Abstract
Heart failure is a growing epidemic that currently affects nearly 6 million people in the USA. Despite the well-documented hemodynamic abnormalities associated with the disease (e.g., elevated systemic vascular resistance), therapies that directly target these derangements have consistently failed to improve important clinical outcomes, unless they also act on the underlying pathophysiology of the disease (e.g., angiotensin-converting enzyme inhibitors). Numerous clinical trials of vasodilators in the treatment of heart failure have resulted in either neutral or negative outcomes suggesting that systemic vascular resistance may be an inappropriate target of therapy. The reasons for failure in these studies are manifold, including a poor understanding of vasodilator agents and their secondary effects, poorly designed studies that include a markedly heterogeneous patient population and a paucity of objective end points that may be used as targets of therapy, to name a few. Future studies of vasodilators will need to consider these issues in trial design.
Financial & competing interests disclosure
The authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.
No writing assistance was utilized in the production of this manuscript.