经放射状途径治疗性神经干预:来自三级保健中心的初步经验

IF 0.3 Q4 SURGERY
V. Bhatia, Ajay Kumar, Mohd Yaqoob Wani, Navneet Singla, A. Prabhakar, M. Karthigeyan, Rajeev Chauhan
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引用次数: 0

摘要

摘要目的本研究的目的是评估放射通路在治疗性神经干预手术中的安全性和可行性。方法回顾性分析我院2021年7月至2022年4月经桡动脉通路治疗性神经干预的20例患者。结果20例患者(年龄24 ~ 74岁;平均年龄48.4岁;13例(65%)女性采用经桡骨入路。桡动脉平均直径2.135 mm。18例(90%)采用右桡骨通路。治疗指征为动脉瘤破裂13例(65%),机械取栓5例(25%),再通动脉瘤分流1例(5%),球囊闭塞试验1例(5%)。经桡骨入路18例(90%)手术成功。有2例患者在转经股动脉入路后手术失败。在这两种情况下,访问转换的原因都是严重的痉挛。在研究队列中未见明显的通路部位并发症。结论桡骨入路是一种成功率高、并发症少的治疗方法。介入医生应该习惯将这种方法作为神经介入的主要或替代途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapeutic Neurointervention through Transradial Approach: Preliminary Experience from a Tertiary Care Center
Abstract Aim  The aim of this study was to assess the safety and feasibility of radial access for therapeutic neurointervention procedures. Methods  The retrospective evaluation of 20 patients taken for therapeutic neurointervention through transradial access at our institute was done from July 2021 to April 2022. Results  Therapeutic neurointervention procedures were attempted in 20 patients (age, 24–74 years; mean age, 48.4 years; 13 (65%) females using a transradial approach. The radial artery's mean diameter was 2.135 mm. The right radial access was taken in 18 (90%) cases. Indications for treatment were ruptured aneurysm in 13 (65%), mechanical thrombectomy in 5 (25%), flow diversion for a recanalized aneurysm in 1 (5%), and balloon occlusion test in 1 (5%) case. The procedure was successful through the transradial approach in 18 (90%) procedures. Failure was seen in two cases that were completed after conversion to the transfemoral approach. The reason for access conversion was a severe spasm in both cases. No significant access site complications were seen in the study cohort. Conclusion  A radial access route is a promising approach for therapeutic interventions with a high success rate and minimal access site complications. Interventionists should get accustomed to this approach as primary or alternative access for neurointervention.
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来源期刊
CiteScore
0.40
自引率
0.00%
发文量
52
审稿时长
12 weeks
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