Evidence map›Paper›PMID 40742123›Full record

Observational studyClinical cardiology2025

Evaluation of the Presence of Native Valvular Disease in Patients With Atrial Fibrillation Using the EHRA (Evaluated Heartvalves, Rheumatic, or Artificial) Classification.

Antonio Escolar Conesa, María Asunción Esteve-Pastor, Vanessa Roldán, Eva Soler Espejo, José Miguel Rivera-Caravaca, Pablo Gil Pérez, Eduardo González Lozano, José María Arribas Leal, Sergio Cánovas López, Daniel Saura Espín and 5 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in Clinical cardiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Antonio Escolar ConesaDepartment of Cardiology, Hospital Comarcal del Noroeste, Murcia, Spain.ORCID https://orcid.org/0000-0002-6811-3373
María Asunción Esteve-PastorDepartment of Cardiology, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain.ORCID https://orcid.org/0000-0003-3104-3460
Vanessa RoldánInstituto Murciano de Investigación Biosanitaria (IMIB-Arrixaca), University of Murcia, Murcia, Spain.
Eva Soler EspejoInstituto Murciano de Investigación Biosanitaria (IMIB-Arrixaca), University of Murcia, Murcia, Spain.ORCID https://orcid.org/0000-0003-4925-4864
José Miguel Rivera-CaravacaInstituto Murciano de Investigación Biosanitaria (IMIB-Arrixaca), University of Murcia, Murcia, Spain.ORCID https://orcid.org/0000-0003-0492-6241
Pablo Gil PérezDepartment of Cardiology, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain.
Eduardo González LozanoDepartment of Clinical Pharmacology, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain.ORCID https://orcid.org/0000-0003-0946-711X
José María Arribas LealDepartment of Cardiovascular Surgery, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain.ORCID https://orcid.org/0000-0003-3001-9960
Sergio Cánovas LópezDepartment of Cardiovascular Surgery, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain.
Daniel Saura EspínDepartment of Cardiology, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain.
María José Oliva SandovalDepartment of Cardiology, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain.
Eduardo Pinar BermúdezDepartment of Cardiology, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain.
Juan García De LaraDepartment of Cardiology, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain.ORCID https://orcid.org/0000-0002-5632-4165
Gregory Y H LipLiverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart & Chest Hospital, Liverpool, UK.ORCID https://orcid.org/0000-0002-7566-1626
Francisco MarínDepartment of Cardiology, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain.

Funding

Project funded by Sociedad Española de Cardiología with a Clinical Research grant Dr. Pedro Zarco.
6 · The paper itself

Abstract

backgroundAtrial fibrillation (AF) in association with native valvular heart disease (VHD) is very common and both entities perpetuate each other due to volume and pressure overload. In 2017, the new EHRA classification (Evaluated Heartvalves, Rheumatic or Artificial) was proposed: EHRA 1 (mechanical prostheses or moderate/severe mitral stenosis), EHRA 2 (native valvular involvement or biological prosthesis) and EHRA 3 (without valve disease). The objective was to analyze the clinical characteristics as well as adverse events in the follow-up of AF patients under oral anticoagulation classified according EHRA classification.

methodsA multicenter retrospective observational descriptive study was designed and collected clinical, analytical, echocardiographic characteristics as well as adverse events in the follow-up of patients with AF who start oral anticoagulation.

results1.399 patients were included (mean age 75.3 ± 9.9 years; 659 (47.1%) male), of whom, 63% were classified as EHRA 2. After a median follow-up of 910 (IQR 730-1018) days, native EHRA 2 patients had higher event rates/patient-year as well as a higher total rate of adverse events such as cardiovascular mortality (5.5% vs. 1.1% event/patient-year; 8.7% vs. 1.1% p < 0.001) and major adverse cardiovascular events (MACE) (8.9% vs. 3.4% event/patient-year; 14.2% vs. 3.1% p < 0.001), compared with EHRA 3 patients. Multivariate logistic regression analysis showed that native EHRA 2 group was independently associated with all major adverse events.

conclusionIn anticoagulated AF patients, those with native valve involvement (EHRA 2) have a worse prognosis than patients without valve involvement (EHRA 3). The presence of native valvular disease is shown as an independent risk factor for all-cause mortality, major bleeding, cardiovascular mortality, ACS, heart failure, and MACE.

Indexed as

Atrial FibrillationHeart Valve DiseasesHeart Valve ProsthesisAgedAged, 80 and overAnticoagulantsEchocardiographyFemaleFollow-Up StudiesHumansMaleRetrospective StudiesRisk AssessmentRisk FactorsTime FactorsAnticoagulants

Identifiers

PMID40742123
PMCPMC12312205

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