Evidence map›Paper›PMID 39945713›Full record

ArticleJACC. Clinical electrophysiology2025

Burden of Premature Ventricular Complexes and Risk of Cardiomyopathy: A Cross-Sectional Study.

Sarah Slaven, Lohit Garg, Rafay Sabzwari, Christopher Barrett, Alexis Tumolo, Lukasz Cerbin, Amneet Sandhu, Matthew Zipse, Wendy Tzou, Michael Rosenberg

Abstract read
In one paragraph

Article in JACC. Clinical electrophysiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
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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

10 authors.

Sarah SlavenDepartment of Medicine-Cardiology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA. Electronic address: sarah.slaven@cuanschutz.edu.
Lohit GargDepartment of Medicine-Cardiology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Rafay SabzwariDepartment of Medicine-Cardiology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Christopher BarrettDivision of Cardiovascular Medicine, Denver Health, Denver, Colorado, USA.
Alexis TumoloDepartment of Medicine-Cardiology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Lukasz CerbinDepartment of Medicine-Cardiology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Amneet SandhuDepartment of Medicine-Cardiology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Matthew ZipseDepartment of Medicine-Cardiology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Wendy TzouDepartment of Medicine-Cardiology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Michael RosenbergDepartment of Medicine-Cardiology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.

Funding

Development of End-To-End Clinical Decision Support Tools To Prevent Cardiotoxic Drug ResponseR01HL146824 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI ROSENBERG, MICHAEL A · 2020 to 2024
$3.9M
NHLBI NIH HHS R01 HL146824
6 · The paper itself

Abstract

backgroundThe association between premature ventricular complexes (PVCs) and ventricular function has been described in several observational studies, where it has been implied that a higher burden of PVCs plays a causative role in reducing left ventricular ejection fraction (LVEF). To date, however, few studies have examined the association of PVCs and cardiomyopathy on a population level.

objectivesIn this treatment-agnostic, cross-sectional study, the authors examined the association of PVC burden with depressed LVEF.

methodsWe performed an analysis of >30,000 ambulatory monitors obtained on patients from April 22, 2017, and February 20, 2023. Subjects with ≥24 hours of monitoring, a PVC burden of ≥5%, and a transthoracic echocardiogram performed within 3 months of monitoring were included. The presence of cardiomyopathy was defined as LVEF <50%. Clinical factors including comorbidities and relevant medications were included and adjusted for.

resultsThe included sample included a total of 1,451 patients, with age 68.2 ± 14.5 years, female sex in 39.6%. The average PVC burden was 12.4% ± 7.4% (5%-43.4%). Of 746 subjects with a transthoracic echocardiogram, the mean LVEF was 55.6% ± 9.2% (25%-76.8%), with 171 subjects (22.9%) having an LVEF <50%. In both unadjusted and adjusted analyses, we found no significant association between percentage of PVCs and LVEF (P = 0.78), nor with PVC burden and depressed left ventricular function (P = 0.13).

conclusionsWe found no evidence that the PVC burden alone is an independent predictor of cardiomyopathy.

Indexed as

CardiomyopathiesVentricular Premature ComplexesAgedCross-Sectional StudiesEchocardiographyFemaleHumansMaleMiddle AgedRisk FactorsStroke VolumeVentricular Dysfunction, Leftambulatory monitoring cardiomyopathyPVC burdenPVC-induced cardiomyopathy

Identifiers

PMID39945713
PMCPMC12119207

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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.