Related Experiment Video
Updated: Aug 6, 2026

Reduction in Left Ventricular Wall Stress and Improvement in Function in Failing Hearts using Algisyl-LVR
Published on: April 8, 2013
Valsartan in the treatment of heart attack survivors
1Walter Mackenzie Health Sciences Centre, Division of Cardiology, Department of Medicine, University of Alberta, Edmonton, Alberta, Canada. bjugdutt@ualberta.ca
Insights
Survivors of myocardial infarction (MI) face high risks. Angiotensin II receptor blockers (ARBs) like valsartan offer effective secondary prevention, reducing mortality and morbidity post-MI.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Survivors of myocardial infarction (MI) are at significant risk for disability and death.
- Infarct-related complications include heart failure, cardiac remodeling, and arrhythmias.
- Angiotensin II (Ang II), a key renin-angiotensin-aldosterone system (RAAS) molecule, contributes to these complications.
Purpose of the Study:
- To review evidence favoring valsartan for secondary prevention in post-MI survivors.
- To compare the efficacy of Angiotensin II receptor blockers (ARBs) with ACE inhibitors.
Main Methods:
- Review of major clinical trials (VALIANT, Val-HeFT).
- Analysis of data comparing ARBs (specifically valsartan) to ACE inhibitors.
- Assessment of outcomes in high-risk post-MI patients with left ventricular systolic dysfunction and/or heart failure.
Main Results:
- Angiotensin receptor blockers (ARBs) provide more complete blockade of Ang II effects at the AT1 receptor.
- Valsartan demonstrated efficacy comparable to ACE inhibitors in reducing mortality and morbidity.
- Evidence supports valsartan's role in secondary prevention for post-MI survivors.
Conclusions:
- RAAS inhibition is crucial for managing post-MI complications.
- Valsartan is a viable and effective option for secondary prevention after myocardial infarction.
- ARBs offer a valuable therapeutic strategy in high-risk post-MI populations.
Abstract:
Survivors of myocardial infarction (MI) are at high risk of disability and death. This is due to infarct-related complications such as heart failure, cardiac remodeling with progressive ventricular dilation, dysfunction, and hypertrophy, and arrhythmias including ventricular and atrial fibrillation. Angiotensin (Ang) II, the major effector molecule of the renin-angiotensin-aldosterone system (RAAS) is a major contributor to these complications. RAAS inhibition, with angiotensin-converting enzyme (ACE) inhibitors were first shown to reduce mortality and morbidity after MI. Subsequently, angiotensin receptor blockers (ARBs), that produce more complete blockade of the effects of Ang II at the Ang II type 1 (AT1) receptor, were introduced and the ARB valsartan was shown to be as effective as an ACE inhibitor in reducing mortality and morbidity in high-risk post-MI survivors with left ventricular (LV) systolic dysfunction and and/or heart failure and in heart failure patients, respectively, in two major trials (VALIANT and Val-HeFT). Both these trials used an ACE inhibitor as comparator on top of background therapy. Evidence favoring the use of valsartan for secondary prevention in post-MI survivors is reviewed.
Related Concept Videos
Antihypertensive Drugs: Angiotensin II Receptor Blockers
Antihypertensive Drugs: Direct Renin Inhibitors
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
Heart Failure Drugs: β-Blockers
Aortic Regurgitation III: Medical Management
Heart Failure V: Medical Management

