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Clinical application of susceptibility-weighted imaging in the evaluation of leptomeningeal collateralization

The feasibility of using susceptibility-weighted imaging (SWI) in a clinical setting was assessed for quantifying leptomeningeal collateralization. Eighteen patients with stroke and acute infarction underwent diffusion-weighted imaging, SWI, perfusion-weighted imaging, and magnetic resonance angiogr...

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Autores principales: Yang, Lijuan, Luo, Song
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320133/
https://www.ncbi.nlm.nih.gov/pubmed/30572437
http://dx.doi.org/10.1097/MD.0000000000013345
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author Yang, Lijuan
Luo, Song
author_facet Yang, Lijuan
Luo, Song
author_sort Yang, Lijuan
collection PubMed
description The feasibility of using susceptibility-weighted imaging (SWI) in a clinical setting was assessed for quantifying leptomeningeal collateralization. Eighteen patients with stroke and acute infarction underwent diffusion-weighted imaging, SWI, perfusion-weighted imaging, and magnetic resonance angiography within 3 days after symptom onset. Lesions were evaluated by the Alberta Stroke Program Early CT score (ASPECTS), based on mean transit time, SWI, and cerebral blood volume (CBV). For evaluating ischemic penumbra and leptomeningeal collateralization, the SWI-ASPECTS significantly correlated, respectively, with mean transit time and CBV-ASPECTS (Spearman test, r = 0.793 and 0.682; P < .001, both). The SWI may be useful to quantify leptomeningeal collateralization in patients with acute cerebral infarction.
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spelling pubmed-63201332019-01-14 Clinical application of susceptibility-weighted imaging in the evaluation of leptomeningeal collateralization Yang, Lijuan Luo, Song Medicine (Baltimore) Research Article The feasibility of using susceptibility-weighted imaging (SWI) in a clinical setting was assessed for quantifying leptomeningeal collateralization. Eighteen patients with stroke and acute infarction underwent diffusion-weighted imaging, SWI, perfusion-weighted imaging, and magnetic resonance angiography within 3 days after symptom onset. Lesions were evaluated by the Alberta Stroke Program Early CT score (ASPECTS), based on mean transit time, SWI, and cerebral blood volume (CBV). For evaluating ischemic penumbra and leptomeningeal collateralization, the SWI-ASPECTS significantly correlated, respectively, with mean transit time and CBV-ASPECTS (Spearman test, r = 0.793 and 0.682; P < .001, both). The SWI may be useful to quantify leptomeningeal collateralization in patients with acute cerebral infarction. Wolters Kluwer Health 2018-12-21 /pmc/articles/PMC6320133/ /pubmed/30572437 http://dx.doi.org/10.1097/MD.0000000000013345 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle Research Article
Yang, Lijuan
Luo, Song
Clinical application of susceptibility-weighted imaging in the evaluation of leptomeningeal collateralization
title Clinical application of susceptibility-weighted imaging in the evaluation of leptomeningeal collateralization
title_full Clinical application of susceptibility-weighted imaging in the evaluation of leptomeningeal collateralization
title_fullStr Clinical application of susceptibility-weighted imaging in the evaluation of leptomeningeal collateralization
title_full_unstemmed Clinical application of susceptibility-weighted imaging in the evaluation of leptomeningeal collateralization
title_short Clinical application of susceptibility-weighted imaging in the evaluation of leptomeningeal collateralization
title_sort clinical application of susceptibility-weighted imaging in the evaluation of leptomeningeal collateralization
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320133/
https://www.ncbi.nlm.nih.gov/pubmed/30572437
http://dx.doi.org/10.1097/MD.0000000000013345
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