Stroke is increasingly treated by removing the vessel obstruction via endovascular thrombectomy. 3T imaging has shown wall enhancement after endovascular thrombectomy, and we hypothesize that 7T MR will be beneficial to visualize this enhancement as the higher field strength allows for higher resolution imaging. Seven patients were examined at 7T within two days after endovascular thrombectomy. Vessel wall images pre- and post-contrast administration were reviewed by two neuroadiologists, who rated the image quality as excellent in all cases. In all patients, wall enhancement was found, and correlated to the site of the stent-retriever rather than the site of the embolus.
Seven patients (age range 55-84 years) treated with endovascular thrombectomy for acute stroke in the anterior circulation were included in the study. All had a CTA verified thrombus in the distal internal carotid artery or M1 or M2 segments of the Middle Cerebral Artery. The study was approved by the local ethics committee and written informed consent was obtained from all patients. A 7T examination (Philips Achieva AS, Best, The Netherlands) was performed within two days after the thrombectomy. Black blood vessel wall images were acquired using a 3D magnetization prepared inversion recovery turbo spin-echo (3D MPIR-TSE [5,6]) with 0.8 mm isotropic resolution. Full brain coverage was obtained in 8:30 min. The vessel wall imaging was performed prior to contrast agent administration (pre-Gd) (0.2 ml/kg bodyweight, Dotarem, Gothia Medical, Sweden), as well as twice post contrast (first and second post-Gd).
To reduce motion artifacts during the long vessel wall scans, prospective motion correction was applied (iMOCO [7,8]). This correction is based on a fat-selective navigator which is played out in each echo train. The navigator image is registered to the first image, and the scan geometry is updated in real-time. If the motion exceeds a set threshold, the last data is required, which prolongs the scan.
Image grading was made independently by two neuroradiologists. First, the images were reviewed for location of any vessel wall enhancement, the amount of motion artifacts was graded on a predefined scale, and over-all image quality was graded in all three contrast phases according to another pre-defined scale. Secondly, the location of Gd-uptake in the vessel wall was correlated to the locations of the embolus, based on the pre-operative CT angiography, and the stent-retriever, based on the pre-operative DSA images.
In general, all patients tolerated the examination well. In three cases, the examination was terminated after the first post-contrast scan due to patient discomfort (two cases) or technical issues (one case).
In all patients, both reviewers agreed that vessel wall enhancement was present and that it correlated to the site of the stent-retriever rather than the site of the embolus.
Figure 1 shows axial images from the first post-Gd vessel wall 3D MPIR-TSE from all seven patients. The wall enhancement at the site of the stent-retriever is marked with an arrow. The images also demonstrate the lack of enhancement on the contralateral side.
The results of the image assessment by the two reviewers are shown in Table 1. Overall image quality was graded highest on a 3-grade scale for all contrast phases, with complete agreement between the reviewers. Motion artifacts was not rated as “impairing the diagnostic quality” for any case by any reviewer. This is noteworthy as there in several cases was considerable patient motion during the long scans, indicating that the prospective motion correction strategy was efficient.
To draw firm conclusions, a larger number of subjects need to be included in the study. Longitudinal data could reveal if the wall enhancement persists for an extended period of time.
Overall, 7T vessel wall imaging in the sub-acute phase following endovascular thrombectomy seems safe, robust and reliably yields excellent diagnostic images. The location of contrast enhancement corresponds with the location of the stent-retriever deployment rather than the location of the embolus.
Lund University Bioimaging Center (LBIC), Lund University is gratefully acknowledged for providing experimental resources.
The authors are grateful to Prof. Dr. J. Hendrikse, UMC Utrecht, for providing the 3D MPIR-TSE sequence.
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