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Effects of Circle of Willis Anatomic Variations on Angiographic and Clinical Outcomes of Coiled Anterior Communicating Artery Aneurysms
Authors:E Tarulli  M Sneade  A Clarke  AJ Molyneux  AJ Fox
Institution:aFrom the Department of Medical Imaging (E.T., A.J.F.), University of Toronto, Ontario, Canada;bOxford Neurovascular and Neuroradiology Research Unit (M.S., A.C., A.J.M.), University of Oxford, Oxford, UK.
Abstract:BACKGROUND AND PURPOSE:Anterior communicating artery aneurysms account for one-fourth of all intracranial aneurysms and frequently occur in the context of A1 vessel asymmetry. The purpose of this study was to correlate circle of Willis anatomic variation association to angiographic and clinical outcomes of anterior communicating aneurysm coiling.MATERIALS AND METHODS:The Cerecyte Coil Trial provides a subgroup of 124 cases with anterior communicating artery aneurysms after endovascular coiling. One hundred seventeen of 124 anterior communicating artery aneurysms had complete imaging and follow-up for clinical outcome analysis, stability of aneurysm coil packing, and follow-up imaging between 5 and 7 months after treatment. Clinical outcomes were assessed by the mRS at 6 months.RESULTS:Anterior cerebral artery trunk-dominance was seen in 91 of 124 (73%) anterior communicating artery aneurysms and codominance in 33 of 124 (27%) anterior communicating artery aneurysms. There was no significant difference (P > .5) in treatment success at 5–7 months for anterior communicating artery aneurysms between the anterior cerebral artery trunk-dominant (49 of 86, 57%) and anterior cerebral artery trunk-codominant (19 of 31) groups. Angiographic follow-up demonstrates a statistically significant increase in neck remnants and progressive aneurysm sac filling with the A1 dominant configuration (n = 21, 24% at follow-up versus n = 11, 12% at immediate posttreatment, P = .035). There was no statistically significant difference in clinical outcomes between types of anterior cerebral artery trunk configuration (P > .5).CONCLUSIONS:Anterior communicating artery aneurysms with anterior cerebral artery trunk-dominant circle of Willis configurations show less angiographic stability at follow-up than those with anterior cerebral artery trunk-codominance similar to other “termination” type aneurysms. This supports the hypothesis that anterior cerebral artery trunk-dominant flow contributes to aneurysm formation, growth, and instability after coiling treatment.

The most common site of intracranial aneurysms is the anterior communicating artery (AcomA). AcomA aneurysms account for approximately one-fourth of all intracranial aneurysms.1 Also very common in the setting of AcomA aneurysms is unilateral anterior cerebral artery trunk (A1) dominance where 1 side supplies both pericallosal artery (A2) arteries, a well-known phenomenon previously shown to be a potent risk factor for AcomA aneurysm formation and rupture.13To what extent vessel dominance influences the long-term result of endovascular packing of these aneurysms with detachable platinum coils and the patients'' clinical outcome is less well known.46 One previous study indicates that vessel dominance is not a major factor in predicting short-term treatment outcome; however, the methodology and definition of vessel dominance as used in this instance was not stated.7 Yet, anterior communicating aneurysms are commonly “termination type” with the aneurysm forming with a relatively wide neck at the site of the inferred jet of flowing blood dynamics, with main branches nearly perpendicular to the parent vessel, also commonly seen for basilar tip, internal carotid tip, and middle cerebral bifurcations.8The Cerecyte Coil Trial (CCT) was a prospective, randomized, controlled study that entered 500 cases comparing endovascular coiling of ruptured and unruptured cerebral aneurysms with either Cerecyte or bare platinum coils that showed no difference between groups.9,10 There was an expected large subset of AcomA aneurysms within the CCT cohort (n = 124).9 Therefore, data from this trial provided a unique opportunity to obtain a large number of AcomA aneurysm cases for determination of A1 dominance in relation to coiling treatment and angiographic outcomes immediately posttreatment and at follow-up. Our goal was to determine the impact of A1 dominance on treatment success, stability, and clinical outcomes of endovascularly coiled AcomA aneurysms.
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