Evidence map›Paper›PMID 40107322›Full record

ArticleESC heart failure2025

Early occurrence of heart failure hospitalization or ventricular arrhythmia re-define the long-term prognosis after CRT.

Anna Zsofia Toth, Laszlo Nagy, Krisztina Maria Szabo, Vivien Racz, Alexandra Kiss, Gabor Sandorfi, Attila Borbely, Tibor Laszlo Nagy, Zoltan Csanadi

Abstract read
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

9 authors.

Anna Zsofia TothDepartment of Cardiology, Division of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.ORCID https://orcid.org/0000-0001-9364-2544
Laszlo NagyDepartment of Cardiology, Division of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Krisztina Maria SzaboDepartment of Cardiology, Division of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Vivien RaczDepartment of Cardiology, Division of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Alexandra KissDepartment of Cardiology, Division of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Gabor SandorfiDepartment of Cardiology, Division of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Attila BorbelyDepartment of Cardiology, Division of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Tibor Laszlo NagyDepartment of Cardiology, Division of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Zoltan CsanadiDepartment of Cardiology, Division of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Funding

National Research, Development and Innovation Fund TKP2021-EGA
6 · The paper itself

Abstract

aimsClassifying patients as responders or non-responders to cardiac resynchronization therapy (CRT) has been recently challenged, suggesting that preventing heart failure (HF) progression may also provide survival benefits. We assessed a novel classification based on echocardiographic left ventricular (LV) reverse remodelling and the occurrence of acute HF hospitalization (HHF) or sustained ventricular arrhythmia (VA) within 1-year post-CRT. METHODS AND

resultsPatients implanted with a CRT defibrillator (CRT-D) at our department between 2010 and 2020 were classified based on the change in LV ejection fraction (LVEF) within 1 year as responders (increase ≥ 10%), non-progressors (increase <10%) or progressors (decline). Patients in each category were further divided based on the occurrence or absence of an HHF/VA event within 1-year post-implantation. Long-term survival free of heart transplantation or LV assist device implantation was calculated for all six subgroups. Cohorts demonstrating no significant between-group differences were grouped together and reclassified as improved, stabilized or worsened. One hundred nineteen responders, 79 non-progressors and 69 progressors were identified based on the echocardiographic response. Long-term event-free survival was higher for responders as compared with non-progressors (hazard ratio [HR] 0.51, P = 0.002) or progressors (HR 0.34, P < 0.0001). Furthermore, non-progressors had better outcome than progressors (HR 0.63, P = 0.03). Long-term prognosis in patients was superior with versus without an HHF/VA event within each group of responders (HR 0.47, P = 0.03), non-progressors (HR 0.31, P = 0.0001) or progressors (HR 0.38, P = 0.0004). No survival difference was found between responders and non-progressors with no event (HR 0.69, P = 0.09), who were recategorized as improved. Long-term prognosis was also similar in responders with any event and in progressors with no event (HR 0.98, P = 0.88; stabilized), as well as in non-progressors and progressors with any event (HR 0.87, P = 0.63; worsened). Median survival rates demonstrated significant differences between the improved, stabilized and worsened groups (102.3, 62.0 and 24.4 months; HR 0.53, P = 0.006 between improved and stabilized; HR 0.41, P < 0.0001 between stabilized and worsened; HR 0.21, P < 0.0001 between improved and worsened cohorts, respectively).

conclusionsLong-term survival can be predicted based on the change in LVEF and on the occurrence of an HHF/VA event within 1-year after CRT-D implantation. Stabilized patients have significantly better prognosis as compared with the worsened group. Patients with strikingly poor prognosis can be identified using this assessment method.

Indexed as

Arrhythmias, CardiacCardiac Resynchronization TherapyHeart FailureHospitalizationVentricular Function, LeftVentricular RemodelingAgedEchocardiographyFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisRetrospective StudiesStroke VolumeCardiac resynchronization therapy (CRT)CRT non‐respondernon‐progressorprogressor

Identifiers

PMID40107322
PMCPMC12287837

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.