Objective: To design and simulate the performance of two spine-specific phased arrays in sonicating targets spanning the thoracic spine, with the objective of efficiently producing controlled foci in the spinal canal.

Methods: Two arrays (256 elements each, 500 kHz) were designed using multi-layered ray acoustics simulation: a four-component array with dedicated components for sonicating via the paravertebral and transvertebral paths, and a two-component array with spine-specific adaptive focusing. Mean array efficiency (canal focus pressure/water focus pressure) was evaluated using forward simulation in neutral and flexed spines to investigate methods that reduce spine-induced insertion loss. Target-specific four-component array reconfiguration and lower frequency sonication (250 kHz) were tested to determine their effects on array efficiency and focal dimensions.

Results: When neutral, two- and four-component efficiencies were [Formula: see text]% and [Formula: see text]%, respectively, spine flexion significantly increased four-component efficiency ([Formula: see text]%), but not two-component efficiency ([Formula: see text]%). Target-specific four-component re-configuration significantly improved efficiency ([Formula: see text]%). Both arrays produced controlled foci centered within the canal with similar 50% pressure contour dimensions: 10.8-11.9 mm (axial), 4.2-5.6 mm (lateral), and 5.9-6.2 mm (vertical). Simulation at 250 kHz also improved two- and four-component efficiency ([Formula: see text]% and [Formula: see text]%, respectively), but doubled the lateral focal dimensions.

Conclusion: Simulation shows that the spine-specific arrays are capable of producing controlled foci in the thoracic spinal canal.

Significance: The complex geometry of the human spine presents geometrical and acoustical challenges for transspine ultrasound focusing, and the design of these spine-specific ultrasound arrays is crucial to the clinical translation of focused ultrasound for the treatment of spinal cord disease.

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http://dx.doi.org/10.1109/TBME.2019.2912146DOI Listing

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