Evidence map›Paper›PMID 40736081›Full record

ArticleESC heart failure2025

Patient-specific modifiers of survival benefit in cardiac resynchronization therapy - A multicentre interaction analysis.

Bert Vandenberk, Marius Brusselmans, Gabor Voros, Pieter Martens, Sebastian Ingelaere, Pascal Betschart, Jens-Uwe Voigt, Matthias Dupont, Alexander Breitenstein, Jan Steffel and 5 more

Abstract readMulticenter Study
In one paragraph

Article in ESC heart failure, 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

15 authors.

Bert VandenberkDepartment of Cardiology, UZ Leuven, Leuven, Belgium.
Marius BrusselmansDepartment of Clinical and Epidemiological Virology, KU Leuven, Leuven, Belgium.
Gabor VorosDepartment of Cardiology, UZ Leuven, Leuven, Belgium.
Pieter MartensDepartment of Cardiology, Ziekenhuis Oost-Limburg, Genk, Belgium.
Sebastian IngelaereDepartment of Cardiovascular Sciences, KU Leuven, Leuven, Belgium.
Pascal BetschartDepartment of Cardiology, University Hospital Zurich, Zurich, Switzerland.
Jens-Uwe VoigtDepartment of Cardiology, UZ Leuven, Leuven, Belgium.
Matthias DupontDepartment of Cardiology, Ziekenhuis Oost-Limburg, Genk, Belgium.
Alexander BreitensteinDepartment of Cardiology, University Hospital Zurich, Zurich, Switzerland.
Jan SteffelDepartment of Cardiology, University Hospital Zurich, Zurich, Switzerland.
Rik WillemsDepartment of Cardiology, UZ Leuven, Leuven, Belgium.
Frank RuschitzkaDepartment of Cardiology, University Hospital Zurich, Zurich, Switzerland.
Wilfried MullensDepartment of Cardiology, Ziekenhuis Oost-Limburg, Genk, Belgium.
Sander TrensonDepartment of Cardiology, UZ Leuven, Leuven, Belgium.
Stephan WinnikDepartment of Cardiology, University Hospital Zurich, Zurich, Switzerland.

Funding

Fonds voor Wetenschappelijk Onderzoek-Vlaanderen 1832922NFrans Van de Werf Fund for Clinical Cardiovascular ResearchFund for Scientific Research Flanders
6 · The paper itself

Abstract

backgroundCardiac resynchronization therapy (CRT) is a key intervention for patients with heart failure. The choice between a CRT with defibrillator therapy (CRT-D) and a CRT with pacemaker (CRT-P) is influenced by individual clinical characteristics. This study explores the interaction between these clinical variables and the benefit of CRT-D versus CRT-P on all-cause mortality.

methodsAll patients who underwent CRT implantation in three European centres were included in a multicentre, retrospective registry. The impact of clinical variables on all-cause mortality was analysed using interaction tests within multivariable Cox proportional hazard models. Significant interactions were explored to assess how patient characteristics modify the effect of CRT-D compared with CRT-P.

resultsA total of 2271 patients with CRT implantation were included. CRT-D was associated with a 35% reduction in all-cause mortality compared with CRT-P [hazard ratio (HR) 0.65; 95% confidence interval (CI) 0.53-0.80]. Significant interactions were observed for left bundle branch block (LBBB) morphology (P = 0.028), left ventricular ejection fraction (LVEF, P = 0.025) and renal function (P = 0.019). The survival benefit of CRT-D was pronounced in patients with LBBB (HR 0.57; 95% CI 0.44-0.73) but was not significant in those without LBBB (HR 0.81; 95% CI 0.59-1.10). For LVEF at implant, CRT-D provided benefit between 17.9% and 37.6%. Similarly, CRT-D improved outcomes in patients with an estimated glomerular filtration rate >31.8 mL/min but not in those with more advanced renal impairment. No interaction was observed with age at implant (P = 0.286).

conclusionsThis study provides insights into the benefits of CRT-D over CRT-P, identifying LBBB morphology, LVEF and renal function as key covariates associated with implantable cardioverter-defibrillator (ICD) therapy's benefit.

Indexed as

Cardiac Resynchronization TherapyDefibrillators, ImplantableHeart FailureRegistriesStroke VolumeVentricular Function, LeftAgedCause of DeathEuropeFemaleFollow-Up StudiesHumansMaleMiddle AgedRetrospective StudiesSurvival Ratecardiac resynchronization therapyheart failureimplantable cardioverter–defibrillatorpacemaker

Identifiers

PMID40736081
PMCPMC12450839

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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.