Evidence map›Paper›PMID 40853721›Full record

ArticlePacing and clinical electrophysiology : PACE2025

The Impact of the Spatial Distribution of Ventricular Extrasystoles on Implantable Cardioverter-Defibrillator Recipients.

Carlos Arthur Hansel Diniz da Costa, Gabriela Menichelli Medeiros Coelho, Rhanniel Theodorus Helhyas Oliveira Shilva Gomes Villar, Gabriela Rodrigues de Oliveira, Pedro Henrique Correia Filgueiras, Enia Lucia Coutinho, Claudio Cirenza, Angelo Amato Vincenzo de Paola

Abstract read
In one paragraph

Article in Pacing and clinical electrophysiology : PACE, 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

8 authors.

Carlos Arthur Hansel Diniz da CostaFederal University of São Paulo, São Paulo, São Paulo, Brazil.ORCID 0009-0008-7253-2635
Gabriela Menichelli Medeiros CoelhoFederal University of São Paulo, São Paulo, São Paulo, Brazil.
Rhanniel Theodorus Helhyas Oliveira Shilva Gomes VillarFederal University of São Paulo, São Paulo, São Paulo, Brazil.
Gabriela Rodrigues de OliveiraFederal University of São Paulo, São Paulo, São Paulo, Brazil.
Pedro Henrique Correia FilgueirasFederal University of São Paulo, São Paulo, São Paulo, Brazil.
Enia Lucia CoutinhoFederal University of São Paulo, São Paulo, São Paulo, Brazil.
Claudio CirenzaFederal University of São Paulo, São Paulo, São Paulo, Brazil.
Angelo Amato Vincenzo de PaolaFederal University of São Paulo, São Paulo, São Paulo, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPremature ventricular complexes (PVC) are a common phenomenon observed in both normal and pathological heart conditions. However, they do not always behave in the same way. Different PVCs present with varying QRS morphologies, mechanisms, and origin sites. These differences may imply distinct prognoses. To date, the impact of the three-dimensional distribution of PVCs across the heart on the prognosis of ICD recipients has not been adequately investigated. MATERIAL AND

methodsWe conducted an ambidirectional cohort study. Patients underwent two twelve-lead ambulatory ECG recordings during follow-up. The spatial distribution of PVCs was analyzed using the algorithm proposed by Kuchar et al. The impact of this spatial distribution on clinical variables was assessed using mixed generalized models.

resultsFifty-five patients were enrolled, with a mean follow-up time of 41.12 ± 13.48 months. All patients underwent two 12-lead ambulatory ECG recordings. The median PVC count was 91.5. PVCs were classified according to the algorithm proposed by Kuchar et al. PVCs arising from exit sites located in the intermediate left ventricle were associated with a higher number of therapies (odds ratio [OR]: 4.78; 95% confidence interval [CI], 1.19-19.26; p = 0.028) and prolonged QRS duration. PVCs with exit sites located in the septal region were associated with higher NYHA functional classes (OR: 2.22 [95% CI: 1.08-4.44]; p = 0.030). No statistically significant interaction was found between PVC topography and gender, number of ATP episodes, ATP success rate, or number of shock episodes.

conclusionThe spatial distribution of PVCs influenced the prognosis of ICD recipients.

Indexed as

Defibrillators, ImplantableVentricular Premature ComplexesAgedAlgorithmsCohort StudiesElectrocardiography, AmbulatoryFemaleHumansMaleMiddle AgedPrognosiscardiomyopathiescohort studyimplantable cardioverter‐defibrillatorpremature ventricular complexesprognosis

Identifiers

PMID40853721
PMCPMC12504925

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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.