Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/136302
Campo DC Valoridioma
dc.contributor.authorMontero-Pérez-Barquero, Manuelen_US
dc.contributor.authorEscobar-Cervantes, Carlosen_US
dc.contributor.authorArévalo-Lorido, José Carlosen_US
dc.contributor.authorConde Martel, Aliciaen_US
dc.contributor.authorSalamanca-Bautista, Pradoen_US
dc.contributor.authorManzano-Espinosa, Luisen_US
dc.contributor.authorFormiga, Francescen_US
dc.contributor.authorDíez-Manglano, Jesúsen_US
dc.contributor.authorCepeda, José Maríaen_US
dc.contributor.authorGonzález-Franco, Alvaroen_US
dc.contributor.authorCasado-Cerrada, Jesúsen_US
dc.date.accessioned2025-02-18T12:33:25Z-
dc.date.available2025-02-18T12:33:25Z-
dc.date.issued2023en_US
dc.identifier.issn1479-6678en_US
dc.identifier.urihttp://hdl.handle.net/10553/136302-
dc.description.abstractAim: To estimate the projected effectiveness of dapagliflozin in subjects with heart failure (HF) with reduced ejection fraction in clinical practice in Spain. Materials & methods: This multicenter cohort study included subjects aged 50 years or older consecutively hospitalized for HF in internal medicine departments in Spain. The projected clinical benefits of dapagliflozin were estimated based on results from the DAPA-HF trial. Results: A total of 1595 patients were enrolled, of whom 1199 (75.2%) were eligible for dapagliflozin. Within 1 year after discharge, 21.6% of patients eligible for dapagliflozin were rehospitalized for HF and 20.5% died. Full implementation of dapagliflozin led to an absolute risk reduction of 3.5% for mortality (number needed to treat = 28) and 6.5% (number needed to treat = 15) for HF readmission. Conclusion: Treatment with dapagliflozin in clinical practice may markedly reduce mortality and readmissions for HF.en_US
dc.languageengen_US
dc.relation.ispartofFuture Cardiologyen_US
dc.sourceFuture Cardiology [ISSN 1479-6678], v. 19(6), pp. 343-351en_US
dc.subject32 Ciencias médicasen_US
dc.subject3205 Medicina internaen_US
dc.subject320501 Cardiologíaen_US
dc.subject.otherDapagliflozinen_US
dc.subject.otherDeathen_US
dc.subject.otherHeart failure with reduced ejection fractionen_US
dc.subject.otherHospitalizationen_US
dc.subject.otherSGLT2 inhibitorsen_US
dc.titleProjected effectiveness of dapagliflozin in heart failure with reduced ejection fraction in clinical practiceen_US
dc.typeArticleen_US
dc.identifier.doi10.2217/fca-2023-0016en_US
dc.identifier.pmid37382223-
dc.identifier.scopus2-s2.0-85167477511-
dc.contributor.orcid0000-0003-4294-1653-
dc.contributor.orcid0000-0001-5584-4735-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.description.lastpage351en_US
dc.identifier.issue6-
dc.description.firstpage343en_US
dc.relation.volume19en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.utils.revisionen_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr0,412
dc.description.sjrqQ3
dc.description.esciESCI
dc.description.miaricds9,7
item.grantfulltextopen-
item.fulltextCon texto completo-
crisitem.author.deptGIR IUIBS: Patología y Tecnología médica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.orcid0000-0002-2540-3880-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameConde Martel, Alicia-
Colección:Artículos
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