Evidence map›Paper›PMID 40320473›Full record

ArticleScientific reports2025

ECG-based evaluation of ventricular synchrony in left bundle branch area pacing through characterization of the activation sequence.

Clara Sales-Belles, Ana Mincholé, Jorge Melero-Polo, Mercedes Cabrera-Ramos, Pablo Vadillo-Martín, Isabel Montilla-Padilla, Laura Sorinas-Villanueva, Inés Julián-García, Gualber Vitto Mayo-Carlos, José Ramón Ruiz-Arroyo and 2 more

Abstract read
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Article in Scientific reports, 2025. 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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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

Who cites it

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

12 authors.

Clara Sales-BellesBSICoS Group, Aragon Institute of Engineering Research, IIS Aragón, University of Zaragoza, Zaragoza, Spain.
Ana MincholéBSICoS Group, Aragon Institute of Engineering Research, IIS Aragón, University of Zaragoza, Zaragoza, Spain.
Jorge Melero-PoloArrhythmias Unit, Cardiology Department, Lozano Blesa Clinical University Hospital, Calle San Juan Bosco 15, 50009, Zaragoza, Spain.
Mercedes Cabrera-RamosArrhythmias Unit, Cardiology Department, Lozano Blesa Clinical University Hospital, Calle San Juan Bosco 15, 50009, Zaragoza, Spain.
Pablo Vadillo-MartínArrhythmias Unit, Cardiology Department, Lozano Blesa Clinical University Hospital, Calle San Juan Bosco 15, 50009, Zaragoza, Spain.
Isabel Montilla-PadillaArrhythmias Unit, Cardiology Department, Lozano Blesa Clinical University Hospital, Calle San Juan Bosco 15, 50009, Zaragoza, Spain.
Laura Sorinas-VillanuevaArrhythmias Unit, Cardiology Department, Lozano Blesa Clinical University Hospital, Calle San Juan Bosco 15, 50009, Zaragoza, Spain.
Inés Julián-GarcíaArrhythmias Unit, Cardiology Department, Lozano Blesa Clinical University Hospital, Calle San Juan Bosco 15, 50009, Zaragoza, Spain.
Gualber Vitto Mayo-CarlosArrhythmias Unit, Cardiology Department, Lozano Blesa Clinical University Hospital, Calle San Juan Bosco 15, 50009, Zaragoza, Spain.
José Ramón Ruiz-ArroyoArrhythmias Unit, Cardiology Department, Lozano Blesa Clinical University Hospital, Calle San Juan Bosco 15, 50009, Zaragoza, Spain.
Esther Pueyo *BSICoS Group, Aragon Institute of Engineering Research, IIS Aragón, University of Zaragoza, Zaragoza, Spain.
Javier Ramos-Maqueda *Arrhythmias Unit, Cardiology Department, Lozano Blesa Clinical University Hospital, Calle San Juan Bosco 15, 50009, Zaragoza, Spain. javierramos.iias@gmail.com.

Funding

Agencia Estatal de Investigación - Ministerio de Ciencia e Innovación (Spain) TED2021-130459B-I00Agencia Estatal de Investigación - Ministerio de Ciencia e Innovación (Spain): PID2019-105674RB-I00Gobierno de Aragón T39\_23R
6 · The paper itself

Abstract

Left bundle branch area pacing (LBBAP) overcomes ventricular dyssynchrony induced by conventional right ventricular pacing (RVP). Despite QRS duration (QRSd) being the standard ECG marker for biventricular synchrony, it lacks insights into the ventricular activation sequence. Our aim is to assess biventricular synchrony by characterizing the ventricular activation sequence and introducing robust markers using the 12-lead ECG. A prospective single-center study was conducted, involving patients with pacemaker indication due to bradycardia. Patients were divided into LBBAP and RVP, and classified by baseline-QRS morphology. To assess biventricular synchrony, low frequency-based QRS analysis was performed to compute the ventricular activation sequence and precordial activation delay (pAD). Additional QRS markers including QRSd, QRS60, and QRS area (QRSa) were calculated. A total of 176 patients (107 LBBAP, 69 RVP) were included. The paced ventricular activation sequence indicated a more physiological pattern after LBBAP than RVP, with lower pAD values in narrow QRS, RBBB, and LBBB subgroups [ - 10( - 20,14) vs. 26(5, 39) ms;  - 18( - 30,  - 8) vs. 34(26, 55) ms; 10( - 14, 25) vs. 32(12, 48) ms] (p < 0.01). In all subgroups, QRS60 showed lower values after LBBAP than RVP [52(41, 62) vs.73(65, 80) ms; 60(55, 66) vs. 77(67, 83) ms; 59(53, 64) vs. 77(74, 82) ms] (p < 0.01) and QRSa were also lower [53(38, 66) vs. 121(92, 143) μVs; 60(50, 89) vs. 124(97, 159) μVs; 62(52, 80) vs. 133(99, 148) μVs] (p < 0.01). pAD provides valuable insights into ventricular activation beyond paced-QRSd. Together with QRS60 and QRSa, pAD could be a promising tool to assess biventricular synchrony.

Indexed as

Bundle-Branch BlockBundle of HisCardiac Pacing, ArtificialElectrocardiographyHeart VentriclesAgedBradycardiaFemaleHumansMaleMiddle AgedProspective StudiesECG markersLeft bundle branch area pacingVentricular activation synchrony

Identifiers

PMID40320473
PMCPMC12050288

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LicenceCC BY-NC-ND
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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.