Magnetic Resonance Imaging Monitoring of Thermal Lesions Produced by Focused Ultrasound

Autor: Anastasia Antoniou, Nikolas Evripidou, Anastasia Nikolaou, Andreas Georgiou, Marinos Giannakou, Antreas Chrysanthou, Leonidas Georgiou, Cleanthis Ioannides, Christakis Damianou
Jazyk: angličtina
Rok vydání: 2024
Předmět:
Zdroj: Journal of Medical Ultrasound, Vol 32, Iss 4, Pp 297-308 (2024)
Druh dokumentu: article
ISSN: 0929-6441
2212-1552
DOI: 10.4103/jmu.jmu_112_23
Popis: Background: The main goal of the study was to find the magnetic resonance imaging (MRI) parameters that optimize contrast between tissue and thermal lesions produced by focused ultrasound (FUS) using T1-weighted (T1-W) and T2-weighted (T2-W) fast spin echo (FSE) sequences. Methods: FUS sonications were performed in ex vivo porcine tissue using a single-element FUS transducer of 2.6 MHz in 1.5 and 3 T MRI scanners. The difference in relaxation times as well as the impact of critical MRI parameters on the resultant contrast-to-noise ratio (CNR) between coagulated and normal tissues were assessed. Discrete and overlapping lesions were inflicted in tissue with simultaneous acquisition of T2-W FSE images. Results: FUS lesions are characterized by lower relaxation times than intact porcine tissue. CNR values above 80 were sufficient for proper lesion visualization. For T1-W imaging, repetition time values close to 1500 ms were considered optimum for obtaining sufficiently high CNR at the minimum time cost. Echo time values close to 50 ms offered the maximum lesion contrast in T2-W FSE imaging. Monitoring of acute FUS lesions during grid sonications was performed successfully. Lesions appeared as hypointense spots with excellent contrast from surrounding tissue. Conclusion: MRI monitoring of signal intensity changes during FUS sonication in grid patterns using optimized sequence parameters can provide useful information about lesion progression and the success of ablation. This preliminary study demonstrated the feasibility of the proposed monitoring method in ex vivo porcine tissue and should be supported by in vivo studies to assess its clinical potential.
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