From the Clinic for Diagnostic and Interventional Radiology, Saarland University Medical Center, Kirrberger Strasse, Geb. 50.1, 66421 Homburg/Saar, Germany.
Radiology. 2017 Aug;284(2):541-551. doi: 10.1148/radiol.2017152742. Epub 2017 Mar 16.
Purpose To evaluate glass-fiber-based guidewires that are safe for magnetic resonance (MR) imaging-guided endovascular interventions by using a phantom and an in vivo swine model. Materials and Methods MR imaging-safe guidewires were made from micropultruded glass and/or aramid fibers and epoxy resin with diameters of 0.89 mm (0.035 inch) for standard and stiff guidewires and 0.36 mm (0.014 inch) for micro guidewires. MR imaging visibility and mechanical properties were assessed in a pulsatile flow model. After approval was obtained from the institutional animal care and use committee, MR imaging guidewires were evaluated for standard endovascular procedures in nine pigs. Real-time steady-state free-precession sequences were used for MR imaging-guided catheterization, balloon dilation, and stent implantation into aorto-iliac/visceral arteries and the vena cava (temporal resolution, five images per second; and spatial resolution, 150-mm field of view, and 128 × 128 matrix) with a 1.5-T clinical imager. Visualization with the guidewires was rated on a four-point scale, handling was rated on a three-point scale, and catheterization times for different vessel regions were determined by two interventional radiologists. Afterward, handling ratings and catheterization times were obtained for standard nitinol guidewires during x-ray-based fluoroscopy. Cannulation times, signal intensity in each vessel region, and visualization and handling ratings were measured for the MR imaging guidewires. Bland-Altman analysis was performed for inter- and intraobserver variability of cannulation time. Spearman rank correlation was used to compare handling of MR imaging guidewires and standard nitinol guidewires. Results MR imaging guidewires were characterized by good to excellent visibility, with a continuous artifact of 2 mm in diameter and 4 × 8-mm ball-shaped tip marker. Stiffness, flexibility, and guidance reflected comparable times for all in vitro and in vivo procedures with both the MR imaging and standard nitinol guidewires. Standard and micro MR imaging guidewires were most suitable for the iliac crossover maneuver. Phantom visceral artery cannulation was easier with standard and micro MR imaging guidewires. The stiff MR imaging guidewire provided the best support for cannulation of the swine aorta and vena cava. All interventional procedures were performed successfully without complications. Conclusion Preliminary results showed that the use of glass-fiber-based guidewires for evaluation of MR imaging-guided endovascular interventions is technically feasible and safe in a swine model, and potentially, in humans. RSNA, 2017 Online supplemental material is available for this article.
目的 使用体模和活体猪模型评估适用于磁共振成像(MR)引导血管内介入的玻璃纤维导丝的安全性。
材料与方法 制造了直径为 0.89 毫米(0.035 英寸)的标准和硬导丝和 0.36 毫米(0.014 英寸)的微导丝的微拉伸玻璃和/或芳纶纤维以及环氧树脂的 MR 成像安全导丝。在脉动流模型中评估了 MR 成像可视性和机械性能。在获得机构动物护理和使用委员会的批准后,在 9 头猪中评估了 MR 成像导丝的标准血管内程序。使用实时稳态自由进动序列进行 MR 成像引导的导管插入术、球囊扩张以及主动脉髂/内脏动脉和腔静脉中的支架植入术(时间分辨率,每秒 5 个图像;和空间分辨率,150 毫米视野和 128×128 矩阵),使用 1.5-T 临床成像仪。使用四点量表对导丝的可视化进行评分,使用三点量表对导丝的操控性进行评分,并由两位介入放射科医生确定不同血管区域的导管插入时间。之后,在基于 X 射线的透视下获取标准镍钛诺导丝的操控评分和导管插入时间。测量 MR 成像导丝在每个血管区域的信号强度、可视化和操控评分。进行 Bland-Altman 分析以评估介入医师间和介入医师内的插管时间变异性。使用 Spearman 秩相关比较 MR 成像导丝和标准镍钛诺导丝的操控性。
结果 MR 成像导丝的可视性良好,直径为 2 毫米,连续伪影为 4×8 毫米的球形尖端标记。体外和体内所有程序的刚性、柔韧性和引导均反映了 MR 成像和标准镍钛诺导丝的可比时间。标准和微 MR 成像导丝最适合髂叉操作。在 MR 成像导丝中,对标准和微 MR 成像导丝进行内脏动脉插管更为容易。刚性 MR 成像导丝为猪主动脉和腔静脉的插管提供了最佳支撑。所有介入程序均成功完成,无并发症。
结论 初步结果表明,在猪模型中,使用玻璃纤维导丝评估 MR 成像引导的血管内介入技术是可行且安全的,并且可能适用于人类。
RSNA,2017 在线补充材料可用于本文。