The field of the invention is systems and methods for focused ultrasound (“FUS”). More particularly, the invention relates to systems and methods for efficiently transmitting focused ultrasound through aberrating media, including skull bone and other tissues that may aberrate ultrasound.
Transcranial focused ultrasound surgery has been clinically investigated for the non-invasive treatment of brain disorders, including chronic pain, essential tremor, and primary brain tumors. Although it is an attractive modality for imaging and therapy in the brain, transcranial ultrasound suffers from the poor propagation of ultrasound through the skull bone, which attenuates and aberrates the beam. At low frequencies, the phase aberrations that result from the heterogeneous and irregular nature of the skull bone are minimal, while at high frequencies phase corrections are required to achieve an ultrasound focus in the brain. The necessary phase delays for these corrections can be determined from computer simulations of the sound propagation through the skull bone, using geometry and bone density information obtained from preoperative computed tomography scans. Even the simplest computational models, however, can take several hours to compute the phase delays.
A simple direct method for measuring phase delays through an aberrator is to place an ultrasound source at the focus and use time-of-flight measurements to calculate the phase delays between transducer elements. Noninvasive realizations of this technique have used bubbles inside the skull cavity as the sound beacon, with the bubbles either induced through acoustic droplet vaporization or transient cavitation. In one study by Gateau et al., computed tomography-based phase correction was utilized for an initial focusing step and then bubble signature-based phase corrections were used to improve the transducer array focusing and to conduct beam steering. The frequency of the transducer array used by Gateau, et al., was 1 MHz, which was too high to create a cavitation event without first using the simulation based phase correction. In addition, the receivers were a subset of the transmit elements, and were sensitive primarily at their driving frequency.
In a study by Haworth, et al., it was proposed that bubble-based phase correction could be performed by first sonicating at low frequencies and then using harmonic imaging to calculate the phase delays and refocus at the higher frequency. A device and strategy to perform such phase corrections, however, were not described. In particular, it has not been addressed that bubble activity at the low frequency could occur anywhere within a fairly large transmit focal zone, which could compound targeting errors.
It would therefore be desirable to provide a system and method for efficiently transmitting focused ultrasound through a medium, such as bone.
The present invention overcomes the aforementioned drawbacks by providing a system and method for efficiently transmitting focused ultrasound through a medium, such as bone, using an adaptive focusing scheme. The focal region of the focused ultrasound is iteratively updated to provide an improved focus through the medium. This method may be carried out using a transducer assembly that includes two or more transmit arrays each operating at a different frequency. An initial focus is set and updated by delivering focused ultrasound with a lower frequency transmit array. The phase corrections determined in the first iteration are applied to subsequently higher frequency transmit arrays and the process repeated until a desired focus is achieved.
It is an aspect of the invention to provide a method for adjusting a focus of a focused ultrasound beam. An initial focal region of an ultrasound transducer assembly having a plurality of transmit arrays each having a different operating frequency is defined by setting an initial focus of the transmit arrays. Ultrasound energy is delivered to the initial focal region to excite a contrast agent present in the initial focal region using one of the plurality of transmit arrays. Signals responsive to the excited contrast agent in the initial focal region are then received using the ultrasound transducer array. An image is produced from the received signals, and a center of the initial focal region is determined from this image. Phase correction values are computed using the determined center of the initial focal region, and are applied to the focused ultrasound transducer assembly to update the initial focus, thereby defining an updated focal region that is more focused than the initial focal region. This process is iteratively repeated until the updated focal region corresponds to a desired focus. During each repetition of this process, ultrasound energy is delivered to the updated focal region to excite a contrast agent present in the updated focal region using a different one of the plurality of transmit arrays that operates at a higher frequency than the previous transmit array.
It is another aspect of the invention to provide a transducer assembly for use with a focused ultrasound system. The transducer assembly includes a plurality of integrated transducer units and a multiplexing circuit in communication with the integrated transducer units. Each integrated transducer unit includes at least two transducer elements that are concentrically nested to form the integrated transducer unit. The multiplexing circuit is configured to connect the transducer elements in each integrated transducer unit to at least one of a transmit line and a receive line.
It is another aspect of the invention to provide a focused ultrasound system that includes a transducer assembly and a processor in communication with the transducer assembly. The transducer assembly includes a plurality of transducer arrays each composed of transducer elements, each transducer array operating at a different frequency. The transducer assembly may include at least one additional receive array composed of receive transducer elements. The processor is configured to set a focal region for the transducer assembly and to iteratively update this focal region for each transmit array in the transducer assembly. In each iteration, the processor selects the transmit array having the lowest remaining operating frequency and directs the selected transmit array to excite the initial focal region for that transmit array and directs the at least one receive array to receive signals from the initial focal region. The processor then reconstructs an image of the focal region from the received signals and computes phase correction values from the reconstructed image. The processor then applies the computed phase correction values to the selected transmit array and to the transmit array having the next highest operating frequency.
The foregoing and other aspects and advantages of the invention will appear from the following description. In the description, reference is made to the accompanying drawings which form a part hereof, and in which there is shown by way of illustration a preferred embodiment of the invention. Such embodiment does not necessarily represent the full scope of the invention, however, and reference is made therefore to the claims and herein for interpreting the scope of the invention.
A system and method for efficiently transmitting focused ultrasound through skull bone using a focused ultrasound (“FUS”) system is provided. Particularly, an ultrasound transducer array design and a method for adaptive ultrasound focusing through the skull bone are provided.
Referring to
The controller 104 generally includes a processor 118, a signal generator 120, and a radio frequency (“RF”) amplifier 122. The signal generator 120 may include, for example, a function generator, and is configured to provide a driving signal that directs the ultrasound transducer 106 to generate ultrasound energy. The driving signal produced by the signal generator 120 is amplified by the RF amplifier 122 before being received by the ultrasound transducer 106. When the FUS system 100 is used during a magnetic resonance guided FUS (“MRgFUS”) application, the controller 104 can be positioned inside or outside of the magnet room of the magnetic resonance imaging (“MRI”) system.
The processor 118 is in communication with the signal generator 120 and directs the signal generator 120 to produce the driving signal that is delivered to the ultrasound transducer 106. As will be described below in detail, the processor 118 may be configured to adjust properties of the driving signal such that the ultrasound energy pressure produced by the ultrasound transducer 106 is adjusted in accordance with embodiments of the present invention.
The processor 118 receives acoustic signals from the signal detector 114. As will be described below in detail, the feedback information provided by the signal detector 114 is utilized by the processor 118 to direct the appropriate adjustments in ultrasound energy. The processor 118 is also in communication with the positioning system 110, and is configured to direct the positioning system 110 to move the position of the ultrasound transducer 106 during a sonication procedure. In the case that the ultrasound transducer 106 is a phased array transducer, the controller 104 may adjust the phase and/or amplitude of the driving RF signal to each transducer element to control the location of the focal spot.
In general, the ultrasound transducer 106 may be referred to as a transducer assembly that includes one or more arrays of ultrasound transducer elements. Each transducer array may include only transmit elements, only receive elements, or both transmit and receive elements. By way of example, the transducer assembly may include multiple integrated transmit and receive arrays. For instance, the transducer assembly may include two or more transmit arrays operating at different frequencies, and one or more receive arrays with resonances at harmonics or sub-harmonics of the transmit arrays. Preferably, the transducer assembly would be a full hemisphere to provide the best focusing capabilities. All of the arrays can be either fully populated or sparse if a reduced number of transducer elements is preferred.
In one configuration, such as the one illustrated in
With reference to
Referring now to
Referring now to
The FUS system 400 includes a processor 418 that is in communication with a multi-channel amplifier 424 and a multi-channel receiver 426. The multi-channel amplifier 424 receives driving signals from the processor 418 and, in turn, directs the transducer elements of the transducer 406 to generate ultrasound energy. The multi-channel receiver 426 receives acoustic signals during sonications and relays these signals to the processor 418 for processing in accordance with embodiments of the present invention. The processor 418 may also be configured to adjust the driving signals in response to the acoustic signals received by the multi-channel receiver 426. For example, the phase and/or amplitude of the driving signals may be adjusted so that ultrasound energy is more efficiently transmitted through the skull of the subject 402 and into the target volume-of-interest 430. Furthermore, the acoustic signals may also be analyzed to determine whether and how the extent of the focal region should be adjusted.
Having described the general structure of a FUS system that implements the present invention, reference is now made to
Using geometric focusing, and ignoring the skull contributions, the ultrasound would be initially focused in the brain using lower frequency ultrasound, as illustrated at step 502. This initial focus would be relatively large due to the low frequency used. The patient may then be administered an ultrasound contrast agent, as illustrated at step 504. This ultrasound contrast agent may be either a microbubble contrast agent or a phase-change droplet contrast agent, and is preferably administered at a very low concentration. For instance, the contrast agent concentration can be sufficiently low as to be able to image individual bubbles in the vasculature.
The low frequency transmit array is then used to excite the individual bubbles, as indicated at step 506. Harmonic emissions that are responsive to this excitation are acquired by one of the receive arrays and beamformed using both phase and amplitude information to produce an initial image of the bubble, as indicated at step 508. The initial beamforming considers only geometric delays and not those produced by the skull. As indicated at decision block 510, the excitation and image reconstruction steps are repeated to create a time series of images depicting bubble activity at the transmit focus. To the extent that additional contrast agent is required, more contrast agent will be administered to the subject.
By examining the spatial extent of the activity and the strength of the bubble responses, the approximate center of the transmit focus can be determined from the time series of images, as indicated at step 512. Using the emissions from one of the bubble events at this location, phase corrections for the transmitted and received beams are calculated, as indicated at step 514. These phase corrections are then applied to the transmit elements to improve the transmit focus, as indicated at step 516. This process can optionally be repeated to improve the estimates of the transmit and receive phase corrections, as indicated at decision block 518.
The phase corrections could then be applied to the transmit array with the next lowest frequency, creating a time series of images with the corresponding receiver array to determine the spatial extent of the transmit focus and to fine-tune the transmit and receive focusing, as indicated at step 520. This process could be iterated at each transmit frequency, and repeated at increasing frequencies to create a sharp treatment focus at high frequencies, as indicated at decision block 522.
In some embodiments, when the bubble signatures recorded at the receivers are very weak, the image quality may be improved by fitting the expected bubble response to the raw data. One implementation of this may include finding an optimal fit by cross-correlating a template of the expected bubble response to the raw data on each line. Thus, in some embodiments the systems and methods of the present invention include providing one or more templates of expected bubble response. Data captured at a low sampling frequency could be up-sampled prior to fitting the template in order to preserve position information.
The present invention provides the ability to perform high resolution vascular mapping of the brain for diagnostic purposes. This can be accomplished by scanning the transmit focus throughout the brain while collecting the scattered signals from microbubbles that are infused into the blood vessels. In this instance, the transmit and receive signal corrections are derived first and then the three-dimensional images of the bubbles (and thus the vasculature) are formed and tracked as a function of time. For this imaging, either standard short ultrasound imaging bursts can be used to provide time-resolved echo location, or long ultrasound imaging bursts using the method described above can be used to form the images. The method of the present invention can also improve ultrasound imaging in other aberrating media, including the breast, the heart, the prostate, and so on. Breast imaging, for example, could be conducted with a similar hemispherical array design as would be used for brain imaging and therapy applications.
The present invention has been described in terms of one or more preferred embodiments, and it should be appreciated that many equivalents, alternatives, variations, and modifications, aside from those expressly stated, are possible and within the scope of the invention.
This application represents the U.S. National Stage of International Application No. PCT/US2014/020279, filed Mar. 4, 2014 which claims the benefit of U.S. Provisional Patent Application Ser. No. 61/771,992, filed on Mar. 4, 2013, and entitled “System and Method for Measuring and Correcting Ultrasound Phase Distortions Induced by Aberrating Media.”
This invention was made with government support under EB003268 and EB009032 awarded by the National Institutes of Health. The government has certain rights in the invention.
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