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Influence of Vertebrobasilar Stenotic Lesion Rigidity on the Outcome of Angioplasty and Stenting

Stenotic lesion rigidity (SLR) has an unclear influence on the outcome of percutaneous transluminal angioplasty and stenting (PTAS) for intracranial arterial stenosis. This study evaluated the outcome of PTAS and the relationship of vertebrobasilar SLR to features on vessel wall MRI (VW-MRI) for ide...

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Autores principales: Chang, Feng-Chi, Luo, Chao-Bao, Chung, Chih-Ping, Kuo, Kuei-Hong, Chen, Ting-Yi, Lee, Han-Jui, Lin, Chung-Jung, Lirng, Jiing-Feng, Guo, Wan-Yuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054424/
https://www.ncbi.nlm.nih.gov/pubmed/32127642
http://dx.doi.org/10.1038/s41598-020-60906-6
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author Chang, Feng-Chi
Luo, Chao-Bao
Chung, Chih-Ping
Kuo, Kuei-Hong
Chen, Ting-Yi
Lee, Han-Jui
Lin, Chung-Jung
Lirng, Jiing-Feng
Guo, Wan-Yuo
author_facet Chang, Feng-Chi
Luo, Chao-Bao
Chung, Chih-Ping
Kuo, Kuei-Hong
Chen, Ting-Yi
Lee, Han-Jui
Lin, Chung-Jung
Lirng, Jiing-Feng
Guo, Wan-Yuo
author_sort Chang, Feng-Chi
collection PubMed
description Stenotic lesion rigidity (SLR) has an unclear influence on the outcome of percutaneous transluminal angioplasty and stenting (PTAS) for intracranial arterial stenosis. This study evaluated the outcome of PTAS and the relationship of vertebrobasilar SLR to features on vessel wall MRI (VW-MRI) for identifying pathologies of vertebrobasilar stenosis (VBS) and evaluating PTAS outcome. We retrospectively evaluated the results of PTAS in 31 patients with severe VBS. Stenotic lesions were classified as soft (based on predilatation pressure [PP] ≦ 4 atm) in 15 patients or hard (PP >4 atm) in 16 patients. We examined the relationship of SLR to clinical and MR findings. Patients with hard vs soft lesions had atherosclerosis (8/16 [50.0%] vs 2/15 [13.3%]), dissection (0/16 [0.0%] vs 12/15 [80.0%]), and dissection in atherosclerosis (8/16 [50.0%] vs 1/15 [6.7%], P < 0.0001); high intensity signal on the T1WI of VW-MRI (5/16 [31.3%] vs 14/15 [93.3%]) and iso- to low intensity signal (11/16 [68.7%] vs 1/15 [6.7], P = 0.001), and significant in-stent restenosis (>50%) in 5/15 (33.3%) vs 0/15 (0.0%) (P = 0.0421) in the 30 patients who successfully completed PTAS. Vertebrobasilar SLR correlated well with lesion etiology, findings on VW-MRI, and PTAS outcome. Patients with hard stenotic lesions need close follow-up after PTAS.
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spelling pubmed-70544242020-03-11 Influence of Vertebrobasilar Stenotic Lesion Rigidity on the Outcome of Angioplasty and Stenting Chang, Feng-Chi Luo, Chao-Bao Chung, Chih-Ping Kuo, Kuei-Hong Chen, Ting-Yi Lee, Han-Jui Lin, Chung-Jung Lirng, Jiing-Feng Guo, Wan-Yuo Sci Rep Article Stenotic lesion rigidity (SLR) has an unclear influence on the outcome of percutaneous transluminal angioplasty and stenting (PTAS) for intracranial arterial stenosis. This study evaluated the outcome of PTAS and the relationship of vertebrobasilar SLR to features on vessel wall MRI (VW-MRI) for identifying pathologies of vertebrobasilar stenosis (VBS) and evaluating PTAS outcome. We retrospectively evaluated the results of PTAS in 31 patients with severe VBS. Stenotic lesions were classified as soft (based on predilatation pressure [PP] ≦ 4 atm) in 15 patients or hard (PP >4 atm) in 16 patients. We examined the relationship of SLR to clinical and MR findings. Patients with hard vs soft lesions had atherosclerosis (8/16 [50.0%] vs 2/15 [13.3%]), dissection (0/16 [0.0%] vs 12/15 [80.0%]), and dissection in atherosclerosis (8/16 [50.0%] vs 1/15 [6.7%], P < 0.0001); high intensity signal on the T1WI of VW-MRI (5/16 [31.3%] vs 14/15 [93.3%]) and iso- to low intensity signal (11/16 [68.7%] vs 1/15 [6.7], P = 0.001), and significant in-stent restenosis (>50%) in 5/15 (33.3%) vs 0/15 (0.0%) (P = 0.0421) in the 30 patients who successfully completed PTAS. Vertebrobasilar SLR correlated well with lesion etiology, findings on VW-MRI, and PTAS outcome. Patients with hard stenotic lesions need close follow-up after PTAS. Nature Publishing Group UK 2020-03-03 /pmc/articles/PMC7054424/ /pubmed/32127642 http://dx.doi.org/10.1038/s41598-020-60906-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chang, Feng-Chi
Luo, Chao-Bao
Chung, Chih-Ping
Kuo, Kuei-Hong
Chen, Ting-Yi
Lee, Han-Jui
Lin, Chung-Jung
Lirng, Jiing-Feng
Guo, Wan-Yuo
Influence of Vertebrobasilar Stenotic Lesion Rigidity on the Outcome of Angioplasty and Stenting
title Influence of Vertebrobasilar Stenotic Lesion Rigidity on the Outcome of Angioplasty and Stenting
title_full Influence of Vertebrobasilar Stenotic Lesion Rigidity on the Outcome of Angioplasty and Stenting
title_fullStr Influence of Vertebrobasilar Stenotic Lesion Rigidity on the Outcome of Angioplasty and Stenting
title_full_unstemmed Influence of Vertebrobasilar Stenotic Lesion Rigidity on the Outcome of Angioplasty and Stenting
title_short Influence of Vertebrobasilar Stenotic Lesion Rigidity on the Outcome of Angioplasty and Stenting
title_sort influence of vertebrobasilar stenotic lesion rigidity on the outcome of angioplasty and stenting
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054424/
https://www.ncbi.nlm.nih.gov/pubmed/32127642
http://dx.doi.org/10.1038/s41598-020-60906-6
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