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The Efficacy of Sacubitril/Valsartan (ARNI) in Decreasing Mortality Among Heart Failure Patients: A Systematic Review
Hashim Talib Hashim1, Mohammedbaqer Ali Al-Ghuraibawi2, Muhammad Hassan Hafeez3
1Department of research, University of Warith Al-Anbiyaa, College of Medicine, Karbala, Iraq.
Insights
Sacubitril/Valsartan significantly reduces NT-proBNP levels and disease events in chronic heart failure (CHF) patients. While effective, monitor for hypotension, as it was the most common adverse event.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Chronic heart failure (CHF) is a major cause of mortality and morbidity worldwide.
- Sacubitril/Valsartan, an angiotensin receptor-neprilysin inhibitor (ARNI), shows promise in improving CHF outcomes.
Purpose of the Study:
- To systematically review and meta-analyze the efficacy and safety of Sacubitril/Valsartan versus conventional therapies in CHF patients.
Main Methods:
- Systematic review following PRISMA 2020 guidelines, searching PubMed, Scopus, and Web of Science.
- Included 10 randomized controlled trials (15,650 patients) comparing Sacubitril/Valsartan with standard therapies.
- Meta-analyses assessed pooled outcomes, including NT-proBNP levels, disease events, and adverse events.
Main Results:
- Sacubitril/Valsartan significantly reduced NT-proBNP levels (SMD = -0.30, p = 0.03) and disease-related events (OR = 0.82, p < 0.00001).
- Hypotension was the most frequent adverse event (OR = 1.57, p < 0.0001).
- No significant differences in hyperkalemia or renal dysfunction compared to controls.
Conclusions:
- Sacubitril/Valsartan improves outcomes and reduces mortality/morbidity in CHF patients.
- The drug has an acceptable safety profile, with hypotension being the primary concern.
- Sacubitril/Valsartan is an effective therapeutic option for managing CHF.
Introduction:
Chronic heart failure (CHF) remains a leading cause of global morbidity and mortality, frequently resulting in hospitalizations and diminished quality of life. Sacubitril/ Valsartan, the first angiotensin receptor-neprilysin inhibitor (ARNI) approved by the FDA, has shown promising effects in reducing mortality and improving clinical outcomes. This systematic review and meta-analysis aimed to evaluate the efficacy and safety of Sacubitril/ Valsartan compared with conventional therapies in patients with CHF.
Methods:
A systematic review was conducted following PRISMA 2020 guidelines. PubMed, Scopus, and Web of Science were searched up to April 18, 2024, using predefined terms. Eligible studies included randomized controlled trials comparing Sacubitril/Valsartan with standard therapies in adult CHF patients. Data extraction was performed independently by multiple reviewers, and study quality was assessed using the JBI checklist. Meta-analyses were conducted to estimate pooled outcomes.
Results:
Ten randomized controlled trials, including 15,650 patients, were analyzed. The mean age across studies was 68.4 years, with males comprising 59.4% of the Sacubitril/Valsartan group and 63.3% of the control group. Sacubitril/Valsartan significantly reduced NT-proBNP levels (SMD = -0.30, 95% CI: -0.58 to -0.03; p = 0.03) and disease-related events (OR = 0.82, 95% CI: 0.76-0.89; p < 0.00001). Hypotension was the most frequently reported adverse event (OR = 1.57, 95% CI: 1.28-1.93; p < 0.0001), whereas hyperkalemia and renal dysfunction did not differ significantly from control groups.
Discussion:
The findings indicate that Sacubitril/Valsartan improves outcomes in patients with CHF and exhibits an acceptable safety profile, although clinicians should monitor for hypotension.
Conclusion:
Sacubitril/Valsartan represents an effective therapeutic option for CHF, providing significant benefits in reducing mortality and morbidity compared with standard therapy.
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