Trend of perceived quality of life and functional capacity in outpatients with chronic heart failure and in treatment with sacubitril/valsartan: a real-life experience.


Journal

Minerva cardiology and angiology
ISSN: 2724-5772
Titre abrégé: Minerva Cardiol Angiol
Pays: Italy
ID NLM: 101776555

Informations de publication

Date de publication:
Oct 2022
Historique:
pubmed: 8 4 2021
medline: 24 9 2022
entrez: 7 4 2021
Statut: ppublish

Résumé

Despite the use of optimal medical therapy, heart failure and reduced left ventricular ejection fraction (HFrEF) remains a leading cause of morbidity, mortality and health care costs. The introduction of angiotensin receptor/neprilysin inhibitors (ARNIs) had a revolutionary impact on the treatment of patients with HFrEF. The aim of the study was to monitor over time the perceived quality of life, the physical performance, the trend of BNP and NT-ProBNP and the NYHA functional class in patients with HFrEF during treatment with sacubitril/valsartan. We enrolled 37 patients (63±10 years old, 76% men) who underwent a total of one-year follow-up. All patients underwent clinical evaluation, 6MWT, blood analysis (in particular, NT-pro-BNP and BNP, renal function test); Kansas City Cardiomyopathy Questionnaire (KCCQ) and the NYHA functional class assessment were also performed, at the beginning of the study and after 3, 6 and 12 months of therapy. We observed at each follow-up a significant improvement of KCCQ score, 6MWT, NT-ProBNP, BNP and NYHA class. However, analyzing the ∆% of variation of each single parameter, the improvement was not uniform in time. We also observed that only 37% of patients tolerated the full recommended dose of sacubitril/valsartan (97/103 mg b.i.d.); of the remaining, 40% tolerated the intermediate dose (49/51 mg b.i.d.) and 23% the minimum (24/26 md b.i.d.). Sacubitril/valsartan therapy improves significantly quality of life, physical effort resistance, BNP and NT-ProBNP and NYHA functional class in patients with HFrEF. Although not all the patients tolerated the maximum recommended dose, the beneficial effects were significant even at lower doses.

Sections du résumé

BACKGROUND BACKGROUND
Despite the use of optimal medical therapy, heart failure and reduced left ventricular ejection fraction (HFrEF) remains a leading cause of morbidity, mortality and health care costs. The introduction of angiotensin receptor/neprilysin inhibitors (ARNIs) had a revolutionary impact on the treatment of patients with HFrEF. The aim of the study was to monitor over time the perceived quality of life, the physical performance, the trend of BNP and NT-ProBNP and the NYHA functional class in patients with HFrEF during treatment with sacubitril/valsartan.
METHODS METHODS
We enrolled 37 patients (63±10 years old, 76% men) who underwent a total of one-year follow-up. All patients underwent clinical evaluation, 6MWT, blood analysis (in particular, NT-pro-BNP and BNP, renal function test); Kansas City Cardiomyopathy Questionnaire (KCCQ) and the NYHA functional class assessment were also performed, at the beginning of the study and after 3, 6 and 12 months of therapy.
RESULTS RESULTS
We observed at each follow-up a significant improvement of KCCQ score, 6MWT, NT-ProBNP, BNP and NYHA class. However, analyzing the ∆% of variation of each single parameter, the improvement was not uniform in time. We also observed that only 37% of patients tolerated the full recommended dose of sacubitril/valsartan (97/103 mg b.i.d.); of the remaining, 40% tolerated the intermediate dose (49/51 mg b.i.d.) and 23% the minimum (24/26 md b.i.d.).
CONCLUSIONS CONCLUSIONS
Sacubitril/valsartan therapy improves significantly quality of life, physical effort resistance, BNP and NT-ProBNP and NYHA functional class in patients with HFrEF. Although not all the patients tolerated the maximum recommended dose, the beneficial effects were significant even at lower doses.

Identifiants

pubmed: 33823573
pii: S2724-5683.20.05494-8
doi: 10.23736/S2724-5683.20.05494-8
doi:

Substances chimiques

Aminobutyrates 0
Angiotensin Receptor Antagonists 0
Biphenyl Compounds 0
Receptors, Angiotensin 0
Tetrazoles 0
sacubitril 17ERJ0MKGI
Valsartan 80M03YXJ7I
Neprilysin EC 3.4.24.11

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

555-562

Auteurs

Giuseppe Dattilo (G)

Section of Cardiology, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Roberto Bitto (R)

Section of Cardiology, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Michele Correale (M)

Unit of Cardiology, Policlinico Riuniti University Hospital, Foggia, Italy - michele.correale@libero.it.

Claudia Morabito (C)

Section of Cardiology, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Vittoria Vaccaro (V)

Section of Cardiology, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Giulia Laterra (G)

Section of Cardiology, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Matteo Casale (M)

Section of Cardiology, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Pasquale Crea (P)

Section of Cardiology, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Gianluca DI Bella (G)

Section of Cardiology, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Francesco Luzza (F)

Section of Cardiology, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Alessandro Migliorato (A)

Section of Cardiology, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Niki Katsiki (N)

School of Medicine, Second Department of Propaedeutic Internal Medicine, Hippocration Hospital, Aristotle University, Thessaloniki, Greece.

Cesare DE Gregorio (C)

Section of Cardiology, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

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Classifications MeSH