Effect of Sacubitril/Valsartan on Patients Having Heart Failure With Preserved Left Ventricular Ejection Fraction

Akira Mima1, Hidemasa Gotoda2, Shinji Lee2

  • 1Department of Nephrology, Osaka Medical and Pharmaceutical University, Osaka, Japan; akira.mima@ompu.ac.jp.

PubMed

Insights

Sacubitril/valsartan (SV) showed a trend towards lowering blood pressure and heart rate in heart failure patients on hemodialysis. However, long-term SV therapy did not significantly improve cardiac function markers like BNP or LVEF in this population.

Area of Science:

  • Cardiology
  • Nephrology
  • Pharmacology

Background:

  • Sacubitril/valsartan (SV) is a novel drug class targeting the neprilysin pathway and renin-angiotensin-aldosterone system.
  • SV is effective in heart failure (HF) management, but its long-term effects in patients with preserved ejection fraction on hemodialysis (HD) are unknown.

Purpose of the Study:

  • To evaluate the long-term efficacy and safety of Sacubitril/valsartan (SV) in patients with HF and preserved left ventricular ejection fraction (LVEF) undergoing hemodialysis (HD).

Main Methods:

  • A single-center retrospective study over 21 months.
  • Included consecutive patients with HF and preserved LVEF on HD, treated with SV (50-200 mg/day).
  • Clinical, biochemical, and echocardiographic parameters were assessed at baseline and during follow-up.

Main Results:

  • Nine patients (median age 76 years, median HD duration 7 years) were included.
  • SV therapy showed a non-significant trend towards decreasing systolic and diastolic blood pressure and heart rate.
  • No significant changes were observed in brain natriuretic peptide (BNP) levels, LVEF, left atrial dimension, or left ventricular mass index.

Conclusions:

  • Sacubitril/valsartan (SV) may help reduce blood pressure and heart rate in HF patients with preserved LVEF on hemodialysis.
  • SV did not demonstrate significant improvements in cardiac function markers (BNP, echocardiography) in this specific patient group.
  • No adverse effects were reported during the study period, suggesting a favorable safety profile.
Abstract

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