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VALIANT (VALsartan In Acute myocardial iNfarcTion) trial
Aldo Pietro Maggioni1, Gianna Fabbri
1ANMCO Research Center, Via La Marmora 34, 50121 Florence, Italy. maggioni@anmco.it
Insights
Valsartan, an angiotensin receptor blocker, is a viable alternative to ACE inhibitors for patients with heart failure or left ventricular dysfunction after myocardial infarction. The VALIANT trial found no significant difference in mortality or adverse cardiovascular events between valsartan and captopril.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Angiotensin-converting enzyme inhibitors (ACE-Is) are standard treatment post-myocardial infarction (MI) for heart failure (HF) or left ventricular systolic dysfunction.
- Complete renin-angiotensin system blockade via angiotensin type 1 receptor blockade presents a potential alternative.
Purpose of the Study:
- To evaluate valsartan, captopril, or their combination in post-MI patients with HF or left ventricular systolic dysfunction.
- To compare the efficacy and safety of valsartan versus ACE-I in this patient population.
Main Methods:
- The VALIANT trial randomized post-MI patients with HF or systolic dysfunction to receive valsartan, captopril, or both.
- Patients were followed for a median of 24.7 months.
Main Results:
- No significant differences in total mortality or the composite endpoint of cardiovascular death, MI, or HF were observed among the three treatment groups.
- Valsartan demonstrated non-inferiority to captopril regarding total mortality and cardiovascular death, MI, and HF.
Conclusions:
- Valsartan can be considered a safe and effective alternative to ACE-Is for patients with post-MI HF or left ventricular systolic dysfunction.
- Angiotensin type 1 receptor blockade offers a comparable therapeutic option to ACE-I in this high-risk population.
Abstract:
Angiotensin-converting enzyme inhibitors (ACE-Is) are an evidence-based treatment for patients who after myocardial infarction (MI) present with either heart failure (HF) or left ventricular systolic dysfunction, or both. An alternative could be a more complete inhibition of the renin-angiotensin system through the blockade of the angiotensin type 1 receptors. The effect of valsartan or captopril, or the combination of the two in post-MI HF or systolic dysfunction or both, has been evaluated in the VALIANT (VALsartan In Acute myocardial iNfarcTion) trial. Total mortality and the combined secondary end point of cardiovascular death, MI or HF were not significantly different in the three groups after 24.7 months of follow-up. Valsartan was not inferior to captopril in terms of total mortality and cardiovascular death, MI and HF. Valsartan can be considered an alternative treatment to ACE-I in these patients.
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