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Effect of haemodynamics on the risk of ischaemic stroke in patients with severe vertebral artery stenosis

OBJECTIVES: Endovascular treatment strategies to optimise individualised care for patients with vertebral artery (VA) stenosis need to be revisited. This study aimed to investigate the relationship between net VA flow volume (NVAFV) and the risk of posterior circulation infarction (PCI) in a high-ri...

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Autores principales: Li, Qing, Zhou, Yinghua, Xing, Yingqi, Yang, Jie, Hua, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9240592/
https://www.ncbi.nlm.nih.gov/pubmed/34952890
http://dx.doi.org/10.1136/svn-2021-001283
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author Li, Qing
Zhou, Yinghua
Xing, Yingqi
Yang, Jie
Hua, Yang
author_facet Li, Qing
Zhou, Yinghua
Xing, Yingqi
Yang, Jie
Hua, Yang
author_sort Li, Qing
collection PubMed
description OBJECTIVES: Endovascular treatment strategies to optimise individualised care for patients with vertebral artery (VA) stenosis need to be revisited. This study aimed to investigate the relationship between net VA flow volume (NVAFV) and the risk of posterior circulation infarction (PCI) in a high-risk patient population. METHODS: We screened 1239 patients with extracranial VA stenosis, of whom 321 patients with severe VA V1 segment stenosis (≥70%) were enrolled in our study. We restratified the patients based on NVAFV and contralateral VA stenosis grades to analyse the proportion of each PCI mechanism—large artery atherosclerosis and branch artery occlusive disease. Furthermore, we estimated the incidence of recurrent ischaemic stroke between groups with different NVAFV over a follow-up period of 2 years. RESULTS: NVAFV was lower in the PCI group. Multiple logistic regression analysis showed that NVAFV is an independent risk factor for PCI and that the OR for PCI for the lowest NVAFV (<112.8 mL/min) was 4.19 (1.76 to 9.95, p=0.001). In patients with severe carotid artery disease, the OR for the lowest NVAFV was 14.03 (3.18 to 61.92, p<0.001). The lower NVAFV group had a higher incidence of recurrent ischaemic stroke events than the higher NVAFV group (HR 2.978, 95% CIs 1.414 to 6.272). CONCLUSION: Our study demonstrated that NVAFV, as estimated by colour duplex ultrasonography, was associated with the incidence of PCI and subsequent ischaemic events and that a high-risk population could be identified for further posterior circulation revascularisation.
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spelling pubmed-92405922022-07-20 Effect of haemodynamics on the risk of ischaemic stroke in patients with severe vertebral artery stenosis Li, Qing Zhou, Yinghua Xing, Yingqi Yang, Jie Hua, Yang Stroke Vasc Neurol Original Research OBJECTIVES: Endovascular treatment strategies to optimise individualised care for patients with vertebral artery (VA) stenosis need to be revisited. This study aimed to investigate the relationship between net VA flow volume (NVAFV) and the risk of posterior circulation infarction (PCI) in a high-risk patient population. METHODS: We screened 1239 patients with extracranial VA stenosis, of whom 321 patients with severe VA V1 segment stenosis (≥70%) were enrolled in our study. We restratified the patients based on NVAFV and contralateral VA stenosis grades to analyse the proportion of each PCI mechanism—large artery atherosclerosis and branch artery occlusive disease. Furthermore, we estimated the incidence of recurrent ischaemic stroke between groups with different NVAFV over a follow-up period of 2 years. RESULTS: NVAFV was lower in the PCI group. Multiple logistic regression analysis showed that NVAFV is an independent risk factor for PCI and that the OR for PCI for the lowest NVAFV (<112.8 mL/min) was 4.19 (1.76 to 9.95, p=0.001). In patients with severe carotid artery disease, the OR for the lowest NVAFV was 14.03 (3.18 to 61.92, p<0.001). The lower NVAFV group had a higher incidence of recurrent ischaemic stroke events than the higher NVAFV group (HR 2.978, 95% CIs 1.414 to 6.272). CONCLUSION: Our study demonstrated that NVAFV, as estimated by colour duplex ultrasonography, was associated with the incidence of PCI and subsequent ischaemic events and that a high-risk population could be identified for further posterior circulation revascularisation. BMJ Publishing Group 2021-12-24 /pmc/articles/PMC9240592/ /pubmed/34952890 http://dx.doi.org/10.1136/svn-2021-001283 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research
Li, Qing
Zhou, Yinghua
Xing, Yingqi
Yang, Jie
Hua, Yang
Effect of haemodynamics on the risk of ischaemic stroke in patients with severe vertebral artery stenosis
title Effect of haemodynamics on the risk of ischaemic stroke in patients with severe vertebral artery stenosis
title_full Effect of haemodynamics on the risk of ischaemic stroke in patients with severe vertebral artery stenosis
title_fullStr Effect of haemodynamics on the risk of ischaemic stroke in patients with severe vertebral artery stenosis
title_full_unstemmed Effect of haemodynamics on the risk of ischaemic stroke in patients with severe vertebral artery stenosis
title_short Effect of haemodynamics on the risk of ischaemic stroke in patients with severe vertebral artery stenosis
title_sort effect of haemodynamics on the risk of ischaemic stroke in patients with severe vertebral artery stenosis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9240592/
https://www.ncbi.nlm.nih.gov/pubmed/34952890
http://dx.doi.org/10.1136/svn-2021-001283
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