2022
DOI: 10.23736/s2724-5683.21.05802-6
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Assessment of sacubitril/valsartan effects on left ventricular dynamics using 3D echocardiography and 3D strain in heart failure with reduced ejection fraction patients

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Cited by 4 publications
(2 citation statements)
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“…Finally, continuous research in pharmacology is providing us with drugs which may more specifically target and slow down myocardial fibrotic processes. Among them, it is worth mentioning sacubitril/valsartan 37 and sodium-glucose co-transporter 2 (SGLT2) inhibitors, 38 which in future clinical trials could be specifically tested with the aim of reducing fibrosis development and progression.…”
Section: Discussionmentioning
confidence: 99%
“…Finally, continuous research in pharmacology is providing us with drugs which may more specifically target and slow down myocardial fibrotic processes. Among them, it is worth mentioning sacubitril/valsartan 37 and sodium-glucose co-transporter 2 (SGLT2) inhibitors, 38 which in future clinical trials could be specifically tested with the aim of reducing fibrosis development and progression.…”
Section: Discussionmentioning
confidence: 99%
“…SV is the first US Food and Drug Administration (FDA)approved drug for the treatment of patients with chronic heart failure who have a reduced ejection fraction in NYHA classes II, III, or IV [6]. Many studies have demonstrated that SV significantly improves LVEF and left ventricular remodeling in patients with heart failure [7][8][9]. SV can also reduce re-hospitalization and mortality rates in patients with acute heart failure with reduced ejection fraction [10][11][12].…”
Section: Introductionmentioning
confidence: 99%