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Published on: April 8, 2013
Optimal Maintenance Strategy for Patients with Improved Left Ventricular Function Following Sacubitril/Valsartan
Yoonjee Park1, Minjung Bak2,3, Heayoung Shin2
1Department of Cardiology, Bucheon Sejong Hospital, 28, Bucheon-si 14754, Republic of Korea.
Insights
Maintaining sacubitril/valsartan (S/V) or switching to a renin-angiotensin system blocker (RASB) is crucial for patients with heart failure with improved ejection fraction (HFimpEF). Discontinuing both therapies significantly increases the risk of heart failure relapse.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Optimal pharmacological management after left ventricular ejection fraction (LVEF) improvement in heart failure (HF) is not well-established.
- Patients with HF and improved EF (HFimpEF) represent a growing population requiring specific treatment strategies.
Purpose of the Study:
- To compare clinical outcomes in HFimpEF patients based on maintaining sacubitril/valsartan (S/V) versus switching to a renin-angiotensin system blocker (RASB).
- To evaluate the impact of discontinuing S/V and RASB on HF relapse in this patient cohort.
Main Methods:
- Retrospective analysis of 354 patients with recovered LVEF (≥40%) after S/V treatment.
- Patients were grouped into: continued S/V (n=294), switched to RASB (n=47), or discontinued both (n=13).
- Primary endpoint: HF relapse (2-fold NT-proBNP increase >400 pg/dL); Secondary endpoints: NT-proBNP level changes.
Main Results:
- No significant difference in HF relapse or NT-proBNP levels between S/V maintenance and RASB switch groups.
- Discontinuation of both S/V and RASB was associated with a significantly higher HF relapse rate (53.8%) compared to maintenance groups (10.6%-16.3%; p=0.001).
- NT-proBNP levels showed a more pronounced increase in the group that discontinued both therapies.
Conclusions:
- Replacing S/V with another RASB is a safe strategy for maintaining remission in HFimpEF patients.
- Discontinuing all guideline-directed medical therapy in HFimpEF significantly elevates the risk of relapse.
- Prospective studies are needed to confirm these findings and optimize long-term management.
Abstract:
Background and Objectives: Optimal pharmacological treatment following left ventricular ejection fraction (LVEF) improvement remains largely unknown. This study compared the clinical outcomes of patients with heart failure (HF) with improved EF (HFimpEF) based on the maintenance of sacubitril/valsartan (S/V) or transition to a renin-angiotensin system blocker (RASB). Material and Method: A total of 354 patients with recovered LVEF of at least 40% after S/V treatment from a single center were retrospectively analyzed. Patients were categorized into three groups: those who continued S/V (n = 294), those who switched to RASB (n = 47), and those who discontinued both S/V and RASB (n = 13). The primary endpoint was HF relapse, defined as a two-fold increase in baseline serum N-terminal-pro hormone B-type natriuretic peptide (NT-proBNP) concentration exceeding 400 pg/dL. Secondary endpoints included the ratio and difference between baseline and peak NT-proBNP levels. Result: Baseline clinical characteristics were well balanced among groups. Over a median follow-up of 399 (252-589) days, HF relapse occurred more frequently in patients who discontinued both S/V and RASB compared to those who maintained either treatment (53.8% vs. 16.3% vs. 10.6%; p = 0.001). NT-proBNP levels also showed a more pronounced increase in this group. However, there were no significant differences in primary or secondary outcomes between the S/V and RASB groups. Conclusions: Our findings suggest that replacing S/V with another RASB does not worsen outcomes in patients with HFimpEF after S/V treatment, whereas discontinuation of both therapies is associated with a significantly higher risk of HF relapse. A prospective trial is warranted to confirm the safety and effectiveness of this approach in maintaining remission.
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