By clicking “Accept”, you agree to the storing of cookies on your device to enhance site navigation, analyze site usage, and assist in our marketing efforts. View our Privacy Policy for more information.
This Product is add-on to
NV Connect
learn more ABOUt NV CONNECT

子宫动脉栓塞

子宫肌瘤栓塞实践训练

learn more
This learning module is designed for:
Interventional radiologists

Mentice 子宫动脉栓塞(UAE),也称为子宫肌瘤栓塞(UFE),旨在让团队学习用于治疗症状性子宫肌瘤疾病的手术步骤。该模块提供了在模拟环境中学习UAE所需的基础知识,并促进了有关在以学习者为中心的无风险培训环境中进入子宫动脉和栓塞术的相关技术的讨论。

由于症状性子宫肌瘤疾病的治疗效果良好,UAE近年来已成为治疗子宫肌瘤的替代方案。该手术需要仔细操作导管,以获得进入子宫动脉的通道。然后通过导管注射颗粒,以阻断流向子宫肌瘤的血液。至关重要的是,由妇科医生和血管内专家以团队方式提供服务。

Features & Benefits

Key Benefits

基于患者场景的手术规划

教授各种粒子栓塞技术的原理

完善UAE的手术步骤

最大限度减少对卵巢的辐射

管理并发症并讨论术后护理

Features & Benefits

• 以患者为导向学习的完整临床场景

• 能够使用真正的临床设备

• 在整个案例中提供指导

• 不同难度的多种解剖结构

•了解真实的设备操作反馈,有助于选择适当的设备

• 使用 DSA 和 3D 叠加进行高级成像

• 推荐的栓塞微导管位置

• 可用于栓塞的不同大小 PVA 颗粒和微球

• 动脉血流取决于栓塞水平

• 接近饱和度时肌瘤会变红

• 回流对栓塞水平和注射速度敏感

• 非靶向栓塞的可视化

• 支持 RUC 导管和 Waltman Loop 技术

• 用于评估和汇报的详细指标

Training Objectives

• 熟悉骨盆血管系统和子宫

• 展示导管插入技能,在内动脉分支中导航

• 操作导管治疗双侧子宫肌瘤

• 选择和改变合适的栓塞颗粒类型和大小

• 执行安全高效的栓塞技术

• 识别和管理潜在的非靶点栓塞

• 能够在漫长而敏感的手术中管理剂量暴露

Workflow

Step 1

Flow Diverter Case planning in Ankyras®

Mentice: Flow Diverter planning in Ankyras
Step 2

Import Case directly into VIST® simulator

Mentice: VIST G7 Virtual Reality Simulation
Step 3

Practice deployment in patient-specific anatomy

Mentice: Wire navigation and flow diverter overlay from Ankyras

Case Layout

共有 3 个不同难度和解剖结构的互动案例

• 1 个全方位指导性案例

For case description, please contact us on the form below
No items found.

Customer Testimonials

Learn more or see a web demo.

Contact us to learn more or see a web demo of this product

Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.

Disclaimer & Regulatory Information

VIST® Ankyras® Flow Diverter Rehearsal is a training solution not intended for clinical use or decision making. Ankyras® is a medical device manufactured by Mentice Spain S.L. Mentice Spain S.L. is ISO 13485 certified. Ankyras® complies with the EU Medical Device Regulation (EU CE Mark, MDR 784032). ANKYRAS® is a medical software intended to assist healthcare professionals in the selection of a proper braided device for treatment of intracranial aneurysms. ANKYRAS® is intended for exclusive use by professional users.