Myocardial stents (both bare metal and drug-eluting varieties) are widely utilized to prevent restenosis following percutaneous transluminal coronary angioplasty (PTCA) and coronary intervention (PCI). Indeed, by 1999 myocardial stents were inserted in 4 of every 5 patients undergoing PCI.1 It now appears what is good for the heart may be good for the brain, too!
Atherosclerotic intracranial arterial stenosis is an important cause of stroke. The WASID (Warfarin Aspirin Symptomatic Intracranial Disease) trial, a double-blind, multicenter clinical trial, evaluated the benefits of best medical therapy (warfarin versus aspirin) in patients with symptomatic intracranial stenoses (50-99%). The primary end point was ischemic stroke, brain hemorrhage, or death from vascular causes other than stroke. During a mean follow-up period of 1.8 years (n=569), the primary end point occurred in 22.1% of the patients in the aspirin group and 21.8% of those in the warfarin group (hazard ratio, 1.04; 95% confidence interval, 0.73- 1.48; P=0.83).2
Because medical treatment of symptomatic intracranial stenosis carries a high risk of stroke, neuro-interventionalists (interventional neurologists, endovascular neurosurgeons, and interventional neuroradiologists) are finding increasing application for stents in cerebral vessels with symptomatic severe stenoses that are refractory to best medical therapy. The main goal of the angioplasty and stent placement is to improve blood flow. Some of these lesions may manifest symptoms only after they become extremely tight, and even relatively minor corrections in the degree of stenosis may improve symptoms and outcomes. Flow is proportional to the fourth power of the vessel’s radius. This means that the flow is approximately doubled when the radius is increased by 20% or the diameter by 10%, so that small increases in the luminal diameter may result in large increases in the flow.
In summary, anesthesia providers should be aware of increasing insertion of metal stents throughout the circulation, including the cerebral circulation. Current trends suggest we will see increasing frequency of neuro-interventional procedures including intracranial angioplasty/stenting. The need for post-procedure antiplatelet therapy is significant, and will likely mirror that noted for myocardial bare metal stents.5,6
Richard C. Prielipp, MD, MBA, FCCM is the J.J. Buckley Professor and Chair of Anesthesiology; Adnan I. Qureshi, MD, is a Stroke and Interventional Neurologist and Professor of Neurology; Steven J Haines, MD, is a Professor of Neurosurgery; and Vallabh Janardhan, MD, is a Stroke and Interventional Neurologist and Assistant Professor of Neurology, Neurosurgery, and Radiology at the University of Minnesota in Minneapolis, MN.
References
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- Chimowitz MI, Lynn MJ, Howlett-Smith H, Stern BJ, Hertzberg VS, Frankel MR, Levine SR, Chaturvedi S, Kasner SE, Benesch CG, Sila CA, Jovin TG, Romano JG; Warfarin-Aspirin Symptomatic Intracranial Disease Trial Investigators. Comparison of warfarin and aspirin for symptomatic intracranial arterial stenosis. N Engl J M
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- Gawaz M, Neumann FJ, Ott I, et al. Platelet activation and coronary stent implantation. Effect of antithrombotic therapy. Circulation 1996;94:279-85.
- Caramori PRA, Lima VC, Seidelin PH, et al. Long-term endothelial dysfunction after coronary stenting. J Am Coll Cardiol 1999;34:1675-9.
- Eagle KA, Berger PB, Calkins H, et al. ACC/AHA guideline update for perioperative cardiovascular evaluation for noncardiac surgery-executive summary: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee to Update the 1996 Guidelines on Perioperative Cardiovascular Evaluation for Noncardiac Surgery). Circulation 2002;105:1257-67.
- Newsome LT, Kutcher MA, Gandhi SK, et al. A protocol for the perioperative management of patients with intracoronary drug-eluting stents. APSF Newsletter 2006-07;21:81-2.