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dc.creatorNtalianis A., Chrysohoou C., Giannakoulas G., Giamouzis G., Karavidas A., Naka A., Papadopoulos C.H., Patsilinakos S., Parissis J., Tziakas D., Kanakakis J.en
dc.date.accessioned2023-01-31T09:40:45Z
dc.date.available2023-01-31T09:40:45Z
dc.date.issued2022
dc.identifier10.1007/s10741-021-10115-8
dc.identifier.issn13824147
dc.identifier.urihttp://hdl.handle.net/11615/77318
dc.description.abstractThe short-term mortality and rehospitalization rates after admission for acute heart failure (AHF) remain high, despite the high level of adherence to contemporary practice guidelines. Observational data from non-randomized studies in AHF strongly support the in-hospital administration of oral evidence-based modifying chronic heart failure (HF) medications (i.e., b-blockers, ACE inhibitors, mineralocorticoid receptor antagonists) to reduce morbidity and mortality. Interestingly, a well-designed prospective randomized multicenter study (PIONEER-HF) showed an improved clinical outcome and stress/injury biomarker profile after in-hospital administration of sacubitril/valsartan (sac/val) as compared to enalapril, in hemodynamically stable patients with AHF. However, sac/val implementation during hospitalization remains suboptimal due to the lack of an integrated individualized plan or well-defined appropriateness criteria for transition to oral therapies, an absence of specific guidelines regarding dose selection and the up-titration process, and uncertainty regarding patient eligibility. In the present expert consensus position paper, clinical practical recommendations are proposed, together with an action plan algorithm, to encourage and facilitate sac/val administration during hospitalization after an AHF episode with the aim of improving efficiencies of care and resource utilization. © 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.en
dc.language.isoenen
dc.sourceHeart Failure Reviewsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85105414137&doi=10.1007%2fs10741-021-10115-8&partnerID=40&md5=67eb4d2222b05cd529cb499fd0ad5341
dc.subjectamino terminal pro brain natriuretic peptideen
dc.subjectangiotensin receptor antagonisten
dc.subjectbeta adrenergic receptor blocking agenten
dc.subjectdipeptidyl carboxypeptidase inhibitoren
dc.subjectdiuretic agenten
dc.subjectmembrane metalloendopeptidaseen
dc.subjectsacubitril plus valsartanen
dc.subjectaminobutyric acid derivativeen
dc.subjectangiotensin derivativeen
dc.subjectangiotensin receptoren
dc.subjectbiphenyl derivativeen
dc.subjectmembrane metalloendopeptidaseen
dc.subjectsacubitrilen
dc.subjectacute heart failureen
dc.subjectclinical studyen
dc.subjectconsensusen
dc.subjectcost effectiveness analysisen
dc.subjectdrug administration routeen
dc.subjectforward heart failureen
dc.subjecthealth care utilizationen
dc.subjectheart failure with reduced ejection fractionen
dc.subjectheart left ventricle ejection fractionen
dc.subjecthospitalen
dc.subjecthospital dischargeen
dc.subjecthospitalizationen
dc.subjecthumanen
dc.subjecthyperkalemiaen
dc.subjecthypotensionen
dc.subjectkidney dysfunctionen
dc.subjectpatient careen
dc.subjectReviewen
dc.subjecttime to treatmenten
dc.subjectunmet medical needen
dc.subjectheart failureen
dc.subjectheart stroke volumeen
dc.subjectmulticenter study (topic)en
dc.subjectprospective studyen
dc.subjectrandomized controlled trial (topic)en
dc.subjecttreatment outcomeen
dc.subjectAminobutyratesen
dc.subjectAngiotensin Receptor Antagonistsen
dc.subjectAngiotensinsen
dc.subjectBiphenyl Compoundsen
dc.subjectConsensusen
dc.subjectHeart Failureen
dc.subjectHumansen
dc.subjectMulticenter Studies as Topicen
dc.subjectNeprilysinen
dc.subjectProspective Studiesen
dc.subjectRandomized Controlled Trials as Topicen
dc.subjectReceptors, Angiotensinen
dc.subjectStroke Volumeen
dc.subjectTreatment Outcomeen
dc.subjectSpringeren
dc.titleAngiotensin receptor-neprilysin inhibition in patients with acute decompensated heart failure: an expert consensus position paperen
dc.typeotheren


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