van Herwaarden Joost A, Jansen Marloes M, Vonken Evert-Jan P A, Bloemert-Tuin Trijntje, Bullens Roland W M, de Borst Gert J, Hazenberg Constantijn E V B
Department of Vascular Surgery, University Medical Center Utrecht, Utrecht, the Netherlands.
Department of Vascular Surgery, University Medical Center Utrecht, Utrecht, the Netherlands.
Eur J Vasc Endovasc Surg. 2021 Feb;61(2):317-325. doi: 10.1016/j.ejvs.2020.10.016. Epub 2020 Nov 29.
Endovascular procedures are conventionally conducted using two dimensional fluoroscopy. A new technology platform, Fiber Optic RealShape (FORS), has recently been introduced allowing real time, three dimensional visualisation of endovascular devices using fiberoptic technology. It functions as an add on to conventional fluoroscopy and may facilitate endovascular procedures. This first in human study assessed the feasibility of FORS in clinical practice.
A prospective cohort feasibility study was performed between July and December 2018. Patients undergoing (regular or complex) endovascular aortic repair (EVAR) or endovascular peripheral lesion repair (EVPLR) were recruited. FORS guidance was used exclusively during navigational tasks such as target vessel catheterisation or crossing of stenotic lesions. Three types of FORS enabled devices were available: a flexible guidewire, a Cobra-2 catheter, and a Berenstein catheter. Devices were chosen at the physician's discretion and could comprise any combination of FORS and non-FORS devices. The primary study endpoint was technical success of the navigational tasks using FORS enabled devices. Secondary study endpoints were user experience and fluoroscopy time.
The study enrolled 22 patients: 14 EVAR and eight EVPLR patients. Owing to a technical issue during start up, the FORS system could not be used in one EVAR. The remaining 21 procedures proceeded without device or technology related complications and involved 66 navigational tasks. In 60 tasks (90.9%), technical success was achieved using at least one FORS enabled device. Users rated FORS based image guidance "better than standard guidance" in 16 of 21 and "equal to standard guidance" in five of 21 procedures. Fluoroscopy time ranged from 0.0 to 52.2 min. Several tasks were completed without or with only minimal X-ray use.
Real time navigation using FORS technology is safe and feasible in abdominal and peripheral endovascular procedures. FORS has the potential to improve intra-operative image guidance. Comparative studies are needed to assess these benefits and potential radiation reduction.
血管内手术传统上使用二维荧光透视法进行。最近引入了一种新技术平台,即光纤真实形状(FORS),它允许使用光纤技术对血管内装置进行实时三维可视化。它作为传统荧光透视法的附加装置发挥作用,可能会促进血管内手术。这项首次人体研究评估了FORS在临床实践中的可行性。
2018年7月至12月进行了一项前瞻性队列可行性研究。招募了接受(常规或复杂)血管内主动脉修复(EVAR)或血管内周围病变修复(EVPLR)的患者。在诸如目标血管插管或穿过狭窄病变等导航任务期间专门使用FORS引导。有三种启用FORS的装置可供使用:一种柔性导丝、一种眼镜蛇2导管和一种贝伦斯坦导管。装置由医生自行决定选择,并且可以包括FORS和非FORS装置的任何组合。主要研究终点是使用启用FORS的装置进行导航任务的技术成功。次要研究终点是用户体验和荧光透视时间。
该研究纳入了22名患者:14名EVAR患者和8名EVPLR患者。由于启动期间的技术问题,FORS系统无法在1例EVAR中使用。其余21例手术未出现与装置或技术相关的并发症,涉及66项导航任务。在60项任务(90.9%)中,使用至少一种启用FORS的装置取得了技术成功。在21例手术中,16例用户将基于FORS的图像引导评为“优于标准引导”,5例评为“等同于标准引导”。荧光透视时间为0.0至52.2分钟。一些任务在未使用或仅使用极少X射线的情况下完成。
在腹部和周围血管内手术中,使用FORS技术进行实时导航是安全可行的。FORS有潜力改善术中图像引导。需要进行比较研究来评估这些益处和潜在的辐射减少情况。