Why the study?
Do additional pharmacotherapies such as ARBs, aldosterone antagonists, or isosorbide dinitrate plus hydralazine improve morbidity and mortality in patients with heart failure involving left ventricular dysfunction who remain symptomatic on or cannot tolerate ACE inhibitors and beta-blockers?
Do additional pharmacotherapies such as ARBs, aldosterone antagonists, or isosorbide dinitrate plus hydralazine improve morbidity and mortality in patients with heart failure involving left ventricular dysfunction who remain symptomatic on or cannot tolerate ACE inhibitors and beta-blockers?
This review highlights the morbidity and mortality benefits of adding ARBs, aldosterone antagonists, or isosorbide dinitrate plus hydralazine to standard ACE inhibitor and beta-blocker therapy for patients with heart failure and left ventricular dysfunction.
Angiotensin-converting enzyme (ACE) inhibitors and beta-blockers make up the cornerstone of therapy for patients with heart failure involving left ventricular dysfunction. These drug classes have been proven to decrease morbidity and mortality in patients with heart failure. Unfortunately, many patients remain symptomatic and experience disease progression despite taking both an ACE inhibitor and a beta-blocker. Others may be unable to tolerate one or both of these agents. In recent years, several other drug classes have been shown to provide additional morbidity and mortality benefits in patients with heart failure. These include angiotensin II receptor blockers (ARBs), aldosterone antagonists, and the combination of isosorbide dinitrate plus hydralazine. To select the most appropriate drug therapy for patients with heart failure, clinicians should consider results from clinical trials in specific patient populations, adverse-event profiles, tolerability, cost, and dosing regimens.
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Norgard et al. (2008) studied this question.
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