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Updated: Sep 7, 2025

Improved Renal Denervation Mitigated Hypertension Induced by Angiotensin II Infusion
Published on: May 26, 2022
[Angiotensine Receptor-Neprilysin Inhibitor combination is not the preferred medication for patients after acute
1Amsterdam UMC, locatie AMC, Amsterdam, Afd. Klinische en Experimentele Cardiologie, Amsterdam Cardiovascular Sciences.
Insights
The PARADISE-MI trial found sacubitril/valsartan did not reduce cardiovascular death or heart failure events compared to ramipril after myocardial infarction. Symptomatic hypotension was more frequent with sacubitril/valsartan.
Area of Science:
- Cardiology
- Clinical Trials
- Pharmacology
Background:
- Acute myocardial infarction (MI) frequently leads to reduced cardiac function and heart failure.
- Standard treatment often involves ACE inhibitors, but newer therapies are being investigated.
Purpose of the Study:
- To compare the efficacy and safety of sacubitril/valsartan (ARNI) versus an ACE inhibitor (ramipril) in patients post-MI.
- To assess the impact on cardiovascular death, rehospitalization, and heart failure-related visits.
Main Methods:
- The PARADISE-MI study randomized 5661 patients with acute MI and reduced ejection fraction to receive either ramipril or sacubitril/valsartan.
- Patients often had concurrent heart failure symptoms and congestion.
Main Results:
- The primary endpoint of a 15% reduction in cardiovascular death, rehospitalization, or extra heart failure visits was not met.
- Symptomatic hypotension occurred in 28.3% of patients on sacubitril/valsartan versus 21.9% on ramipril.
Conclusions:
- Sacubitril/valsartan did not demonstrate superiority over ramipril in this post-MI population.
- Increased symptomatic hypotension necessitates a cautious approach with ARNIs in this setting.
- ACE inhibitors remain a recommended first-choice treatment in the initial weeks following myocardial infarction.
Abstract:
The PARADISE-MI study compared standard treatment with an ACE inhibitor (ramipril) after an acute myocardial infarction with the newer sacubitril/ valsartan combination (so-called ARNI) medication in 5661 patients. Most patients had a reduced cardiac function (40% ejection fraction or less) and in about 50% of patients it was accompanied by complaints of congestion. The expected 15% reduction in primary endpoint cardiovascular death or rehospitalization or extra visits for heart failure was not met after 22 months. The study is characterized by an increased incidence of symptomatic hypotension of 28,3% in the group treated with the ARNI, compared to an incidence of 21,9% in the group treated with the ACE inhibitor. The interpretation of the trial is hampered by the mixed design of prevention and treatment trial for heart failure. A continuing careful approach is advised with ACE inhibitors as first choice in the first week(s) after myocardial infarction.
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