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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorCesareo, Marco Riccardo
dc.contributor.authorRódenas-Alesina, Eduard
dc.contributor.authorCasas, Guillem
dc.contributor.authorVallelonga, Fabrizio
dc.contributor.authorFerreira González, Ignacio
dc.contributor.authorGuala, Andrea
dc.contributor.authorLozano Torres, Jordi
dc.contributor.authorRodríguez Palomares, José F
dc.date.accessioned2024-07-22T06:30:20Z
dc.date.available2024-07-22T06:30:20Z
dc.date.issued2024-06-30
dc.identifier.citationCesareo M, Ródenas-Alesina E, Guala A, Lozano-Torres J, Casas G, Vallelonga F, et al. Echocardiography-Derived Hemodynamic Forces Are Associated with Clinical Outcomes in Patients with Non-Ischemic Dilated Cardiomyopathy. J Clin Med. 2024 Jun 30;13(13):3862.
dc.identifier.issn2077-0383
dc.identifier.urihttps://hdl.handle.net/11351/11751
dc.descriptionDilated cardiomyopathy; Echocardiography; Hemodynamic forces
dc.description.abstractIntroduction: Non-ischemic dilated cardiomyopathy (NIDCM) is characterized by a reduced left ventricular (LV) ejection fraction (LVEF, <50%) and a high risk for heart failure (HF) and death. Echocardiography-derived hemodynamic forces (HDFs) may provide important information on LV mechanics, but their prognostic value is unknown. Aim: To explore the features of echocardiography-derived HDFs in NIDCM and their association with clinical endpoints. Methods: Asymptomatic, non-hospitalized NIDCM patients free from coronary artery disease and moderate or severe valvular heart disease were included in this single-center observational retrospective longitudinal study. Those with atrial fibrillation and a follow-up <12 months were excluded. Major adverse cardiovascular events (MACE) were defined as a composite of all-cause death, HF hospitalization, and ambulatory intravenous diuretics administration. LV HDFs were analyzed with a prototype software. Apex-base (HDFs-ab), lateral-septal (HDFs-ls), and HDFs-angle were computed. Results: Ninety-seven patients were included, sixty-seven (69%) were males, mean age was 62 ± 14 years, and mean LVEF was 39.2 ± 8.6%. During a median follow-up of 4.2 (3.1–5.1) years, 19 (20%) patients experienced MACE. These patients had a higher HDFs-angle (71.0 (67.0–75.0) vs. 68.0 (63.0–71.0)°, p = 0.005), lower HDFs-ls (1.36 (1.01–1.85) vs. 1.66 ([1.28–2.04])%, p = 0.015), but similar HDFs-ab (5.02 (4.39–6.34) vs. 5.66 (4.53–6.78)%, p = 0.375) compared to those without MACE. in a Cox regression analysis, HDFs-angle (HR 1.16 (95%-CI 1.04–1.30), p = 0.007) was associated with MACE, while other conventional echocardiography parameters, including LVEF and LV longitudinal strain, were not. Conclusions: HDFs-angle is associated with clinical endpoints in NIDCM. A higher HDFs-angle may be a marker of impaired myocardial performance in patients with reduced LVEF.
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofseriesJournal of Clinical Medicine;13(13)
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectCor - Ventricle esquerre - Malalties - Factors de risc
dc.subjectEcocardiografia
dc.subjectMiocardi - Malalties - Imatgeria
dc.subjectCor - Hipertròfia
dc.subjectHemodinàmica
dc.subject.meshHemodynamics
dc.subject.meshCardiomyopathy, Dilated
dc.subject.mesh/diagnostic imaging
dc.subject.meshEchocardiography
dc.subject.meshVentricular Dysfunction, Left
dc.titleEchocardiography-Derived Hemodynamic Forces Are Associated with Clinical Outcomes in Patients with Non-Ischemic Dilated Cardiomyopathy
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3390/jcm13133862
dc.subject.decshemodinámica
dc.subject.decsmiocardiopatía dilatada
dc.subject.decs/diagnóstico por imagen
dc.subject.decsecocardiografía
dc.subject.decsdisfunción ventricular izquierda
dc.relation.publishversionhttps://doi.org/10.3390/jcm13133862
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Cesareo M] Hypertension Unit, Division of Internal Medicine, University Hospital Città della Salute e della Scienza of Turin, Turin, Italy. Department of Medical Sciences, University of Turin, Turin, Italy. [Ródenas-Alesina E, Rodriguez-Palomares JF] Servei de Cardiologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Departament de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Spain. Centro de Investigación Biomédica en Red-Enfermedades Cardiovaculares (CIBERCV), Madrid, Spain. [Guala A] Centro de Investigación Biomédica en Red-Enfermedades Cardiovaculares (CIBERCV), Madrid, Spain. Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. [Lozano-Torres J] Servei de Cardiologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Casas G] Servei de Cardiologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Centro de Investigación Biomédica en Red-Enfermedades Cardiovaculares (CIBERCV), Madrid, Spain. [Vallelonga F] Department of Medical Sciences, University of Turin, Turin, Italy. Division of Internal Medicine, Candiolo Cancer Institute-Fondazione del Piemonte per l’Oncologia (FPO)-Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Turin, Italy. [Ferreira-González I] Servei de Cardiologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Departament de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Spain. Consorcio de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), Madrid, Spain
dc.identifier.pmid38999432
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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