Key result
Sacubitril/valsartan cuts CV death or HF hospitalization by ~20% vs. enalapril in HFrEF.
Why the study?
Does sacubitril/valsartan improve clinical outcomes in patients with heart failure compared to standard ACE inhibitor therapy?
Does sacubitril/valsartan improve clinical outcomes in patients with heart failure compared to standard ACE inhibitor therapy?
Sacubitril/valsartan is a foundational therapy for HFrEF that provides superior morbidity and mortality benefits compared to ACE inhibitors, though its generalizability to all real-world populations requires ongoing study.
Affirms sacubitril/valsartan superiority in HFrEF; leaves open real-world generalizability questions.
With an estimated prevalence of 5.8 million in the USA and over 23 million people worldwide, heart failure (HF) is growing in epidemic proportions. Despite the use of guideline-directed medical therapies such as angiotensin-converting enzyme inhibitors, beta-adrenergic blockers, angiotensin receptor blockers, and mineralocorticoid receptor antagonists for chronic systolic HF for almost two decades, HF remains a leading cause of morbidity, mortality, and health care expenditures. The Prospective Comparison of Angiotensin Receptor-Neprilysin Inhibitor with Angiotensin-Converting Enzyme Inhibitor to Determine Impact on Global Mortality and Morbidity in Heart Failure (PARADIGM-HF) trial provided compelling evidence for the cardiovascular and mortality benefit of sacubitril/valsartan when compared to enalapril in patients with heart failure and reduced ejection fraction (HFrEF). Sacubitril/valsartan performed better than enalapril across various HFrEF patient characteristics and showed substantial benefit in patients with other common comorbidities. Following the trial, the US Food and Drug Administration approved this drug for the treatment of HF. Various international HF consensus guidelines endorse sacubitril/valsartan as a class I recommendation for the management of symptomatic HFrEF. Although this high-quality clinical study is the largest and the most globally represented trial in HFrEF patients, concerns have been raised regarding the generalizability of the trial results in real-world HF population. The gaps in US Food and Drug Administration labeling and guideline recommendations might lead to this medication being used in a larger population than it was studied in. In this review, we will discuss the current role of sacubitril/valsartan in the management of HF, concerns related to PARADIGM-HF and answers, shortcomings of this novel drug, effects on patient characteristics, real-world eligibility, and the role of ongoing and further investigations to clarify the profile of sacubitril/valsartan in the management of HF.
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Yandrapalli et al. (2017) conducted a review in Heart failure with reduced ejection fraction (HFrEF) (n=8,442). Sacubitril/valsartan vs. Enalapril 10 mg twice daily was evaluated on Composite of death from cardiovascular causes or hospitalization for heart failure (20% decrease). Sacubitril/valsartan reduced the composite primary endpoint of cardiovascular death or heart failure hospitalization by 20% compared to enalapril in patients with HFrEF.
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