From the Guidelines
The management of compensated heart failure should prioritize the use of ACE inhibitors, beta-blockers, and diuretics as the cornerstone of treatment, with consideration of additional therapies such as ARBs, aldosterone receptor antagonists, and hydralazine/isosorbide dinitrate in specific patient populations, as recommended by the 2013 ACCF/AHA guideline for the management of heart failure 1.
Key Components of Treatment
- ACE inhibitors (like lisinopril 10-40mg daily or enalapril 2.5-20mg twice daily) or ARBs (such as losartan 25-100mg daily) to reduce afterload and remodeling, as supported by the guideline's Class I recommendation for ACE inhibitors in all patients with HFrEF 1.
- Beta-blockers (metoprolol succinate 12.5-200mg daily or carvedilol 3.125-25mg twice daily) to reduce workload on the heart, with a Class I recommendation for their use in all stable patients with HFrEF 1.
- Diuretics (furosemide 20-80mg daily or as needed) to manage fluid retention, recommended for patients with HFrEF and fluid retention, with a Class I recommendation 1.
Additional Therapies
- Aldosterone receptor antagonists (such as spironolactone 12.5-50mg daily) are beneficial for patients with NYHA class II-IV and LVEF ≤35%, with a Class I recommendation 1.
- The combination of hydralazine and isosorbide dinitrate is recommended for African Americans with NYHA class III-IV HFrEF on GDMT, with a Class I recommendation 1.
- Omega-3 PUFA supplementation is reasonable to use as adjunctive therapy in HFrEF or HFpEF patients, with a Class IIa recommendation 1.
Lifestyle Modifications
- Sodium restriction (<2g daily)
- Fluid restriction if needed
- Regular moderate exercise
- Smoking cessation
- Limiting alcohol intake
Monitoring and Follow-Up
Regular monitoring of weight, symptoms, and medication adherence helps prevent decompensation. This comprehensive approach addresses the neurohormonal and hemodynamic abnormalities in heart failure, reducing symptoms and improving long-term outcomes, as supported by the guideline's recommendations 1.
From the FDA Drug Label
The primary objective of PARADIGM-HF was to determine whether sacubitril and valsartan, a combination of sacubitril and an RAS inhibitor (valsartan), was superior to an RAS inhibitor (enalapril) alone in reducing the risk of the combined endpoint of cardiovascular (CV) death or hospitalization for heart failure (HF) PARADIGM-HF demonstrated that sacubitril and valsartan, an combination of sacubitril and a RAS inhibitor (valsartan), was superior to a RAS inhibitor (enalapril), in reducing the risk of the combined endpoint of cardiovascular death or hospitalization for heart failure, based on a time-to-event analysis (hazard ratio [HR] 0.8; 95% confidence interval [CI], 0.73,0.87, p < 0. 0001)
Compensated Heart Failure Management: Sacubitril and valsartan is superior to enalapril in reducing the risk of cardiovascular death or hospitalization for heart failure in patients with symptomatic chronic heart failure (NYHA class II to IV) and systolic dysfunction (left ventricular ejection fraction ≤40%) 2.
- The treatment effect reflected a reduction in both cardiovascular death and heart failure hospitalization.
- Sacubitril and valsartan also improved overall survival (HR 0.84; 95% CI [0.76,0.93], p = 0. 0009) 2.
From the Research
Compensated Heart Failure Management
- Heart failure is a chronic condition that affects the heart's functional capacity, resulting in symptoms such as fatigue, edema, and dyspnea 3.
- The American College of Cardiology (ACC) provides guidelines for the pharmacotherapy of heart failure, which include the use of beta-blockers, angiotensin-converting enzyme inhibitors, and angiotensin receptor blockers 3, 4.
- The use of sacubitril-valsartan has been shown to improve clinical outcomes in patients with heart failure and ejection fraction at or less than 60% compared to angiotensin converting enzyme inhibitor or angiotensin receptor blocker 5.
- A mnemonic device, BANDAID, has been developed to summarize the evidence-based treatments for systolic heart failure, which includes beta-blocker, angiotensin-converting enzyme inhibitor/angiotensin receptor blocker, nitrate-hydralazine, diuretics, aldosterone antagonist, ivabradine, devices, and digoxin 4.
- The addition of an angiotensin receptor blocker to patients already receiving an angiotensin-converting enzyme inhibitor plus an aldosterone antagonist, with or without a beta blocker, has been shown to be effective and tolerable in patients with heart failure 6.
Treatment Options
- Beta-blockers are recommended for patients with heart failure to reduce mortality and hospitalization rates 3, 4.
- Angiotensin-converting enzyme inhibitors and angiotensin receptor blockers are also recommended to reduce mortality and hospitalization rates in patients with heart failure 3, 4.
- Sacubitril-valsartan has been shown to be effective in reducing morbidity and mortality in patients with heart failure and ejection fraction at or less than 60% 5.
- Diuretics, aldosterone antagonists, and ivabradine are also used in the treatment of heart failure to reduce symptoms and improve outcomes 4.
Clinical Outcomes
- The use of sacubitril-valsartan has been shown to improve 6- and 12-month clinical outcomes, including heart failure hospitalization, all-cause hospitalization, and all-cause mortality, compared to angiotensin converting enzyme inhibitor or angiotensin receptor blocker 5.
- The addition of an angiotensin receptor blocker to patients already receiving an angiotensin-converting enzyme inhibitor plus an aldosterone antagonist, with or without a beta blocker, has been shown to reduce cardiovascular death or heart failure hospitalization 6.
- The use of beta-blockers, angiotensin-converting enzyme inhibitors, and angiotensin receptor blockers has been shown to reduce mortality and hospitalization rates in patients with heart failure 3, 4.