The Impact of Sacubitril/Valsartan on Heart Failure Patient with Reduced Left Ventricular Ejection Fraction: Single Center Retrospective Study in Saudi Arabia.

Drug Healthc Patient Saf

Department of Pharmaceutical Care, King Abdulaziz Medical City, Ministry of the National Guard-Health Affairs, Riyadh, Saudi Arabia.

Published: September 2024

AI Article Synopsis

  • Sacubitril/valsartan (S/V) is a medication for heart failure with reduced ejection fraction (HFrEF), aimed at improving heart function and reducing hospitalizations.* -
  • A study with 107 patients showed no significant improvement in left ventricular ejection fraction (LVEF) after using S/V, although hospitalizations due to heart failure symptoms decreased numerically.* -
  • Overall, S/V was well tolerated but did not demonstrate a strong benefit for LVEF improvement, suggesting that heart failure clinics should carefully manage dosing for optimal results.*

Article Abstract

Background: Sacubitril/valsartan (S/V) is used in managing heart failure with reduced ejection fraction (HFrEF), reducing morbidity and mortality while improving symptoms and prognosis. This study aims to evaluate the effectiveness of S/V in patients with reduced left ventricular ejection fraction (LVEF) and its safety.

Methods:  This retrospective cohort study included adult patients aged ≥18 years diagnosed with HFrEF, receiving S/V, and followed up at a tertiary hospital in Riyadh. Primary outcomes included improvements in LVEF on echocardiography and the number of hospitalizations due to acute decompensated heart failure (ADHF). Secondary outcomes assessed the safety profile of S/V. Multinomial logistic regression analysis was performed with statistical significance set at P < 0.05. .

Results: The study included 107 patients: 80 with LVEF < 30% and 27 with LVEF 30-40%. Six-month follow-up, LVEF improvement was categorized into three groups: no improvement, LVEF increased by 1 to <10 points, and LVEF increased by ≥10 points. The LVEF was similar across groups (P = 0.59). Although hospitalizations due to ADHF were not significantly different between groups, they numerically decreased after initiating S/V (P = 0.1). S/V was generally well tolerated.

Conclusion: This study suggests no significant benefit from S/V regarding LVEF improvement. It is recommended that heart failure clinics assess and titrate S/V to the maximum tolerated dose.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11451457PMC
http://dx.doi.org/10.2147/DHPS.S471867DOI Listing

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