Evidence map›Paper›PMID 40833627›Full record

Trial reportClinical research in cardiology : official journal of the German Cardiac Society2026

A novel measure of AV-conduction predicts clinical outcomes and benefit from CRT-D in non-LBBB patients with wide QRS and a low left ventricular ejection fraction.

Anika Sophie Beierle, Wojciech Zareba, Richard E Auge, Spencer Z Rosero, Scott McNitt, Fabian Knebel, Martin A Stockburger, Valentina Kutyifa, MADIT-CRT Investigators

Abstract readMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Clinical research in cardiology : official journal of the German Cardiac Society, 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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1 · What the graph read from it

What it found

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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

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.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Anika Sophie BeierleCardiology, Havelland Kliniken, Academic Teaching Hospital of Charité, Universitätsmedizin Berlin, Berlin, Germany.
Wojciech ZarebaClinical Cardiovascular Research Center, Cardiology Division, University of Rochester Medical Center, 265 Crittenden Blvd, Box 653, Rochester, NY, 14642, USA.
Richard E AugeCardiology, Havelland Kliniken, Academic Teaching Hospital of Charité, Universitätsmedizin Berlin, Berlin, Germany.
Spencer Z RoseroClinical Cardiovascular Research Center, Cardiology Division, University of Rochester Medical Center, 265 Crittenden Blvd, Box 653, Rochester, NY, 14642, USA.
Scott McNittClinical Cardiovascular Research Center, Cardiology Division, University of Rochester Medical Center, 265 Crittenden Blvd, Box 653, Rochester, NY, 14642, USA.
Fabian KnebelSana Klinikum Berlin Lichtenberg, Berlin, Germany.
Martin A Stockburger *Cardiology, Havelland Kliniken, Academic Teaching Hospital of Charité, Universitätsmedizin Berlin, Berlin, Germany.
Valentina Kutyifa *Clinical Cardiovascular Research Center, Cardiology Division, University of Rochester Medical Center, 265 Crittenden Blvd, Box 653, Rochester, NY, 14642, USA. Valentina.Kutyifa@heart.rochester.edu.ORCID http://orcid.org/0000-0002-0016-289X
MADIT-CRT Investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPR-interval reflects atrioventricular timing but does not well characterize adverse hemodynamics. Novel ECG parameters of conduction may identify benefit from non-dyssynchronous ventricular pacing to correct long atrioventricular conduction delays.

objectiveEvaluating novel ECG parameters to identify risk of heart failure (HF)/death and benefit vs harm by CRT-D in MADIT-CRT non-LBBB patients.

methodsWe analyzed intervals from ECGs in 535 non-LBBB patients enrolled in MADIT-CRT, using ImageJ. Onset of atrial activation, P wave zero crossing in V1, latest P offset, earliest QRS onset, and time to the first R peak in V1 and V6 were determined. Endpoints included HF or death. Associations between novel conduction measures and clinical outcomes in ICD patients (n = 209), and CRT-D (n = 326) vs. ICD benefit, were assessed using Kaplan-Meier and multivariable Cox regression analyses.

resultsWe identified the delay from P zero crossing to the first R peak in V1 (P0PV1) at quintile 5 as the strongest risk predictor in ICD patients (n = 159, 30%), over PR-interval, for all endpoints (p < 0.001), with a more than threefold risk increase. In this group, CRT-D was associated with a 66% lower risk of HF/Death (95% CI: 0.22-0.68, p = 0.001) vs. an ICD. However, in patients with a P0PV1 < 201 ms, CRT-D vs. an ICD was associated with a 64% increased risk of HF/death (95% CI: 1.12-2.55, p = 0.012), with significant bidirectional interaction (p-value < 0.001).

conclusionsWe propose a novel variable, P0PV1, to identify risk and benefit vs. harm from CRT-D in HF patients with non-LBBB. Prospective studies are warranted to confirm our findings.

Indexed as

Cardiac Resynchronization TherapyElectrocardiographyHeart FailureStroke VolumeVentricular Function, LeftAgedDefibrillators, ImplantableFemaleFollow-Up StudiesHumansMaleMiddle AgedPredictive Value of TestsRetrospective StudiesRisk FactorsTreatment OutcomeAV-conductionCardiac resynchronization therapyPredictor

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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.