Early in-hospital initiation of angiotensin-receptor-neprilysin inhibitor in post-acute myocardial infarction patients with impaired left ventricular systolic function: a systematic review and meta-analysis of randomized controlled trials
In brief
Early in-hospital ARNI prevents one major cardiac event per 7 patients
Starting an angiotensin-receptor-neprilysin inhibitor during the index admission for myocardial infarction reduced major adverse cardiovascular events by about 40% (NNT≈7) and halved ventricular arrhythmias, while modestly improving ejection fraction and lowering NT-proBNP. The benefit came with a slight rise in symptomatic hypotension, so close monitoring is needed, and longer-term outcomes remain unknown.
- Journal
- Frontiers in cardiovascular medicine (Q1)
- Published
- 21 July 2026
- Study design
- Systematic review / meta-analysis of RCTs
- Evidence level
- Level 1, High (CEBM 1a)
- Authors
- Quynh Nguyen, Trang Thi Quynh Tran, Chia-Te Liao, Chung-Lieh Hung, Hung-Yu Chang, Chih-Wei Chen, et al.
- PMID
- 42553042
- DOI
- 10.3389/fcvm.2026.1877075
Why clinicians should know about it
- Picked for Cardiology and Cardiovascular Medicine (top studies of the week, 9 August 2026).
- Picked for Epidemiology (top studies of the week, 9 August 2026).
- Picked for Neurology (clinical) (top studies of the week, 9 August 2026).
Abstract
AIMS: Heart failure (HF) is a common and serious complication following acute myocardial infarction (AMI), particularly in patients with impaired left ventricular systolic function [left ventricular ejection fraction (LVEF) < 50%] during hospitalization. Although angiotensin-receptor-neprilysin inhibitor (ARNI) therapy has proven benefit in chronic HF, evidence supporting its initiation during the index AMI admission remains limited. This study systematically evaluated the effects of early in-hospital initiation of ARNI therapy compared with angiotensin-converting enzyme (ACE) inhibitor or angiotensin receptor blocker (ARB) therapy on cardiovascular outcomes in post- AMI patients with impaired systolic function. METHODS: This systematic review and meta-analysis was prospectively registered in the International Prospective Register of Systematic Reviews (PROSPERO CRD420251007504). A comprehensive search was completed on 30 August 2025. We included randomized controlled trials (RCTs) enrolling hospitalized AMI patients with impaired systolic function (LVEF <50%) who initiated ARNI therapy during the index admission. The primary outcome was major adverse cardiovascular events (MACEs), defined as HF hospitalization, all-cause mortality, or recurrent acute coronary syndrome. Secondary outcomes included incidence of ventricular arrhythmia, cardiovascular death, stroke, changes in left-ventricular ejection fraction, NT-proBNP levels, and adverse events (AEs). Prespecified subgroup analyses and meta-regression were performed. RESULTS: Twelve RCTs comprising 7,539 patients (ARNI: n = 3,771; ACEI/ARB: n = 3,768) were included, with a mean follow-up of approximately 6 months. Early in-hospital ARNI initiation significantly reduced MACEs [risk ratio (RR) 0.58; 95% CI 0.41-0.83; number-needed-to-treat (NNT) ≈ 7] and ventricular arrhythmia (RR 0.51; 95% CI 0.35-0.75; NNT ≈ 25). ARNI therapy improved LVEF (mean difference +2.54%; 95% CI +1.34 to +3.75) and reduced NT-proBNP levels (mean difference -424 pg/mL; 95% CI -779 to -68). However, ARNI was associated with higher rates of AEs (RR 1.16; 95% CI 1.14-1.19), primarily symptomatic hypotension (RR 1.32; 95% CI 1.20-1.46). Results were consistent across subgroups, with greater incremental benefit observed among patients who underwent successful primary percutaneous coronary intervention. CONCLUSIONS: Among hospitalized post-AMI patients with impaired left ventricular systolic function, early in-hospital initiation of ARNI reduces MACEs, lowers the incidence of ventricular arrhythmia, and improves ventricular function compared with ACEI/ARB therapy, although careful monitoring for hypotension is required. These findings support early in-hospital ARNI adoption in this high-risk population and underscore the need for longer-term outcome studies.
Abstract as published, via PubMed.
For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.