian ChowNational Heart and Lung Institute Hammersmith Hospital London United Kingdom.ORCID 0000-0003-2454-7644
Kevin M W LeongNational Heart and Lung Institute Hammersmith Hospital London United Kingdom.ORCID 0000-0003-3208-2592
Matthew J Shun-ShinNational Heart and Lung Institute Hammersmith Hospital London United Kingdom.ORCID 0000-0002-1179-0867
Julian O M OrmerodOxford University Hospitals National Health Service Trust Oxford United Kingdom.ORCID 0000-0003-1612-8992
Michael Koa-WingNational Heart and Lung Institute Hammersmith Hospital London United Kingdom.
David C LefroyNational Heart and Lung Institute Hammersmith Hospital London United Kingdom.
Phang Boon LimNational Heart and Lung Institute Hammersmith Hospital London United Kingdom.
Nicholas W F LintonNational Heart and Lung Institute Hammersmith Hospital London United Kingdom.ORCID 0000-0002-5712-849X
Fu Siong NgNational Heart and Lung Institute Hammersmith Hospital London United Kingdom.ORCID 0000-0002-8681-4368
Norman A QureshiNational Heart and Lung Institute Hammersmith Hospital London United Kingdom.
Zachary I WhinnettNational Heart and Lung Institute Hammersmith Hospital London United Kingdom.ORCID 0000-0002-2775-5126
Nicholas S PetersNational Heart and Lung Institute Hammersmith Hospital London United Kingdom.ORCID 0000-0002-3581-8078
Darrel P FrancisNational Heart and Lung Institute Hammersmith Hospital London United Kingdom.ORCID 0000-0002-3410-0814
Amanda M VarnavaNational Heart and Lung Institute Hammersmith Hospital London United Kingdom.ORCID 0000-0003-0651-0303
Prapa KanagaratnamNational Heart and Lung Institute Hammersmith Hospital London United Kingdom.ORCID 0000-0003-3593-2185
Hammersmith Hospital · GBNational Health Service · GB

Funding

British Heart Foundation PG/15/20/31339
6 · The paper itself

Abstract

Background Idiopathic ventricular fibrillation (VF) is a diagnosis of exclusion following normal cardiac investigations. We sought to determine if exercise-induced changes in electrical substrate could distinguish patient groups with various ventricular arrhythmic pathophysiological conditions and identify patients susceptible to VF. Methods and Results Computed tomography and exercise testing in patients wearing a 252-electrode vest were combined to determine ventricular conduction stability between rest and peak exercise, as previously described. Using ventricular conduction stability, conduction heterogeneity in idiopathic VF survivors (n=14) was compared with those surviving VF during acute ischemia with preserved ventricular function following full revascularization (n=10), patients with benign ventricular ectopy (n=11), and patients with normal hearts, no arrhythmic history, and negative Ajmaline challenge during Brugada family screening (Brugada syndrome relatives; n=11). Activation patterns in normal subjects (Brugada syndrome relatives) are preserved following exercise, with mean ventricular conduction stability of 99.2±0.9%. Increased heterogeneity of activation occurred in the idiopathic VF survivors (ventricular conduction stability: 96.9±2.3%) compared with the other groups combined (versus 98.8±1.6%;

Indexed as

Brugada SyndromeVentricular Premature ComplexesElectrocardiographyHeart Conduction SystemHumansSurvivorsVentricular Fibrillationexercise testingidiopathic ventricular fibrillationmyocardial ischemiapremature ventricular complex

Identifiers

PMID37042261
PMCPMC10227238
OpenAlexW4365135498

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.