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Circle of Willis Variants: Fetal PCA
We sought to determine the prevalence of fetal posterior cerebral artery (fPCA) and if fPCA was associated with specific stroke etiology and vessel territory affected. This paper is a retrospective review of prospectively identified patients with acute ischemic stroke from July 2008 to December 2010...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3618940/ https://www.ncbi.nlm.nih.gov/pubmed/23577277 http://dx.doi.org/10.1155/2013/105937 |
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author | Shaban, Amir Albright, Karen C. Boehme, Amelia K. Martin-Schild, Sheryl |
author_facet | Shaban, Amir Albright, Karen C. Boehme, Amelia K. Martin-Schild, Sheryl |
author_sort | Shaban, Amir |
collection | PubMed |
description | We sought to determine the prevalence of fetal posterior cerebral artery (fPCA) and if fPCA was associated with specific stroke etiology and vessel territory affected. This paper is a retrospective review of prospectively identified patients with acute ischemic stroke from July 2008 to December 2010. We defined complete fPCA as absence of a P1 segment linking the basilar with the PCA and partial fPCA as small segment linking the basilar with the PCA. Patients without intracranial vascular imaging were excluded. We compared patients with complete fPCA, partial fPCA, and without fPCA in terms of demographics, stroke severity, distribution, and etiology and factored in whether the stroke was ipsilateral to the fPCA. Of the 536 included patients, 9.5% (n = 51) had complete fPCA and 15.1% (n = 81) had partial fPCA. Patients with complete fPCA were older and more often female than partial fPCA and no fPCA patients, and significant variation in TOAST classification was detected across groups (P = 0.023). Patients with complete fPCA had less small vessel and more large vessel strokes than patients with no fPCA and partial fPCA. Fetal PCA may predispose to stroke mechanism, but is not associated with vascular distribution, stroke severity, or early outcome. |
format | Online Article Text |
id | pubmed-3618940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-36189402013-04-10 Circle of Willis Variants: Fetal PCA Shaban, Amir Albright, Karen C. Boehme, Amelia K. Martin-Schild, Sheryl Stroke Res Treat Clinical Study We sought to determine the prevalence of fetal posterior cerebral artery (fPCA) and if fPCA was associated with specific stroke etiology and vessel territory affected. This paper is a retrospective review of prospectively identified patients with acute ischemic stroke from July 2008 to December 2010. We defined complete fPCA as absence of a P1 segment linking the basilar with the PCA and partial fPCA as small segment linking the basilar with the PCA. Patients without intracranial vascular imaging were excluded. We compared patients with complete fPCA, partial fPCA, and without fPCA in terms of demographics, stroke severity, distribution, and etiology and factored in whether the stroke was ipsilateral to the fPCA. Of the 536 included patients, 9.5% (n = 51) had complete fPCA and 15.1% (n = 81) had partial fPCA. Patients with complete fPCA were older and more often female than partial fPCA and no fPCA patients, and significant variation in TOAST classification was detected across groups (P = 0.023). Patients with complete fPCA had less small vessel and more large vessel strokes than patients with no fPCA and partial fPCA. Fetal PCA may predispose to stroke mechanism, but is not associated with vascular distribution, stroke severity, or early outcome. Hindawi Publishing Corporation 2013 2013-03-21 /pmc/articles/PMC3618940/ /pubmed/23577277 http://dx.doi.org/10.1155/2013/105937 Text en Copyright © 2013 Amir Shaban et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Shaban, Amir Albright, Karen C. Boehme, Amelia K. Martin-Schild, Sheryl Circle of Willis Variants: Fetal PCA |
title | Circle of Willis Variants: Fetal PCA |
title_full | Circle of Willis Variants: Fetal PCA |
title_fullStr | Circle of Willis Variants: Fetal PCA |
title_full_unstemmed | Circle of Willis Variants: Fetal PCA |
title_short | Circle of Willis Variants: Fetal PCA |
title_sort | circle of willis variants: fetal pca |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3618940/ https://www.ncbi.nlm.nih.gov/pubmed/23577277 http://dx.doi.org/10.1155/2013/105937 |
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