Key result
This review discusses strategies to improve nitric oxide bioavailability after vascular procedures to reduce the risk of thrombosis and restenosis.
Why the study?
Does improving nitric oxide bioavailability reduce the risk of thrombosis and restenosis after vascular procedures in patients with peripheral arterial disease?
Does improving nitric oxide bioavailability reduce the risk of thrombosis and restenosis after vascular procedures in patients with peripheral arterial disease?
Improving nitric oxide bioavailability at the site of vascular injury is a key research target to reduce neointimal hyperplasia, thrombosis, and restenosis following revascularization procedures.
Answers are grounded in this paper and cite their sources.
Should not yet change practice; leaves open targeted nitric oxide strategies for randomized trials in PAD.
Atherosclerosis in the form of peripheral arterial disease results in significant morbidity and mortality. Surgical treatment options for peripheral arterial disease include angioplasty with and without stenting, endarterectomy, and bypass grafting. Unfortunately, all of these procedures injure the vascular endothelium, which impairs its ability to produce nitric oxide (NO) and ultimately leads to neointimal hyperplasia and restenosis. To improve on current patency rates after vascular procedures, investigators are engaged in research to improve the bioavailability of NO at the site of vascular injury in an attempt to reduce the risk of thrombosis and restenosis after successful revascularization. This article reviews some of the previous research that has aimed to improve NO bioavailability after vascular procedures whether through systemic or local delivery, as well as to describe some of the NO-releasing products that are currently undergoing study for use in clinical practice.
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Popowich et al. (2007) conducted a review in Peripheral arterial disease. Nitric oxide (NO) bioavailability improvement strategies was evaluated. This review discusses strategies to improve nitric oxide bioavailability after vascular procedures to reduce the risk of thrombosis and restenosis.
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