Lizzi Frederic L, Muratore Robert, Deng Cheri X, Ketterling Jeffrey A, Alam S Kaisar, Mikaelian Samuel, Kalisz Andrew
Biomedical Engineering Laboratories, Riverside Research Institute, New York, NY 10038, USA.
Ultrasound Med Biol. 2003 Nov;29(11):1593-605. doi: 10.1016/s0301-5629(03)01052-4.
This report describes a monitoring technique for high-intensity focused ultrasound (US), or HIFU, lesions, including protein-denaturing lesions (PDLs) and those made for noninvasive cardiac therapy and tumor treatment in the eye, liver and other organs. Designed to sense the increased stiffness of a HIFU lesion, this technique uniquely utilizes the radiation force of the therapeutic US beam as an elastographic push to detect relative stiffness changes. Feasibility was demonstrated with computer simulations (treating acoustically induced displacements, concomitant heating, and US displacement-estimation algorithms) and pilot in vitro experimental studies, which agree qualitatively in differentiating HIFU lesions from normal tissue. Detectable motion can be induced by a single 5 ms push with temperatures well below those needed to form a lesion. Conversely, because the characteristic heat diffusion time is much longer than the characteristic relaxation time following a push, properly timed multiple therapy pulses will form lesions while providing precise control during therapy.
本报告描述了一种用于高强度聚焦超声(HIFU)损伤的监测技术,包括蛋白质变性损伤(PDL)以及用于眼部、肝脏和其他器官的非侵入性心脏治疗和肿瘤治疗所造成的损伤。该技术旨在感知HIFU损伤增加的硬度,独特地利用治疗性超声束的辐射力作为弹性成像推力来检测相对硬度变化。通过计算机模拟(处理声学诱导位移、伴随加热和超声位移估计算法)和初步体外实验研究证明了其可行性,这些研究在定性区分HIFU损伤与正常组织方面达成了一致。单次5毫秒的推力就能在远低于形成损伤所需温度的情况下诱导出可检测到的运动。相反,由于特征热扩散时间远长于推力后的特征弛豫时间,适当定时的多个治疗脉冲将形成损伤,同时在治疗过程中提供精确控制。