Vertebral artery diseases, including atherosclerotic stenosis, dissections and aneurysms, can lead to ischemia of the posterior cerebral circulation. Conventional management of extracranial vertebral artery diseases may include medical therapy such as antiplatelet or anticoagulant medications, medications to reduce atherosclerotic disease risk (e.g., statins), and/or surgical revascularization. Endovascular therapies, to include percutaneous transluminal angioplasty (PTA) with or without stenting, have been investigated as an alternative to conventional management.
Ischemia of the vertebrobasilar circulation accounts for about 20% of all strokes. Posterior circulation strokes may arise from occlusion of the innominate and subclavian arteries, the extracranial vertebral arteries, or the intracranial vertebral, basilar or posterior cerebral arteries. Compared with carotid artery disease, relatively little is known about the true prevalence of specific causes of posterior circulation strokes, particularly the prevalence of vertebral artery disease. Reports from one stroke registry have estimated that, in 9% of cases, posterior circulation strokes are due to stenosis of the proximal vertebral artery. Individuals who experience strokes or transient ischemic attacks of the vertebrobasilar circulation face a 25 - 35% risk of stroke within the subsequent five years.
Endovascular therapies, including percutaneous transluminal angioplasty with or without stenting, for the treatment or management of extracranial vertebral artery disease is considered investigational.
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Randomized controlled trials have found no advantage for PTA with or without stenting in individuals diagnosed with extracranial vertebral artery stenosis compared to medical therapy alone. For PTA with stent implantation for extracranial vertebral artery aneurysm(s), dissection(s), and arteriovenous (AV) fistula(e), the evidence includes small case series and case reports. Given the lack of data comparing endovascular therapies to alternative treatment, the evidence is insufficient to determine the net health outcome.
American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines, and the American Stroke Association. (2011). Guideline on the management of patients with extracranial carotid and vertebral artery disease. Retrieved July 14, 2015 from http://circ.ahajournals.org.
American Heart Association and American Stroke Association. (2014). Guidelines for the prevention of stroke in patients with stroke and transient ischemic attack. Retrieved December 14, 2020 from https://www.ahajournals.org.
BlueCross BlueShield Association. Evidence Positioning System. (6:2020). Endovascular therapies for extracranial vertebral artery disease. (7.01.148). Retrieved December 14, 2020 from http://www.evidencepositioningsystem.com. (24 articles and/or guidelines reviewed)
Centers for Medicare & Medicaid Services.CMS.gov. NCD for percutaneous transluminal angioplasty (20.7). Retrieved June 26, 2015 from http://www.cms.hhs.gov.
Compter, A., Van der Worp, H.B., Schonewille, W.J., Vos, J.A., Boiten, J., Uyttenboogaart, M., et al. (2015). Stenting versus medical treatment in patients with symptomatic vertebral artery stenosis: a randomized open-label phase 2 trial. Lancet Neurology, 14 (6), 606-614. Abstract retrieved May 24, 2018 from PubMed database.
Liu, X., Dai, Q., Ye, R., Zi, W., Liu, Y., Wang, H., et al. (2020). Endovascular treatment versus standard medical treatment for vertebrobasilar artery occlusion (BEST): an open-label, randomised controlled trial. Lancet Neurology, 19 (2), 115-122. Abstract retrieved December 14, 2020 from PubMed database.
Markus, H.S., Larsson, S.C., Kuker, W., Schulz, U.G., Ford, I., Rothwell, P.M., & Clifton, A. (2017). Stenting for symptomatic vertebral artery stenosis: the vertebral artery ischaemia stenting trial. Neurology, 89 (12), 1229-1236. (Level 1 evidence)
U. S. Food and Drug Administration. (August 2002). Center for Devices and Radiological Health. Humanitarian Device Exemption (HDE) for Neurolink® System Retrieved May 28, 2015 from http://www.fda.gov.
U. S. Food and Drug Administration. (August 2005). Center for Devices and Radiological Health. Humanitarian Device Exemption (HDE) for Wingspan Stent System. Retrieved May 28, 2015 from http://www.fda.gov.
ORIGINAL EFFECTIVE DATE: 11/14/2015
MOST RECENT REVIEW DATE: 2/11/2021
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