Key result
Compared with ACEI/ARB, sacubitril-valsartan did not reduce cardiovascular mortality but decreased hospitalization for heart failure.
Why the study?
It was unknown whether sacubitril-valsartan could further improve prognosis, cardiac function, and left ventricular remodelling in patients following acute myocardial infarction.
Does sacubitril-valsartan reduce cardiovascular mortality, myocardial reinfarction, and heart failure hospitalization in adult patients following acute myocardial infarction compared to ACEI/ARB?
Meta-Analysis (n=1,358)
Does sacubitril-valsartan reduce cardiovascular mortality, myocardial reinfarction, and heart failure hospitalization in adult patients following acute myocardial infarction compared to ACEI/ARB?
In patients following acute myocardial infarction, early administration of sacubitril-valsartan significantly reduces the risk of heart failure hospitalization and improves left ventricular remodeling compared to conventional ACEI/ARB therapy, though it does not significantly reduce cardiovascular mortality.
Answers are grounded in this paper and cite their sources.
May support early sacubitril-valsartan over ACEI/ARB post-AMI; extends prior HF trial benefits to acute infarction.
AIMS: We aimed to investigate whether sacubitril-valsartan could further improve the prognosis, cardiac function, and left ventricular (LV) remodelling in patients following acute myocardial infarction (AMI). METHODS AND RESULTS: We searched the PubMed, Embase, Cochrane Library, and China National Knowledge Infrastructure (CNKI) from inception to 10 May 2021 to identify potential articles. Randomized controlled trials (RCTs) meeting the inclusion criteria were included and analysed. Thirteen RCTs, covering 1358 patients, were analysed. Compared with angiotensin-converting enzyme inhibitors (ACEI)/angiotensin receptor blockers (ARB), sacubitril-valsartan did not significantly reduced the cardiovascular mortality [risk ratio (RR) 0.65, 95% confidence interval (CI) 0.22 to 1.93, P = 0.434] and the rate of myocardial reinfarction (RR 0.65, 95% CI 0.29 to 1.46, P = 0.295) of patients following AMI, but the rate of hospitalization for heart failure (HF) (RR 0.48, 95% CI 0.35 to 0.66, P < 0.001) and the change of LV ejection fraction (LVEF) [weighted mean difference (WMD) 5.49, 95% CI 3.62 to 7.36, P < 0.001] were obviously improved. The N-terminal pro-brain natriuretic peptide (NT-ProBNP) level (WMD -310.23, 95% CI -385.89 to -234.57, P < 0.001) and the LV end-diastolic dimension (LVEDD) (WMD -3.16, 95% CI -4.59 to -1.73, P < 0.001) were also significantly lower in sacubitril-valsartan group than in ACEI/ARB group. Regarding safety, sacubitril-valsartan did not increase the risk of hypotension, hyperkalaemia, angioedema, and cough. CONCLUSIONS: This meta-analysis suggests that early administration of sacubitril-valsartan may be superior to conventional ACEI/ARB to decrease the risk of hospitalization for HF, improve the cardiac function, and reverse the LV remodelling in patients following AMI.
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Xiong et al. (2021) conducted a meta-analysis in Acute myocardial infarction (AMI) (n=1,358). Sacubitril-valsartan vs. ACEI/ARB was evaluated on Cardiovascular mortality (RR 0.65, 95% CI 0.22 to 1.93, p=0.434). Compared with ACEI/ARB, sacubitril-valsartan did not reduce cardiovascular mortality but decreased hospitalization for heart failure.
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