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dc.contributor.authorPardo-Martínez, Patricia
dc.contributor.authorBarge-Caballero, Eduardo
dc.contributor.authorBouzas-Mosquera, Alberto
dc.contributor.authorBarge-Caballero, Gonzalo
dc.contributor.authorCouto-Mallón, David
dc.contributor.authorPaniagua-Martín, María J.
dc.contributor.authorSagastagoitia-Fornie, Marta
dc.contributor.authorPrada-Delgado, Óscar
dc.contributor.authorMuñiz, Javier
dc.contributor.authorAlmenar-Bonet, Luis
dc.contributor.authorVázquez Rodríguez, José Manuel
dc.contributor.authorCrespo-Leiro, María Generosa
dc.date.accessioned2022-02-18T11:20:22Z
dc.date.issued2022-01-06
dc.identifier.citationPardo-Martínez P, Barge-Caballero E, Bouzas-Mosquera A, Barge-Caballero G, Couto-Mallón D, Paniagua-Martín MJ, et al. Real world comparison of spironolactone and eplerenone in patients with heart failure. Eur J Intern Med.2022;97:86-94es_ES
dc.identifier.issn0953-6205
dc.identifier.urihttp://hdl.handle.net/2183/29814
dc.description.abstract[Abstract] Aims. In the absence of previous direct comparative studies, we aimed to evaluate the effectiveness of spironolactone and eplerenone in patients with heart failure and reduced ejection fraction (HFrEF) in a real-world clinical setting. Methods. Using Fine-Gray´s competing risk regression, we compared the clinical outcomes of 293 patients with chronic HF and left ventricular ejection fraction <40% treated with eplerenone and 293 propensity-score matched individuals treated with spironolactone. Study subjects were selected from a prospective cohort of 1404 ambulatory patients with HFrEF seen since 2010 to 2019 in a single specialized HF clinic, among which 992 received a mineralocorticoid receptor antagonist at baseline. Median follow-up was 3.95 years. Results. No statistically significant differences between patients treated with eplerenone versus spironolactone were observed with regard to the risk of the primary composite end-point cardiovascular death or HF hospitalization (HR 0.95; 95% CI 0.73–1.23; p= 0.677). However, eplerenone use was associated to lower cardiovascular mortality (HR 0.55; 95% CI 0.35–0.85; p= 0.008) and lower all-cause mortality (HR 0.67; 95% CI 0.47–0.95; p= 0.027). The incidence of drug suspension due to side effects (HR 0.58, 95% CI 0.40–0.85; p= 0.005) and drug suspension due to any reason (HR 0.70, 95% CI 0.51–0.97; p= 0.033) were lower among patients treated with eplerenone. Conclusions. In this observational, real-world, propensity-score matched study of patients with HFrEF, eplerenone was associated to lower cardiovascular mortality and lower all-cause mortality than spironolactone.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.relation.urihttps://doi.org/10.1016/j.ejim.2021.12.027es_ES
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs 4.0 International Licence (CC-BY-NC-ND 4.0)es_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectHeart failurees_ES
dc.subjectReduced ejection fractiones_ES
dc.subjectSpironolactonees_ES
dc.subjectEplerenonees_ES
dc.subjectSurvivales_ES
dc.subjectOutcomeses_ES
dc.titleReal World Comparison of Spironolactone and Eplerenone in Patients With Heart Failurees_ES
dc.typejournal articlees_ES
dc.rights.accessRightsembargoed accesses_ES
dc.date.embargoEndDate2023-01-06es_ES
dc.date.embargoLift2023-01-06
UDC.journalTitleEuropean Journal of Internal Medicinees_ES
UDC.coleccionInvestigaciónes_ES
UDC.departamentoCiencias da Saúdees_ES
UDC.grupoInvGrupo de Investigación Cardiovascular (GRINCAR)es_ES


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