Despite significant therapeutic advances, patients with chronic heart failure and reduced ejection fraction (HFrEF) remain at high risk for heart failure progression and death. The PARADIGM-HF study, the largest outcome trial in HFrEF, has shown improved cardiovascular outcomes with sacubitril/valsartan (Entresto®, Novartis), previously known as LCZ696, compared with angiotensin-converting enzyme (ACE) inhibitor therapy, possibly leading us to a new era for heart failure treatment. Sacubitril/valsartan represents a first-in-class drug acting through inhibition of angiotensin receptor and neprilysin, thus modulating the renin-angiotensin-aldosterone system and vasoactive substances such as natriuretic peptides. This approach can be considered a "paradigm shift" from neurohumoral inhibition to neurohumoral modulation. Based on the PARADIGM-HF results, the European Society of Cardiology and the American Heart Association/American College of Cardiology guidelines proposed a substitution of ACE-inhibitor/angiotensin receptor blocker therapy rather than an "add-on" strategy in HFrEF. Sacubitril/valsartan can be considered a milestone in cardiovascular therapy, like aspirin, statins, beta-blockers. Of course there are many questions that arise spontaneously from this trial, three recognized experts can help us to answer them.

[Sacubitril/valsartan, a new and effective treatment for heart failure with reduced ejection fraction] [Sacubitril/valsartan, una nuova ed efficace terapia dello scompenso cardiaco a funzione sistolica ridotta] / Senni, Michele; Trimarco, Bruno; Emdin, Michele; De Biase, Luciano. - In: GIORNALE ITALIANO DI CARDIOLOGIA. - ISSN 1827-6806. - 18:1(2017), pp. S3-S11. [10.1714/2654.27228]

[Sacubitril/valsartan, a new and effective treatment for heart failure with reduced ejection fraction] [Sacubitril/valsartan, una nuova ed efficace terapia dello scompenso cardiaco a funzione sistolica ridotta]

De Biase, Luciano
Membro del Collaboration Group
2017

Abstract

Despite significant therapeutic advances, patients with chronic heart failure and reduced ejection fraction (HFrEF) remain at high risk for heart failure progression and death. The PARADIGM-HF study, the largest outcome trial in HFrEF, has shown improved cardiovascular outcomes with sacubitril/valsartan (Entresto®, Novartis), previously known as LCZ696, compared with angiotensin-converting enzyme (ACE) inhibitor therapy, possibly leading us to a new era for heart failure treatment. Sacubitril/valsartan represents a first-in-class drug acting through inhibition of angiotensin receptor and neprilysin, thus modulating the renin-angiotensin-aldosterone system and vasoactive substances such as natriuretic peptides. This approach can be considered a "paradigm shift" from neurohumoral inhibition to neurohumoral modulation. Based on the PARADIGM-HF results, the European Society of Cardiology and the American Heart Association/American College of Cardiology guidelines proposed a substitution of ACE-inhibitor/angiotensin receptor blocker therapy rather than an "add-on" strategy in HFrEF. Sacubitril/valsartan can be considered a milestone in cardiovascular therapy, like aspirin, statins, beta-blockers. Of course there are many questions that arise spontaneously from this trial, three recognized experts can help us to answer them.
2017
heart failure with reduced ejection fraction; sacubitril/valsartan; aminobutyrates; cardiovascular agents; drug combinations; heart failure; humans; renin-angiotensin system; stroke volume; tetrazoles; treatment outcome; valsartan
01 Pubblicazione su rivista::01a Articolo in rivista
[Sacubitril/valsartan, a new and effective treatment for heart failure with reduced ejection fraction] [Sacubitril/valsartan, una nuova ed efficace terapia dello scompenso cardiaco a funzione sistolica ridotta] / Senni, Michele; Trimarco, Bruno; Emdin, Michele; De Biase, Luciano. - In: GIORNALE ITALIANO DI CARDIOLOGIA. - ISSN 1827-6806. - 18:1(2017), pp. S3-S11. [10.1714/2654.27228]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1550406
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