MR-guided cardiovascular interventions do not use ionizing radiation, provide excellent soft tissue contrast, and enable functional measurements. The feasibility of MR-guided percutaneous coronary intervention has been demonstrated in animal trials using metallic stents. Recently, bio-resorbable vascular scaffolds have been introduced for stenting of coronary arteries. These scaffolds enable artifact-free MR imaging of the coronary artery segment that the result of the intervention can be readily assessed via MR imaging. We show the first fully MR-guided PCI with a bioresorbable scaffold in the LCA of a pig at 3T using dedicated active guiding catheters, an MR-safe guidewire and BVS delivery system.
MR-guided cardiovascular interventions do not use ionizing radiation, provide excellent soft tissue contrast, offer arbitrary slice orientations and enable functional measurements as well as tissue characterization of the myocardium. Although MR-guided catheterizations of the heart are already performed in humans1, percutaneous coronary interventions (PCI) are still challenging to perform under MR guidance due to limited spatial and temporal resolution. However, animal trials at 1.5T demonstrated the feasibility of MR-guided PCI2,3, and recent developments in coronary MRI4 as well as real-time imaging techniques5 may help to overcome current limitations. Furthermore, dedicated active guiding catheters and MR-visible guidewires were developed to enable the engagement of the coronary artery under MR guidance6,7.
Recently, bio-resorbable vascular scaffolds (BVS) have been introduced for stenting of coronary arteries. BVS are free of metal and thus enable artifact-free MR imaging of the scaffolded coronary artery segment8 which is desirable for MR-guided PCI as the result of the intervention can be readily assessed via MR imaging.
In this study, we show the first MR-guided implantation of a BVS in a pig at 3T using an active guiding catheter and an MR-safe guidewire and BVS delivery system.
For engagement of the left coronary artery (LCA), an 8F catheter with non-metallic braiding and Tiger tip shape was designed as a guiding catheter. The distal end was equipped with a 2cm-long single-loop coil to allow for visualization of the catheter tip during real-time MR imaging. The coil was connected to one receive channel of the MR system via a coaxial cable embedded in the catheter’s wall and a tune/match circuit with variable attenuation9.
For BVS implantation a non-metallic BVS delivery system (Abbott Vascular, Wetzlar, Germany) was used in combination with an MR-safe 0.014” guidewire (MaRVis Interventional GmbH, Frechen, Germany) which was doped with iron microparticles for MR visibility.
The MR-guided PCI was performed in a female Göttingen minipig on a clinical 3T MR system (Siemens PRISMA). A 10F sheath was placed in the right femoral artery for arterial access. The pig was mechanically ventilated and general anesthesia was maintained by isoflurane inhalation. Initial localization of the coronary arteries was done via a whole-heart 3D navigator-gated FLASH sequence (fat saturation, T2 preparation, TE/TR: 1.6/3.5 ms, FA: 16°, FoV: 2822x102 mm³, matrix: 1762x64, TET2prep: 40 ms, R = 2). A radial bSSFP sequence was used for real-time imaging during the engagement of the LCA with the active guiding catheter (TE/TR: 1.4/2.8 ms, spokes: 105, FA: 40°, FoV: 2752x7 mm³, matrix: 160x160, fat saturation).
Once the catheter tip was in the LCA, contrast-enhanced MR angiography images were acquired during infusion of a 5 ml bolus (5% Gd-DTPA solution) through the guiding catheter. Contrast enhancement in the myocardium was imaged using an ECG-triggered FLASH acquisition with saturation recovery in short-axis view (TE/TR: 1.1/2.2 ms, TSR: 102 ms, FA: 8°, FoV: 225x300 mm³, matrix: 120x160, R = 2). Then, the guidewire was advanced into the LCA followed by the BVS delivery catheter. The balloon was dilated to place an 18mm-long BVS (Ø 3 mm) in the artery. For visualization of the balloon, a 1% Gd-DTPA solution was used in combination with the real-time radial bSSFP sequence as before with an additional saturation pulse (TSR = 170 ms).
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