WO2010058292A2 - Closed-loop clot lysis - Google Patents

Closed-loop clot lysis Download PDF

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Publication number
WO2010058292A2
WO2010058292A2 PCT/IB2009/007674 IB2009007674W WO2010058292A2 WO 2010058292 A2 WO2010058292 A2 WO 2010058292A2 IB 2009007674 W IB2009007674 W IB 2009007674W WO 2010058292 A2 WO2010058292 A2 WO 2010058292A2
Authority
WO
WIPO (PCT)
Prior art keywords
clot
transducer
correction factors
blood vessel
blood flow
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/IB2009/007674
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English (en)
French (fr)
Other versions
WO2010058292A3 (en
Inventor
Eyal Zadicario
Arik Hananel
Gilat Schiff
Javier Grinfeld
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Insightec Ltd
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Insightec Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Insightec Ltd filed Critical Insightec Ltd
Priority to CN2009801539971A priority Critical patent/CN102292123A/zh
Priority to JP2011536968A priority patent/JP2012509126A/ja
Priority to EP09801547.2A priority patent/EP2358437B1/en
Publication of WO2010058292A2 publication Critical patent/WO2010058292A2/en
Publication of WO2010058292A3 publication Critical patent/WO2010058292A3/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N7/00—Ultrasound therapy
    • A61N7/02—Localised ultrasound hyperthermia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
    • A61B90/36—Image-producing devices or illumination devices not otherwise provided for
    • A61B90/37—Surgical systems with images on a monitor during operation
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/02—Detecting, measuring or recording for evaluating the cardiovascular system, e.g. pulse, heart rate, blood pressure or blood flow
    • A61B5/026—Measuring blood flow
    • A61B5/0263—Measuring blood flow using NMR
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N7/00—Ultrasound therapy
    • A61N7/02—Localised ultrasound hyperthermia
    • A61N7/022—Localised ultrasound hyperthermia intracavitary

Definitions

  • the present invention relates generally to systems and methods for performing noninvasive procedures using acoustic energy, and, more particularly, to systems and methods for focusing ultrasonic energy to treat thrombotic disease.
  • Tissue such as a benign or malignant tumor or blood clot within a skull or other region of a patient' s body may be treated invasively by surgically removing the tissue, or non- invasively by using effects of focused ultrasound. Both approaches may effectively treat certain localized conditions within the brain, but involve delicate procedures in which it is desired to avoid destroying or damaging otherwise healthy tissue. These treatments may not be appropriate for conditions in which diseased tissue is integrated into healthy tissue, unless destroying the healthy tissue is unlikely to affect neurological function significantly.
  • HIFU High-intensity focused ultrasound
  • tPA tissue plasminogen activator
  • Focused ultrasound has particular appeal for treating tissue within the brain because it generally does not disturb intervening or surrounding healthy tissue. Focused ultrasound may also be attractive because acoustic energy generally penetrates well through soft tissues and ultrasonic energy, in particular, may be focused toward focal zones having a cross-section of only a few millimeters due to relatively short wavelengths (e.g., as small as 1.5 millimeters (mm) in cross-section at one Megahertz (1 MHz)). Thus, ultrasonic energy may be focused at a small target in order to ablate the tissue without significantly damaging surrounding healthy tissue.
  • a piezoelectric transducer having a number of transducer elements such that constructive interference occurs at a "focal zone.”
  • sufficient acoustic energy may be delivered either to heat tissue until necrosis occurs, or mechanically disrupt its structure until the tissue is destroyed.
  • tissue along the path through which the acoustic energy passes (the "pass zone") outside the focal zone is heated only minimally, if at all, thereby minimizing damage to tissue outside the focal zone.
  • Stroke is the third leading cause of death in the United States and a leading cause of adult disability.
  • strokes can be classified as either ischemic or hemorrhagic.
  • ischemic strokes the blockage of blood flow results from a clot in intracerebral vessels, whereas hemorrhagic strokes are caused by ruptured blood vessels.
  • Several clinical trials were initiated to evaluate the safety and efficacy of ultrasound-assisted tPA approach to treat stroke patients. However, these trials were generally unsuccessful due to adverse events associated with bleeding that were triggered outside the target area.
  • the present invention provides procedures and systems that facilitate non-invasive, focused clot lysis.
  • the technique uses a closed-loop approach such that immediate feedback is provided to an operator or to an automatic control system.
  • One application directs ultrasound energy at the clot so as to cause it to become smaller (typically through liquefaction) while sparing adjacent tissue.
  • blood flow is monitored in the vicinity of the blocked vessel, or, in the case of hemorrhagic stroke, the liquefaction of the clot is monitored.
  • images are taken of the area surrounding the clot and displayed to an operator so as to provide a real-time indication of blood flow in and/or around the affected blood vessel or the content of the hemorrhage (i.e., solid versus liquid).
  • alterations to the treatment regimen can be administered by increasing or decreasing the overall pressure, energy and changing temporal or spatial characteristics of the acoustic beam (i.e., on/off timing, location).
  • the energy transmitted to the clot may be increased or decreased and/or the focus of the ultrasound transducer may be adjusted by modifying various operational parameters of the individual transducer elements.
  • control is automated — that is, a controller responds to the measured blood flow (and changes therein), and/or the content of the hemorrhage and alters the intensity, pressure and/or direction of the ultrasound energy accordingly.
  • a system for delivering acoustic energy to a clot within a blood vessel or a hemorrhage includes a high-intensity focused ultrasound phased- array transducer, means for monitoring blood flow (such as a visual display providing magnetic resonance images, computer tomography images and/or ultrasound images) in the vicinity of the blood vessel as ultrasound energy is directed at the blood vessel, and a controller for operating the transducer and adjusting transducer operation based on the monitored blood flow.
  • the system also includes a processor for generating correction factors based on the monitored blood flow, and the controller responds to the processor by implementing the correction factors (and, based thereon, adjusting the application of the acoustic energy).
  • a beam former may also be used to drive the transducer elements according to the correction factors.
  • the controller may also allow an operator to manually override the correction factors.
  • the phased- array transducer may include numerous transducer elements, each of which can deliver ultrasound energy independent of the others.
  • the images may, in some cases, provide an indication of blood flow and/or oxygen level in blood vessels about the clot, and in certain within the specific blood vessel containing the clot. In other instances, the focal quality of the images being used to monitor the blood flow may be used to determine one or more adjustments.
  • the correction factors may include phase correction factors for each (or a group of) transducer elements.
  • the controller may also include a phase adjuster for adjusting the excitation signals provided to the transducer elements based on the correction factors.
  • the controller may include amplifiers coupled to the phase adjuster for amplifying the excitation signals provided to respective transducer elements based upon amplitude and/or phase correction factors.
  • the processor constructs an acoustic transmission regime that includes a series of treatment parameters optimized to perform clot lysis. In such cases, the correction factors influence the treatment parameters, thereby adjusting the delivery of ultrasound energy to the clot.
  • a system for treating a clot within a blood vessel includes a focused ultrasound energy transducer, means for monitoring the liquid content of the blood vessel as energy is delivered to the clot (by an operator using a visual display, for example), and a controller for adjusting the transducer operation based on the monitored liquid content.
  • the system also includes a processor for generating correction factors based on the liquefaction information.
  • the controller is responsive to the processor and implements the correction factors, thereby influencing the application of acoustic energy to the clot.
  • a method for treating a clot within a blood vessel includes applying focused ultrasound energy to the blood vessel using a focused ultrasound phased-array transducer, monitoring blood flow in a vicinity of the blood vessel, and operating the transducer including adjusting the transducer operation based on the monitored blood flow.
  • the method also includes obtaining subsequent images (e.g., magnetic resonance images, computer tomography images and/or ultrasound images) of the blood vessel during the application of the ultrasound energy and generating correction factors based on the images for transducer elements that comprise the transducer array.
  • the focal quality of the images used to monitor the blood flow may also be used to determine or influence the correction factors.
  • the correction factors are then used to create excitation signals based upon the correction factors to focus acoustic energy from the transducer elements at the clot.
  • the above technique may be repeated until the clot is substantially liquefied.
  • the correction factors may include phase correction factors for each (or a group of) transducer elements.
  • the excitation signals may be adjusted based on the correction factors, and may further be amplified prior to being provided to respective transducer elements based upon amplitude correction factors.
  • an acoustic transmission regime that includes a series of treatment parameters optimized to perform clot lysis may be provided.
  • the correction factors influence the treatment parameters, thereby adjusting the delivery of ultrasound energy to the clot.
  • a method for treating a clot within a blood vessel includes applying focused ultrasound energy to the blood vessel using a focused ultrasound phased-array transducer, monitoring liquid content of the clot in a vicinity of the blood vessel, and operating the transducer including adjusting the transducer operation based on the monitored liquid content.
  • images may be used to monitor the liquid content of the clot, and correction factors may be determined based on the liquefaction information as provided in the images.
  • Fig. 1 schematically illustrates a system for monitoring physiological effects of ultrasound treatment in accordance with various embodiments of the invention.
  • Fig. 2 is a flow chart illustrating a method for administering ultrasound therapy in accordance with various embodiments of the invention.
  • a system for quickly treating a patient P suffering from a stroke and/or an intracranial clot C includes a high-intensity focused-ultrasound phased-array transducer 105 (which is driven by one or more drivers 110), a controller 120, and one or more imagers 130 for monitoring clinical parameters related to the clot C.
  • the parameters are detectable via the imaging apparatus 130 and can be used to monitor the successful liquefaction of the clot C. Examples of such parameters include blood flow in the vicinity of a blood vessel being treated and/or liquification of the clot C.
  • the system may also include a processor 140 and a display 150.
  • the system may also include a user interface 160, such as a touch screen, a keyboard, and/or a mouse.
  • a user interface 160 such as a touch screen, a keyboard, and/or a mouse.
  • the system is configured for delivering ultrasonic energy between ten kilohertz (0.01 MHz) and ten Megahertz (10 MHz) to tissue within the skull or other anatomical regions.
  • ultrasonic energy between ten kilohertz (0.01 MHz) and ten Megahertz (10 MHz) to tissue within the skull or other anatomical regions.
  • Such a system may be used to treat blood clots lodged within blood vessels of a patient or a clot outside blood vessels (generated by ruptured blood vessels) by delivering acoustic energy to the clot.
  • the clot may be partially or completely blocking a blood vessel in the patient's cranium, or applying intra cranial pressure in case of hemorrhagic clot and causing life-threatening conditions such as a stroke.
  • blood flow (as well as other clinical parameters) in and/or around the affected blood vessel is monitored, and adjustments made to one or more treatment parameters based thereon.
  • the adjustments may be automatic or manual. For example, various images of the patient' s anatomy surrounding the clot may be viewed on a display, and adjustments made based on automated or human analysis of the images.
  • the transducer 105 may include "n" (where n > 1) transducer elements, thereby providing a multiple-element transducer array.
  • the transducer 105 may include a flexible or semi-rigid base or panel conforming to the shape of patient's anatomy, such as the skull if being used to treat cranial blood clots.
  • the transducer 105 may be pre-curved (e.g. biased to a spherical or other concave shape), such that the transducer may be placed on or near a portion of a skull.
  • the transducer 105 may be planar, parabolic, or any other suitable shape, e.g., circular, elliptical, and the like.
  • Suitable HIFU phased-array transducers are known in the art. See, e.g., co-pending, commonly-owned U.S. Patent Application Serial No. 10/328,584, entitled “Tissue Aberration Corrections in Ultrasound Therapy.”
  • the system may obtain, process and present images of the interior anatomy of the patient P, including the area surrounding the clot C.
  • the images may be taken using a magnetic resonance imaging (MRI) device, a computer tomography (CT) device, or an ultrasound imaging device.
  • the images processed by the processor 140 and presented on the display 150 indicate the state of blood flow and/or liquification of tissue about the clot C, either within the specific blood vessel in which the clot is lodged, or, in some cases, in blood vessels surrounding the clot or a general measure of perfusion surrounding the clot C or within the hemorrhagic clot.
  • an operator views the images in real-time or pseudo-real time (e.g., a delay of less than five seconds), and thus is able to see the effects of the ultrasound on the clot and the resulting improvement of blood flow or perfusion.
  • the effects of reflow or liquefaction maybe also assessed directly or by other bio-imaging parameters.
  • a processor 140 may generate correction factors to be applied to the signals that drive the transducers 105.
  • the processor 140 may, for example, determine the correction factors by automatically analyzing images and estimating blood flow or liquid content (and, in some embodiments, identifying tissue characteristics of interest) from the images. Sufficient information is provided by the images (or other monitoring modality) to facilitate determination of the correction factors. Alternatively, a user may manually analyze the images and observe blood flow or liquid content and identify tissue characteristics, or a combination of automatic and manual analysis may be used. In some instances, the focal quality of the images themselves may be determined and used to influence the correction factors. For example, if a particular image is know to be of poor quality, its contribution to the correction factor(s) may be down-weighted.
  • the processor 140 may, for example, receive instructions as input by the operator, or, in some cases, automatically recognize an increase in blood flow, perfusion (or lack thereof), and/or liquid content based, for example, on the images.
  • the correction factors can be applied to treatment parameters that govern the application of HIFU energy, thereby influencing subsequent ultrasound applications.
  • the processor 140 includes a number of amplifiers and/or phase shifters that are coupled in respective sets.
  • the amplifiers provide amplified excitation signals to the transducer elements 105, e.g., via coaxial cables or other connections, which may individually connect the amplifiers and respective transducer elements.
  • the correction factors allow the acoustic energy transmitted by the transducer elements to be steered such that the "focal zone" (the region in space toward which the acoustic energy is focused) can be moved, along the z axis (i.e., an axis extending orthogonally from the transmission surface of the transducer into the skull) and/or along the x or y axes.
  • the component of each phase-shift factor associated with steering may be computed using known techniques, e.g., using the average speed of sound in the body (possibly adjusted for different tissue types) and the distance from each transducer element to a target site of interest (the intended focal zone within a tissue region).
  • the correction factors may also compensate for phase distortion of the ultrasonic energy transmitted by each transducer element that occurs when the acoustic energy passes through the skull.
  • the component of each correction factor associated with phase distortion may compensate for perturbations and distortions introduced by the bone of the skull, the skin/skull interface, the dura matter/skull interface, by variations in skull thickness or density, and/or by structural considerations such as air-filled or liquid-filled pockets in the skull.
  • the two components that make up the phase-shift factors i.e., the steering components and the phase-distortion components, are summed to determine the composite phase- shift factors for the respective channels in order to focus ultrasonic energy at a desired location.
  • the processor 140 or the operator may also construct an initial treatment regime describing various treatment parameters (e.g., pressure, temporal structure, frequency, energy, etc.) that creates a sharp focus (e.g., less than 5 mm) of the ultrasound energy, thereby facilitating clot lysis in a targeted manner.
  • various treatment parameters e.g., pressure, temporal structure, frequency, energy, etc.
  • a sharp focus e.g., less than 5 mm
  • the correction factors determined during treatment may be applied to the treatment regime in real-time.
  • the phase-shift factors may, in some cases, be determined by the processor 140 and/ or the system image and display computer, which may be coupled to the controller 120 and to an imager 130.
  • the controller 120 itself may include all necessary hardware components and/or software modules to determine the correction factors instead of requiring a separate computer.
  • the system may include one or more software modules, hardware components, firmware, hardwiring, or any combinations of these.
  • the processor may be a general or special purpose digital data processor programmed with software to generate the phase shift factors, which may be transferred to the controller for subsequent transfer to the phase shifters or directly to the phase shifters based upon images shown on the display.
  • various embodiments of the invention provide methods for treating stroke victims using such a system as described below and illustrated in FIG. 2.
  • an imager Upon initial examination, an imager is used to acquire one or more images (STEP 205) of a clot area within a patient's brain.
  • the imager may be any of a variety of imaging devices, such as an MRI device, a CT device, or an ultrasound device or a combination/fusion of images.
  • Data representing the images are transferred to a processor (STEP 210), and presented on a display (STEP 215).
  • the transfer of image data may occur immediately upon acquiring the images from the patient in order to provide treatment quickly. The transfer may be completed automatically or may occur only upon instruction from a physician or other operator.
  • correction factors and other potential adjustments may be determined (STEP 220) for treatment of the clot.
  • the correction factors may account for different speeds of sound that are encountered as the acoustic energy passes through different tissue types in respective segmented tissue regions.
  • the correction factors may account for aberrations generated by the skull or at boundaries of the segmented tissue regions, as explained further below.
  • the resulting correction factors may be used to assist a particular course of treatment, preferably focusing acoustic energy at the clot.
  • the correction factors may be provided to the controller which, in turn, provides excitation signals (STEP 225) to the transducer array.
  • the focused ultrasound system uses the correction factors to control a beam former or signal adjuster which delivers excitation or drive signals to the transducer based upon the correction factors for application of the ultrasound treatment (STEP 230).
  • one or more base signals may be supplied to a signal adjuster and split into a plurality of channels, preferably into individual channels corresponding to respective transducer elements or transducer element groupings of the transducer array.
  • the phase of the signals for the respective channels may be adjusted by the signal adjuster according to phase correction factors received by the controller.
  • the phases may be adjusted to compensate for acoustic energy from respective transducer elements passing through different tissue types and/or encountering one or more tissue boundaries.
  • the amplitude adjustments may be done to compensate for a known or calculated skull temperature or to generate desired skull temperature.
  • Such an approach may be implemented a priori based, for example, on an acoustic-bio-heat simulation or based on actual skull temperature measurements. In some cases, the system may assume an even temperature distribution on the skull.
  • phase-adjusted signals may be amplified based upon amplitude correction factors, e.g., by amplifiers, which may amplify the excitation signals.
  • the signals for the respective channels may be amplified before they are phase- adjusted.
  • the amplified and phase-adjusted excitation signals may be delivered to the transducer to drive the respective transducer elements.
  • the transducer elements convert the excitation signals into acoustic energy that is transmitted from the respective transducer elements of the transducer into the blood vessel containing the clot or hemorrhage inside the brain (or its general area) through any intervening tissue and/or bone, such as the skull.
  • additional images may be acquired (STEP 235) using the same or a different imager than used to acquire reference image data to monitor the progress of the treatment.
  • the images may be transferred to the processor and/or rendered on a display for real-time or nearly real-time monitoring.
  • the images acquired during treatment may be compared with the previously acquired reference images to determine if, for example, the blood flow within the blood vessel has improved or the hemorrhage has been liquefied. This comparison may be made by the operator or in an automated fashion using image-analysis software configured to recognize fluid flow through or liquid content of a clot.
  • the treatment parameters may be adjusted, e.g., by providing further amplitude and/or phase correction factors, to modify the energy delivered to the tissue region and reflect events as they unfold, e.g., to increase monitored blood flow or liquid content. Treatment is thereby delivered in a controlled, closed-loop manner that considers how the treatment is affecting the physiological characteristics of the clot and/or the treatment zone surrounding the clot.
  • phase settings are adjusted based on the quality of the focus.
  • the focal quality may be sensed using regular imaging or, in some cases, unique modes of imaging tailored to assess focus quality such as acoustic radiation force imaging.
  • the phases are dithered to identify optimal focus that defines the phase setting.

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  • Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
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  • Radiology & Medical Imaging (AREA)
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  • Engineering & Computer Science (AREA)
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  • Oral & Maxillofacial Surgery (AREA)
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PCT/IB2009/007674 2008-11-19 2009-11-19 Closed-loop clot lysis Ceased WO2010058292A2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
CN2009801539971A CN102292123A (zh) 2008-11-19 2009-11-19 闭环凝块消散
JP2011536968A JP2012509126A (ja) 2008-11-19 2009-11-19 閉ループ血塊溶解
EP09801547.2A EP2358437B1 (en) 2008-11-19 2009-11-19 Closed-loop clot lysis

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US11611108P 2008-11-19 2008-11-19
US61/116,111 2008-11-19

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WO2010058292A2 true WO2010058292A2 (en) 2010-05-27
WO2010058292A3 WO2010058292A3 (en) 2010-10-28

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US (1) US8425424B2 (enExample)
EP (1) EP2358437B1 (enExample)
JP (1) JP2012509126A (enExample)
CN (1) CN102292123A (enExample)
WO (1) WO2010058292A2 (enExample)

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US20100125193A1 (en) 2010-05-20
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