Renal effects of guideline-directed medical therapies in heart failure: a consensus document from the Heart Failure Association of the European Society of Cardiology

dc.contributor.authorMullens, Wilfried
dc.contributor.authorMartens, Pieter
dc.contributor.authorTestani, Jeffrey Moore
dc.contributor.authorTang, W. H.wlison
dc.contributor.authorSkouri, Hadi N.
dc.contributor.authorVerbrugge, Frederik Hendrik
dc.contributor.authorFudim, Marat
dc.contributor.authorIacoviello, Massimo
dc.contributor.authorFranke, Jennifer C.
dc.contributor.authorFlammer, Andreas J.
dc.contributor.authorPalazzuoli, Alberto
dc.contributor.authorBarragan, Paola Morejon
dc.contributor.authorThum, Thomas
dc.contributor.authorMarcos, Marta Cobo
dc.contributor.authorMiró, Ò.
dc.contributor.authorRossignol, Patrick
dc.contributor.authorMetra, Marco
dc.contributor.authorLassus, Johan P.E.
dc.contributor.authorOrso, Francesco
dc.contributor.authorJankowska, Ewa Anita
dc.contributor.authorChioncel, O. Dragomir
dc.contributor.authorMiličić, Davor
dc.contributor.authorHill, Loreena Michelle
dc.contributor.authorSeferović, Petar M.
dc.contributor.authorRosano, Giuseppe Massimo Claudio
dc.contributor.authorCoats, Andrew J.S.
dc.contributor.authorDamman, Kevin
dc.contributor.departmentInternal Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:44:23Z
dc.date.available2025-01-24T11:44:23Z
dc.date.issued2022
dc.description.abstractNovel pharmacologic treatment options reduce mortality and morbidity in a cost-effective manner in patients with heart failure (HF). Undisputedly, the effective implementation of these agents is an essential element of good clinical practice, which is endorsed by the European Society of Cardiology (ESC) guidelines on acute and chronic HF. Yet, physicians struggle to implement these therapies as they have to balance the true and/or perceived risks versus their substantial benefits in clinical practice. Any worsening of biomarkers of renal function is often perceived as being disadvantageous and is in clinical practice one of the most common reasons for ineffective drug implementation. However, even in this context, they clearly reduce mortality and morbidity in HF with reduced ejection fraction (HFrEF) patients, even in patients with poor renal function. Furthermore these agents are also beneficial in HF with mildly reduced ejection fraction (HFmrEF) and sodium–glucose cotransporter 2 (SGLT2) inhibitors more recently demonstrated a beneficial effect in HF with preserved ejection fraction (HFpEF). The emerge of several new classes (angiotensin receptor–neprilysin inhibitor [ARNI], SGLT2 inhibitors, vericiguat, omecamtiv mecarbil) and the recommendation by the 2021 ESC guidelines for the diagnosis and treatment of acute and chronic HF of early initiation and titration of quadruple disease-modifying therapies (ARNI/angiotensin-converting enzyme inhibitor + beta-blocker + mineralocorticoid receptor antagonist and SGLT2 inhibitor) in HFrEF increases the likelihood of treatment-induced changes in renal function. This may be (incorrectly) perceived as deleterious, resulting in inertia of starting and uptitrating these lifesaving therapies. Therefore, the objective of this consensus document is to provide advice of the effect HF drugs on renal function. © 2022 European Society of Cardiology.
dc.identifier.doihttps://doi.org/10.1002/ejhf.2471
dc.identifier.eid2-s2.0-85127333715
dc.identifier.pmid35239201
dc.identifier.urihttp://hdl.handle.net/10938/30442
dc.language.isoen
dc.publisherJohn Wiley and Sons Ltd
dc.relation.ispartofEuropean Journal of Heart Failure
dc.sourceScopus
dc.subjectHeart failure
dc.subjectPharmacological therapy
dc.subjectRenal function
dc.subjectAngiotensin receptor antagonists
dc.subjectAngiotensin-converting enzyme inhibitors
dc.subjectCardiology
dc.subjectChronic disease
dc.subjectConsensus
dc.subjectHumans
dc.subjectKidney
dc.subjectSodium-glucose transporter 2 inhibitors
dc.subjectStroke volume
dc.subjectVentricular dysfunction, left
dc.subjectAldosterone
dc.subjectAngiotensin i
dc.subjectAngiotensin ii
dc.subjectAngiotensin receptor
dc.subjectAngiotensin receptor antagonist
dc.subjectBeta adrenergic receptor blocking agent
dc.subjectDipeptidyl carboxypeptidase
dc.subjectDipeptidyl carboxypeptidase inhibitor
dc.subjectDiuretic agent
dc.subjectEnkephalinase inhibitor
dc.subjectIvabradine
dc.subjectMineralocorticoid antagonist
dc.subjectMineralocorticoid receptor
dc.subjectNatriuretic factor
dc.subjectOmecamtiv mecarbil
dc.subjectSacubitril plus valsartan
dc.subjectSodium glucose cotransporter 2
dc.subjectSodium glucose cotransporter 2 inhibitor
dc.subjectVericiguat
dc.subjectArticle
dc.subjectChronic kidney failure
dc.subjectClinical outcome
dc.subjectClinical practice
dc.subjectDrug dose titration
dc.subjectEuropean
dc.subjectGlomerulus filtration rate
dc.subjectHuman
dc.subjectKidney function
dc.subjectKidney tubule function
dc.subjectMedical society
dc.subjectMorbidity
dc.subjectMortality
dc.subjectNonhuman
dc.subjectPathophysiology
dc.subjectPractice guideline
dc.subjectPrognosis
dc.subjectRenin angiotensin aldosterone system
dc.subjectDrug therapy
dc.subjectHeart left ventricle function
dc.subjectHeart stroke volume
dc.subjectPhysiology
dc.titleRenal effects of guideline-directed medical therapies in heart failure: a consensus document from the Heart Failure Association of the European Society of Cardiology
dc.typeArticle

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