Single-center experience of endovascular treatment for patients with progressive posterior circulation cerebral infarction exceeding 24 h.

IF 0.4 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Guangfeng Zhao, Xiongjun He, Yajie Liu, Liang Zhang, Kaifeng Li
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引用次数: 0

Abstract

Background: Evidence of endovascular treatment (ET) for patients with progressive infarction of the posterior circulation exceeding 24 h is lacking.

Objective: To evaluate the efficacy and safety of ET for progressive posterior circulation cerebral infarction.

Methods: This retrospective study evaluated the ET for 18 patients with posterior circulation infarction caused by vertebrobasilar artery occlusion from July 2017 to November 2018. The conditions of patients worsened despite receiving intravenous thrombolysis or combination therapy with clopidogrel and aspirin. The time from the onset of cerebral infarction to puncture was >24 h. The preoperative National Institutes of Health Stroke Scale (NIHSS), modified Rankin Scale (mRS), and related risk factors of patients at 3 months were analyzed postoperatively.

Results: The preoperative NIHSS score was 10.6 (IQR: 6.5), and the time from onset to puncture was 163.5 ± 144.7 h. Postoperative blood flow was modified thrombolysis in cerebral infarction (mTICI) grade 2b or above. During the follow-up period, 1 patient died of basilar artery re-occlusion and pulmonary infection, and 1 died of postoperative hyperperfusion hemorrhage, with a mortality rate of 11.1% (2/18). No recurrent ischemic events were observed in any of the 16 patients during the 3-month follow-up period. The mean mRS score was 1.3 (IQR: 2.3), and 75% patients (12/16) had an mRS score of 0-2. There were no significant differences in age, gender, clinical characteristics, and stroke subtype between patients with mRS scores ≤2 and >2.

Conclusion: In patients with progressive posterior circulation cerebral infarction caused by vertebral basilar artery occlusion, ET is effective and safe even if the time from onset to puncture exceeds 24 h.

Abstract Image

超过24小时进行性后循环脑梗死患者血管内治疗的单中心经验。
背景:对于后循环进展性梗死超过24小时的患者,尚缺乏血管内治疗(ET)的证据。目的:评价ET治疗进行性后循环脑梗死的疗效和安全性。方法:回顾性研究2017年7月至2018年11月18例椎基底动脉闭塞性后循环梗死患者的ET。尽管接受静脉溶栓或氯吡格雷和阿司匹林联合治疗,患者的病情仍恶化。从脑梗死发病到穿刺时间均>24 h。术后3个月采用美国国立卫生研究院卒中量表(NIHSS)、改良Rankin量表(mRS)及相关危险因素进行分析。结果:术前NIHSS评分为10.6 (IQR: 6.5),从发病到穿刺时间为163.5±144.7 h。术后血流量为改良型脑梗死溶栓(mTICI) 2b级及以上。随访期间,1例患者死于基底动脉再闭塞及肺部感染,1例患者死于术后高灌注出血,死亡率为11.1%(2/18)。在3个月的随访期间,16例患者均未观察到复发性缺血事件。平均mRS评分为1.3 (IQR: 2.3),其中75%(12/16)的患者mRS评分为0-2。mRS评分≤2分与>2分的患者在年龄、性别、临床特征、脑卒中亚型等方面均无显著差异。结论:对于椎基底动脉闭塞致进行性后循环脑梗死患者,即使从发病到穿刺时间超过24 h, ET也是安全有效的。
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来源期刊
Asian Biomedicine
Asian Biomedicine 医学-医学:研究与实验
CiteScore
1.20
自引率
0.00%
发文量
24
审稿时长
6-12 weeks
期刊介绍: Asian Biomedicine: Research, Reviews and News (ISSN 1905-7415 print; 1875-855X online) is published in one volume (of 6 bimonthly issues) a year since 2007. [...]Asian Biomedicine is an international, general medical and biomedical journal that aims to publish original peer-reviewed contributions dealing with various topics in the biomedical and health sciences from basic experimental to clinical aspects. The work and authorship must be strongly affiliated with a country in Asia, or with specific importance and relevance to the Asian region. The Journal will publish reviews, original experimental studies, observational studies, technical and clinical (case) reports, practice guidelines, historical perspectives of Asian biomedicine, clinicopathological conferences, and commentaries Asian biomedicine is intended for a broad and international audience, primarily those in the health professions including researchers, physician practitioners, basic medical scientists, dentists, educators, administrators, those in the assistive professions, such as nurses, and the many types of allied health professionals in research and health care delivery systems including those in training.
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