Evaluation of the EMBOPIPE flow diverter device: in vivo and in vitro experiments.

Yongnan Zhu, Fanyan Zeng, Jian Liu, Shiqing Mu, Ying Zhang, Xinjian Yang
{"title":"Evaluation of the EMBOPIPE flow diverter device: in vivo and in vitro experiments.","authors":"Yongnan Zhu, Fanyan Zeng, Jian Liu, Shiqing Mu, Ying Zhang, Xinjian Yang","doi":"10.1186/s41016-024-00360-9","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Although flow diverter device (FDD) has brought revolutionized advances in endovascular treatment of intracranial aneurysms, it also presents considerable drawbacks as well, as the innovation for novel device has never stopped. This preclinical research aims to evaluate the safety and efficacy of a newly developed FDD, the EMBOPIPE, through in vivo and in vitro experiments.</p><p><strong>Methods: </strong>Aneurysms were induced in 20 New Zealand white rabbits which were randomized to three follow-up groups according to the time elapsed after EMBOPIPE implantation (28, 90, and 180 days). Additional EMBOPIPEs were implanted in the abdominal aorta to cover the renal artery in nine rabbits. Angiography was performed immediately after device placement in all groups. Aneurysm occlusion, patency of renal arteries, and pathological outcomes were assessed. For the in vitro experiments, we measured the thrombogenic potential of EMBOPIPEs (n = 5) compared with bare stents (n = 5) using the Chandler loop model. Evaluation indicators were the platelet counts, macroscopic observations and scanning electron microscopy.</p><p><strong>Results: </strong>EMBOPIPEs were successfully deployed in 19 of 20 rabbit aneurysms (95.0%). The rates of complete or near-complete aneurysm occlusion were 73.3%, 83.3%, and 100% in the 28-, 90-, and 180-day groups, respectively. All renal arteries covered by EMBOPIPEs remained patent, and the mean difference in renal artery diameter before and after the device placement in the three groups was 0.07 mm, 0.10 mm, and 0.10 mm, respectively (p = 0.77). Renal pathology was normal in all cases. The pathological findings of the aneurysms were as follows: thickened and adequate neointimal coverage at the aneurysm neck, minimal inflammatory response, near-complete smooth muscle cell layer, and endothelialization along the device. In vitro experiments showed that the platelet counts were significantly higher in EMBOPIPE blood samples than in bare stent samples and that platelet adhesion to the device was lower in the EMBOPIPE stent struts compared with bare stent struts through macroscopic observations and scanning electron microscopy.</p><p><strong>Conclusions: </strong>The EMBOPIPE can achieve high rates of aneurysm occlusion while maintaining excellent branch artery patency. It exhibited wonderful pathological results. This novel device with phosphorylcholine surface modification could reduce platelet thrombus attached to the stent struts.</p>","PeriodicalId":36700,"journal":{"name":"Chinese Neurosurgical Journal","volume":"10 1","pages":"8"},"PeriodicalIF":0.0000,"publicationDate":"2024-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10929142/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Neurosurgical Journal","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s41016-024-00360-9","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Although flow diverter device (FDD) has brought revolutionized advances in endovascular treatment of intracranial aneurysms, it also presents considerable drawbacks as well, as the innovation for novel device has never stopped. This preclinical research aims to evaluate the safety and efficacy of a newly developed FDD, the EMBOPIPE, through in vivo and in vitro experiments.

Methods: Aneurysms were induced in 20 New Zealand white rabbits which were randomized to three follow-up groups according to the time elapsed after EMBOPIPE implantation (28, 90, and 180 days). Additional EMBOPIPEs were implanted in the abdominal aorta to cover the renal artery in nine rabbits. Angiography was performed immediately after device placement in all groups. Aneurysm occlusion, patency of renal arteries, and pathological outcomes were assessed. For the in vitro experiments, we measured the thrombogenic potential of EMBOPIPEs (n = 5) compared with bare stents (n = 5) using the Chandler loop model. Evaluation indicators were the platelet counts, macroscopic observations and scanning electron microscopy.

Results: EMBOPIPEs were successfully deployed in 19 of 20 rabbit aneurysms (95.0%). The rates of complete or near-complete aneurysm occlusion were 73.3%, 83.3%, and 100% in the 28-, 90-, and 180-day groups, respectively. All renal arteries covered by EMBOPIPEs remained patent, and the mean difference in renal artery diameter before and after the device placement in the three groups was 0.07 mm, 0.10 mm, and 0.10 mm, respectively (p = 0.77). Renal pathology was normal in all cases. The pathological findings of the aneurysms were as follows: thickened and adequate neointimal coverage at the aneurysm neck, minimal inflammatory response, near-complete smooth muscle cell layer, and endothelialization along the device. In vitro experiments showed that the platelet counts were significantly higher in EMBOPIPE blood samples than in bare stent samples and that platelet adhesion to the device was lower in the EMBOPIPE stent struts compared with bare stent struts through macroscopic observations and scanning electron microscopy.

Conclusions: The EMBOPIPE can achieve high rates of aneurysm occlusion while maintaining excellent branch artery patency. It exhibited wonderful pathological results. This novel device with phosphorylcholine surface modification could reduce platelet thrombus attached to the stent struts.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
EMBOPIPE 分流装置的评估:体内和体外实验。
背景:尽管血流分流装置(FDD)为颅内动脉瘤的血管内治疗带来了革命性的进步,但由于新型装置的创新从未停止,因此它也存在相当大的缺陷。这项临床前研究旨在通过体内和体外实验评估新开发的 FDD(EMBOPIPE)的安全性和有效性:方法:用 20 只新西兰白兔诱发动脉瘤,根据 EMBOPIPE 植入后的时间(28、90 和 180 天)将其随机分为三个随访组。另外还在 9 只兔子的腹主动脉中植入了 EMBOPIPE,以覆盖肾动脉。所有组别均在植入装置后立即进行血管造影。对动脉瘤闭塞情况、肾动脉通畅情况和病理结果进行评估。在体外实验中,我们使用钱德勒循环模型测量了 EMBOPIPE(5 个)与裸支架(5 个)的血栓形成潜能。评价指标包括血小板计数、宏观观察和扫描电子显微镜:结果:在 20 个兔动脉瘤中,有 19 个成功植入了 EMBOPIPE(95.0%)。28天、90天和180天组的动脉瘤完全或接近完全闭塞率分别为73.3%、83.3%和100%。EMBOPIPE 覆盖的所有肾动脉均保持通畅,三组患者置入装置前后肾动脉直径的平均差异分别为 0.07 毫米、0.10 毫米和 0.10 毫米(P = 0.77)。所有病例的肾脏病理结果均正常。动脉瘤的病理结果如下:动脉瘤颈部增厚且有足够的新内膜覆盖,炎症反应轻微,平滑肌细胞层近乎完整,沿装置内皮化。体外实验表明,通过宏观观察和扫描电子显微镜,EMBOPIPE 血液样本中的血小板数量明显高于裸支架样本,而且与裸支架相比,EMBOPIPE 支架支架上的血小板附着力更低:结论:EMBOPIPE 能实现较高的动脉瘤闭塞率,同时保持良好的分支动脉通畅。结论:EMBOPIPE 可实现较高的动脉瘤闭塞率,同时保持良好的分支动脉通畅,其病理结果也非常出色。这种表面经过磷酰胆碱修饰的新型装置可以减少附着在支架支柱上的血小板血栓。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
2.70
自引率
0.00%
发文量
224
审稿时长
10 weeks
期刊最新文献
Nonadjustable state of programmable shunt valve: obstruction of middle cranial fossa arachnoid cyst-peritoneal shunt. Emergency neurosurgical hybrid operating platform for acute intracranial hemorrhage (E-HOPE). Extubation timing and risk of extubation failure in aneurysmal subarachnoid hemorrhage patients. Radiographic predictors of peritumoral brain edema in intracranial meningiomas: a review of current controversies and illustrative cases. Comparison of ketorolac intravenous versus acetaminophen intravenous in treating headache following head trauma: a semi-experimental study.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1