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The editorial discusses the role and dosing of angiotensin-receptor blockade in patients with acute myocardial infarction and heart failure.
This editorial discusses the rationale for angiotensin-receptor blockade dosing in patients with acute myocardial infarction and heart failure, noting that ACE inhibitors block only a fraction of cardiac angiotensin II production.
Beta-blockers, angiotensin-converting–enzyme (ACE) inhibitors, and aldosterone antagonists have been shown to reduce the overall risk of death as well as the risk of major nonfatal cardiovascular events when they are administered to patients with acute myocardial infarction who also have left ventricular systolic dysfunction, clinical evidence of heart failure, or both.1,2 However, there remains a sizable subgroup of patients in whom clinical heart failure worsens despite optimal medical therapy after acute myocardial infarction. Relevant to this discussion is the observation that ACE inhibitors block only 13 percent of the total production of angiotensin II in the human heart3 because . . .
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Mann et al. (2003) conducted an editorial in Acute myocardial infarction with left ventricular systolic dysfunction or heart failure. Angiotensin-Receptor Blockade was evaluated. The editorial discusses the role and dosing of angiotensin-receptor blockade in patients with acute myocardial infarction and heart failure.
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