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N-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.

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.contributor.funderRochees_ES
dc.date.accessioned2024-07-03T08:58:38Z
dc.date.available2024-07-03T08:58:38Z
dc.date.issued2024-04
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.peerreviewedes_ES
dc.description.sponsorshipThis work has been supported by a non-conditional grant from Roche Diagnostics.es_ES
dc.format.number4es_ES
dc.format.page776es_ES
dc.format.volume26es_ES
dc.identifier.citationEur J Heart Fail. 2024 Apr;26(4):776-784.es_ES
dc.identifier.doi10.1002/ejhf.3222es_ES
dc.identifier.e-issn1879-0844es_ES
dc.identifier.journalEuropean journal of heart failurees_ES
dc.identifier.pubmedID38606524es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/19927
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.relation.publisherversion10.1002/ejhf.3222es_ES
dc.repisalud.institucionCNICes_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Imagen Cardiovascular y Estudios Poblacionaleses_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.meshHeart Failurees_ES
dc.subject.meshNatriuretic Peptide, Braines_ES
dc.subject.meshPeptide Fragmentses_ES
dc.subject.meshStroke Volumees_ES
dc.subject.meshPatient Dischargees_ES
dc.subject.meshBiomarkerses_ES
dc.subject.meshHumanses_ES
dc.subject.meshFemalees_ES
dc.subject.meshMalees_ES
dc.subject.meshAgedes_ES
dc.subject.meshMiddle Agedes_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.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublicatione15445a1-38b4-496b-86ca-6992a03bed1a
relation.isAuthorOfPublication52ada1ee-7241-4738-b46d-90a5ccc14894
relation.isAuthorOfPublication.latestForDiscoverye15445a1-38b4-496b-86ca-6992a03bed1a

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