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dc.contributor.authorPascual-Figal, Domingo A 
dc.contributor.authorHernández-Vicente, Alvaro
dc.contributor.authorPastor-Pérez, Francisco
dc.contributor.authorMartínez-Sellés, Manuel
dc.contributor.authorSolé-González, Eduard
dc.contributor.authorAlvarez-García, Jesús
dc.contributor.authorGarcia-Pavia, Pablo 
dc.contributor.authorVarela-Román, Alfonso
dc.contributor.authorSánchez, Pedro Luis
dc.contributor.authorDelgado, Juan F
dc.contributor.authorNoguera-Velasco, Jose A
dc.contributor.authorBayes-Genis, Antoni
dc.date.accessioned2024-07-03T08:58:38Z
dc.date.available2024-07-03T08:58:38Z
dc.date.issued2024-04
dc.identifier.citationEur J Heart Fail. 2024 Apr;26(4):776-784.es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/19927
dc.description.abstractAIMS There is a lack of specific studies assessing the impact of natriuretic peptide monitoring in the post-discharge management of patients with heart failure (HF) and preserved ejection fraction (HFpEF), throughout the vulnerable phase following acute HF hospitalization. The NICE study aims to assess the clinical benefit of incorporating N-terminal pro-B-type natriuretic peptide (NT-proBNP) into the post-discharge management of HFpEF patients. METHODS AND RESULTS Individuals admitted with HFpEF (left ventricular ejection fraction >50%) were included in a multicentre randomized controlled study employing an open-label design with event blinding (NCT02807168). Upon discharge, 157 patients were randomly allocated to either NT-proBNP monitoring (n = 79) or no access to NT-proBNP (control group, n = 78) during pre-scheduled visits at 2, 4 and 12 weeks. Clinical endpoints were evaluated at 6 months. The primary endpoint of HF rehospitalizations occurred in 12.1% patients, without significant differences observed between the NT-proBNP monitoring group (12.8%) and the control group (11.4%) (hazard ratio [HR] 1.15, 95% confidence interval [CI] 0.47-2.81, p = 0.760). Regarding secondary endpoints, the NT-proBNP monitoring group demonstrated a significantly lower risk of death (1.3% vs. 10.1%; HR 0.12, 95% CI 0.02-0.98; p = 0.048), whereas non-HF hospitalizations (12.8% vs. 19.0%, p = 0.171) and any adverse clinical event (26.9% vs. 36.7%, p = 0.17) did not reach statistical significance [Correction added on 29 April 2024, after first online publication: In the preceding sentence, "95% CI 0.02 - 0.09" has been corrected to "95% CI 0.02 - 0.98; p = 0.048" in this version.]. Awareness of NT-proBNP levels were associated with higher doses of diuretics and renin-angiotensin system inhibitors (angiotensin-converting enzyme inhibitors/angiotensin II receptor blockers) in the NT-proBNP monitoring group. CONCLUSIONS Post-discharge monitoring of NT-proBNP in HFpEF patients did not exhibit an association with reduced rates of HF hospitalization in this study. Nonetheless, it appears to enhance global clinical management by optimizing medical therapies and contributing to improved overall survival.es_ES
dc.description.sponsorshipThis work has been supported by a non-conditional grant from Roche Diagnostics.es_ES
dc.language.isoenges_ES
dc.publisherWiley es_ES
dc.type.hasVersionVoRes_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.meshHeart Failure es_ES
dc.subject.meshNatriuretic Peptide, Braines_ES
dc.subject.meshPeptide Fragments es_ES
dc.subject.meshStroke Volume es_ES
dc.subject.meshPatient Discharge es_ES
dc.subject.meshBiomarkers es_ES
dc.subject.meshHumans es_ES
dc.subject.meshFemale es_ES
dc.subject.meshMale es_ES
dc.subject.meshAged es_ES
dc.subject.meshMiddle Aged es_ES
dc.subject.meshAged, 80 and over es_ES
dc.subject.meshPatient Readmission es_ES
dc.subject.meshMonitoring, Physiologices_ES
dc.subject.meshHospitalization es_ES
dc.titleN-terminal pro-B-type natriuretic peptide post-discharge monitoring in the management of patients with heart failure and preserved ejection fraction - a randomized trial: The NICE study.es_ES
dc.typejournal articlees_ES
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.identifier.pubmedID38606524es_ES
dc.format.volume26es_ES
dc.format.number4es_ES
dc.format.page776es_ES
dc.identifier.doi10.1002/ejhf.3222es_ES
dc.contributor.funderRoche es_ES
dc.description.peerreviewedes_ES
dc.identifier.e-issn1879-0844es_ES
dc.relation.publisherversion10.1002/ejhf.3222es_ES
dc.identifier.journalEuropean journal of heart failurees_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Imagen Cardiovascular y Estudios Poblacionaleses_ES
dc.repisalud.institucionCNICes_ES
dc.rights.accessRightsopen accesses_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Este Item está sujeto a una licencia Creative Commons: Attribution-NonCommercial-NoDerivatives 4.0 Internacional