Bioresorbable Vascular Scaffolds (BVS) provide a new and rapidly evolving alternative to drug eluting metal stents (DES) in the treatment of coronary artery disease. Besides potential advantages over DES in the restoration of the vessel function and reduction of post-interventional angina BVS allow for artifact-free coronary MRI of scaffolded arteries. In this study, we demonstrate that MRI for non-invasive monitoring of coronary arteries after BVS implantation is feasible by assessing coronary patency in a group of 11 patients initially and one year post-intervention.
Coronary MRI is a non-invasive and radiation-free imaging technique that allows for the assessment of vascular patency and detection of stenoses in patients with coronary artery disease (CAD).1 After treatment of CAD patients with percutaneous coronary intervention (PCI), about 30% of these patients re-develop symptoms of angina pectoris within the first year post-intervention.2 Thus, coronary MRI would be desirable for the follow-up of vascular patency after PCI. However, imaging of arteries treated with metallic drug eluting stents (DES) is not feasible due to strong imaging artifacts.3
Bioresorbable Vascular Scaffolds (BVS) provide a new and rapidly evolving alternative to DES in the treatment of CAD. Besides potential advantages over DES in the restoration of the vessel function and reduction of post-interventional angina, BVS allow for artifact-free coronary MRI of scaffolded arteries. This has been shown in proof-of-concept studies at 1.5T and 3T4-6.In this work, we further assess coronary patency in a group of 11 patients one year after the treatment with BVS and demonstrate the applicability of coronary flow measurements in the presence of BVS for myocardial blood flow quantification.
Eleven patients were included that received one or more BVS in proximal segments of the left anterior descending (LAD), left circumflex (LCX) or right coronary artery (RCA). The baseline MR exam was performed within three days post-intervention and all patients were imaged again after 12 months with the same MR protocol.
All MR image data were acquired using ECG triggering, and 3D acquisitions were additionally gated to end-expiration. Coronary arteries were localized using a whole-heart low-resolution 3D navigator-gated bSSFP sequence with fat-saturation. This was followed by a targeted 3D bright-blood navigator-gated FLASH sequence with 1.08 mm isotropic resolution, fat saturation and T2 preparation (TE/TR: 1.9/3.1 ms, FoV: 28x277x295x28 mm³, TET2prep: 40 ms, R = 2).
In a subgroup of 5 patients the ejection fraction was measured with a multi-slice cine-bSSFP sequence in short-axis view. To demonstrate proof-of-concept of coronary flow measurements in the proximity of the scaffold, time-resolved blood flow velocity quantification via phase-contrast MRI was performed in one patient both at baseline and after 12 months. Therefore, a cross-sectional 2D single slice positioned proximal to the scaffolded vessel area was acquired with through-plane velocity-encoding using spiral sampling, prospective ECG-triggering and respiratory navigator gating as well as a 1-2-1 binomial water selective RF excitation pulse (TE/TR: 4.8/15.2 ms, 16 interleaves, SL: 8 mm, FoV: 200x200 mm³, VENC: 35 cm/s).7
To evaluate lumen diameters and assess potential re-stenoses in the scaffolded segment of the artery, all bright-blood image sets were manually reformatted along the course of the vessel (IMPAX EE Extended Multi-planar Reconstruction, AGFA Healthcare). Based on these reformats, the lumen diameter was measured as the FWHM and averaged over the scaffolded segment.
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