Systems and methods for cosmetic ultrasound treatment of skin

Information

  • Patent Grant
  • 11241218
  • Patent Number
    11,241,218
  • Date Filed
    Monday, August 14, 2017
    6 years ago
  • Date Issued
    Tuesday, February 8, 2022
    2 years ago
Abstract
Embodiments of a dermatological cosmetic treatment and/or imaging system and method adapted for dithering ultrasound beams from a transducer to alter placement and position of one or multiple cosmetic treatment zones in tissue, simultaneous multi-focus therapy using multi-channel signal mixing, and/or dithering ultrasound beams from a transducer to alter placement and position of one or multiple cosmetic treatment zones in tissue, configured for using imaging for improved ultrasound therapy efficacy, and/or adapted for imaging with multiple focal zone sequencing and triggering for mechanically translated and/or steered ultrasound transducers are provided herein. The system can include a hand wand, a removable transducer module, and a control module. In some embodiments, the cosmetic treatment system may be used in various cosmetic procedures.
Description
BACKGROUND
Field

Several embodiments of the invention relate to energy-based noninvasive treatments for obtaining aesthetically and/or cosmetically enhancing effects on skin and/or tissue near the skin of a human face, head, neck, and/or body.


Description of the Related Art

Some cosmetic procedures involve invasive procedures that may require invasive surgery. Patients not only have to endure weeks of recovery time, but also are frequently required to undergo risky anesthetic procedures. Non-invasive energy-based therapeutic devices and methods are available, but may have various shortcomings with respect to efficiency and effectiveness. Some cosmetic procedures create a sequential series of treatment points or lines. In those procedures, the period of time for treatment is the sum of the sequential treatments.


SUMMARY

In several embodiments, provided are systems and methods that successfully achieve an aesthetic effect using targeted and precise ultrasound to cause a visible and effective cosmetic result via a thermal pathway by splitting an ultrasound therapy beam to two, three, four, or more simultaneous focal zones for performing various treatment and/or imaging procedures. In various embodiments, an ultrasound system is configured for focusing ultrasound to produce localized, mechanical motion within tissues and cells for the purpose of producing either localized heating for tissue coagulation or for mechanical cellular membrane disruption intended for non-invasive aesthetic use. In various embodiments, an ultrasound system is configured for lifting a brow (e.g., an eyebrow). In various embodiments, an ultrasound system is configured for lifting lift lax tissue, such as submental (beneath the chin) and neck tissue. In various embodiments, an ultrasound system is configured for improving lines and wrinkles of the décolleté. In various embodiments, an ultrasound system is configured for reducing fat. In various embodiments, an ultrasound system is configured for reducing the appearance of cellulite.


In various embodiments, an ultrasound system is configured for imaging to visualize tissue (e.g., dermal and subdermal layers of tissue) to ensure proper coupling of the transducer to the skin. In various embodiments, an ultrasound system is configured for imaging to visualize tissue (e.g., dermal and subdermal layers of tissue) to confirm appropriate depth of treatment such as to avoid certain tissues (e.g., bone).


In various embodiments, treating tissue, such as skin tissue, with multiple beams provides one or more advantages, such as, for example, reducing treatment time, creating unique heating patterns, leveraging multiple channels for greater power, the option to treat skin at two or more depths with the same or different power levels, (e.g., a thermal coagulation point in the superficial muscular aponeurotic system (“SMAS”) and another defocused energy at the surface of the skin, or other combinations), optional simultaneous treatment at different depths (e.g., such as at depths below a skin surface of 3 mm and 4.5 mm thermal coagulation points simultaneously or in an overlapping time period); and/or treatment with one, two, or more simultaneous linear or line focuses, such as at different depths below the skin surface or spaced apart. In some embodiments simultaneous multi-focus therapy uses dithering.


In several embodiments, provided are systems and methods that successfully improve the effectiveness and/or efficiency of an aesthetic effect using targeted and precise ultrasound to cause a visible and effective cosmetic result via a thermal pathway. In some embodiments, a single focal zone targeted. In some embodiments an ultrasound therapy beam is split into two, three, four, or more simultaneous focal zones for performing various treatment and/or imaging procedures. In particular, embodiments of the invention improve effectiveness and/or efficiency in confirming the proper coupling between the treatment device and tissue for treatment in a treatment zone.


In several embodiments, provided are systems and methods that successfully improve the effectiveness and/or efficiency of an aesthetic effect using targeted and precise ultrasound to cause a visible and effective cosmetic result via a thermal pathway by splitting an ultrasound therapy beam to two, three, four, or more simultaneous focal zones for performing various treatment and/or imaging procedures.


According to one embodiment, an ultrasound treatment system creates two or more simultaneous therapeutic treatment points and/or focal zones under the skin surface for a cosmetic treatment, wherein the treatment points are enlarged by dithering the ultrasound beams. In one embodiment, a focal zone is a point. In one embodiment, a focal zone is a line. In one embodiment, a focal zone is a plane. In one embodiment, a focal zone is a three-dimensional volume or shape. The dithering of the ultrasound beam focus points enlarges the treatment area by shaking, blurring, or splattering the focus point or focus zone (e.g., a focus point, line, plane, or volume) like paint through an air brush by mechanically and/or electronically scattering the location of the focus points by varying the frequency, and therefore focal point, of the ultrasound treatment beams. In some embodiments, dithering increases efficacy by making a larger treatment points and/or focal zones. In some embodiments, dithering reduces pain since the temperature of the hot spot is spread over a larger volume of tissue, allowing a potential reduction in dose. In some embodiments, mechanical dithering is one method of spreading the acoustic energy from the ultrasound beam so there is less reliance on tissue thermal conduction away from the focus. In one embodiment of mechanical dithering, the therapy transducer is moved locally around the intended center of the thermal coagulation point (TCP). The acoustic beam movement can be side-to-side, up-down, and/or angular. In one embodiment of mechanical dithering, the movement of the motion mechanism is sufficiently fast enough to create a flatter temperature profile around the intended TCP which either allows a reduction of total acoustic energy for the same effected tissue volume or the same total acoustic energy for a larger effected tissue volume or any combination thereof.


In accordance with various embodiments, frequency modulation modifies the location of a focal zone and/or spacing between the focal zones, such that electronic dithering of beam via modulation of the frequency precisely alters and/or moves the position of the beam focus point(s). For example, in one embodiment, a spacing of 1.5 mm can be dithered with +/−0.1 mm using a small frequency swing. In various embodiments, any one or more spacings of 0.5, 0.75, 1.0, 1.2, 1.5, 2.0 mm can be dithered with +/−0.01, 0.05, 0.1, 0.12, 0.15, 0.20, 0.25, 0.30 mm using a frequency swing. In various embodiments, a frequency is modulated by 1-200% (e.g., 1%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%. 100%, 120%, 150%, 180%, 200% and any range therein).


Several embodiments relate to devices, systems and methods for providing one or more (e.g., a plurality or multiple) focus zones and/or ultrasound treatment points in performing various ultrasound treatment and/or imaging procedures quickly, safely, efficiently, and effectively. In some embodiments, no imaging is used. Some embodiments relate to splitting an ultrasound therapy beam to two, three, four, or more focal zones from a single ultrasound transducer and/or single ultrasound transduction element. In some embodiments, multiple ultrasound beams are electronically manipulated with frequency modulation. In some embodiments, dithering (e.g., electronic dithering) of multiple and/or split ultrasound beam apertures using frequency modulation provide treatment zones or points in multiple locations. In some embodiments, dithering relates to intentional movement of the position/location of a focal point of an energy beam. For example, in one embodiment, dithering involves shaking, moving, vibrating, altering the location and/or position of a single focal zone, and/or a relative spacing between two or more focal zones. In various embodiments, the relative position of a focal zones is dithered by 1-50% (e.g., 1%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50% and any range therein, such as a percentage of a mean location by a certain percentage). In various embodiments, spacing between focal zones is dithered by a range of between 1-50% (e.g., 1%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50% and any range therein). In some embodiments, dithering may be achieved through mechanical, electronic, or combinations of mechanical and electronic means depending on the system design. In one embodiment of mechanical dithering, the ultrasound beam is moved locally around the intended TCP center through a mechanical translation or tilt of the therapy transducer or patient or any combination thereof. The mechanical translation and/or tilt enable(s) the spread of the acoustic energy such that thermal conduction limitations of tissue are overcome. This creates a flatter temperature profile in tissue to either reduce the total acoustic energy to create the same effected tissue volume or have the same total acoustic energy to increase the effected tissue volume when compared to a stationary ultrasound therapy device. In various embodiments of electronic dithering, frequency, phase, amplitude modulations or time based techniques are used to in combination with a uniquely defined transducer to move the ultrasound beam in tissue without any mechanical movement. In one embodiment, electronic movement of the ultrasound beam occurs significantly faster than mechanical movement to overcome the thermal conductivity limitation of tissue. In various embodiments, a ratio of relative focal zone positioning via dithering is 1:1000, 1:500, 1:200; 1:100, 1:50, 1:25, 1:10, 1:2 or any ratio between 1:1000 and 1:1. In various embodiments, a ratio of spacing between relative focal zone positioning via dithering is 1:1000, 1:500, 1:200; 1:100, 1:50, 1:25, 1:10, 1:2 or any ratio between 1:1000 and 1:1. For example, in some embodiments, a focal zone is activated at “1” and an open spacing ratio of untreated tissue is provided in the second number of the ratio. For example, in one embodiment, a dithering spacing is e.g., 1 mm, and a dithering distance is 0.1 mm, so a ratio is 1:10. In various embodiments, a ratio of spacing between focal zones via dithering is 1:1000, 1:500, 1:200; 1:100, 1:50, 1:25, 1:10, 1:2 or any ratio between 1:1000 and 1:1. In some embodiments, the spacing of simultaneous focal zones is dithered. In some embodiments, the treatment points and/or zones are formed simultaneously in tissue. In various embodiments, dithering for performing various treatment and/or imaging procedures is with modulated and/or multiphased with controlled variance in frequency. Some embodiments relate to splitting an ultrasound therapy beam to two, three, four, or more focal zones for performing various treatment with, for example, dithering, poling, phasing, and/or modulation techniques and/or imaging procedures.


In several embodiments disclosed herein, non-invasive ultrasound systems are adapted to be used in achieving one or more of the following beneficial aesthetic and/or cosmetic improvement effects: a face lift, a brow lift, a chin lift, an eye treatment (e.g., malar bags, treat infraorbital laxity), a wrinkle reduction, fat reduction (e.g., treatment of adipose and/or cellulite), cellulite (which may be called gynoid lipodystrophy) treatment (e.g., dimple or non-dimple type female gynoid lipodystrophy), décolletage improvement (e.g., upper chest), a buttock lift (e.g., buttock tightening), skin tightening (for example, treating laxity to cause tightening on the face or body, such as the face, neck, chest, arms, thighs, abdomen, buttocks, etc.), a scar reduction, a burn treatment, a tattoo removal, a vein removal, a vein reduction, a treatment on a sweat gland, a treatment of hyperhidrosis, a sun spot removal, an acne treatment, a pimple reduction. Several embodiments of the invention are particularly advantageous because they include one, several or all of the following benefits: faster treatment time, (ii) less pain during treatment, (iii) less pain after treatment, (iv) shorter recovery time, (v) more efficient treatment, (vi) higher customer satisfaction, (vii) less energy to complete a treatment, and/or (viii) larger treatment area by dithered focal regions.


In accordance with various embodiments, a cosmetic ultrasound treatment system and/or method can non-invasively produce single or multiple dithered cosmetic treatment zones and/or thermal coagulation points where ultrasound is focused in one or more locations in a region of treatment in tissue under a skin surface, and moved via changes in frequency (e.g., via frequency modulation). Some systems and methods provide cosmetic treatment at different locations in tissue, such as at different depths, heights, widths, and/or positions. In one embodiment, a method and system comprise a multiple depth/height/width transducer system configured for providing ultrasound treatment to one or more region of interest, such as between at least one depth of treatment region of interest, a superficial region of interest, and/or a subcutaneous region of interest. In one embodiment, a method and system comprise a transducer system configured for providing ultrasound treatment to more than one region of interest, such as between at least two points in various locations (e.g. at a fixed or variable depth, height, width, and/or orientation, etc.) in a region of interest in tissue. Some embodiments can split a beam to focus at two, three, four, or more focal points (e.g., multiple focal points, multi-focal points) for cosmetic treatment zones and/or for imaging in a region of interest in tissue. Position and/or dithering of the focal points can be positioned axially, laterally, or otherwise within the tissue. Some embodiments can be configured for spatial control, such as by the location and/or dithering of a focus point, changing the distance from a transducer to a reflecting surface, and/or changing the angles of energy focused or unfocused to the region of interest, and/or configured for temporal control, such as by controlling changes in the frequency, drive amplitude and timing of the transducer. In some embodiments the position and/or dithering of multiple treatment zones or focal points is achieved with poling, phasic poling, biphasic poling, and/or multi-phasic poling. In some embodiments the position of multiple treatment zones or focal points with phasing, such as in one embodiment, electrical phasing. As a result, changes in the location of the treatment region, the number, shape, size and/or volume of treatment zones or lesions in a region of interest, as well as the thermal conditions, can be dynamically controlled over time.


In accordance with various embodiments, a cosmetic ultrasound treatment system and/or method can create multiple cosmetic treatment zones using one or more of frequency modulation, phase modulation, poling, nonlinear acoustics, and/or Fourier transforms to create any spatial periodic pattern with one or multiple ultrasound portions. In one embodiment, a system simultaneously or sequentially delivers single or multiple treatment zones using poling at a ceramic level. In one embodiment, a poling pattern is function of focal depth and frequency, and the use of odd or even functions. In one embodiment, a poling pattern, which can be a combination of odd or even functions, is applied, and based on focal depth and/or frequency. In one embodiment, a process can be used in two or more dimensions to create any spatial periodic pattern. In one embodiment, an ultrasound beam is split axially and laterally to significantly reduce treatment time through the use of nonlinear acoustics and Fourier transforms. In one embodiment, modulation from a system and amplitude modulation from a ceramic or a transducer can be used to place multiple treatments zones in tissue, either sequentially or simultaneously.


In one embodiment, an aesthetic imaging and treatment system includes an ultrasonic probe that includes an ultrasound transducer configured to apply ultrasonic therapy to tissue at a plurality of locations at a focal depth with electronic dithering of multiple energy beam apertures with frequency modulation. In one embodiment, the system includes a control module coupled to the ultrasonic probe for controlling the ultrasound transducer.


In one embodiment, the system includes dithering configured to provide variable spacing between a plurality of individual cosmetic treatment zones. In one embodiment, a sequence of individual cosmetic treatment zones has a treatment spacing in a range from about 0.01 mm to about 25 mm (e.g., 1 mm, 1.5 mm, 2 mm, 2.5 mm, 3 mm, 5 mm, 10 mm, 20 mm and any value ranges therein), with a dithering alteration of the spacing by 1-50% (e.g., 1%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50% and any range therein). In one embodiment, a sequence of individual cosmetic treatment zones has a treatment spacing in a range from about 0.01 mm to about 100 mm (e.g., 1 mm, 1.5 mm, 2 mm, 2.5 mm, 3 mm, 5 mm, 10 mm, 20 mm, 25 mm, 30 mm, 35 mm, 40 mm, 45, mm, 50 mm, 60 mm, 70 mm, 80 mm, 90 mm, and 100 mm, and any value ranges therein), with a dithering alteration of the spacing by 1-50% (e.g., 1%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50% and any range therein).


In one embodiment, the system further includes a movement mechanism configured to be programmed to provide constant or variable spacing between the plurality of individual cosmetic treatment zones. In one embodiment, a sequence of individual cosmetic treatment zones has a treatment spacing in a range from about 0.01 mm to about 25 mm (e.g., 0.1, 0.5, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 19 mm or any range or value therein). In one embodiment, a sequence of individual cosmetic treatment zones has a treatment spacing in a range from about 0.01 mm to about 100 mm (e.g., 0.1, 0.5, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30, 35, 40, 50, 100 mm or any range or value therein). In one embodiment, treatment zones are provided along a distance of about 25 mm. In one embodiment, treatment zones are provided along a distance of about 50 mm. In various embodiments, treatment zones are provided along a distance of 5 mm to 100 mm (e.g., 10 mm, 20 mm, 25 mm, 35 mm, 50 mm, 75 mm, 100 mm, and any amounts or ranges therein. In various embodiments, treatment zones are provided along a linear and/or curved distance.


For example, in some non-limiting embodiments transducers can be configured for a tissue depth of 0.5 mm, 1.0 mm, 1.5 mm, 2 mm, 3 mm, 4.5 mm, 6 mm, less than 3 mm, between 0.5 mm and 5 mm, between 1.5 mm and 4.5 mm, more than more than 4.5 mm, more than 6 mm, and anywhere in the ranges of 0.1 mm-3 mm, 0.1 mm-4.5 mm, 0.1 mm-25 mm, 0.1 mm-100 mm, and any depths therein (e.g., 6 mm, 10 mm, 13 mm, 15 mm). In several embodiments, tissue is treated at a depth below a skin surface and the skin surface is not impaired. Instead, the therapeutic effect achieved at the depth below the skin surface results in a favorable cosmetic appearance of the skin surface. In other embodiments, the skin surface is treated with ultrasound (e.g., at a depth less than 0.5 mm).


One benefit of a motion mechanism is that it can provide for a more efficient, accurate and precise use of an ultrasound transducer, for imaging and/or therapy purposes. One advantage this type of motion mechanism has over conventional fixed arrays of multiple transducers fixed in space in a housing is that the fixed arrays are a fixed distance apart. In one embodiment, the transducer module is configured to provide an acoustic power of the ultrasonic therapy in a range of between about 1 W to about 100 W (e.g., 3-30 W, 7-30 W, 21-33 W) and a frequency of about 1 MHz to about 10 MHz to thermally heat the tissue to cause coagulation. In one embodiment, the transducer module is configured to provide an acoustic power of the ultrasonic therapy in a range of between about 1 W to about 500 W for peak or average energy, (e.g., 3-30 W, 7-30 W, 21-33 W, 100 W, 220 W, or more) and a frequency of about 1 MHz to about 10 MHz to thermally heat the tissue to cause coagulation. In some embodiments, an instantaneous energy is delivered. In some embodiments, an average energy is delivered. In one embodiment, the acoustic power can be from a range of 1 W to about 100 W in a frequency range from about 1 MHz to about 12 MHz (e.g., 1 MHz, 3 MHz, 4 MHz, 4.5 MHz, 7 MHz, 10 MHz, 2-12 MHz), or from about 10 W to about 50 W at a frequency range from about 3 MHz to about 8 MHz (e.g., 3 MHz, 4 MHz, 4.5 MHz, 7 MHz). In one embodiment, the acoustic power can be from a range of 1 W to about 500 W in a frequency range from about 1 MHz to about 12 MHz (e.g., 1 MHz, 4 MHz, 7 MHz, 10 MHz, 2-12 MHz), or from about 10 W to about 220 W at a frequency range from about 3 MHz to about 8 MHz, or 3 MHz to 10 MHz. In one embodiment, the acoustic power and frequencies are about 40 W at about 4.3 MHz and about 30 W at about 7.5 MHz. An acoustic energy produced by this acoustic power can be between about 0.01 joule (“J”) to about 10 J or about 2 J to about 5 J. An acoustic energy produced by this acoustic power can be between about 0.01 J to about 60,000 J (e.g., via bulk heating, for body shaping, submental fat, abdomen and/or flanks, arms, inner thigh, outer thigh, buttocks, abdominal laxity, cellulite), about 10 J or about 2 J to about 5 J. In one embodiment, the acoustic energy is in a range less than about 3 J. In various embodiments, a treatment power is 1 kW/cm2 to 100 kW/cm2, 15 kW/cm2 to 75 kW/cm2, 1 kW/cm2 to 5 kW/cm2, 500 W/cm2 to 10 kW/cm2, 3 kW/cm2 to 10 kW/cm2, 15 kW/cm2 to 50 kW/cm2, 20 kW/cm2 to 40 kW/cm2, and/or 15 kW/cm2 to 35 kW/cm2.


In various embodiments, an ultrasound treatment system for dithering multiple simultaneous focus points from an ultrasound transducer includes an ultrasonic probe and a control module coupled to the ultrasonic probe for controlling the ultrasound transducer. The ultrasonic probe includes an ultrasound transducer with a single transduction element adapted to simultaneously apply ultrasonic therapy to tissue at a plurality of spaced locations at a focal depth. The ultrasound transducer is poled with at least a first poling configuration and a second poling configuration. The control module modifies the spacing between the spaced locations via dithering of a first focal zone and a second focal zone, such that dithering via modulation of a frequency precisely moves a position of a beam focus point at the spaced locations.


In one embodiment, the plurality of locations are positioned in a linear sequence within a cosmetic treatment zone, wherein the spaced locations are separated with a spacing dithered via a frequency swing. In one embodiment, a first set of locations is positioned within a first cosmetic treatment zone and a second set of locations is positioned within a second cosmetic treatment zone, the first zone being different from the second zone. In one embodiment, the ultrasound transducer is adapted to apply ultrasonic therapy using amplitude modulation whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of amplitudes of acoustic intensity, wherein a first amplitude is different than a second amplitude. In one embodiment, at least one portion of the ultrasonic transducer is adapted to emit ultrasonic therapy at two or more amplitudes of acoustic intensity, and wherein the amplitude of ultrasonic therapy emitted by the at least one portion of the piezoelectric varies over time. In one embodiment, the ultrasound transducer comprises piezoelectric material and the plurality of portions of the ultrasound transducer are adapted to create a plurality of corresponding piezoelectric material variations in response to an electric field applied to the ultrasound transducer. In one embodiment, the plurality of piezoelectric material variations comprise at least one of expansion of the piezoelectric material and contraction of the piezoelectric material. In one embodiment, the ultrasound transducer is adapted to apply ultrasonic therapy via phase shifting whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of phases of acoustic intensity, wherein a first phase is different than a second phase. In one embodiment, the plurality of phases comprises discrete phase values. In one embodiment, the ultrasound transducer is adapted to apply ultrasonic therapy using amplitude modulation whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of amplitudes of acoustic intensity, wherein a first amplitude is different than a second amplitude, and apply ultrasonic therapy whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of phases of acoustic intensity, wherein a first phase is different than a second phase. In various embodiments, the ultrasonic treatment is at least one of: a face lift, a brow lift, a chin lift, an eye treatment (e.g., malar bags, treat infraorbital laxity), a wrinkle reduction, a décolletage improvement, a buttock lift, a scar reduction, a burn treatment, a skin tightening (e.g., abdominal laxity treatment or treating laxity in other locations), a blood vessel reduction, a treatment of a sweat gland, a sun spot removal, a fat treatment, and a cellulite treatment. Skin tightening by reducing skin laxity is accomplished in some embodiments to treat subject with excess or loose skin post weight loss, whether such weight loss occurs naturally or is performed surgically.


In various embodiments, an ultrasound treatment system for use in cosmetic treatment for dithering multiple simultaneous focal points from an ultrasound transducer includes an ultrasonic probe including a control module adapted to modify a spacing between a first focal zone and a second focal zone via dithering, a switch operably controlling an ultrasonic treatment function for providing an ultrasonic treatment, and a movement mechanism adapted to direct ultrasonic treatment in at least one pair of simultaneous sequences of individual thermal cosmetic treatment zones, and a transducer module adapted to apply ultrasonic therapy. The transducer module is adapted for both ultrasonic imaging and ultrasonic treatment. The transducer module is adapted for coupling to the ultrasonic probe. The transducer module includes an ultrasound transducer adapted to apply ultrasonic therapy to tissue at a plurality of locations at a focal depth. The transducer module is adapted to be operably coupled to at least one of the switch and the movement mechanism. The control module includes a processor and a display for controlling the transducer module.


In one embodiment, the transducer module is adapted to apply ultrasonic therapy using amplitude modulation whereby a plurality of portions of the transducer module are adapted to emit ultrasonic therapy at a plurality of amplitudes of acoustic intensity, wherein a first amplitude is different than a second amplitude. In one embodiment, the transducer module is adapted to apply ultrasonic therapy whereby a plurality of portions of the transducer module are adapted to emit ultrasonic therapy at a plurality of phases of acoustic intensity, wherein a first phase is different than a second phase.


In various embodiments, an ultrasound treatment system for dithering multi-focus treatment includes a module comprising an ultrasound transducer. The ultrasound transducer is adapted to simultaneously apply ultrasonic therapy to tissue at a plurality of spaced locations in tissue, wherein the module modifies a spacing between the plurality of spaced locations via dithering of a first focal zone and a second focal zone, such that dithering via modulation of a frequency precisely moves a position of a beam focus point at the plurality of spaced locations, wherein the module further comprises an interface guide designed to for removable coupling to a hand wand to provide electronic communication and power between the module and the hand wand.


In one embodiment, the ultrasound transducer is adapted to apply ultrasonic therapy using amplitude modulation whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of amplitudes of acoustic intensity, wherein a first amplitude is different than a second amplitude. In one embodiment, the ultrasound transducer is adapted to apply ultrasonic therapy whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of phases of acoustic intensity, wherein a first phase is different than a second phase. In one embodiment, the ultrasound transducer comprises piezoelectric material and the plurality of portions of the ultrasound transducer are adapted to create a plurality of corresponding piezoelectric material variations in response to an electric field applied to the ultrasound transducer. In one embodiment, at least one portion of the ultrasonic transducer is adapted to emit ultrasonic therapy at two or more amplitudes of acoustic intensity, and wherein the amplitude of ultrasonic therapy emitted by the at least one portion of the ultrasonic transducer remains constant over time. In one embodiment, the ultrasonic treatment is at least one of a face lift, a brow lift, a chin lift, an eye treatment (e.g., malar bags, treat infraorbital laxity), a wrinkle reduction, a décolletage improvement, a buttock lift, a scar reduction, a burn treatment, a tattoo removal, a skin tightening (e.g., abdominal laxity treatment or tightening of the skin on other areas of the body and face, such as any excess skin or tissue, such as during or after weight loss, such as, for example, the abdomen, buttocks, thighs, arms, and other areas), a vein removal, a vein reduction, a treatment on a sweat gland, a treatment of hyperhidrosis, a sun spot removal, a fat treatment, a vaginal rejuvenation, and an acne treatment.


In various embodiments, a method of dithering simultaneous focused ultrasound treatment beams includes providing an ultrasonic probe comprising an ultrasound transducer comprising a single transduction element adapted to simultaneously apply ultrasonic therapy to tissue at a plurality of spaced locations at a focal depth and a control module coupled to the ultrasonic probe for controlling the ultrasound transducer, and dithering the spacing between the spaced locations of a first focal zone and a second focal zone via modulation of a frequency to move a position of an ultrasound focus point at the spaced locations.


In one embodiment, the method includes imaging the first focal zone with an ultrasound imaging element. In one embodiment, the method includes imaging the second focal zone with an ultrasound imaging element. In one embodiment, the spacing between the first focal zone and the second focal zone is dithered in a range of between 1-50%. In one embodiment, the spacing between the first focal zone and the second focal zone is 1.5 mm and is by 0.1 mm. In one embodiment, the modulation of frequency is in a range of between 1-50%. In one embodiment, the ultrasound treatment is at least one of a face lift, a brow lift, a chin lift, an eye treatment (e.g., malar bags, treat infraorbital laxity), a wrinkle reduction, a décolletage improvement, a buttock lift, a scar reduction, a burn treatment, a tattoo removal, a skin tightening (e.g., treating laxity on the face and body, such as abdominal laxity treatment, tightening of the skin on other areas of the body and face, such as any excess skin or tissue, such as during or after weight loss, such as, for example, the abdomen, buttocks, thighs, arms, and other areas), a vein removal, a vein reduction, a treatment on a sweat gland, a treatment of hyperhidrosis, a sun spot removal, a fat treatment, a vaginal rejuvenation, and an acne treatment.


In various embodiments, a method of dithering a focused ultrasound beam includes providing an ultrasonic probe comprising a single transduction element and a control module, wherein the single transduction element is adapted to apply ultrasonic therapy to tissue at a focal zone at a focal depth, wherein the control module is coupled to the ultrasonic probe for controlling the single transduction element, and dithering the focal zone via modulation of a frequency to alter a size of the focal zone at the tissue.


In one embodiment, the relative position of the focal zone is dithered in a range of between 1-50%. In one embodiment, a second focal zone is emitted simultaneously from the single transduction element. In one embodiment, the method includes imaging the focal zone with an ultrasound imaging element. In one embodiment, the modulation of the frequency is in a range of between 1-50%.


In several of the embodiments described herein, the procedure is entirely cosmetic and not a medical act. For example, in one embodiment, the methods described herein need not be performed by a doctor, but at a spa or other aesthetic institute. In some embodiments, a system can be used for the non-invasive cosmetic treatment of skin.


In some embodiments simultaneous multi-focus therapy using multi-channel signal mixing. In several embodiments, a treatment system utilizes multiple therapy channels to enable electronic focusing and/or steering. For example, a treatment system that utilizes multiple therapy channels to enable electronic focusing and/or steering allows for faster electronic dithering to either create more thermal coagulation using the same amount of energy as other treatment devices or equal thermal coagulation using electronic dithering with less energy than other treatment devices.


In various embodiments, an ultrasound treatment system configured for generating multiple simultaneous focus points from an ultrasound transducer includes an ultrasonic probe comprising an ultrasound transducer with a multiple transduction elements adapted to simultaneously apply ultrasonic therapy to tissue at a plurality of spaced locations, wherein each transduction element comprises a channel wherein the ultrasonic probe has a geometric focus; wherein the ultrasonic probe has a first electronic focus; and wherein the ultrasonic probe has a second electronic focus; a control module coupled to the ultrasonic probe for controlling the ultrasound transducer, wherein the control module modifies the spacing between the spaced locations via dithering of a first focal zone and a second focal zone, such that dithering via an excitation function that moves a position of a beam focus point at the spaced locations.


In one embodiment, the plurality of locations are positioned in a linear sequence within a cosmetic treatment zone, wherein the spaced locations are separated. In one embodiment, a first set of locations is positioned within a first cosmetic treatment zone and a second set of locations is positioned within a second cosmetic treatment zone, the first zone being different from the second zone. In one embodiment, the ultrasound transducer is adapted to apply ultrasonic therapy whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of amplitudes of acoustic intensity, wherein a first amplitude is different than a second amplitude. In one embodiment, at least one portion of the ultrasonic transducer is adapted to emit ultrasonic therapy at two or more amplitudes of acoustic intensity, and wherein the amplitude of ultrasonic therapy emitted by the at least one portion of the piezoelectric varies over time. In one embodiment, the ultrasound transducer comprises piezoelectric material and the plurality of portions of the ultrasound transducer are adapted to create a plurality of corresponding piezoelectric material variations in response to an electric field applied to the ultrasound transducer. In one embodiment, the plurality of piezoelectric material variations comprise at least one of expansion of the piezoelectric material and contraction of the piezoelectric material. In one embodiment, the ultrasound transducer is adapted to apply ultrasonic therapy via phase shifting whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of phases of acoustic intensity, wherein a first phase is different than a second phase. In one embodiment, the plurality of phases comprises discrete phase values. In one embodiment, the ultrasound transducer is adapted to apply ultrasonic therapy using amplitude modulation whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of amplitudes of acoustic intensity, wherein a first amplitude is different than a second amplitude; and apply ultrasonic therapy whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of phases of acoustic intensity, wherein a first phase is different than a second phase.


In various embodiments, the ultrasonic treatment is at least one of: a face lift, a brow lift, a chin lift, an eye (e.g., malar bags, treat infraorbital laxity) treatment, a wrinkle reduction, a décolletage improvement, a buttock lift, a scar reduction, a burn treatment, a skin tightening (e.g., abdominal, thigh, buttock, arm, neck or other laxity treatment), a blood vessel reduction, a treatment of a sweat gland, a sun spot removal, a fat treatment, and a cellulite treatment.


In various embodiments, an ultrasound treatment system for use in cosmetic treatment for forming multiple simultaneous focal zones from an ultrasound transducer, the system includes an ultrasonic probe including a control module adapted to modify a spacing between a first focal zone and a second focal zone, a switch operably controlling an ultrasonic treatment function for providing an ultrasonic treatment; and a movement mechanism adapted to direct ultrasonic treatment in at least one pair of simultaneous sequences of individual thermal cosmetic treatment zones; and a transducer module adapted to apply ultrasonic therapy, wherein the transducer module is adapted for ultrasonic imaging and/or ultrasonic treatment, wherein the transducer module is adapted for coupling to the ultrasonic probe, wherein the transducer module comprises an ultrasound transducer adapted to simultaneously apply ultrasonic therapy to tissue at a plurality of locations, wherein the transducer module is adapted to be operably coupled to at least one of the switch and the movement mechanism; and wherein the control module comprises a processor and a display for controlling the transducer module.


In one embodiment, the transducer module is adapted to apply ultrasonic therapy whereby a plurality of portions of the transducer module are adapted to emit ultrasonic therapy at a plurality of amplitudes of acoustic intensity, wherein a first amplitude is different than a second amplitude. In one embodiment, the transducer module is adapted to apply ultrasonic therapy whereby a plurality of portions of the transducer module are adapted to emit ultrasonic therapy at a plurality of acoustic intensities. In various embodiments, an ultrasound treatment system for generating a multi-focus treatment using multi-channel signal mixing including a module comprising an ultrasound transducer, wherein the ultrasound transducer is adapted to simultaneously apply ultrasonic therapy to tissue at a plurality of spaced locations in tissue, wherein the module modifies a spacing between the plurality of spaced locations between a first focal zone and a second focal zone, such that multi-channel signal mixing precisely moves a position of a beam focus point at the plurality of spaced locations, wherein the module further comprises an interface guide designed to for removable coupling to a hand wand to provide electronic communication and power between the module and the hand wand. In one embodiment, the ultrasound transducer is adapted to apply ultrasonic therapy whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of amplitudes of acoustic intensity, wherein a first amplitude is different than a second amplitude. In one embodiment, the ultrasound transducer is adapted to apply ultrasonic therapy whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of phases of acoustic intensity, wherein a first phase is different than a second phase. In one embodiment, the ultrasound transducer comprises piezoelectric material and the plurality of portions of the ultrasound transducer are adapted to create a plurality of corresponding piezoelectric material variations in response to an electric field applied to the ultrasound transducer. In one embodiment, at least one portion of the ultrasonic transducer is adapted to emit ultrasonic therapy at two or more amplitudes of acoustic intensity, and wherein the amplitude of ultrasonic therapy emitted by the at least one portion of the ultrasonic transducer remains constant over time. In one embodiment, the ultrasonic treatment is at least one of a face lift, a brow lift, a chin lift, an eye treatment (e.g., malar bags, treat infraorbital laxity), a wrinkle reduction, a décolletage improvement, a buttock lift, a scar reduction, a burn treatment, a tattoo removal, a skin tightening (e.g., a laxity treatment, a tissue laxity treatment, an abdominal laxity treatment, and any tightening of the skin on other areas of the body and face, such as any excess skin or tissue, such as during or after weight loss, such as, for example, the abdomen, buttocks, thighs, arms, and other areas) a vein removal, a vein reduction, a treatment on a sweat gland, a treatment of hyperhidrosis, a sun spot removal, a fat treatment, a vaginal rejuvenation, and an acne treatment. In various embodiments, a method of generating simultaneous focused ultrasound treatment beams using multi-channel signal mixing includes providing an ultrasonic probe comprising an ultrasound transducer comprising a plurality of transduction elements adapted to simultaneously apply ultrasonic therapy to tissue at a plurality of spaced locations at a plurality of focal depths and a control module coupled to the ultrasonic probe for controlling the ultrasound transducer, and modifying the spacing between the spaced locations of a first focal zone and a second focal zone via multi-channel signal mixing to move a position of an ultrasound focus point at the spaced locations. In one embodiment, the method includes imaging the first focal zone with an ultrasound imaging element. In one embodiment, the method includes imaging the second focal zone with an ultrasound imaging element. In one embodiment, the spacing between the first focal zone and the second focal zone is varied in a range of between 1-50%. In one embodiment, the spacing between the first focal zone and the second focal zone is 1.5 mm and is by 0.1 mm. In one embodiment, the spacing between electrical foci ranges of between 10-50% of the nominal distance between the electrical foci. In one embodiment, the ultrasound treatment is at least one of a face lift, a brow lift, a chin lift, an eye treatment, a wrinkle reduction, a décolletage improvement, a buttock lift, a scar reduction, a burn treatment, a tattoo removal, a skin tightening (e.g., tightening of tissue on a human or an abdominal laxity treatment), a vein removal, a vein reduction, a treatment on a sweat gland, a treatment of hyperhidrosis, a sun spot removal, a fat treatment, a vaginal rejuvenation, and an acne treatment.


In various embodiments, a method of generating simultaneous focused ultrasound beams includes providing an ultrasonic probe comprising an array of transduction elements and a control module, wherein the array of transduction elements is adapted to apply ultrasonic therapy to tissue at a focal zone at a plurality of foci, wherein the control module is coupled to the ultrasonic probe for controlling the array of transduction elements, and moving the focal zone.


In one embodiment, the relative position of the focal zone is moved in a range of between 10-50%. In one embodiment, a second focal zone is emitted simultaneously from the single transduction element. In one embodiment, the method includes imaging the focal zone with an ultrasound imaging element. In one embodiment, the system is designed to work non-invasively to treat tissue. In one embodiment, the method functions in a non-invasive manner to treat tissue.


In various embodiments, ultrasound imaging is employed to ensure sufficient acoustic coupling during delivery of an ultrasound therapy treatment. In various embodiments, ultrasound imaging is employed to prevent treatment at an undesired area in a body, such as a bone or an implant. Sound, unlike light, needs a medium for propagation. In an embodiment, an ultrasound treatment system acoustically couples ultrasound energy from the transducer to the body through an acoustic window using gel. In this embodiment, the gel is the medium which mimics the acoustic impedance properties of tissue so there is efficient transfer of energy from the device into tissue. Unfortunately, any pockets of air between the transducer and tissue prevent proper coupling and can therefore cause an inadequate transfer of the ultrasound therapy energy. The ultrasound imaging checks this coupling. Inadequate coupling may show up as shadows or vertical stripes in the ultrasound images or a completely dark image. Even if there is sufficient coupling, tissues or objects, such as bone or an implant can cause challenges since these objects can have a different acoustic impedance and absorption characteristics than soft tissue (e.g. skin, muscle). Because of this, objects (such as bone or an implant) in between the device and intended therapy focus may cause significant reflection and the appearance heating at a shallower depth than intended. Objects (e.g., bone, etc.) slightly beyond the focus may also cause issues since the object reflects and readily absorbs the ultrasound from the soft tissue. The reflected energy may inadvertently add to the energy already at the therapy focus causing a higher temperature rise than intended. The absorbed energy at the bone may cause heating or discomfort in the bone.


In various embodiments, advantages of the present invention include using image to assess coupling of an ultrasound therapy beam to the intended treatment tissue. In various embodiments, higher resolution imaging is advantageous to provide more detail in an image of the tissue in and near the target tissue for treatment. In various embodiments, the invention improves safety characteristics, improves efficacy performance, provides a component of safety and efficacy for bulk heating devices (such as a band treatment, a linear focal treatment zone, a cylindrical focal line, a plane and/or a volume, etc.) for body shaping, submental fat, abdomen and/or flanks, arms, inner thigh, outer thigh, buttocks, laxity, abdominal laxity, etc., provides qualitative and/or quantitative assessment of coupling, provides for blending of high resolution image(s) with coupling image(s), is employed for assessing out-of-plane impediments post-focally (e.g. bone, intestine, implants), and/or can be used to reduce the need for sonographer equivalent skills.


In various embodiments, an ultrasound treatment and imaging system includes an ultrasonic probe comprising an ultrasound therapy transducer adapted to apply ultrasonic therapy to tissue, an ultrasound imaging transducer adapted for imaging the tissue, and an acoustic window, wherein the ultrasound imaging transducer comprises an annular imaging array; wherein the ultrasound imaging transducer comprises a plurality of transmit channels; wherein the ultrasound imaging transducer comprises a plurality of receive channels; wherein the ultrasound imaging transducer is configured for focusing at a location proximate the ultrasound imaging transducer with respect to a distance between the ultrasound imaging transducer and the acoustic window; and a control module coupled to the ultrasonic probe for controlling the ultrasound imaging transducer, wherein the ultrasound imaging transducer is configured to interrogate more than 40% of the acoustic window.


In various embodiments, an ultrasound treatment and imaging system includes an ultrasonic probe comprising an ultrasound therapy transducer adapted to apply ultrasonic therapy to tissue, an ultrasound imaging transducer adapted for imaging the tissue, and an acoustic window, wherein the ultrasound imaging transducer comprises an annular imaging array; wherein the ultrasound imaging transducer comprises a plurality of transmit channels; wherein the ultrasound imaging transducer comprises a plurality of receive channels; wherein the wherein the ultrasound imaging transducer operates at an imaging frequency of between 8 MHz to 50 MHz, wherein the ultrasound imaging transducer is configured to image tissue at a depth of up to 25 mm (e.g., 5 mm, 8 mm, 10 mm, 12 mm, 15 mm, 20 mm) below a skin surface; wherein the ultrasound imaging transducer is configured for focusing at a location behind the ultrasound imaging transducer with respect to the acoustic window; and a control module coupled to the ultrasonic probe for controlling the ultrasound imaging transducer, wherein the ultrasound imaging transducer is configured to interrogate more than 10% of the acoustic window.


In various embodiments, an ultrasound treatment and imaging system includes an ultrasonic probe comprising an ultrasound therapy transducer adapted to apply ultrasonic therapy to tissue, an ultrasound imaging transducer adapted for imaging the tissue, and an acoustic window, wherein the ultrasound imaging transducer comprises an annular or a linear imaging array; wherein the ultrasound imaging transducer comprises a plurality of transmit channels; wherein the ultrasound imaging transducer comprises a plurality of receive channels; wherein the wherein the ultrasound imaging transducer operates at an imaging frequency of between 8 MHz to 50 MHz, wherein the ultrasound imaging transducer is configured to image tissue at a depth of up to 25 mm below a skin surface; wherein the ultrasound imaging transducer is configured for focusing at a location proximate the ultrasound imaging transducer with respect to a distance between the ultrasound imaging transducer and the acoustic window; and a control module coupled to the ultrasonic probe for controlling the ultrasound imaging transducer, wherein the ultrasound imaging transducer is configured to interrogate more than 15% of the acoustic window.


In one embodiment, an imaging beam width from the ultrasound imaging transducer is at least 20% the cross-sectional size of a therapy beam width from the ultrasound therapy transducer. In one embodiment, an imaging beam width from the ultrasound imaging transducer is at least 30% the cross-sectional size of a therapy beam width from the ultrasound therapy transducer. In one embodiment, an imaging beam width from the ultrasound imaging transducer is at least 40% the cross-sectional size of a therapy beam width from the ultrasound therapy transducer. In one embodiment, an imaging beam width from the ultrasound imaging transducer is at least 50% the cross-sectional size of a therapy beam width from the ultrasound therapy transducer. In one embodiment, an imaging beam width from the ultrasound imaging transducer is at least 80% the cross-sectional size of a therapy beam width from the ultrasound therapy transducer.


In one embodiment, a coupling of the imaging of the ultrasound imaging transducer provides an indication of the coupling for the treatment by the ultrasound therapy transducer. In one embodiment, the ultrasound imaging transducer is configured to interrogate more than 80% of the acoustic window. In one embodiment, the ultrasound imaging transducer is configured to interrogate more than 90% of the acoustic window. In one embodiment, the annular imaging array is positioned in the ultrasound therapy transducer.


In one embodiment, the control module controls the ultrasound imaging transducer for vector imaging. In one embodiment, the control module controls the ultrasound imaging transducer for defocused vector imaging.


In one embodiment, the ultrasound therapy transducer is configured for treatment of tissue at a first set of locations that is positioned within a first cosmetic treatment zone and a second set of locations that is positioned within a second cosmetic treatment zone, the first zone being different from the second zone. In one embodiment, the ultrasound therapy transducer is adapted to apply ultrasonic therapy using amplitude modulation whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of amplitudes of acoustic intensity, wherein a first amplitude is different than a second amplitude. In one embodiment, at least one portion of the ultrasonic transducer is adapted to emit ultrasonic therapy at two or more amplitudes of acoustic intensity, and wherein the amplitude of ultrasonic therapy emitted by the at least one portion of the piezoelectric varies over time. In one embodiment, the ultrasound transducer comprises piezoelectric material and the plurality of portions of the ultrasound transducer are adapted to create a plurality of corresponding piezoelectric material variations in response to an electric field applied to the ultrasound transducer. In one embodiment, plurality of piezoelectric material variations comprise at least one of expansion of the piezoelectric material and contraction of the piezoelectric material. In one embodiment, the ultrasound transducer is adapted to apply ultrasonic therapy via phase shifting whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of phases of acoustic intensity, wherein a first phase is different than a second phase. In one embodiment, the plurality of phases comprises discrete phase values. In one embodiment, the ultrasound transducer is adapted to apply ultrasonic therapy using amplitude modulation whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of amplitudes of acoustic intensity, wherein a first amplitude is different than a second amplitude; and apply ultrasonic therapy whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of phases of acoustic intensity, wherein a first phase is different than a second phase.


In various embodiments, the ultrasonic treatment is at least one of a face lift, a brow lift, a chin lift, an eye treatment, a wrinkle reduction, a décolletage improvement, a buttock lift, a scar reduction, a burn treatment, a skin tightening (e.g., an abdominal laxity treatment), a blood vessel reduction, a treatment of a sweat gland, a sun spot removal, a fat treatment, and a cellulite treatment.


In various embodiments, a method of confirming coupling between an ultrasound probe and tissue for treatment includes providing an ultrasonic probe comprising an acoustic window, an ultrasound transducer comprising an ultrasound therapy transduction element adapted to apply ultrasonic therapy to a tissue, a plurality of imaging transduction elements in an array for imaging the tissue, and a control module coupled to the ultrasonic probe for controlling the ultrasound transducer, and interrogating at least 20% of the acoustic window with an imaging beam from the plurality of imaging transduction elements.


In one embodiment, the plurality of imaging transduction elements interrogates at least 30% of the acoustic window. In one embodiment, the plurality of imaging transduction elements interrogates at least 40% of the acoustic window. In one embodiment, the plurality of imaging transduction elements interrogates at least 50% of the acoustic window.


In one embodiment, the plurality of imaging transduction elements interrogates at least 60% of the acoustic window. In one embodiment, the plurality of imaging transduction elements interrogates at least 70% of the acoustic window. In one embodiment, the method further includes vector imaging. In one embodiment, the method further includes defocused vector imaging. In one embodiment, the method further includes imaging a first focal zone in the tissue with the plurality of imaging transduction elements. In one embodiment, the method further includes imaging a second focal zone in the tissue with the plurality of imaging transduction elements. In various embodiments, the ultrasound treatment is at least one of a face lift, a brow lift, a chin lift, an eye treatment, a wrinkle reduction, a décolletage improvement, a buttock lift, a scar reduction, a burn treatment, a tattoo removal, a skin tightening, (e.g., a laxity treatment), a vein removal, a vein reduction, a treatment on a sweat gland, a treatment of hyperhidrosis, a sun spot removal, a fat treatment, a vaginal rejuvenation, and an acne treatment.


In several of the embodiments described herein, the procedure is entirely cosmetic and not a medical act. For example, in one embodiment, the methods described herein need not be performed by a doctor, but at a spa or other aesthetic institute. In some embodiments, a system can be used for the non-invasive cosmetic treatment of skin.


In several embodiments, provided are systems and methods that successfully improve the ultrasound imaging of tissue while moving, such as when an imaging transducer is on a motion mechanism. In various embodiments, higher resolution is achieved. In various embodiments, better imaging signal quality is obtained. In various embodiments, ultrasound imaging is used with a therapeutic tissue treatment.


In various embodiments, an ultrasound treatment and imaging system configured for reducing imaging misalignment, including an ultrasonic probe comprising an ultrasound therapy transducer adapted to apply ultrasonic therapy to tissue, an ultrasound imaging transducer adapted for imaging the tissue, and a motion mechanism for moving the ultrasound imaging transducer in a first direction and a second direction. In an embodiment, the ultrasound imaging transducer is mechanically attached to the motion mechanism. In an embodiment, the first direction is linear. In an embodiment, the second direction is linear. In an embodiment, the first direction is parallel to the second direction. In an embodiment, the first direction is opposite the second direction. In an embodiment, the ultrasound imaging transducer images with a first focal zone sequence order (f1, f2) when travelling in the first direction, the ultrasound imaging transducer images with a second focal zone sequence order (f2, f1) when travelling in the second direction, and a spatial registration between the first direction imaging and the second direction imaging is improved by staggering a triggering location. In an embodiment, a control module is coupled to the ultrasonic probe for controlling the ultrasound imaging transducer.


In various embodiments, an ultrasound treatment and imaging system configured for reducing imaging misalignment, includes an ultrasonic probe comprising an ultrasound therapy transducer adapted to apply ultrasonic therapy to tissue, an ultrasound imaging transducer adapted for imaging the tissue, and a motion mechanism for moving the ultrasound imaging transducer in a first direction and a second direction. In an embodiment, the ultrasound imaging transducer is mechanically attached to the motion mechanism, wherein the first direction is linear, wherein the second direction is linear, wherein the first direction is parallel to the second direction, wherein the first direction is opposite the second direction, wherein the ultrasound imaging transducer images with a first focal zone sequence order (f1, f2, f3, f4) when travelling in the first direction, wherein the ultrasound imaging transducer images with a second focal zone sequence order (f4, f3, f2, f1) when travelling in the second direction, wherein a spatial registration between the first direction imaging and the second direction imaging is improved by staggering a triggering location, wherein the imaging system employs a sequence of two consecutive A-lines following progression of (line 1: f1, f2, f3, f4; line2: f4, f3, f2, f1) continuously; and a control module coupled to the ultrasonic probe for controlling the ultrasound imaging transducer.


In various embodiments, an ultrasound treatment and imaging system configured for reducing imaging misalignment, includes an ultrasonic probe comprising an ultrasound therapy transducer adapted to apply ultrasonic therapy to tissue, an ultrasound imaging transducer adapted for imaging the tissue, and a motion mechanism for moving the ultrasound imaging transducer in a first direction and a second direction. In an embodiment, the ultrasound imaging transducer is mechanically attached to the motion mechanism. In an embodiment, the first direction is opposite the second direction. In an embodiment, the ultrasound imaging transducer images with a focal zone sequence order (f1, . . . , fN), where N>1 when travelling in the first direction. In an embodiment, the ultrasound imaging transducer images with a second focal zone sequence order (fN, . . . , f1) when travelling in the second direction. In an embodiment, a spatial registration between the first direction imaging and the second direction imaging is improved by staggering a triggering location. In an embodiment, the imaging system employs a directionally dependent focal zone sequencing with alternating between (f1- . . . -fN) and (fN- . . . -f1) on consecutive A-lines; and a control module coupled to the ultrasonic probe for controlling the ultrasound imaging transducer.


In an embodiment, the first direction of motion of the transducer is any one or more of the group consisting of: linear, rotational, and curved. In an embodiment, the second direction is the reversed path of the first direction. In an embodiment, the first direction of motion occurs in multiple dimensions and the second direction is the reversed path of the first direction. In an embodiment, the ultrasound imaging transducer images with a first focal zone sequence order is specified as (f1, . . . , fN), where N>1. In an embodiment, the ultrasound therapy transducer is configured for treatment of tissue at a first set of locations that is positioned within a first cosmetic treatment zone and a second set of locations that is positioned within a second cosmetic treatment zone, the first zone being different from the second zone. In an embodiment, the ultrasound therapy transducer is adapted to apply ultrasonic therapy using amplitude modulation whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of amplitudes of acoustic intensity, wherein a first amplitude is different than a second amplitude. In an embodiment, at least one portion of the ultrasonic transducer is adapted to emit ultrasonic therapy at two or more amplitudes of acoustic intensity, and wherein the amplitude of ultrasonic therapy emitted by the at least one portion of the piezoelectric varies over time. In an embodiment, the ultrasound transducer comprises piezoelectric material and the plurality of portions of the ultrasound transducer are adapted to create a plurality of corresponding piezoelectric material variations in response to an electric field applied to the ultrasound transducer. In an embodiment, the plurality of piezoelectric material variations comprise at least one of expansion of the piezoelectric material and contraction of the piezoelectric material. In an embodiment, the ultrasound transducer is adapted to apply ultrasonic therapy via phase shifting whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of phases of acoustic intensity, wherein a first phase is different than a second phase. In an embodiment, the plurality of phases comprises discrete phase values. In an embodiment, the ultrasound transducer is adapted to apply ultrasonic therapy using amplitude modulation whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of amplitudes of acoustic intensity, wherein a first amplitude is different than a second amplitude; and apply ultrasonic therapy whereby a plurality of portions of the ultrasound transducer are adapted to emit ultrasonic therapy at a plurality of phases of acoustic intensity, wherein a first phase is different than a second phase. In various embodiments, the ultrasonic treatment is at least one of: a face lift, a brow lift, a chin lift, an eye treatment, a wrinkle reduction, a décolletage improvement, a buttock lift, a scar reduction, a burn treatment, a skin tightening (e.g., a laxity treatment), a blood vessel reduction, a treatment of a sweat gland, a sun spot removal, a fat treatment, a cellulite treatment, a vaginal rejuvenation, and an acne treatment.


In various embodiments, a method of reducing imaging misalignment in a moving ultrasound probe, including staggering a triggering location of a spatial registration between a first direction imaging and a second direction imaging with an ultrasonic probe, the ultrasound probe comprising an ultrasound therapy transducer adapted to apply ultrasonic therapy to tissue, an ultrasound imaging transducer adapted for imaging the tissue, and a motion mechanism for moving the ultrasound imaging transducer in a first direction and a second direction, wherein the ultrasound imaging transducer is mechanically attached to the motion mechanism, wherein the first direction is opposite the second direction, wherein the ultrasound imaging transducer images with a focal zone sequence order (f1, . . . , fN), with N>1, wherein the ultrasound imaging transducer images with a first focal zone sequence order (f1, . . . , fN) when travelling in the first direction, wherein the ultrasound imaging transducer images with a second focal zone sequence order (fN, . . . , f1) when travelling in the second direction.


In an embodiment, N=any one of the group consisting of: 2, 3, 4, 5, 6, 7, 8, 9, and 10. In an embodiment, N=4. In various embodiments, the ultrasound treatment is at least one of a face lift, a brow lift, a chin lift, an eye treatment, a wrinkle reduction, a décolletage improvement, a buttock lift, a scar reduction, a burn treatment, a tattoo removal, a skin tightening (e.g., an abdominal laxity treatment), a vein removal, a vein reduction, a treatment on a sweat gland, a treatment of hyperhidrosis, a sun spot removal, a fat treatment, a vaginal rejuvenation, and an acne treatment.


The methods summarized above and set forth in further detail below describe certain actions taken by a practitioner; however, it should be understood that they can also include the instruction of those actions by another party. Thus, actions such as “dithering an energy beam” include “instructing the dithering of an energy beam.”


In some embodiments, the system comprises various features that are present as single features (as opposed to multiple features). For example, in one embodiment, the system includes a single transduction element that produces two simultaneous treatment focus points that are dithered. Multiple features or components are provided in alternate embodiments. In various embodiments, the system comprises, consists essentially of, or consists of one, two, three, or more embodiments of any features or components disclosed herein. In some embodiments, a feature or component is not included and can be negatively disclaimed from a specific claim, such that the system is without such feature or component.


Further, areas of applicability will become apparent from the description provided herein. It should be understood that the description and specific examples are intended for purposes of illustration only and are not intended to limit the scope of the embodiments disclosed herein.





BRIEF DESCRIPTION OF THE DRAWINGS

The drawings described herein are for illustration purposes only and are not intended to limit the scope of the present disclosure in any way. Embodiments of the present invention will become more fully understood from the detailed description and the accompanying drawings wherein:



FIG. 1A is a schematic illustration of an ultrasound system according to various embodiments of the present invention.



FIG. 1B is a schematic illustration of an ultrasound system according to various embodiments of the present invention.



FIG. 1C is a schematic illustration of an ultrasound system according to various embodiments of the present invention.



FIG. 2 is a schematic illustration of an ultrasound system coupled to a region of interest according to various embodiments of the present invention.



FIG. 3 is a schematic illustration of a portion of a transducer according to various embodiments of the present invention.



FIG. 4 is a partial cut away side view of an ultrasound system according to various embodiments of the present invention.



FIG. 5 is table illustrating foci separation for apertures with different spatial frequencies according to various embodiments of the present invention.



FIG. 6 is plot illustrating foci separation for apertures with different aperture spatial frequencies according to various embodiments of the present invention.



FIG. 7 is plot illustrating foci separation for apertures with different aperture spatial frequencies according to various embodiments of the present invention.



FIG. 8 is a schematic representation of aperture poling with a spatial frequency that can be modified by excitation of channels according to various embodiments of the present invention.



FIG. 9 is a schematic representation of a poled ceramic with a spatial frequency that can be modified by excitation of channels covering two poled areas of the ceramic according to various embodiments of the present invention.



FIG. 10 is a schematic representation of an embodiment of array transducer with an imaging transducer.



FIG. 11 is a schematic representation of an embodiment of the array transducer of FIG. 10 with a mechanical focus, a first electronic focus, and a second electric focus.



FIG. 12 is a schematic representation of an embodiment of an intensity map of a treatment with two foci at 15 mm and 17 mm.



FIG. 13 is a schematic representation of an embodiment of an embodiment of an intensity map of a treatment with two foci at 15 mm and 19 mm.



FIG. 14 is a schematic representation of the cross-section of the difference between the size of an ultrasound therapy beam compared to an ultrasound imaging beam according to various embodiments of the present invention.



FIG. 15 is a schematic representation of a linear array according to various embodiments of the present invention.



FIG. 16 is a schematic representation of an annular array according to various embodiments of the present invention.



FIG. 17 is a schematic representation of an annular array compared to a linear array according to various embodiments of the present invention.



FIG. 18 is a schematic representation of an annular array with a virtual focus behind the array according to various embodiments of the present invention.



FIG. 19 is a schematic representation of an annular array with a virtual focus between the array and acoustic window according to various embodiments of the present invention.



FIG. 20 is a schematic representation of time progression of the transmit-receive vectors for ordinary B-mode imaging according to various embodiments of the present invention.



FIG. 21 is a schematic representation of an interleaved imaging approach according to various embodiments of the present invention.



FIG. 22 is a schematic representation of an imaging approach with synthetic transmit and receive aperture methods according to various embodiments of the present invention.



FIG. 23 is a schematic representation of an imaging diagnostic ultrasound system according to various embodiments of the present invention.



FIG. 24 is a schematic representation of bidirectional imaging at the same lateral location according to various embodiments of the present invention.



FIG. 25 is a schematic representation of directionally dependent focal zone sequencing according to various embodiments of the present invention.



FIG. 26 is a schematic representation of directionally dependent focal zone sequencing with different triggering locations according to various embodiments of the present invention.



FIG. 27 is a schematic representation of directionally dependent focal zone sequencing with alternating between (f1-f2-f3-f4) & (f4-f3-f2-f1) on consecutive A-lines according to various embodiments of the present invention.



FIG. 28 is schematic views of a transducer as viewed from a convex side, side view cross section, and concave side various embodiments of the present invention.



FIG. 29 is schematic views of a transducer as viewed from a convex side, side view cross section, and concave side various embodiments of the present invention.



FIG. 30 is schematic views of a transducer as viewed from a convex side, side view cross section, and concave side various embodiments of the present invention.



FIG. 31 is schematic views of a transducer as viewed from a convex side, side view cross section, and concave side various embodiments of the present invention.



FIG. 32 is schematic views of a transducer as viewed from a convex side, side view cross section, and concave side various embodiments of the present invention.



FIG. 33 is schematic views of a transducer as viewed from a convex side, side view cross section, and concave side various embodiments of the present invention.





DETAILED DESCRIPTION

The following description sets forth examples of embodiments, and is not intended to limit the present invention or its teachings, applications, or uses thereof. It should be understood that throughout the drawings, corresponding reference numerals indicate like or corresponding parts and features. The description of specific examples indicated in various embodiments of the present invention are intended for purposes of illustration only and are not intended to limit the scope of the invention disclosed herein. Moreover, recitation of multiple embodiments having stated features is not intended to exclude other embodiments having additional features or other embodiments incorporating different combinations of the stated features. Further, features in one embodiment (such as in one figure) may be combined with descriptions (and figures) of other embodiments.


In various embodiments, systems and methods for ultrasound treatment of tissue are adapted for and/or configured to provide cosmetic treatment. In some embodiments, devices and methods of directing ultrasound therapy to a single focus point or multiple, simultaneous focus points, employing ultrasound imaging to confirm sufficient acoustic coupling to a treatment area for improving performance or providing improved correlation between movement in a first and second direction when forming images in cosmetic and/or medical procedures are provided in several embodiments. In some embodiments, devices and methods of employing ultrasound imaging to confirm sufficient acoustic coupling to a treatment area for improving performance and safety when directing ultrasound therapy to a single focus point or multiple, simultaneous focus points in cosmetic and/or medical procedures are provided in several embodiments. In some embodiments, devices and methods of improved ultrasound imaging provide better correlation between movement in a first and second direction when forming images. Embodiments of the invention provide better imaging correlation between a first moving direction and a second moving direction, (e.g., better correlation between left-traveling & right-traveling formed images). Devices and methods of improved ultrasound imaging improve effect B-mode imaging faster (e.g., 1.5×, 2×, 3×, 5× times the scanning rate). In various embodiments, tissue below or even at a skin surface such as epidermis, dermis, fascia, muscle, fat, and superficial muscular aponeurotic system (“SMAS”), are treated non-invasively with ultrasound energy. The ultrasound energy can be focused at one or more treatment points and/or zones, can be unfocused and/or defocused, and can be applied to a region of interest containing at least one of epidermis, dermis, hypodermis, fascia, muscle, fat, cellulite, and SMAS to achieve a cosmetic and/or therapeutic effect. In various embodiments, systems and/or methods provide non-invasive dermatological treatment to tissue through thermal treatment, coagulation, ablation, and/or tightening. In several embodiments disclosed herein, non-invasive ultrasound is used to achieve one or more of the following effects: a face lift, a brow lift, a chin lift, an eye treatment (e.g., malar bags, treat infraorbital laxity), a wrinkle reduction, fat reduction (e.g., treatment of adipose and/or cellulite), cellulite treatment (e.g., dimple or non-dimple type female gynoid lipodystrophy), décolletage improvement (e.g., upper chest), a buttock lift (e.g., buttock tightening), a skin laxity treatment (e.g., treatment of tissue for tightening or an abdominal laxity treatment), a scar reduction, a burn treatment, a tattoo removal, a vein removal, a vein reduction, a treatment on a sweat gland, a treatment of hyperhidrosis, sun spot removal, an acne treatment, and a pimple removal. In one embodiment, fat reduction is achieved. In various embodiments, cellulite (e.g., dimple or non-dimple type gynoid lipodystrophy) reduction or amelioration of one or more characteristics (such as dimples, nodularity, “orange peel” appearance, etc., is achieved by about 10-20%, 20-40%, 40-60%, 60-80% or higher (as well as overlapping ranging therein) as compared to, for example, untreated tissue. In one embodiment, décolletage is treated. In some embodiments, two, three or more beneficial effects are achieved during the same treatment session, and may be achieved simultaneously.


Various embodiments of the present invention relate to devices or methods of controlling the delivery of energy to tissue. In various embodiments, various forms of energy can include acoustic, ultrasound, light, laser, radio-frequency (RF), microwave, electromagnetic, radiation, thermal, cryogenic, electron beam, photon-based, magnetic, magnetic resonance, and/or other energy forms. Various embodiments of the present invention relate to devices or methods of splitting an ultrasonic energy beam into multiple beams. In various embodiments, devices or methods can be used to alter the delivery of ultrasound acoustic energy in any procedures such as, but not limited to, therapeutic ultrasound, diagnostic ultrasound, ultrasonic welding, any application that involves coupling mechanical waves to an object, and other procedures. Generally, with therapeutic ultrasound, a tissue effect is achieved by concentrating the acoustic energy using focusing techniques from the aperture. In some instances, high intensity focused ultrasound (HIFU) is used for therapeutic purposes in this manner. In one embodiment, a tissue effect created by application of therapeutic ultrasound at a particular depth to can be referred to as creation of a thermal coagulation point (TCP). In some embodiments, a zone can include a point. In some embodiments, a zone is a line, plane, spherical, elliptical, cubical, or other one-, two-, or three-dimensional shape. It is through creation of TCPs at particular positions that thermal and/or mechanical ablation of tissue can occur non-invasively or remotely. In some embodiments, an ultrasound treatment does not include cavitation and/or shock waves. In some embodiments, an ultrasound treatment includes cavitation and/or shock waves.


In one embodiment, TCPs can be created in a linear or substantially linear, curved or substantially curved, zone or sequence, with each individual TCP separated from neighboring TCPs by a treatment spacing. In one embodiment, multiple sequences of TCPs can be created in a treatment region. For example, TCPs can be formed along a first sequence and a second sequence separated by a treatment distance from the first sequence. Although treatment with therapeutic ultrasound can be administered through creation of individual TCPs in a sequence and sequences of individual TCPs, it may be desirable to reduce treatment time and corresponding risk of pain and/or discomfort experienced by a patient. Therapy time can be reduced by forming multiple TCPs simultaneously, nearly simultaneously, or sequentially. In some embodiments, a treatment time can be reduced 10%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80% or more by creating multiple TCPs.


Various embodiments of the present invention address potential challenges posed by administration of ultrasound therapy. In various embodiments, time for effecting the formation of TCPs for a desired cosmetic and/or therapeutic treatment for a desired clinical approach at a target tissue is reduced. In various embodiments, target tissue is, but is not limited to, any of skin, eyelids, eye lash, eye brow, caruncula lacrimalis, crow's feet, wrinkles, eye, nose, mouth (e.g., nasolabial fold, perioral wrinkles), tongue, teeth, gums, ears, brain, heart, lungs, ribs, abdomen (e.g., for abdominal laxity), stomach, liver, kidneys, uterus, breast, vagina, prostrate, testicles, glands, thyroid glands, internal organs, hair, muscle, bone, ligaments, cartilage, fat, fat labuli, adipose tissue, subcutaneous tissue, implanted tissue, an implanted organ, lymphoid, a tumor, a cyst, an abscess, or a portion of a nerve, or any combination thereof.


Various embodiments of ultrasound treatment and/or imaging devices are described in U.S. application Ser. No. 12/996,616, which published as U.S. Publication No. 2011-0112405 A1 on May 12, 2011, which is a U.S. National Phase under 35 U.S.C. § 371 of International Application No. PCT/US2009/046475, filed on Jun. 5, 2009 and published in English on Dec. 10, 2009, which claims the benefit of priority from U.S. Provisional No. 61/059,477 filed Jun. 6, 2008, each of which is incorporated in its entirety by reference, herein. Various embodiments of ultrasound treatment and/or imaging devices are described in U.S. application Ser. No. 14/193,234, which published as U.S. Publication No. 2014/0257145 on Sep. 11, 2014, which is incorporated in its entirety by reference, herein. Various embodiments of ultrasound treatment and/or imaging devices are described in International App. PCT/US15/25581, which published as WO 2015/160708 on Oct. 22, 2015 with a national phase U.S. application Ser. No. 15/302,436, which published as U.S. Publication No. 2017/0028227 on Feb. 2, 2017, each of which is incorporated in its entirety by reference, herein.


System Overview


With reference to the illustration in FIGS. 1A, 1B, and 1C, various embodiments of an ultrasound system 20 includes a hand wand (e.g., handpiece) 100, module (e.g., transducer module, cartridge, probe) 200, and a controller (e.g., console) 300. In some embodiments, a console 300 comprises a communication system (e.g., wifi, Bluetooth, modem, etc. to communicate with another party, a manufacturer, a supplier, a service provider, the Internet, and/or a cloud. In some embodiments, a cart 301 provides mobility and/or position of the system 20, and can include wheels, surfaces to write on or place components, and/or compartments 302 (e.g., drawers, containers, shelves, etc.) to, for example, store or organize components. In some embodiments, the cart has a power supply, such as a power connection to a battery and/or one or more cords to connect power, communications (e.g., Ethernet) to the system 20. In some embodiments, the system 20 comprises a cart 301. In some embodiments, the system 20 does not comprise a cart 301. The hand wand 100 can be coupled to the controller 300 by an interface 130, which may be a wired or wireless interface. The interface 130 can be coupled to the hand wand 100 by a connector 145. The distal end of the interface 130 can be connected to a controller connector on a circuit 345 (not shown). In one embodiment, the interface 130 can transmit controllable power from the controller 300 to the hand wand 100. In an embodiment, the system 20 has multiple imaging channels (e.g., 8 channels) for ultra-clear HD (high definition) visualization of subcutaneous structures to improve imaging. In an embodiment, the system 20 multiple therapy channels (e.g., 8 channels) and a precision linear-drive motor that doubles treatment accuracy while increasing speed (e.g., by 25%, 40%, 50%, 60%, 75%, 100% or more). Together, these features establish one of the most versatile system platforms in the industry and provide a foundation for unprecedented future possibilities.


In various embodiments, the controller 300 can be adapted to and/or configured for operation with the hand wand 100 and the module 200, as well as the overall ultrasound system 20 functionality. In various embodiments, multiple controllers 300, 300′, 300″, etc. can be adapted to and/or configured for operation with multiple hand wands 100, 100′, 100″, etc. and or multiple modules 200, 200′, 200″, etc. The controller 300 can include connectivity to one or more interactive graphical display 310, which can include a touchscreen monitor and Graphic User Interface (GUI) that allows the user to interact with the ultrasound system 20. In one embodiment, a second smaller, more mobile display that allows the user to more easily position and view the treatment screen. In one embodiment, a second display that allows the system user to view a treatment screen (e.g., on a wall, on a mobile device, large screen, remote screen). In one embodiment the graphical display 310 includes a touchscreen interface 315 (not shown). In various embodiments, the display 310 sets and displays the operating conditions, including equipment activation status, treatment parameters, system messages and prompts, and ultrasound images. In various embodiments, the controller 300 can be adapted to and/or configured to include, for example, a microprocessor with software and input/output devices, systems and devices for controlling electronic and/or mechanical scanning and/or multiplexing of transducers and/or multiplexing of transducer modules, a system for power delivery, systems for monitoring, systems for sensing the spatial position of the probe and/or transducers and/or multiplexing of transducer modules, and/or systems for handling user input and recording treatment results, among others. In various embodiments, the controller 300 can include a system processor and various analog and/or digital control logic, such as one or more of microcontrollers, microprocessors, field-programmable gate arrays, computer boards, and associated components, including firmware and control software, which may be capable of interfacing with user controls and interfacing circuits as well as input/output circuits and systems for communications, displays, interfacing, storage, documentation, and other useful functions. System software running on the system process may be adapted to and/or configured to control all initialization, timing, level setting, monitoring, safety monitoring, and all other ultrasound system functions for accomplishing user-defined treatment objectives. Further, the controller 300 can include various input/output modules, such as switches, buttons, etc., that may also be suitably adapted to and/or configured to control operation of the ultrasound system 20.


In one embodiment, the hand wand 100 includes one or more finger activated controllers or switches, such as 150 and 160. In various embodiments, one or more thermal treatment controllers 160 (e.g., switch, button) activates and/or stops treatment. In various embodiments, one or more imaging controllers 150 (e.g., switch, button) activates and/or stops imaging. In one embodiment, the hand wand 100 can include a removable module 200. In other embodiments, the module 200 may be non-removable. In various embodiments, the module 200 can be mechanically coupled to the hand wand 100 using a latch or coupler 140. In various embodiments, an interface guide 235 or multiple interface guides 235 can be used for assisting the coupling of the module 200 to the hand wand 100. The module 200 can include one or more ultrasound transducers 280. In some embodiments, an ultrasound transducer 280 includes one or more ultrasound elements. The module 200 can include one or more ultrasound elements. The hand wand 100 can include imaging-only modules, treatment-only modules, imaging-and-treatment modules, and the like. In various embodiments, the ultrasound transducer 280 is movable in one or more directions 290 within the module 200. The transducer 280 is connected to a motion mechanism 400. In various embodiments, the motion mechanism comprises zero, one, or more bearings, shafts, rods, screws, lead screws 401, encoders 402 (e.g., optical encoder to measure position of the transducer 280), motors 403 (e.g., a step motor) to help ensure accurate and repeatable movement of the transducer 280 within the module 200. In various embodiments, module 200 can include a transducer 280 which can emit energy through an acoustically transparent member 230. In one embodiment, the control module 300 can be coupled to the hand wand 100 via the interface 130, and the graphic user interface 310 can be adapted to and/or configured for controlling the module 200. In one embodiment, the control module 300 can provide power to the hand wand 100. In one embodiment, the hand wand 100 can include a power source. In one embodiment, the switch 150 can be adapted to and/or configured for controlling a tissue imaging function and the switch 160 can be adapted to and/or configured for controlling a tissue treatment function. In various embodiments, delivery of emitted energy 50 at a suitable focal depth, distribution, timing, and energy level is provided by the module 200 through controlled operation by the control system 300 of the transducer 280 to achieve the desired therapeutic effect with a thermal coagulation zone 550.


In one embodiment, the module 200 can be coupled to the hand wand 100. The module 200 can emit and receive energy, such as ultrasonic energy. The module 200 can be electronically coupled to the hand wand 100 and such coupling may include an interface which is in communication with the controller 300. In one embodiment, the interface guide 235 can be adapted to and/or configured to provide electronic communication between the module 200 and the hand wand 100. The module 200 can comprise various probe and/or transducer configurations. For example, the module 200 can be adapted to and/or configured for a combined dual-mode imaging/therapy transducer, coupled or co-housed imaging/therapy transducers, separate therapy and imaging probes, and the like. In one embodiment, when the module 200 is inserted into or connected to the hand wand 100, the controller 300 automatically detects it and updates the interactive graphical display 310.


In some embodiments, an access key 320 (e.g., a secure USB drive, key) is removably connected to a system 20 to permit the system 20 to function. In various embodiments, the access key is programmed to be customer specific, and serves multiple functions, including system security, country/region specific access to treatment guidelines and functionality, software upgrades, support log transfers and/or credit transfer and/or storage. In various embodiments, the system 20 has internet and/or data connectivity. In an embodiment, connectivity provides a method by which data is transferred between the system 20 provider and the customer. In various embodiments, data includes credits, software updates and support logs. Connectivity is divided into different model embodiments, based on how a user's console is connected to the internet. In one embodiment, Disconnected Model connectivity comprises a console that is disconnected from the internet and customer doesn't have internet access. Credit transfers and software upgrades are conducted by shipping access key(s), (e.g., USB drives) to the customer. In one embodiment, Semi-Connected Model connectivity comprises a console that is disconnected from the internet but customer has internet access. Credit transfers, software upgrades and support log transfers are conducted using the customer's personal computer, smart phone, or other computing device in conjunction with the system access key to transfer data. In one embodiment, Fully-Connected Model connectivity comprises a console that is wirelessly connected to the internet using wifi, cellular modem, Bluetooth, or other protocol. Credit transfers, software upgrades and support log transfers are made directly between the console and the cloud. In various embodiments, the system 20 connects to an online portal, for streamlined inventory management, on-demand treatment purchases and business analytics insights to drive customer aesthetic treatment business to the next level.


In various embodiments, tissue below or even at a skin surface such as epidermis, dermis, hypodermis, fascia, and superficial muscular aponeurotic system (“SMAS”), and/or muscle are treated non-invasively with ultrasound energy. Tissue may also include blood vessels and/or nerves. The ultrasound energy can be focused, unfocused or defocused and applied to a region of interest containing at least one of epidermis, dermis, hypodermis, fascia, and SMAS to achieve a therapeutic effect. FIG. 2 is a schematic illustration of the ultrasound system 20 coupled to a region of interest 10. In various embodiments, tissue layers of the region of interest 10 can be at any part of the body of a subject. In one embodiment, the tissue layers are in the head and face region of the subject. The cross-sectional portion of the tissue of the region of interest 10 includes a skin surface 501, an epidermal layer 502, a dermal layer 503, a fat layer 505, a superficial muscular aponeurotic system 507 (hereinafter “SMAS 507”), and a muscle layer 509. The tissue can also include the hypodermis 504, which can include any tissue below the dermal layer 503. The combination of these layers in total may be known as subcutaneous tissue 510. Also illustrated in FIG. 2 is a treatment zone 525 which is below the surface 501. In one embodiment, the surface 501 can be a surface of the skin of a subject 500. Although an embodiment directed to therapy at a tissue layer may be used herein as an example, the system can be applied to any tissue in the body. In various embodiments, the system and/or methods may be used on tissue (including but not limited to one or a combination of muscles, fascia, SMAS, dermis, epidermis, fat, adipose cells, cellulite, which may be called gynoid lipodystrophy, (e.g., non-dimple type female gynoid lipodystrophy), collagen, skin, blood vessels, of the face, neck, head, arms, legs, or any other location on or in the body (including bodily cavities). In various embodiments, cellulite (e.g., non-dimple type female gynoid lipodystrophy) reduction is achieved in an amount of 2%, 5%, 10%, 15%, 20%, 25%, 30%, 40%, 50%, 75%, 80%, 90%, 95%, and any ranges therein.


With reference to the illustration in FIG. 2, an embodiment of the ultrasound system 20 includes the hand wand 100, the module 200, and the controller 300. In one embodiment, the module 200 includes a transducer 280. FIG. 3 illustrates an embodiment of an ultrasound system 20 with a transducer 280 adapted to and/or configured to treat tissue at a focal depth 278. In one embodiment, the focal depth 278 is a distance between the transducer 280 and the target tissue for treatment. In one embodiment, a focal depth 278 is fixed for a given transducer 280. In one embodiment, a focal depth 278 is variable for a given transducer 280. In one embodiment, a transducer 280 is configured to treat simultaneously at multiple depths below a skin surface (e.g., 1.5 mm, 3.0 mm, 4.5 mm, or other depths).


With reference to the illustration in FIG. 4, the module 200 can include a transducer 280 which can emit energy through an acoustically transparent member 230. In various embodiments, a depth may refer to the focal depth 278. In one embodiment, the transducer 280 can have an offset distance 270, which is the distance between the transducer 280 and a surface of the acoustically transparent member 230. In one embodiment, the focal depth 278 of a transducer 280 is a fixed distance from the transducer. In one embodiment, a transducer 280 may have a fixed offset distance 270 from the transducer to the acoustically transparent member 230. In one embodiment, an acoustically transparent member 230 is adapted to and/or configured at a position on the module 200 or the ultrasound system 20 for contacting the skin surface 501. In various embodiments, the focal depth 278 exceeds the offset distance 270 by an amount to correspond to treatment at a target area located at a tissue depth 279 below a skin surface 501. In various embodiments, when the ultrasound system 20 placed in physical contact with the skin surface 501, the tissue depth 279 is a distance between the acoustically transparent member 230 and the target area, measured as the distance from the portion of the hand wand 100 or module 200 surface that contacts skin (with or without an acoustic coupling gel, medium, etc.) and the depth in tissue from that skin surface contact point to the target area. In one embodiment, the focal depth 278 can correspond to the sum of an offset distance 270 (as measured to the surface of the acoustically transparent member 230 in contact with a coupling medium and/or skin 501) in addition to a tissue depth 279 under the skin surface 501 to the target region. In various embodiments, the acoustically transparent member 230 is not used.


Coupling components can comprise various substances, materials, and/or devices to facilitate coupling of the transducer 280 or module 200 to a region of interest. For example, coupling components can comprise an acoustic coupling system adapted to and/or configured for acoustic coupling of ultrasound energy and signals. Acoustic coupling system with possible connections such as manifolds may be utilized to couple sound into the region of interest, provide liquid- or fluid-filled lens focusing. The coupling system may facilitate such coupling through use of one or more coupling media, including air, gases, water, liquids, fluids, gels, solids, non-gels, and/or any combination thereof, or any other medium that allows for signals to be transmitted between the transducer 280 and a region of interest. In one embodiment one or more coupling media is provided inside a transducer. In one embodiment a fluid-filled module 200 contains one or more coupling media inside a housing. In one embodiment a fluid-filled module 200 contains one or more coupling media inside a sealed housing, which is separable from a dry portion of an ultrasonic device. In various embodiments, a coupling medium is used to transmit ultrasound energy between one or more devices and tissue with a transmission efficiency of 100%, 99% or more, 98% or more, 95% or more, 90% or more, 80% or more, 75% or more, 60% or more, 50% or more, 40% or more, 30% or more, 25% or more, 20% or more, 10% or more, and/or 5% or more.


In various embodiments, the transducer 280 can image and treat a region of interest at any suitable tissue depths 279. In one embodiment, the transducer module 280 can provide an acoustic power in a range of about 1 W or less, between about 1 W to about 100 W, and more than about 100 W, e.g., 200 W, 300 W, 400 W, 500 W. In one embodiment, the transducer module 280 can provide an acoustic power at a frequency of about 1 MHz or less, between about 1 MHz to about 10 MHz (e.g., 3 MHz, 4 MHz, 4.5 MHz, 7 MHz, 10 MHz), and more than about 10 MHz. In one embodiment, the module 200 has a focal depth 278 for a treatment at a tissue depth 279 of about 4.5 mm below the skin surface 501. In one embodiment, the module 200 has a focal depth 278 for a treatment at a tissue depth 279 of about 3 mm below the skin surface 501. In one embodiment, the module 200 has a focal depth 278 for a treatment at a tissue depth 279 of about 1.5 mm below the skin surface 501. Some non-limiting embodiments of transducers 280 or modules 200 can be adapted to and/or configured for delivering ultrasonic energy at a tissue depth of 1.5 mm, 3 mm, 4.5 mm, 6 mm, 7 mm, less than 3 mm, between 3 mm and 4.5 mm, between 4.5 mm and 6 mm, more than more than 4.5 mm, more than 6 mm, etc., and anywhere in the ranges of 0-3 mm, 0-4.5 mm, 0-6 mm, 0-25 mm, 0-100 mm, etc. and any depths therein. In one embodiment, the ultrasound system 20 is provided with two or more transducer modules 280. For example, a first transducer module can apply treatment at a first tissue depth (e.g., about 4.5 mm) and a second transducer module can apply treatment at a second tissue depth (e.g., of about 3 mm), and a third transducer module can apply treatment at a third tissue depth (e.g., of about 1.5-2 mm). In one embodiment, at least some or all transducer modules can be adapted to and/or configured to apply treatment at substantially same depths.


In various embodiments, changing the number of focus point locations (e.g., such as with a tissue depth 279) for an ultrasonic procedure can be advantageous because it permits treatment of a patient at varied tissue depths even if the focal depth 278 of a transducer 270 is fixed. This can provide synergistic results and maximizing the clinical results of a single treatment session. For example, treatment at multiple depths under a single surface region permits a larger overall volume of tissue treatment, which results in enhanced collagen formation and tightening. Additionally, treatment at different depths affects different types of tissue, thereby producing different clinical effects that together provide an enhanced overall cosmetic result. For example, superficial treatment may reduce the visibility of wrinkles and deeper treatment may induce formation of more collagen growth. Likewise, treatment at various locations at the same or different depths can improve a treatment.


Although treatment of a subject at different locations in one session may be advantageous in some embodiments, sequential treatment over time may be beneficial in other embodiments. For example, a subject may be treated under the same surface region at one depth in time one, a second depth in time two, etc. In various embodiments, the time can be on the order of nanoseconds, microseconds, milliseconds, seconds, minutes, hours, days, weeks, months, or other time periods. The new collagen produced by the first treatment may be more sensitive to subsequent treatments, which may be desired for some indications. Alternatively, multiple depth treatment under the same surface region in a single session may be advantageous because treatment at one depth may synergistically enhance or supplement treatment at another depth (due to, for example, enhanced blood flow, stimulation of growth factors, hormonal stimulation, etc.). In several embodiments, different transducer modules provide treatment at different depths. In one embodiment, a single transducer module can be adjusted or controlled for varied depths. Safety features to minimize the risk that an incorrect depth will be selected can be used in conjunction with the single module system.


In several embodiments, a method of treating the lower face and neck area (e.g., the submental area) is provided. In several embodiments, a method of treating (e.g., softening) mentolabial folds is provided. In other embodiments, a method of treating the eye region (e.g., malar bags, treat infraorbital laxity) is provided. Upper lid laxity improvement and periorbital lines and texture improvement will be achieved by several embodiments by treating at variable depths. By treating at varied locations in a single treatment session, optimal clinical effects (e.g., softening, tightening) can be achieved. In several embodiments, the treatment methods described herein are non-invasive cosmetic procedures. In some embodiments, the methods can be used in conjunction with invasive procedures, such as surgical facelifts or liposuction, where skin tightening is desired. In various embodiments, the methods can be applied to any part of the body.


In one embodiment, a transducer module 200 permits a treatment sequence at a fixed depth at or below the skin surface. In one embodiment, a transducer module permits a treatment sequence at one, two, or more variable or fixed depths below the dermal layer. In several embodiments, the transducer module comprises a movement mechanism adapted to and/or configured to direct ultrasonic treatment in a sequence of individual thermal lesions (hereinafter “thermal coagulation points” or “TCPs”) at a fixed focal depth. In one embodiment, the sequence of individual TCPs has a treatment spacing in a range from about 0.01 mm to about 25 mm (e.g., 1 mm, 1.5 mm, 2 mm, 2.5 mm, 3 mm, 5 mm, 10 mm, 20 mm and any value ranges therein), with a dithering alteration of the spacing by 1-50% (e.g., 1%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50% and any range therein). For example, the spacing can be 1.1 mm or less, 1.5 mm or more, between about 1.1 mm and about 1.5 mm, etc. In one embodiment, the individual TCPs are discrete. In one embodiment, the individual TCPs are overlapping. In one embodiment, the movement mechanism is adapted to and/or configured to be programmed to provide variable spacing between the individual TCPs. In one embodiment, the dithering can be adapted to and/or configured to provide variable spacing between the individual TCPs. In several embodiments, a transducer module comprises a movement mechanism adapted to and/or configured to direct ultrasonic treatment in a sequence so that TCPs are formed in linear or substantially linear sequences separated by a treatment distance. For example, a transducer module can be adapted to and/or configured to form TCPs along a first linear sequence and a second linear sequence separated by a treatment distance from the first linear sequence. In one embodiment, treatment distance between adjacent linear sequences of individual TCPs is in a range from about 0.01 mm to about 25 mm. In one embodiment, treatment distance between adjacent linear sequences of individual TCPs is in a range from about 0.01 mm to about 50 mm. For example, the treatment distance can be 2 mm or less, 3 mm or more, between about 2 mm and about 3 mm, etc. In several embodiments, a transducer module can comprise one or more movement mechanisms 400 adapted to and/or configured to direct ultrasonic treatment in a sequence so that TCPs are formed in linear or substantially linear sequences of individual thermal lesions separated by a treatment distance from other linear sequences. In one embodiment a treatment is applied in a first direction 290 (e.g., push). In one embodiment, a treatment is applied opposite the first direction 290 (e.g., pull). In one embodiment, treatment is applied in both a first direction 290 and opposite the first direction (e.g., push and pull). In one embodiment, the treatment distance separating linear or substantially linear TCPs sequences is the same or substantially the same. In one embodiment, the treatment distance separating linear or substantially linear TCPs sequences is different or substantially different for various adjacent pairs of linear TCPs sequences.


In one embodiment, first and second removable transducer modules are provided. In one embodiment, each of the first and second transducer modules are adapted to and/or configured for both ultrasonic imaging and ultrasonic treatment. In one embodiment, a transducer module is adapted to and/or configured for treatment only. In one embodiment, an imaging transducer may be attached to a handle of a probe or a hand wand. The first and second transducer modules are adapted to and/or configured for interchangeable coupling to a hand wand. The first transducer module is adapted to and/or configured to apply ultrasonic therapy to a first layer of tissue, while the second transducer module is adapted to and/or configured to apply ultrasonic therapy to a second layer of tissue. The second layer of tissue is at a different depth than the first layer of tissue.


As illustrated in FIG. 3, in various embodiments, delivery of emitted energy 50 at a suitable focal depth 278, distribution, timing, and energy level is provided by the module 200 through controlled operation by the control system 300 to achieve the desired therapeutic effect of controlled thermal injury to treat at least one of the epidermis layer 502, dermis layer 503, fat layer 505, the SMAS layer 507, the muscle layer 509, and/or the hypodermis 504. FIG. 3 illustrates one embodiment of a depth that corresponds to a depth for treating muscle. In various embodiments, the depth can correspond to any tissue, tissue layer, skin, epidermis, dermis, hypodermis, fat, SMAS, muscle, blood vessel, nerve, or other tissue. During operation, the module 200 and/or the transducer 280 can also be mechanically and/or electronically scanned along the surface 501 to treat an extended area. Before, during, and after the delivery of ultrasound energy 50 to at least one of the epidermis layer 502, dermis layer 503, hypodermis 504, fat layer 505, the SMAS layer 507 and/or the muscle layer 509, monitoring of the treatment area and surrounding structures can be provided to plan and assess the results and/or provide feedback to the controller 300 and the user via a graphical interface 310.


In one embodiment, an ultrasound system 20 generates ultrasound energy which is directed to and focused below the surface 501. This controlled and focused ultrasound energy 50 creates the thermal coagulation point or zone (TCP) 550. In one embodiment, the ultrasound energy 50 creates a void in subcutaneous tissue 510. In various embodiments, the emitted energy 50 targets the tissue below the surface 501 which cuts, ablates, coagulates, micro-ablates, manipulates, and/or causes a TCP 550 in the tissue portion 10 below the surface 501 at a specified focal depth 278. In one embodiment, during the treatment sequence, the transducer 280 moves in a direction denoted by the arrow marked 290 at specified intervals 295 to create a series of treatment zones 254 each of which receives an emitted energy 50 to create one or more TCPs 550. In one embodiment, an arrow marked 291 illustrates an axis or direction that is orthogonal to arrow 290, and a spacing of TCP's 550 show TCP's can be spaced orthogonally to the motion direction of the transducer 280. In some embodiments, an orientation of the spaced TCP's can be set at any angle 0-180 degrees from arrow 290. In some embodiments, an orientation of the spaced TCP's can be set at any angle 0-180 degrees based on the orientation of poled areas on the transducer 280.


In various embodiments, transducer modules can comprise one or more transduction elements. The transduction elements can comprise a piezoelectrically active material, such as lead zirconante titanate (PZT), or any other piezoelectrically active material, such as a piezoelectric ceramic, crystal, plastic, and/or composite materials, as well as lithium niobate, lead titanate, barium titanate, and/or lead metaniobate. In various embodiments, in addition to, or instead of, a piezoelectrically active material, transducer modules can comprise any other materials adapted to and/or configured for generating radiation and/or acoustical energy. In various embodiments, transducer modules can be adapted to and/or configured to operate at different frequencies and treatment depths. Transducer properties can be defined by an outer diameter (“OD”) and focal length (FL). In one embodiment, a transducer can be adapted to and/or configured to have OD=19 mm and FL=15 mm. In other embodiments, other suitable values of OD and FL can be used, such as OD of less than about 19 mm, greater than about 19 mm, etc. and FL of less than about 15 mm, greater than about 15 mm, etc. Transducer modules can be adapted to and/or configured to apply ultrasonic energy at different target tissue depths. As described above, in several embodiments, transducer modules comprise movement mechanisms adapted to and/or configured to direct ultrasonic treatment in a linear or substantial liner sequence of individual TCPs with a treatment spacing between individual TCPs. For example, treatment spacing can be about 1.1 mm, 1.5 mm, etc. In several embodiments, transducer modules can further comprise movement mechanisms adapted to and/or configured to direct ultrasonic treatment in a sequence so that TCPs are formed in linear or substantially linear sequences separated by a treatment spacing. For example, a transducer module can be adapted to and/or configured to form TCPs along a first linear sequence and a second linear sequence separated by treatment spacing between about 2 mm and 3 mm from the first linear sequence. In one embodiment, a user can manually move the transducer modules across the surface of a treatment area so that adjacent linear sequences of TCPs are created. In one embodiment, a movement mechanism can automatically move the transducer modules across the surface of a treatment area so that adjacent linear sequences of TCPs are created.


Aperture Spatial Frequency Analysis and Fourier Transform


In various embodiments, spatial frequency analysis techniques based on Fourier analysis and Fourier optics can be used to increase efficiency of therapeutic treatment. When a system that has an impulse response h(t) is excited by a stimulus x(t), the relationship between the input x(t) and output y(t) is related by the convolution function as follows:

y(t)=x(t)*h(t)=∫−∞x(τ)h(t−τ)  (1)


In various embodiments, Fourier transform can be applied to compute the convolution of equation (1). Continuous one-dimensional Fourier transform can be defined at:

y(f)=F(y(t)=∫−∞y(t)e−j2πftdt  (2)


Here f is frequency, t is time. It can be shown that convolution in the time domain is equivalent to multiplication in the frequency domain:

F(x(t)*h(t))=X(f)H(f)=Y(f)  (3)


In various embodiments, the Fraunhofer approximation can be used for deriving a relationship between a transducer opening or aperture and a resulting ultrasonic beam response. Derivation of the Fraunhofer approximation is described in Joseph Goodman, Introduction to Fourier Optics (3d ed. 2004), which is incorporated in its entirety by reference, herein. According to the Fraunhofer approximation, a far-field complex amplitude pattern produced by a complex aperture is equal to a two-dimensional Fourier transform of the aperture amplitude and phase. In several embodiments, this relationship in optics can be extended to ultrasound since linear wave equations can be used to represent both light propagation and sound propagation. In the case of optics and/or ultrasound, the two-dimensional Fourier transform can determine a sound wave pressure amplitude distribution at the focus of a transducer.


For a focused system, the variable z which represents depth can be replaced with zf which represents a focal distance.










f
x

=


x
0


λ






z
f







(

4

a

)







f
y

=


y
0


λ






z
f







(

4

b

)







In various embodiments, Fourier optics and Fourier transform identities (some of which are listed in Table 1, below) can be used for ultrasound transducers in order to determine the intensity distribution corresponding to a transducer design. For example, Fourier transform of a rectangle rect(ax) is a sinc function. As another example, Fourier transform of a two dimensional circle of uniform amplitude is a first order Bessel function which can be represented as J1.











TABLE 1






Aperture Function
Fourier Transform







1
rect(ax)





1


a









sinc


(

ξ
a

)











2
δ(x)
1





3
cos(ax)






δ


(

ξ
-

a

2

π



)


+

δ


(

ξ
+

a

2

π



)



2









4
sin(ax)






δ


(

ξ
-

a

2

π



)


-

δ


(

ξ
+

a

2

π



)




2

j










5 (two- dimensional transform
circ({square root over (x2+y2)})






j
1



(

2

π




ξ
x
2

+

ξ
y
2




)





ξ
x
2

+

ξ
y
2









pair







6
f(x) * g(x)
F(ξ)G(ξ)


7
f(x)g(x)
F(ξ) * G(ξ)









In several embodiments, an ultrasound transducer can have a rectangular aperture of suitable dimensions and focal length. In several embodiments, an ultrasound transducer can have a circular aperture with suitable dimensions and focal length. In one embodiment, a transducer can have a circular aperture with an outer radius of approximately 9.5 mm, an inner diameter of approximately 2 mm, and focal length of approximately 15 mm. The aperture of a circular transducer may be described as:










f


(

x
,
y

)


=


circ






(

r
a

)


-

circ






(

r
b

)







(

5

a

)






r
=



x
2

+

y
2







(

5

b

)







For example, in one embodiment, the variable ‘a’ can be approximately 9.5 mm and the variable ‘b’ in equation (5a) can be approximately 2 mm. Applying Fourier transform to equation (5a) can provide an estimate of the sound wave pressure distribution at the focus.











F

x
,
y




(

f


(

x
,
y

)


)


=


F


(


ξ
x

,

ξ
y


)


=









(

2

π





a




ξ
x
2

+

ξ
y
2




)





ξ
x
2

+

ξ
y
2




-








(

2

π





b




ξ
x
2

+

ξ
y
2




)





ξ
x
2

+

ξ
y
2










(
6
)







where ξx and ξy are same as fx and fy of equations (4a) and (4b). Equation (6) demonstrates that the sound wave pressure distribution of a transducer with a circular aperture is a first order Bessel function. In one embodiment, a substantial majority of the energy is concentrated at the focus (e.g., 15 mm away from the aperture). The width of a main ultrasonic beam and the distribution of energy away from the main beam can be expressed as a function of the operating frequency as is expressed in equations (4a) and (4b).


In various embodiments, two identical or nearly identical beams could be created at the focus if the aperture was modulated (e.g., multiplied) by a correct function. In one embodiment, a cosine function can be applied to a circular aperture as follows:










g


(

x
,
y

)


=


cos


(
cx
)




(


circ


(

r
a

)


-

circ


(

r
b

)



)






(
7
)







An energy distribution or beam response at the focus of the modulated aperture of equation (7) is the convolution of the Fourier transform of the two functions of the aperture:










G


(


ξ
x

,

ξ
y


)


=


(



δ


(


ξ
x

-

c

2

π



)


+

δ


(


ξ
x

+

c

2

π



)



2

)



F


(


ξ
x

,

ξ
y


)







(
8
)







Equation (8) can be simplified into the summation of two separate functions applying the Fourier Transform identity for a Dirac delta function (e.g., identity 2 in Table 2):










G


(


ξ
x

,

ξ
y


)


=


1
2



(


F


(



ξ
x

-

c

2

π



,

ξ
y


)


+

F


(



ξ
x

+

c

2

π



,

ξ
y


)



)






(
9
)







Equation (9) shows that two beams appearing at the focus are spatially shifted by






±

c

2

π







compared to the original, non-modulated beam. In several embodiments, one or more other modulation functions, such as sine function, can be used to achieve a desired beam response. In several embodiments, aperture can be modulated such that more than two foci are created. For example, three, four, five, etc. foci can be created. In several embodiments, aperture can be modulated such that foci are created sequentially or substantially sequentially rather than simultaneously.


In several embodiments, therapy transducer modules comprise movement mechanisms configured to direct ultrasonic treatment in a linear or substantial liner sequence of individual TCPs with a treatment spacing between individual TCPs. For example, treatment spacing can be about 1.1 mm, 1.5 mm, etc. In several embodiments, transducer modules can further comprise movement mechanisms configured to direct ultrasonic treatment in a sequence so that TCPs are formed in linear or substantially linear sequences separated by a treatment spacing. For example, a transducer module can be configured to form TCPs along a first linear sequence and a second linear sequence separated by treatment spacing between about 2 mm and 3 mm from the first linear sequence. According to equation (9), a simultaneous or substantially simultaneous split in the ultrasonic beam may be achieved at the focus (or before the focus) if the aperture is modulated by a cosine and/or sine function of a desired spatial frequency. In one embodiment, two simultaneous or nearly simultaneous focused beams separated by about 1.1 mm treatment spacing can be created in a linear or substantially linear sequence. At 7 MHz frequency of ultrasound, the wavelength λ of ultrasound wave in water is approximately 0.220 mm. Accordingly, spatial frequencies ξx and ξy at the focus are represented as:










ξ
x

=



x
o


15
*
0.220


=


x
0

3.3






(

10

a

)







ξ
y

=



y
0


15
*
0.220


=


y
0

3.3






(

10

b

)







In order to place two foci separated by about 1.1 mm, then the spatial frequency for modulating the aperture is calculated as follows. Using identities 3 and 4 in Table 2, the Fourier transformation of a sine or cosine function is a Dirac delta function with the argument:









arg
=



x
0

3.3

-


k
x


2

π







(

11

a

)







In one embodiment, equation (11a) can solved for kx when argument is 0:










k
x

=


2

π






x
0


3.3





(

11

b

)







Further, xo can be replaced by half of the separation distance (e.g., 1.1 mm):










k
x

=



Z





π


s
2




z
f


λ


=



Z





π


1.1
2


3.5

=

1.04






mm

-
1









(

11

c

)







In several embodiments, a transducer with circular aperture emitting ultrasonic energy at various operating frequencies can be modulated by a sine and/or cosine functions at spatial frequencies listed in Table 2. Modulated aperture of the transducer can produce a simultaneously or substantially simultaneously split beam with two foci having different separation distances, as is indicated in Table 2. In one embodiment, the transducer can have OD of about 19 mm and a focal length of about 15 mm.











TABLE 2







Ultrasound
Separation Distance Between Foci












Frequency
1.1 mm
1.5 mm
2 mm
3 mm














4 MHz
0.60
0.82
1.09
1.63


7 MHz
1.04
1.43
1.90
2.86


10 MHz 
1.50
2.04
2.72
3.08









As is shown in Table 2, in several embodiments, a spatial frequency of an aperture modulation function increases as the ultrasonic operating frequency increases for a given foci separation distance. In addition, the spatial frequency increases as the desired foci separation distance increases.


In one embodiment, higher spatial frequency can result in amplitude transitions in the aperture occurring more rapidly. Due to transducer processing limitations, rapid amplitude variations in the aperture can make the aperture less efficient as there may be a variance in an amount of sound pressure produced by different parts of the aperture. In one embodiment, using spatial frequencies to simultaneously or nearly simultaneously split the beam can reduce the overall focal gain of each beam. As is shown in equation (9), a field pressure at the focus of each beam is reduced by a factor of two in comparison with an unmodulated beam. In one embodiment, the sound pressure or ultrasound intensity from the aperture can be increased to obtain similar or substantially similar intensities at the focal plane. However, in one embodiment, increasing the pressure at the aperture may not be limited by system and/or transducer processing limitations. In one embodiment, an increase in the pressure at the aperture can increase the overall intensity in the near field, which may increase the possibility of excessively heating treatment area tissue(s) that is located before focus. In one embodiment, the possibility of additional heating of the pre-focal tissue(s) may be limited or eliminated by using a lower ultrasound treatment frequency.


In one embodiment, applying aperture modulation function as is shown in equation (7) results in two simultaneous or substantially simultaneous ultrasound beams at the focus. In various embodiments, ultrasound beam can be split multiple times, such as three, four, five, etc. times, such that multiple simultaneous or nearly simultaneous beams are created. In one embodiment, four equally spaced beams along one dimension can be generated by modulating or multiplying the aperture by two separate spatial frequencies:















g


(

x
,
y

)


=


(


cos


(
cx
)


+

cos


(
dx
)



)



(


circ


(

r
a

)


-

circ


(

r
b

)



)







(

12

a

)







G


(


ξ
x

,

ξ
y


)


=


1
2



(


F


(



ξ
x

-

c

2

π



,

ξ
y


)


+

F


(



ξ
x

+

c

2

π



,

ξ
y


)


+

F


(



ξ
x

-

d

2

π



,

ξ
y


)


+

F


(



ξ
x

-

d

2

π



,

ξ
y


)



)






(

12

b

)







As is shown in equation (12b), unmodulated beam at the focus can be created at four different locations along the x-axis. In one embodiment, a constant or DC term, Cl, may be added to the amplitude modulation function to maintain placement of energy at the original focal location:















g


(

x
,
y

)


=


(


cos


(
cx
)






cos


(
dx
)






C
1


)



(




circ


(

r
a

)





circ


(

r
b

)





)







(

13

a

)







G


(


ξ
x

,

ξ
y


)


=



1
2



(


F


(



ξ
x

-

c

2

π



,

ξ
y


)


+

F


(



ξ
x

+

c

2

π



,

ξ
y


)


+

F


(



ξ
x

-

d

2

π



,

ξ
y


)


+

F


(



ξ
x

-

d

2

π



,

ξ
y


)



)


+


C
1



F


(


ξ
x

,

ξ
y


)








(

13

b

)







In one embodiment, aperture modulation of equations (12) and (13), whereby the beam can be placed at multiple locations simultaneously or nearly simultaneously, may be have limited applicability due to system, material, and/or tissue limitations. In one embodiment, due to the possibility of heating treatment area tissue(s) located before focus, the frequency of ultrasound therapy may be adjusted, such as lowered, in order to limit and/or eliminate such possibility. In one embodiment, nonlinear techniques can be applied at the focus in order to limit and/or eliminate the possibility of heating of the pre-focal tissue(s). In one embodiment, the sound pressure or ultrasound intensity from the aperture can be increased to obtain similar or substantially similar intensities at the focal plane.


In various embodiments, if the amplitude and phase functions at the aperture are separable, the two-dimensional Fourier transform of a sound pressure function U(x1, y1) can be expressed as a product of a one-dimensional Fourier transform of two functions in x and y. In various embodiments, it may be advantageous to create multiple TCPs in a linear or substantially linear sequence as well as to create multiple linear sequences simultaneously or nearly simultaneously.


Electronic Dithering of Multiple Beam Splitting Apertures Using Frequency Modulation


In various embodiments, Table 2 illustrates aperture spatial frequency for achieving a specific distance between two simultaneous foci for a given operational frequency (e.g. in various embodiments, 4 MHz, 7 MHz, 10 MHz). Equation (11c) shows that the separation distance between the foci is also a function operational frequency. For example, in one embodiment the spatial frequency of the aperture (kx) is fixed to 1.0 mm−1 and the operational frequency is allowed to vary. Equation 11c can be rewritten to show how the foci separation distance can be modulated through operation frequency.

s=(kxzfvc)/(πfop)  (14)


where kx is the spatial frequency in mm−1, zf is the focal depth of the aperture in mm, vc is the velocity of ultrasound in the propagating medium (e.g. water) in mm/μsec and fop is the operational frequency of the aperture in MHz. In one embodiment, the following substitution is made in equation 11c:

λ=vc/fop  (15)


As Equation (14) shows, the separation distance of the foci is a function of the operational frequency. Further, the rate in change of the separation distance to the operational frequency is:

ds/dfop=−(kxZfVc)/(πfop2)  (16)


Equation (16) shows that the separation distance decreases as the operational frequency increases. Table 3 (below) shows the rate in change of separation distance as a function of operational frequency for the different spatial frequencies (e.g., in various embodiments, 4 MHz, 7 MHz, 10 MHz).











TABLE 3







Ultrasound
Derivative of Equation (16) [mm/MHz]












Frequency
1.1 mm
1.5 mm
2 mm
3 mm














4 MHz
−0.269
−0.367
−0.488
−0.730


7 MHz
−0.152
−0.209
−0.278
−0.418


10 MHz 
−0.107
−0.146
−0.195
−0.221









As shown in Table 3, as the operational frequency increases, the foci get closer together and as the operational frequency decreases the foci get farther apart without the need to change the phase or mechanically move the transducer. This is a unique method of electronically moving the beam to spread the energy without relying on thermal conduction in tissue. The benefits include a reduction or a minimization of the maximum temperature and an increase in the thermal coagulation volume of the lesion without the need for additional system channels.


The amount of movement from a main operational frequency can be determined by using equation (14). In one embodiment, the main operational frequency of an aperture is 5 MHz and the focal length is 15 mm. In some embodiments, the operational frequency is called the aperture center frequency. In one embodiment, the operational frequency is 5 MHz. In one embodiment, Table 4 at FIG. 5 shows the amount of foci separation for apertures with different spatial frequencies (kx=0.5, 1.0, 1.5, 2.0 in mm−1) as designed for a center frequency of 5 MHz. It also calculates the amount of spread from the foci of the center frequency at 5 MHz. According to one embodiment, the spacing decreases for higher frequencies relative to 5 MHz and increases for lower frequencies relative to 5 MHz.



FIG. 6 shows the spacing difference for all operational frequencies of the aperture for different aperture spatial frequencies. As FIG. 6 shows, the separation distance increases as the frequency decreases.


In one embodiment, the separation distance is relative to a frequency 5 MHz. In one embodiment, one way to estimate the electronic dithering from frequency modulation can be determined by referencing all movement to the initial separation at 5 MHz. As FIG. 7 shows, the spread of the separation distance between the foci can easily vary by over 1 mm.


In various embodiments, the range of possible operational frequencies from one aperture can be described in terms of the transducer bandwidth. In one embodiment, a larger transducer bandwidth results in an aperture that has a wider range of operational frequencies. Transducer bandwidth can be described as a percent fraction of the aperture center frequency by locating the frequency where the transmit intensity decreases to −3 dB of the peak transmit intensity. In one embodiment the −3 dB high frequency is designated as f−3 db,H and the −3 dB low frequency is designated as f−3 dB,L for the transmit response of a transducer aperture. The −3 dB center frequency in [MHz] is described as:

f−3 dB,center=(f−3 dB,H+f−3 dB,L)/2  (17)


The −3 dB percent bandwidth is described as:

BW−3 dB=100%*(f−3 dB,H+f−3 dB,L)/((f−3 dB,H+f−3 dB,L)/2)  (18)


In some embodiments, increasing the range of operational frequencies possible within one aperture may be achieved (but not limited to) by the use of backing layers, matching layers, multiple piezoelectric layers, electrical matching, piezoelectric composites, and/or a single crystal piezoceramic. In one embodiment, as the transducer bandwidth increases, the range of possible separation distance increases. Table 5 (below) shows how based on percent bandwidth the foci spread can vary if the aperture center frequency is 5 MHz. The foci separation distance for 5 MHz is 0.72 mm, 1.43 mm, 2.15 mm and 2.86 mm respectively for spatial frequencies of 0.5 mm−1, 1.00 mm−1, 1.50 mm−1, 2.00 mm−1. If the spatial frequency at the aperture is 1.50 mm−1 and the transducer bandwidth is 60%, then the separation distance between the foci varies by 1.42 mm which is a distance greater than the lateral resolution of the beam at 5 MHz.









TABLE 5







Additional Spread from 5 MHz Center Frequency in [mm]











Band-
kx =
kx =
kx =
kx =


width
0.5 mm−1
1.0 mm−1
1.5 mm−1
2.0 mm−1














20%
0.14
0.29
0.43
0.58


40%
0.30
0.60
0.90
1.19


60%
0.47
0.94
1.42
1.89


80%
0.68
1.36
2.05
2.73


100% 
0.95
1.91
2.86
3.82









In one embodiment, as the frequency is changed, the depth-of-field will also change as well as lateral resolution and focal gain. In one embodiment, as the frequency is changed, the depth-of-field, lateral resolution and focal gain will also change. Therefore, in one embodiment, the intensity at the aperture may change depending in the heating rate goals. Also, in some embodiments, it may be advantageous to send multiple operational frequencies at the same time to spread the energy immediately or near-immediately. For example, transmit excitation of the aperture may include excitation at 4 MHz, 5 MHz and 6 MHz all at the same time.


Multiple Foci by Changing the Aperture Spatial Frequency


As Equation 11c shows, the higher the aperture spatial frequency, the greater the separation distance between the foci. In one embodiment, an aperture is poled with a spatial frequency of kx. The spatial frequency can be easily doubled or decreased to zero by connecting individual electrical excitation channels that have the ability to modify the phase to 0 degrees or 180 degrees, as shown in the embodiments in FIG. 8. For example, if the phase on channels 1 through 16 is 0 degrees, then the aperture spatial frequency is kx. In an embodiment, as the phase on each channel is varied from 0 degrees to 180 degrees such that odd channels are at 0 degrees and even channels are at 180 degrees, then the spatial frequency at the aperture is ½ kx. In an embodiment, if the phase repeats every two channels such that channel 1 and channel 2 is 0 degrees and channel 3 and channel 4 is 180 degrees and so on, then the spatial frequency at the aperture is 0. If channel 1 is 0 degrees, channel 2 is 180 degrees, channel 3 is 180 degrees, channel 4 is 0 degrees and so on, then the spatial frequency at the aperture is 2kx. In this case, seven unique foci can be created. As noted in Table 4 (at FIG. 5), if the aperture center frequency is 5 MHz, and the aperture frequency is any of 0 mm−1, 0.5 mm−1, 1.0 mm−1, or 2.0 mm−1, the corresponding separation distances are 0 mm, 0.72 mm, 1.43 mm and 2.86 mm, which yield seven unique focal positions separated by 0.36 mm. In various embodiments, intermediate phases between 0 degrees and 180 degrees would further allow the two foci to be tilted such that a line of foci could be created at the focal plane. Ultimately, the tilting, modulation of focal position, and frequency modulation enables the heating and possible coagulation of an entire line with a length of approximately 2.86 mm.


In one embodiment, a poled ceramic has a spatial frequency of 2kx, as shown in FIG. 9. In this case, each electrical channel covers two poled areas in the ceramic (e.g., a piezoceramic). If channel 1 through channel 8 have the same electrical phase, then the spatial frequency of the aperture is 2kx. If the phase alternates such that odd channels have a phase of 0 degrees and even channels have a phase of 180 degrees, then the spatial frequency of the aperture is kx. In one embodiment, this configuration of only two phases are possible on the channels enables four unique foci. In various embodiments, if additional phases are allowable then it is possible to tilt the two foci to many different focal positions. This configuration limits the number of required electronic channels to get multiple foci positions.


Multiple Foci Using Multi-Channel Signal Mixing


In several embodiments, a treatment system utilizes multiple therapy channels to enable electronic focusing and/or steering. For example, a treatment system that utilizes multiple therapy channels to enable electronic focusing and/or steering allows for faster electronic dithering to either create more thermal coagulation using the same amount of energy as other treatment devices or equal thermal coagulation using electronic dithering with less energy than other treatment devices. This technique broadens the efficacy and comfort continuum that the device offers. In addition to electronic dithering, the multiple therapy channels also offer the possibility to move the beam to different depth locations such that two conventional transducers such as the DS7-4.5 (7 MHz at 4.5 mm depth) and DS7-3.0 (7 MHz at 3.0 mm depth) could be replaced by one single device that moves between the two different depths.


In one embodiment, a transducer 280 with multiple therapy channels 281 connected to move the beam axially (e.g. annular array) would typically create a TCP 550 at a deep depth first and then move to the shallower depth. In another embodiment, a TCP 550 is created at a shallow depth and then at a deeper depth below the skin surface. This creates the TCP 550 sequentially and would cause the treatment time to be extended. For example, in one embodiment, if the time for the deep TCP 550 is tdeep and the time for the shallow TCP 550 is tshallow, then the total treatment time for the two TCPs 550 is the sum of the two treatment times, tdeep plus tshallow. In one embodiment, total treatment time is reduced by forming multiple (two, or more) TCP's 550 simultaneously using signal mixing techniques which uses both signal apodization (shading) and phase control at each channel. In one embodiment, the total treatment time is the maximum of tdeep and tshallow:


Treatment time, conventional approach: ttreatment=tdeep+tshallow


Treatment time, signal mixing: ttreatment=max(tdeep, tshallow)


In an embodiment, an annular array design 280 enables the electronic movement of the therapy beam in depth (e.g., by changing depth of the TCP 550 below the skin surface). In one embodiment, a transducer 280 includes an eight therapy channel annular transducers elements 281 with a fixed mechanical focus. FIG. 10 shows a top view of one embodiment of this ceramic annular array design 280 with an imaging transducer 285 at the center of the howl. In this embodiment, the therapy annular transducer 280 has eight rings identified as Tx0 though Tx7, corresponding to the elements 281. FIG. 11 shows a side view of the same eight channel annular transducer 280 with hash marks signifying the boundaries between rings. In this embodiment, eight separate excitation sources have been connected to the individual annular rings 281. In addition to the electrical excitations, the geometric focus 551 and two electronic foci 552, 552′ have been identified.


In one embodiment, there is a unique amplitude ‘A’ and phase ‘8’ applied to each therapy channel and corresponding annular ring 281 for each focus at a given therapy frequency ‘w’. The excitation function for a channel can be generalized to the following form:

fn,m(t)=An,m sin(ωt+θn,m)  (19)


where n is the ring or channel number and m is the focus number.


In the case of creating a TCP at the geometric focus, the phase is zero and equation (19) can be rewritten as:

fn,1(t)=An,1 sin(ωt)  (20)


where the ‘1’ in the subscript signifies the geometric focus.


In the case of creating a TCP 550 at electronic focus #2, the phase of the rings must be adjusted to focus the ultrasound at the spatial point using bowl geometry and time delay estimates. The excitation function can be written as:

fn,2(t)=An,2 sin(ωt+θn,2)  (21)


where the ‘2’ in the subscript signifies the electronic focus #2 and the angle is the required phasing for the ring.


Now, in the conventional case, the two TCP's would be created sequentially with typically the deeper TCP generated first and then the shallow TCP. However, signal mixing allows the two excitation signals to be represented as one signal such that both TCPs could be generated simultaneously.

fn,total(t)=fn,1(t)+fn,2(t)=An,1 sin(ωt)+An,2 sin(ωt+θn,2)
fn,total(t)=c sin(ωt+ϕ)  (22a)
where c=sqrt(An,12+An,22+2An,1An,2 cos(θn,2)) and
ϕ=a tan 2(An,2 sin(θn,2),An,1+An,2 cos(θn,2))  (22b)


The amplitude and phase at each ring is modified to support the focusing at two locations simultaneously.


In some embodiments, the time to deliver the dose for one focus will be slightly different than the second focus. In one embodiment, the excitation may start or end on the focus with the longer dosing time with excitation modified to support the dosing at two foci simultaneously using Equation (22b) during the other times. For example, in one embodiment, for fn,1 a total dosing time of 30 msec is required whereas for fn,2 a total dosing time of 60 msec is required. In order to satisfy this, many different excitations scenarios could be used:

fn,2(t) for 30 msec and then fn,total(t) for 30 msec  (23a)
fn,total(t) for 30 msec and then fn,2(t) for 30 msec  (23b)
fn,2(t) for 15 msec and then fn,total(t) for 30 msec and fn,2(t) for 15 msec  (23c)


In one embodiment, this concept can be further generalized to more than two simultaneous foci. Suppose the excitation on one ring is the following:












f

n
,
total




(
t
)


=





i
=
1

m




A

n
,
i




sin


(


ω





t

+

θ

n
,
i



)




=


A

n
,
total




sin


(


ω





t

+

φ
n


)












A

n
,
total

2

=




i
=
1

m






j
=
1

m




A

n
,
i




A

n
,
j




cos


(


θ

n
,
i


-

θ

n
,
j



)













tan


(

φ
n

)


=





i
=
1

m




A

n
,
i




sin


(

θ

n
,
i


)








i
=
1

m




A

n
,
i




cos


(

θ

n
,
i


)










(
224
)







where n is the ring number and m is the number of simultaneous foci. This generalization to more than two foci enables the geometric focus, shallow electronic focus and deep electronic focus to be delivered at the same time.


In one embodiment, an experiment was conducted using simulations of two simultaneous foci were completed to show that when this theory is applied that two foci appear. The simulations attempted to place a therapy focus at 15 mm and 17 mm simultaneously. FIG. 12 shows the intensity map in azimuth and depth for this simultaneous excitation. The intensity map clearly shows two foci appearing at 15 mm and 17 mm. Another simulation was done with the foci at 15 mm and 19 mm respectively. FIG. 13 shows the results. In various embodiments, this technique can be applied to any array. The array can be annular, linear, or any electronically controlled array transducer.


Ultrasound Imaging for Improving Ultrasound Therapy Treatments


In an embodiment, the imaging resolution is improved via electronic focusing on the beam axis in transmit and receive signals. In various embodiments, imaging resolution is improved by 10%, 20%, 40%, or 50%, 10%-50%, or any values therein. In an embodiment, increasing imaging resolution may not interrogate as well the coupling between the therapy transducer and the skin since the cross-section of the therapy beam is much wider than the imaging beam at this tissue interface.



FIG. 14 illustrates an embodiment of a cross-section of a therapy beam 281 from a therapy transducer 280 through an acoustic window interface compared to the cross-section of the imaging beam 286 from an imaging transducer 285. In this figure, the movement of the transducer 280 is in-and-out of the page. As FIG. 14 shows, the OD of the therapy cross-section is significantly greater than the imaging cross-section. Analysis using trigonometry and simple ray tracing shows that for a therapy transducer with a 4 MHz therapy beam directed to a depth of 4.5 mm below the skin surface (DS 4-4.5) has a therapy beam OD 281 of 8 mm whereas the imaging beam OD 286 is expected to be approximately 0.25 mm. In this case, if the small imaging beam is used to check for proper coupling, only approximately 0.1% of the therapy beam through the acoustic window is interrogated. In an embodiment, this estimate may be slightly underestimated due to diffraction effects of the therapy beam.


In an embodiment, an imaging beam 286 is extended to a larger (e.g., 10%, 15%. 25%, 50%, 75%, 90%, 100%) entire image frame to cover more, or all, of the therapy beam 281 cross section. In an embodiment, an image has a width of 25 mm. If the areas are calculated and compared (e.g. slice thickness and width), then the imaging plane only interrogates approximately 2.5% of the total therapy area cross-section at the acoustic window. Although this is improved over the initial calculation, it is still significantly below 100% coverage. In various embodiments, imaging provides for properly interrogate more (e.g., 10%, 15%. 25%, 50%, 75%, 90%, 100%) the coupling using an imaging system with an annular array. In some embodiments, image processing enables proper interpretation by the operator.


Linear Imaging Array


In various embodiments, an ultrasound treatment system comprises an imaging module and an imaging array 285. In various embodiments, the imaging array 285 is a linear array, such as shown in the embodiment at FIG. 15. In one embodiment, a method for detecting the amount of acoustic coupling between tissue and the ultrasound treatment systems is to use a linear array which is oriented in the transducer module such that electronic steering and focusing of the beam is along the y and z dimensions. This is orthogonal to the direction of motion with a motion mechanism. In this embodiment, the linear array focuses the imaging beam in the imaging plane multiple times as the transducer is moved along the x-axis which generates a high resolution ultrasound image. As the linear array translates along the x-axis, an imaging beam can also be steered and focused away from the imaging plane to better assess the coupling of the therapy beam cross-section into tissue. In some cases, this may give an even better spatial determination of poor coupling regions than the annular array due to the spatial specificity of the imaging beam. This is especially true if the linear array is a 1.25D, 1.5D, 1.75D, or 2D array.


Annular Imaging Array


In various embodiments, an ultrasound treatment system comprises an imaging module and an imaging array 285. In various embodiment, the imaging module has multiple (e.g., 2, 4, 8) transmit channels and multiple (e.g., 2, 4, 8) receive channels that operate from between 8 MHz to 50 MHz (e.g., 8, 9, 10, 12, 15, 20, 22, 25, 28, 30, 40 or 50 MHz and any ranges therein) for purposes of imaging the skin to approximately 25 mm in depth. In one embodiment, the imaging module has eight transmit channels and eight receive channels that operate from 8 MHz to 50 MHz for purposes of imaging the skin to approximately 25 mm in depth. The eight channels enable unique imaging aperture designs with elements that offer electronic steering and focusing in transmit and receive. One of these types of apertures is an annular array (FIG. 16).


In some embodiments, the annular array 285 contains rings of equal element areas that permit electronic focusing along the beam axis. In one embodiment, a mechanically scanned annular array 285 offers superior imaging performance over a more technically advanced, electronically controlled linear array 285′. This is because an annular array 285 focuses the beam along the beam axis in azimuth and elevation. The radial symmetry produces a high resolution beam with equivalent beamwidth. The linear array 285′ uses electronic focusing in azimuth and mechanical focusing in elevation which is equivalent to a compound lens. The resolution of the beam in azimuth can match the performance of the annular array 285; however, the resolution of the beam in elevation underperforms the annular array 285 due to the mechanical lens having only one focal depth.



FIG. 17 shows an embodiment of the focusing capability of an annular array 285 when compared to a linear array 285′ in elevation. The beamwidth 286 remains narrow throughout the depth for the annular array 285. However, this narrow beamwidth 286 limits an acceptable level of interrogation of the therapy beam both pre-focally (e.g. at tissue coupling) and post-focally (e.g., at bone).


In one embodiment, the annular array 285 is superior to standard imaging transducers because it can focus on the beam axis in transmit and receive. Just as the annular array 285 can focus in tissue, it can also effectively focus behind the transducer 285. This focus behind the imaging array 285 defocuses the acoustic energy propagating toward the tissue such that it is possible to better interrogate the coupling of the therapy behind at the acoustic window as well as the possibility of obstructions (e.g., bone) behind the therapy focus. FIG. 18 shows an embodiment of a virtual focus behind the annular imaging array 285 and the effective response toward the tissue. The defocused beam 286 spreads from the imaging array 285 toward the acoustic window such that a much larger percentage (e.g., 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, and any ranges or values therein) of the coupling for the therapy beam is interrogated. Another transmit focus depending on the specific beamwidth and penetration characteristics may be used to defocus the beam behind the therapy focus. This may be accomplished by placing a virtual focus behind the annular array 285 or a focus immediately in front to meet the required point-spread-function beamwidth when compared to the therapy beam. FIG. 19 shows an embodiment of a therapy beam 286 that quickly spreads behind the focus and the width of the imaging beam 286 may need to be slightly larger to search for tissues or implants that do not readily couple ultrasound energy (e.g. bone, intestines). In some embodiments, the goal is to better probe the acoustic window prior to the therapy focus and tissue behind the therapy focus to insure safe and efficacious treatment.


Vector Imaging


In some embodiments, defocusing the beam at the acoustic window and behind the therapy focus is advantageous to test for coupling and potential tissue impediments (e.g., bone, intestines) or implants. The processing and display of this information can be used by the system operator to make appropriate decisions without interfering with normal imaging. In one embodiment, in order to provide the information in a timely manner, the transmit-receive events with the defocused beam are be interwoven with standard imaging. This form of imaging enables the frame rates for regular B-mode imaging and the coupling pulses.



FIG. 20 shows an embodiment the time progression of the transmit-receive vectors for ordinary B-mode imaging. In standard imaging, the transmit-receive events occur when the annular array 285 is at the appropriate azimuth location (e.g. P1). In one embodiment, an ultrasound imaging and treatment system will utilize 1 to 4 transmit foci per imaging vector to generate a high resolution frame. FIG. 20 represents the position vector with a ‘P’ and then a number. In one embodiment, P1 has three transmits: TR1, TR2, and TR3. DF1 is an interrogation pulse to check if the system properly coupled to the tissue to be treated. In one embodiment, for 25 mm, the scan will consist of 501 vectors separated by 0.050 mm for a total imaging width of 25 mm. The transmit-receive event is represented with a ‘TR’ and then a number. FIG. 20 shows that three transmit-receive events are associated with each position, or in other words, there are three transmit foci for each vector position. When applying the defocused beam, it is not necessary to transmit at every position. This is because the beam has a much larger beamwidth than the sample spacing of 0.050 mm. Further, in one embodiment, the imaging beam width at the acoustic window for the defocused transmit is approximately 5 mm, then possibly the window is sampled every 0.5 mm. This is because there is really no additional information acquired by finer sampling. This type of imaging involves an interleaved (e.g., overlapping, etc.) imaging approach as shown in FIG. 21.


The vector imaging is similar in FIG. 21 as in FIG. 20 except that at P1 and then every 10 positions after than a defocused vector is acquired. Therefore, there are still 501 vectors acquired for the high resolution image. However, in addition to these 501 vectors, 51 vectors are acquired using the defocused transmit to assess coupling at the acoustic window. The 501 vectors and corresponding transmit-receive events are processed differently than the 51 vectors used to assess coupling. Note that this is only one method of vector sequencing. Because the high resolution imaging is oversampled laterally by approximately four to five beamwidths, it is possible to drop one sequence at a position and just perform defocused imaging. Averaging may be applied where defocused imaging is applied to interpolate between vectors. This would permit a shallow (e.g. at the acoustic window) and deep assessment (e.g. behind the focus) of the coupling and tissue to assess the safety and efficacy of therapy energy delivery. The type of sequencing is analogous to duplex imaging which perform B-mode and Doppler imaging simultaneously.


In embodiments where there is sufficient transmit sensitivity and receive signal-to-noise ratio, synthetic transmit and receive aperture imaging may be utilized to achieve optimal resolution in the ultrasound image and permit ample means to determine if there is sufficient coupling for the therapy transducer. FIG. 21 shows an embodiment where defocused transmit-receive events are interwoven with three standard focused transmit-receive events. This method may cause a compromise with the ultrasound image resolution. In one embodiment, illustrated at FIG. 22, a method transmits on each imaging array element separately and receive on the individual receive elements. After the data is digitized and stored for each of the eight transmit receive sequences as shown in the timing diagram, synthetic transmit and receive aperture methods are used to generate the optimal resolution for the ultrasound image and develop ideal beam widths to assess the coupling of the therapy transducer. Synthetic transmit and receive aperture methods simultaneously apply transmit and receive delays on post processed data for every spatial point in the ultrasound image. This technique yields ideal resolution throughout the entire ultrasound image when there is sufficient receive SNR at the cost of a reduced frame rate. The same method can be applied when interrogating the therapy beam cross-section.


Image Processing


In one embodiment, an advantage of using the defocused beam are to help the operator assess coupling and the tissue behind the acoustic focus. In one embodiment, a method to display the information includes calculating a brightness variance across the top of the image. A significant brightness variance off of the dermis strongly suggests insufficient coupling whereas uniform brightness suggests uniform coupling across the majority of the therapy beam. A brightness variance calculation would be the second moment of the speckle brightness over a specific depth such as 1 mm to 2 mm from the acoustic window.


In one embodiment, a two-dimensional (2D) filtering function is used to reduce the brightness variation that naturally occurs from the speckle. In one embodiment, a quantitative or qualitative variable is presented to the user along with the high resolution image to suggest the quality of coupling at the acoustic window or tissue behind the focus.


In one embodiment, the coupling assessment image is combined with the high resolution image. For example, the two images could be multiplied together. This will provide one image to the operator without removing any of the information from the high resolution image. The 2D multiplication (pixel-by-pixel) will show the shadowing from poor coupling on top of the high resolution image. The operator can then decide whether treatment is appropriate based on the amount of brightness shadowing. In one embodiment, the two images are blended together like an overlay which permits greater emphasis on either the high resolution image or the coupling assessment image. In one embodiment, overlapping images can be configured in a manner like images presented to radiologists when combining registered images from different systems (e.g. MRI and ultrasound).


Multifocal Zone Sequencing


In various embodiments, ultrasound imaging is used with a therapeutic tissue treatment. According to various embodiments, an ultrasound treatment system creates one, two or more simultaneous therapeutic treatment points and/or focal zones under the skin surface for a cosmetic treatment. In one embodiment, a treatment comprises mechanical dithering in which the therapy transducer is moved locally around the intended center of the thermal coagulation point (TCP). The acoustic beam movement can be side-to-side, up-down, and/or angular. In one embodiment of mechanical dithering, the movement of the motion mechanism is sufficiently fast enough to create a flatter temperature profile around the intended TCP which either allows a reduction of total acoustic energy for the same effected tissue volume or the same total acoustic energy for a larger effected tissue volume or any combination thereof. In accordance with various embodiments, frequency modulation modifies the location of a focal zone and/or spacing between the focal zones, such that electronic dithering of beam via modulation of the frequency precisely alters and/or moves the position of the beam focus point(s). For example, in one embodiment, a spacing of 1.5 mm can be dithered with +/−0.1 mm using a small frequency swing. In various embodiments, any one or more spacings of 0.5, 0.75, 1.0, 1.2, 1.5, 2.0 mm can be dithered with +/−0.01, 0.05, 0.1, 0.12, 0.15, 0.20, 0.25, 0.30 mm using a frequency swing. In various embodiments, a frequency is modulated by 1-200% (e.g., 1%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%. 100%, 120%, 150%, 180%, 200% and any range therein).


In various embodiments for improved ultrasound imaging, multiple focal zones are employed to obtain better signal quality and resolution through depth. For traditional, conventional diagnostic ultrasound scanners (linear, curvilinear, phased arrays, etc.), where the 2-D ultrasound images are formed without having to move the transducer, the sequence of acquiring these multiple focal zones are relatively inconsequential as precise placement of these focal zones can be controlled electronically. FIG. 23 illustrates a focal zone imaging that does not move while imaging, with electronically steered/translated aperture. For non-moving imaging transducers, focal zone positioning is precise, therefore focal zone sequencing is not employed. In traditional multiple focal zone imaging sequences, the order of the focal zone interrogation does vary. For example, a 4-focal zone sequence will follow the progression (f1, f2, f3, f4) independent of location and direction of motion.


However, for moving imaging transducers (e.g., mechanically translated or steered arrays), this becomes problematic, due to the positional differences of the transducer as it scans through the multiple focal zones. This positional mis-registration is particularly magnified when forming imaging bidirectionally (forming both left-to-right and right-to-left images), as the region of interrogation between the two images will be different. This principle is demonstrated in FIG. 24 in a linearly translating circumstance, but the disclosure applies to all types of motion, including but not limited to translational, rotational, and two-dimensional, or any combination thereof.


Embodiments of the imaging system disclosed herein address these misalignments. FIG. 24 illustrates bidirectional imaging at the same lateral location. In instances, spatial mis-registration occurs due to the fact that the transducer is moving while imaging. In particular, focal zone 4 (Fz4) can be seen to be farthest apart between the two images, although they should be interrogating the same region of interest. When forming a 2-D image with a mechanically translated/steered transducer, the transmit/receive position of the transducer will vary, due to the fact that during the propagation time associated with an ultrasound signal, the transducer has also moved.


In one embodiment, an alternative sequence is proposed such that the first direction-traveling (outbound) sequence shall proceed in order (f1, f2, f3, f4), but the second direction-traveling (returning) sequence is reversed (f4, f3, f2, f1), thereby allowing better registration of two images. In one embodiment, an alternative sequence is proposed such that the right-traveling (outbound) sequence shall proceed in order (f1, f2, f3, f4), but the left-traveling (returning) sequence is reversed (f4, f3, f2, f1), thereby allowing better registration of two images (FIG. 25). In various embodiments, a direction can be left, right, forward, backward, up, or down.



FIG. 25 illustrates an embodiment of directionally dependent focal zone sequencing. The left-traveling sequence is in reverse order relative to the right-traveling sequence. As a result, the focal zone alignment has been improved. Further, the positions of acquisitions can be staggered, such that the same regions of interest are better registered between these two images (FIG. 26).



FIG. 26 illustrates an embodiment of a directionally dependent focal zone sequencing with different triggering locations. The spatial registration between right traveling and left traveling A-lines has been further improved by staggering the triggering locations.


In an embodiment, an imaging system employs a novel sequence of two consecutive A-lines following progression of (line 1: f1, f2, f3, f4; line2: f4, f3, f2, f1) continuously. This sequence can be repeated across the entire field of view, and assuming an even number of vectors within the field of view, the returning sequence can have the exact same alternating pattern focal zone sequence, and the two images would be registered (FIG. 27).



FIG. 27 illustrates an embodiment of a directionally dependent focal zone sequencing with alternating between (f1-f2-f3-f4) and (f4-f3-f2-f1) on consecutive A-lines. If the entire field of view is spanned by an even number of A-lines, then the left-traveling and right-traveling focal sequences are the same. Triggering locations still vary between the two images.


In various embodiments, the multifocal zone imaging provides advantages for better correlation between first direction-traveling and second direction-traveling formed images.


In various embodiments, the multifocal zone imaging provides advantages for improved effectiveness of B-mode imaging at faster (e.g., 2×, 3×, 4×) the scanning rate.


In various embodiments, multifocal zone imaging is applied to any number of focal zones greater than one. In various embodiments, the number of focal zones is two, three, four, five, six, seven, eight, nine, ten, or more.


Transducers


In various embodiments, transducer 280 comprises a convex side 282 and a concave side 283. In various embodiments, a transducer 280 comprises a convex side 282 and a concave side 283 with features that provide for any one or more of variable depth, variable spacing, variable focus positioning, with one, two, three, four, or more simultaneous focus zones. FIG. 28 illustrates an embodiment of a transducer 280 comprising a single element with a convex side 282 and a concave side 283. FIG. 29 illustrates an embodiment of a transducer 280 comprising a solid, coated a convex side 282 and a striped a concave side 283, where the stripes comprise first poled and second poled regions, wherein a poled region is a positive, negative, or unpoled. FIG. 29 illustrates an embodiment of a transducer 280 comprising a solid, coated a convex side 282 and a striped a concave side 283, where the stripes comprise first regions and second regions, wherein a region can comprising a coating or no coating.



FIG. 30 illustrates an embodiment of a transducer 280 comprising a striped convex side 282 and a solid, coated concave side 283, where the stripes comprise first poled and second poled regions, wherein a poled region is a positive, negative, or unpoled. FIG. 30 illustrates an embodiment of a transducer 280 comprising a striped convex side 282 and a solid, coated concave side 283, where the stripes comprise first regions and second regions, wherein a region can comprising a coating or no coating.



FIG. 31 illustrates an embodiment of a transducer 280 comprising a striped convex side 282 and a striped concave side 283, where the stripes comprise first poled and second poled regions, wherein a poled region is a positive, negative, or unpoled, wherein the striped regions are rotated in an orientation of about 90 degrees with respect to each other. FIG. 31 illustrates an embodiment of a transducer 280 comprising a striped convex side 282 and a solid, coated concave side 283, where the stripes comprise first regions and second regions, wherein a region can comprising a coating or no coating, and wherein the stripes are rotated about 90 degrees with respect to each other.



FIG. 32 illustrates an embodiment of a transducer 280 comprising an annular convex side 282 and a striped concave side 283, where the stripes comprise first poled and second poled regions, wherein a poled region is a positive, negative, or unpoled. FIG. 32 illustrates an embodiment of a transducer 280 comprising an annular convex side 282 and a striped concave side 283, where the stripes comprise first regions and second regions, wherein a region can comprising a coating or no coating.



FIG. 33 illustrates an embodiment of a transducer 280 comprising a striped convex side 282 and an annular concave side 283, where the stripes comprise first poled and second poled regions, wherein a poled region is a positive, negative, or unpoled. FIG. 33 illustrates an embodiment of a transducer 280 comprising a striped convex side 282 and an annular concave side 283, where the stripes comprise first regions and second regions, wherein a region can comprising a coating or no coating. In some embodiments, the system comprises various features that are present as single features (as opposed to multiple features). For example, in one embodiment, the system comprises, consists essentially of, or consists of a single ultrasound transduction element that is adapted to provide two simultaneous treatment zones via dithering. Multiple features or components are provided in alternate embodiments.


Some embodiments and the examples described herein are examples and not intended to be limiting in describing the full scope of compositions and methods of these invention. Equivalent changes, modifications and variations of some embodiments, materials, compositions and methods can be made within the scope of the present invention, with substantially similar results.


While the invention is susceptible to various modifications, and alternative forms, specific examples thereof have been shown in the drawings and are herein described in detail. It should be understood, however, that the invention is not to be limited to the particular forms or methods disclosed, but to the contrary, the invention is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the various embodiments described and the appended claims. Any methods disclosed herein need not be performed in the order recited. The methods disclosed herein include certain actions taken by a practitioner; however, they can also include any third-party instruction of those actions, either expressly or by implication. For example, actions such as “coupling a transducer module with an ultrasonic probe” include “instructing the coupling of a transducer module with an ultrasonic probe.” The ranges disclosed herein also encompass any and all overlap, sub-ranges, and combinations thereof. Language such as “up to,” “at least,” “greater than,” “less than,” “between,” and the like includes the number recited. Numbers preceded by a term such as “about” or “approximately” include the recited numbers. For example, “about 25 mm” includes “25 mm.”

Claims
  • 1. An ultrasound treatment and imaging system configured for reducing imaging misalignment and further configured for applying precise ultrasonic therapy for lifting a brow, comprising: an ultrasonic probe adapted for placement at a skin surface of a face at the brow, the ultrasonic probe comprising:a hand wand and a removable transducer module,the removable transducer module configured for interchangeable coupling to the hand wand,the removable transducer module comprising an ultrasound therapy transducer,the ultrasound therapy transducer comprising a piezoelectrically active material,the piezoelectrically active material having a focal length, adapted to focus ultrasonic therapy to a tissue below the skin surface of the brow, the tissue comprising one or more of: a dermis, a hypodermis, a superficial muscular aponeurotic system (“SMAS”), and a muscle,wherein the ultrasound therapy transducer is configured to focus the ultrasonic therapy at a thermal coagulation point with an acoustic power in a range of 1 W to 100 W at a treatment frequency range selected from the group consisting of: 4 MHz, 7 MHz, and 10 MHz to thermally heat the tissue to cause coagulation to form a lesion at the thermal coagulation point,an ultrasound imaging transducer adapted for imaging the tissue at the brow,wherein the ultrasonic therapy is applied at the thermal coagulation point to form the lesion based on precise imaging alignment of the imaging of the tissue from the ultrasound imaging transducer to improve the effectiveness and safety of the ultrasonic therapy at the tissue at the brow comprising the one or more of: the dermis, the hypodermis, the SMAS, and the muscle;wherein the ultrasound therapy transducer and ultrasound imaging transducer are co-housed imaging/therapy transducers in an imaging-and-treatment module; anda motion mechanism configured for moving the co-housed imaging/therapy transducers within the imaging-and-treatment module in a first direction and a second direction configured for forming a plurality of the thermal coagulation points at the tissue at the brow, wherein the plurality of thermal coagulation points forms a plurality of the lesions at the tissue at the brow with a treatment spacing in a range from 0.01 mm to 25 mm,wherein the co-housed imaging/therapy transducers within the imaging-and-treatment module are mechanically attached to the motion mechanism,wherein the first direction is linear,wherein the second direction is linear,wherein the first direction is parallel to the second direction,wherein the first direction is opposite the second direction,wherein the ultrasound imaging transducer images with a first focal zone sequence order (f1, . . . , fN) or (fN, . . . , f1), where N>1 when travelling in the first direction,wherein the ultrasound imaging transducer images with a second focal zone sequence order (fN, . . . , f1) or (f1, . . . , fN) when travelling in the second direction,wherein a spatial registration between the ultrasound imaging transducer images with the first focal zone sequence order (f1, . . . , fN) or (fN, . . . , f1) in the first direction and the ultrasound imaging transducer images with the second focal zone sequence order (fN, . . . , f1) or (f1, . . . , fN) in the second direction is improved by staggering a triggering location,wherein the spatial registration improved by staggering the triggering location provides a better correlation between the ultrasound imaging transducer images at the brow with the first focal zone sequence order (f1, . . . , fN) or (fN, . . . , f1) in the first direction and the ultrasound imaging transducer images with the second focal zone sequence order (fN, . . . , f1) or (f1, . . . , fN) in the second direction,wherein the staggering comprises triggering an image acquisition at the brow at the triggering location over a time period,wherein the imaging-and-treatment module employs a directionally dependent focal zone sequencing of (f1- . . . -fN) and (f1- . . . -fN) or alternating between (f1- . . . -fN) and (fN- . . . -f1) on consecutive A-lines; anda control module coupled to the ultrasonic probe configured for controlling the ultrasound therapy transducer for treatment at the tissue at the brow and the ultrasound imaging transducer for imaging the tissue at the brow.
  • 2. The ultrasound treatment and imaging system of claim 1, wherein the second direction is the reversed path of the first direction,wherein the coagulation occurs at a treatment depth selected from the group consisting of: 4.5 mm, 3 mm, and 1.5 mm.
  • 3. The ultrasound treatment and imaging system of claim 1, wherein the first direction of motion occurs in multiple dimensions and the second direction is the reversed path of the first direction.
  • 4. The ultrasound treatment and imaging system of claim 1, wherein the ultrasound imaging transducer images with the first focal zone sequence order is specified as (f1, . . . , fN), where N>2.
  • 5. The ultrasound treatment and imaging system of claim 1, wherein the ultrasound therapy transducer is configured for treatment of tissue at a first set of locations that is positioned within a first cosmetic treatment zone and a second set of locations that is positioned within a second cosmetic treatment zone, the first zone being different from the second zone.
  • 6. The ultrasound treatment and imaging system of claim 1, wherein the ultrasound therapy transducer is adapted to apply the ultrasonic therapy using amplitude modulation whereby a plurality of portions of the ultrasound therapy transducer are adapted to emit ultrasonic therapy at a plurality of amplitudes of acoustic intensity, wherein a first amplitude is different than a second amplitude.
  • 7. The ultrasound treatment and imaging system of claim 6, wherein at least one portion of the ultrasound therapy transducer is adapted to emit the ultrasonic therapy at two or more amplitudes of acoustic intensity, and wherein the amplitude of the ultrasonic therapy emitted by the at least one portion of the ultrasound therapy transducer varies over time.
  • 8. The ultrasound treatment and imaging system of claim 6, wherein the plurality of portions of the ultrasound therapy transducer are adapted to create a plurality of corresponding piezoelectric material variations in response to an electric field applied to the ultrasound therapy transducer.
  • 9. The ultrasound treatment and imaging system of claim 8, wherein the plurality of piezoelectric material variations comprise at least one of expansion of the piezoelectrically active material of the plurality of portions of the ultrasound therapy transducer and contraction of the piezoelectrically active material of the plurality of portions of the ultrasound therapy transducer.
  • 10. The ultrasound treatment and imaging system of claim 1, wherein the ultrasound therapy transducer is adapted to apply the ultrasonic therapy via phase shifting whereby a plurality of portions of the ultrasound therapy transducer are adapted to emit the ultrasonic therapy at a plurality of phases of acoustic intensity, wherein a first phase is different than a second phase.
  • 11. The ultrasound treatment and imaging system of claim 1, wherein the ultrasound therapy transducer is adapted to apply an ultrasonic therapy using amplitude modulation, whereby a plurality of portions of the ultrasound therapy transducer are adapted to emit ultrasonic therapy at a plurality of amplitudes of acoustic intensity, wherein a first amplitude is different than a second amplitude; andwhereby the plurality of portions of the ultrasound therapy transducer are adapted to emit ultrasonic therapy at a plurality of phases of acoustic intensity, wherein a first phase is different than a second phase.
  • 12. The ultrasound treatment and imaging system of claim 1, wherein the ultrasound imaging transducer images with the first focal zone sequence order is specified as (f1, . . . , fN), where N>3.
  • 13. A method of reducing imaging misalignment in a bidirectionally moving ultrasound probe and performing precise ultrasonic therapy for lifting a brow, comprising: placing an ultrasound probe at a skin surface of a face at the brow, the ultrasound probe comprising a hand wand and a removable transducer module,the removable transducer module configured for interchangeable coupling to the hand wand,the removable transducer module comprising an ultrasound therapy transducer and an ultrasound imaging transducer;the ultrasound therapy transducer comprising a piezoelectrically active material,staggering a triggering location of a spatial registration between images from an ultrasound imaging transducer with a first focal zone sequence order (f1, . . . , fN) or (fN, . . . , f1) in a first direction and with a second focal zone sequence order (fN, . . . , f1) or (f1, . . . , fN) in a second direction with the ultrasound imaging transducer,wherein the staggering comprises triggering an image acquisition at the triggering location over a time period to improve the spatial registration by providing a better correlation between the ultrasound imaging transducer images with the first focal zone sequence order (f1, . . . , fN) or (fN, . . . , f1) in the first direction and the ultrasound imaging transducer images with the second focal zone sequence order (fN, . . . , f1) or (f1, . . . , fN) in the second direction,applying ultrasonic therapy to tissue below the skin surface at the brow, wherein the ultrasonic therapy is applied based on precise imaging alignment of the imaging of the tissue from the ultrasound imaging transducer to improve the effectiveness and safety of the ultrasonic therapy at the tissue below the skin surface at the brow, thereby thermally heating the tissue to cause coagulation at a thermal coagulation point to form a lesion by applying an acoustic power from the ultrasound therapy transducer in a range of 1 W to 100 W at a treatment frequency range selected from the group consisting of: 4 MHz, 7 MHz, and 10 MHz,wherein the ultrasound therapy transducer and ultrasound imaging transducer are co-housed imaging/therapy transducers, and a motion mechanism is configured for moving the co-housed imaging/therapy transducers in the first direction and the second direction,wherein the co-housed imaging/therapy transducers is mechanically attached to the motion mechanism,wherein the first direction is linear,wherein the second direction is linear,wherein the first direction is parallel to the second direction,wherein the first direction is opposite the second direction,wherein the ultrasound imaging transducer images with the first focal zone sequence order (f1, . . . , fN) or (fN, . . . , f1), with N>2, when travelling in the first direction,wherein the ultrasound imaging transducer images with the second focal zone sequence order (fN, . . . , f1) or (f1, . . . , fN) when travelling in the second direction,wherein the staggering comprises such that a region of interest is registered between the first focal zone sequence order (f1, . . . , fN) or (fN, . . . , ft) and the second focal zone sequence order (f N, . . . , f1) or (f1, . . . , fN).
  • 14. The method of claim 13, wherein N=any one of the group consisting of: 3, 4, 5, 6, 7, 8, 9, and 10,wherein the coagulation occurs at a treatment depth selected from the group consisting of: 4.5 mm, 3 mm, and 1.5 mm.
  • 15. The method of claim 13, wherein the ultrasound therapy transducer is adapted to apply ultrasonic therapy via phase shifting whereby a plurality of portions of the ultrasound therapy transducer are adapted to emit the ultrasonic therapy at a plurality of phases of acoustic intensity, wherein a first phase is different than a second phase.
  • 16. An ultrasound module configured for reducing imaging misalignment and further configured for applying precise ultrasonic therapy for lifting a brow on a face, comprising: an ultrasound therapy transducer adapted for placement at a skin surface on the face at the brow, the ultrasound therapy transducer being adapted to apply ultrasonic therapy to tissue below the brow, the tissue comprising one or more of: an epidermis, a dermis, a hypodermis, and a superficial muscular aponeurotic system (“SMAS”),wherein the ultrasound therapy transducer is configured to apply the ultrasonic therapy at an acoustic power in a range of 1 W to 100 W at a frequency range selected from the group consisting of: 4 MHz, 7 MHz, and 10 MHz to thermally heat the tissue below the brow to cause coagulation forming a lesion at a thermal coagulation point,wherein the ultrasonic therapy is applied based on precise imaging alignment of the imaging of the tissue from an ultrasound imaging transducer to improve the effectiveness and safety of the ultrasonic therapy at the tissue comprising the one or more of: the dermis, the hypodermis, the fascia, and the superficial muscular aponeurotic system;the ultrasound imaging transducer adapted for imaging the tissue,wherein the ultrasound therapy transducer and ultrasound imaging transducer are co-housed imaging/therapy transducers in an imaging-and-treatment module; anda linear motion mechanism configured for moving the co-housed imaging/therapy transducers in a first linear direction and a second linear direction,wherein the co-housed imaging/therapy transducers are mechanically attached to the linear motion mechanism,wherein the linear motion mechanism forms a plurality of the thermal coagulation points, wherein the plurality of thermal coagulation points forms a plurality of the lesions with a treatment spacing in a range from 0.01 mm to 25 mm,wherein the first linear direction is opposite the second linear direction,wherein the ultrasound imaging transducer images with a first focal zone sequence order (f1, . . . , fN) or (fN, . . . , f1), where N>1 when travelling in the first linear direction,wherein the ultrasound imaging transducer images with a second focal zone sequence order (fN, . . . , f1) or (f1, . . . , fN) when travelling in the second linear direction,wherein a spatial registration between imaging in the first linear direction and the second linear direction is improved by staggering a triggering location such that a region of interest is registered between the first focal zone sequence order (f1, . . . , fN) and the second focal zone sequence order (fN, . . . , f1) or (f1, . . . , fN),wherein the spatial registration improved by staggering the triggering location provides a better correlation between the ultrasound imaging transducer images with the first focal zone sequence order (f1, . . . , fN) or (fN, . . . , f1) in the first linear direction and the ultrasound imaging transducer images with the second focal zone sequence order (fN, . . . , f1) or (f1, fN) in the second linear direction,wherein the staggering comprises triggering an image acquisition at the triggering location over a time period,wherein the ultrasound module employs a directionally dependent focal zone sequencing of (f1- . . . -fN) and (f1- . . . -fN) or alternating between (f1- . . . -fN) and (fN- . . . -f1) on consecutive A-lines.
  • 17. The ultrasound module of claim 16, wherein the ultrasound therapy transducer is adapted to apply ultrasonic therapy using amplitude modulation whereby a plurality of portions of the ultrasound therapy transducer are adapted to emit ultrasonic therapy at a plurality of amplitudes of acoustic intensity, wherein a first amplitude is different than a second amplitude.
  • 18. The ultrasound module of claim 16, wherein the ultrasound therapy transducer is adapted to apply ultrasonic therapy via phase shifting whereby a plurality of portions of the ultrasound therapy transducer are adapted to emit ultrasonic therapy at a plurality of phases of acoustic intensity, wherein a first phase is different than a second phase.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a U.S. National Phase of PCT Application No. PCT/US2017/046703, filed Aug. 14, 2017, which claims the benefit of priority from U.S. Provisional Application No. 62/375,607 filed Aug. 16, 2016, U.S. Provisional Application No. 62/482,476 filed Apr. 6, 2017, U.S. Provisional Application No. 62/482,440 filed Apr. 6, 2017, and U.S. Provisional Application No. 62/520,055 filed Jun. 15, 2017, each of which is incorporated in its entirety by reference, herein. Any and all priority claims identified in the Application Data Sheet, or any correction thereto, are hereby incorporated by reference under 37 CFR 1.57.

PCT Information
Filing Document Filing Date Country Kind
PCT/US2017/046703 8/14/2017 WO 00
Publishing Document Publishing Date Country Kind
WO2018/035012 2/22/2018 WO A
US Referenced Citations (1223)
Number Name Date Kind
2427348 Bond et al. Sep 1947 A
2792829 Calosi Feb 1952 A
3913386 Saglio Oct 1975 A
3965455 Hurwitz Jun 1976 A
3992925 Perilhou Nov 1976 A
4039312 Patru Aug 1977 A
4059098 Murdock Nov 1977 A
4101795 Fukumoto Jul 1978 A
4151834 Sato et al. May 1979 A
4166967 Benes et al. Sep 1979 A
4211948 Smith et al. Jul 1980 A
4211949 Brisken et al. Jul 1980 A
4213344 Rose Jul 1980 A
4276491 Daniel Jun 1981 A
4315514 Drewes et al. Feb 1982 A
4325381 Glenn Apr 1982 A
4343301 Indech Aug 1982 A
4372296 Fahim Feb 1983 A
4379145 Masuho et al. Apr 1983 A
4381007 Doss Apr 1983 A
4381787 Hottinger May 1983 A
4397314 Vaguine Aug 1983 A
4409839 Taenzer Oct 1983 A
4417170 Benisncasa Nov 1983 A
4431008 Wanner et al. Feb 1984 A
4441486 Pounds Apr 1984 A
4452084 Taenzer Jun 1984 A
4484569 Driller Nov 1984 A
4507582 Glenn Mar 1985 A
4513749 Kino Apr 1985 A
4513750 Heyman et al. Apr 1985 A
4527550 Ruggera et al. Jul 1985 A
4528979 Marchenko Jul 1985 A
4534221 Fife et al. Aug 1985 A
4566459 Umemura et al. Jan 1986 A
4567895 Putzke Feb 1986 A
4586512 Do-Huu May 1986 A
4587971 Stolfi May 1986 A
4601296 Yerushalmi Jul 1986 A
4620546 Aida et al. Nov 1986 A
4637256 Sugiyama et al. Jan 1987 A
4646756 Watmough Mar 1987 A
4663358 Hyon May 1987 A
4668516 Duraffourd et al. May 1987 A
4672591 Breimesser et al. Jun 1987 A
4680499 Umemura et al. Jul 1987 A
4697588 Reichenberger Oct 1987 A
4754760 Fukukita et al. Jul 1988 A
4757820 Itoh Jul 1988 A
4771205 Mequio Sep 1988 A
4801459 Liburdy Jan 1989 A
4803625 Fu et al. Feb 1989 A
4807633 Fry Feb 1989 A
4817615 Fukukita et al. Apr 1989 A
4858613 Fry Aug 1989 A
4860732 Hasegawa et al. Aug 1989 A
4865041 Hassler Sep 1989 A
4865042 Umemura Sep 1989 A
4867169 Machida Sep 1989 A
4874562 Hyon Oct 1989 A
4875487 Seppi Oct 1989 A
4881212 Takeuchi Nov 1989 A
4891043 Zeimer et al. Jan 1990 A
4893624 Lele Jan 1990 A
4896673 Rose Jan 1990 A
4900540 Ryan et al. Feb 1990 A
4901729 Saitoh Feb 1990 A
4917096 Englehart Apr 1990 A
4932414 Coleman et al. Jun 1990 A
4938216 Lele Jul 1990 A
4938217 Lele Jul 1990 A
4947046 Kawabata et al. Aug 1990 A
4951653 Fry Aug 1990 A
4955365 Fry Sep 1990 A
4958626 Nambu Sep 1990 A
4976709 Sand Dec 1990 A
4979501 Valchanov Dec 1990 A
4992989 Watanabe et al. Feb 1991 A
5012797 Liang May 1991 A
5018508 Fry et al. May 1991 A
5030874 Saito et al. Jul 1991 A
5036855 Fry Aug 1991 A
5040537 Katakura Aug 1991 A
5054310 Flynn Oct 1991 A
5054470 Fry Oct 1991 A
5054491 Saito et al. Oct 1991 A
5070879 Herres Dec 1991 A
5088495 Miyagawa Feb 1992 A
5115814 Griffith May 1992 A
5117832 Sanghvi Jun 1992 A
5123418 Saurel Jun 1992 A
5142511 Kanai et al. Aug 1992 A
5143063 Fellner Sep 1992 A
5143074 Dory Sep 1992 A
5149319 Unger Sep 1992 A
5150711 Dory Sep 1992 A
5150714 Green Sep 1992 A
5152294 Mochizuki et al. Oct 1992 A
5156144 Iwasaki Oct 1992 A
5158536 Sekins Oct 1992 A
5159931 Pini Nov 1992 A
5163421 Bernstein Nov 1992 A
5163436 Saitoh et al. Nov 1992 A
5178135 Uchiyama et al. Jan 1993 A
5190518 Takasu Mar 1993 A
5190766 Ishihara Mar 1993 A
5191880 McLeod Mar 1993 A
5205287 Erbel et al. Apr 1993 A
5209720 Unger May 1993 A
5212671 Fujii et al. May 1993 A
5215680 D'Arrigo Jun 1993 A
5224467 Oku Jul 1993 A
5230334 Klopotek Jul 1993 A
5230338 Allen et al. Jul 1993 A
5247924 Suzuki et al. Sep 1993 A
5255681 Ishimura et al. Oct 1993 A
5257970 Dougherty Nov 1993 A
5265614 Hayakawa Nov 1993 A
5267985 Shimada Dec 1993 A
5269297 Weng Dec 1993 A
5282797 Chess Feb 1994 A
5295484 Marcus Mar 1994 A
5295486 Wollschlager et al. Mar 1994 A
5304169 Sand Apr 1994 A
5305756 Entrekin et al. Apr 1994 A
5321520 Inga et al. Jun 1994 A
5323779 Hardy et al. Jun 1994 A
5327895 Hashimoto et al. Jul 1994 A
5329202 Garlick et al. Jul 1994 A
5348016 Unger et al. Sep 1994 A
5358466 Aida et al. Oct 1994 A
5360268 Hayashi Nov 1994 A
5370121 Reichenberger Dec 1994 A
5370122 Kunig Dec 1994 A
5371483 Bhardwaj Dec 1994 A
5375602 Lancee et al. Dec 1994 A
5379773 Hornsby Jan 1995 A
5380280 Peterson Jan 1995 A
5380519 Schneider et al. Jan 1995 A
5383917 Desai et al. Jan 1995 A
5391140 Schaetzle et al. Feb 1995 A
5391197 Burdette et al. Feb 1995 A
5392259 Bolorforosh Feb 1995 A
5396143 Seyed-Bolorforosh et al. Mar 1995 A
5398689 Connor et al. Mar 1995 A
5406503 Williams Apr 1995 A
5413550 Castel May 1995 A
5417216 Tanaka May 1995 A
5423220 Finsterwald et al. Jun 1995 A
5435311 Umemura Jul 1995 A
5438998 Hanafy Aug 1995 A
5443068 Cline et al. Aug 1995 A
5445611 Eppstein et al. Aug 1995 A
5458596 Lax Oct 1995 A
5460179 Okunuki et al. Oct 1995 A
5460595 Hall et al. Oct 1995 A
5419327 Rohwedder Nov 1995 A
5469854 Unger et al. Nov 1995 A
5471488 Fujio Dec 1995 A
5472405 Buchholtz et al. Dec 1995 A
5487388 Rello et al. Jan 1996 A
5492126 Hennige Feb 1996 A
5496256 Bock Mar 1996 A
5501655 Rolt Mar 1996 A
5503152 Oakley et al. Apr 1996 A
5503320 Webster et al. Apr 1996 A
5507790 Weiss Apr 1996 A
5511296 Dias et al. Apr 1996 A
5520188 Hennige May 1996 A
5522869 Burdette Jun 1996 A
5523058 Umemura et al. Jun 1996 A
5524620 Rosenchein Jun 1996 A
5524624 Tepper Jun 1996 A
5524625 Okazaki Jun 1996 A
5526624 Berg Jun 1996 A
5526812 Dumoulin et al. Jun 1996 A
5526814 Cline et al. Jun 1996 A
5526815 Granz Jun 1996 A
5529070 Augustine et al. Jun 1996 A
5540235 Wilson Jul 1996 A
5558092 Unger Sep 1996 A
5560362 Sliwa et al. Oct 1996 A
5573497 Chapelon Nov 1996 A
5575291 Hayakawa Nov 1996 A
5575807 Faller Nov 1996 A
5577502 Darrow et al. Nov 1996 A
5577507 Snyder et al. Nov 1996 A
5577991 Akui et al. Nov 1996 A
5580575 Unger et al. Dec 1996 A
5643179 Fujimoto Jan 1997 A
5601526 Chapelon Feb 1997 A
5603323 Pflugrath et al. Feb 1997 A
5605154 Ries et al. Feb 1997 A
5609562 Kaali Mar 1997 A
5615091 Palatnik Mar 1997 A
5618275 Bock Apr 1997 A
5620479 Diederich Apr 1997 A
5622175 Sudol et al. Apr 1997 A
5617858 Taverna et al. May 1997 A
5638819 Manwaring et al. Jun 1997 A
5644085 Lorraine et al. Jul 1997 A
5647373 Paltieli Jul 1997 A
5655535 Frlemel et al. Aug 1997 A
5655538 Lorraine Aug 1997 A
5657760 Ying Aug 1997 A
5658328 Johnson Aug 1997 A
5660836 Knowlton Aug 1997 A
5662116 Kondo Sep 1997 A
5665053 Jacobs Sep 1997 A
5665141 Vago Sep 1997 A
5671746 Dreschel et al. Sep 1997 A
5673699 Trahey et al. Oct 1997 A
5676692 Sanghvi Oct 1997 A
5677491 Ishrak Oct 1997 A
5685820 Riek et al. Nov 1997 A
5690608 Watanabe Nov 1997 A
5694936 Fujimoto Dec 1997 A
5697897 Buchholtz Dec 1997 A
5701900 Shehada et al. Dec 1997 A
5704361 Seward et al. Jan 1998 A
5706252 Le Verrier et al. Jan 1998 A
5706564 Rhyne Jan 1998 A
5715823 Wood et al. Feb 1998 A
5720287 Chapelon et al. Feb 1998 A
5722411 Suzuki Mar 1998 A
5727554 Kalend et al. Mar 1998 A
5735280 Sherman et al. Apr 1998 A
5740804 Cerofolini Apr 1998 A
5743863 Chapelon Apr 1998 A
5746005 Steinberg May 1998 A
5746762 Bass May 1998 A
5748767 Raab May 1998 A
5749364 Sliwa et al. May 1998 A
5755228 Wilson et al. May 1998 A
5755753 Knowlton May 1998 A
5762066 Law Jun 1998 A
5763886 Schulte Jun 1998 A
5769790 Watkins Jun 1998 A
5779644 Eberle et al. Jul 1998 A
5792058 Lee Aug 1998 A
5795297 Daigle Aug 1998 A
5795311 Wess Aug 1998 A
5810009 Mine et al. Sep 1998 A
5810888 Fenn Sep 1998 A
5814599 Mitragotri et al. Sep 1998 A
5817013 Ginn et al. Oct 1998 A
5817021 Reichenberger Oct 1998 A
5820564 Slayton Oct 1998 A
5823962 Schaetzle Oct 1998 A
5827204 Grandia et al. Oct 1998 A
5840032 Hatfield et al. Nov 1998 A
5844140 Seale Dec 1998 A
5853367 Chalek et al. Dec 1998 A
5866024 de Villeneuve Feb 1999 A
5869751 Bonin Feb 1999 A
5871524 Knowlton Feb 1999 A
5873902 Sanghvi Feb 1999 A
5876341 Wang et al. Mar 1999 A
5879303 Averkiou et al. Mar 1999 A
5882557 Hayakawa Mar 1999 A
5891034 Bucholz Apr 1999 A
5895356 Andrus et al. Apr 1999 A
5899861 Friemel et al. May 1999 A
5904659 Duarte May 1999 A
5919219 Knowlton Jul 1999 A
5923099 Bilir Jul 1999 A
5924989 Polz Jul 1999 A
5928169 Schatzle et al. Jul 1999 A
5931805 Brisken Aug 1999 A
5938606 Bonnefous Aug 1999 A
5938612 Kline-Schoder Aug 1999 A
5948011 Knowlton Sep 1999 A
5957844 Dekel Sep 1999 A
5957882 Nita et al. Sep 1999 A
5957941 Ream Sep 1999 A
5964707 Fenster et al. Oct 1999 A
5967980 Ferre et al. Oct 1999 A
5968034 Fullmer Oct 1999 A
5971949 Levin Oct 1999 A
5977538 Unger et al. Nov 1999 A
5984881 Ishibashi et al. Nov 1999 A
5984882 Rosenchein Nov 1999 A
5990598 Sudol et al. Nov 1999 A
5997471 Gumb et al. Dec 1999 A
5997497 Nita et al. Dec 1999 A
5999843 Anbar Dec 1999 A
6004262 Putz et al. Dec 1999 A
6007499 Martin et al. Dec 1999 A
6013032 Savord Jan 2000 A
6014473 Hossack et al. Jan 2000 A
6016255 Bolan et al. Jan 2000 A
6019724 Gronningsaeter et al. Feb 2000 A
6022308 Williams Feb 2000 A
6022317 Cruanas et al. Feb 2000 A
6022327 Chang Feb 2000 A
6030374 McDaniel Feb 2000 A
6036646 Barthe Mar 2000 A
6039048 Silberg Mar 2000 A
6039689 Lizzi Mar 2000 A
6042556 Beach Mar 2000 A
6049159 Barthe Apr 2000 A
6050943 Slayton Apr 2000 A
6059727 Fowlkes May 2000 A
6071239 Cribbs Jun 2000 A
6080108 Dunham Jun 2000 A
6083148 Williams Jul 2000 A
6086535 Ishibashi Jul 2000 A
6086580 Mordon et al. Jul 2000 A
6090054 Tagishi Jul 2000 A
6093148 Fujimoto Jul 2000 A
6093883 Sanghvi Jul 2000 A
6100626 Frey et al. Aug 2000 A
6101407 Groezinger Aug 2000 A
6106469 Suzuki et al. Aug 2000 A
6113558 Rosenchein Sep 2000 A
6113559 Klopotek Sep 2000 A
6120452 Barthe Sep 2000 A
6123081 Durette Sep 2000 A
6126619 Peterson et al. Oct 2000 A
6135971 Hutchinson Oct 2000 A
6139499 Wilk Oct 2000 A
6159150 Yale et al. Dec 2000 A
6171244 Finger et al. Jan 2001 B1
6176840 Nishimura Jan 2001 B1
6183426 Akisada Feb 2001 B1
6183502 Takeuchi Feb 2001 B1
6183773 Anderson Feb 2001 B1
6190323 Dias Feb 2001 B1
6190336 Duarte Feb 2001 B1
6193658 Wendelken Feb 2001 B1
6198956 Dunne Mar 2001 B1
6210327 Brackett et al. Apr 2001 B1
6213948 Barthe Apr 2001 B1
6216029 Paltieli Apr 2001 B1
6233476 Strommer et al. May 2001 B1
6234990 Rowe et al. May 2001 B1
6241753 Knowlton Jun 2001 B1
6246898 Vesely et al. Jun 2001 B1
6251074 Averkiou et al. Jun 2001 B1
6251088 Kaufman et al. Jun 2001 B1
6268405 Yao Jul 2001 B1
6273864 Duarte Aug 2001 B1
6280402 Ishibashi et al. Aug 2001 B1
6287257 Matichuk Sep 2001 B1
6287304 Eggers et al. Sep 2001 B1
6296619 Brisken Oct 2001 B1
6301989 Brown et al. Oct 2001 B1
6307302 Toda Oct 2001 B1
6309355 Cain et al. Oct 2001 B1
6311090 Knowlton Oct 2001 B1
6315741 Martin Nov 2001 B1
6322509 Pan et al. Nov 2001 B1
6322532 D'Sa Nov 2001 B1
6325540 Lounsberry et al. Dec 2001 B1
6325758 Carol et al. Dec 2001 B1
6325769 Klopotek Dec 2001 B1
6325798 Edwards et al. Dec 2001 B1
6338716 Hossack et al. Jan 2002 B1
6350276 Knowlton Feb 2002 B1
6356780 Licato et al. Mar 2002 B1
6361531 Hissong Mar 2002 B1
6370411 Osadchy et al. Apr 2002 B1
6375672 Aksan Apr 2002 B1
6377854 Knowlton Apr 2002 B1
6377855 Knowlton Apr 2002 B1
6381497 Knowlton Apr 2002 B1
6381498 Knowlton Apr 2002 B1
6387380 Knowlton May 2002 B1
6390982 Bova et al. May 2002 B1
6405090 Knowlton Jun 2002 B1
6409720 Hissong Jun 2002 B1
6413216 Cain et al. Jul 2002 B1
6413253 Koop Jul 2002 B1
6413254 Hissong Jul 2002 B1
6419648 Vitek Jul 2002 B1
6423007 Lizzi et al. Jul 2002 B2
6425865 Salcudean Jul 2002 B1
6425867 Vaezy Jul 2002 B1
6425912 Knowlton Jul 2002 B1
6428477 Mason Aug 2002 B1
6428532 Doukas Aug 2002 B1
6430446 Knowlton Aug 2002 B1
6432057 Mazess et al. Aug 2002 B1
6432067 Martin Aug 2002 B1
6432101 Weber Aug 2002 B1
6436061 Costantino Aug 2002 B1
6438424 Knowlton Aug 2002 B1
6440071 Slayton Aug 2002 B1
6440121 Weber Aug 2002 B1
6443914 Costantino Sep 2002 B1
6447443 Keogh et al. Sep 2002 B1
6450979 Miwa et al. Sep 2002 B1
6451013 Bays et al. Sep 2002 B1
6453202 Knowlton Sep 2002 B1
6461304 Tanaka et al. Oct 2002 B1
6461378 Knowlton Oct 2002 B1
6470216 Knowlton Oct 2002 B1
6485420 Bullis Nov 2002 B1
6488626 Lizzi Dec 2002 B1
6491657 Rowe Dec 2002 B2
6500121 Slayton Dec 2002 B1
6500141 Irion Dec 2002 B1
6506171 Vitek et al. Jan 2003 B1
6508774 Acker Jan 2003 B1
6511427 Sliwa, Jr. et al. Jan 2003 B1
6511428 Azuma Jan 2003 B1
6514244 Pope Feb 2003 B2
6517484 Wilk Feb 2003 B1
6524250 Weber Feb 2003 B1
6666835 Martin Mar 2003 B2
6540679 Slayton Apr 2003 B2
6540685 Rhoads et al. Apr 2003 B1
6540700 Fujimoto et al. Apr 2003 B1
6547788 Maguire et al. Apr 2003 B1
6554771 Buil et al. Apr 2003 B1
6569099 Babaev May 2003 B1
6569108 Sarvazyan et al. May 2003 B2
6572552 Fukukita Jun 2003 B2
6575956 Brisken et al. Jun 2003 B1
6595934 Hissong Jul 2003 B1
6599256 Acker Jul 2003 B1
6605043 Dreschel Aug 2003 B1
6605080 Altshuler et al. Aug 2003 B1
6607498 Eshel Aug 2003 B2
6618620 Freundlich et al. Sep 2003 B1
6623430 Slayton Sep 2003 B1
6626854 Friedman Sep 2003 B2
6626855 Weng Sep 2003 B1
6638226 He et al. Oct 2003 B2
6645145 Dreschel et al. Nov 2003 B1
6645150 Angelsen et al. Nov 2003 B2
6645162 Friedman Nov 2003 B2
6662054 Kreindel Dec 2003 B2
6663627 Francischelli Dec 2003 B2
6665806 Shimizu Dec 2003 B1
6669638 Miller Dec 2003 B1
6685639 Wang et al. Feb 2004 B1
6685640 Fry Feb 2004 B1
6692450 Coleman Feb 2004 B1
6699237 Weber Mar 2004 B2
6716184 Vaezy et al. Apr 2004 B2
6719449 Laughlin Apr 2004 B1
6719694 Weng Apr 2004 B2
6726627 Lizzi et al. Apr 2004 B1
6733449 Krishnamurthy et al. May 2004 B1
6749624 Knowlton Jun 2004 B2
6772490 Toda Aug 2004 B2
6773409 Truckai et al. Aug 2004 B2
6775404 Pagoulatos et al. Aug 2004 B1
6790187 Thompson et al. Sep 2004 B2
6824516 Batten et al. Nov 2004 B2
6825176 White et al. Nov 2004 B2
6835940 Morikawa et al. Dec 2004 B2
6846290 Lizzi et al. Jan 2005 B2
6875176 Mourad et al. Apr 2005 B2
6882884 Mosk et al. Apr 2005 B1
6887239 Elstrom May 2005 B2
6887260 McDaniel May 2005 B1
6889089 Behl May 2005 B2
6896657 Willis May 2005 B2
6902536 Manna Jun 2005 B2
6905466 Salgo Jun 2005 B2
6918907 Kelly Jul 2005 B2
6920883 Bessette Jul 2005 B2
6921371 Wilson Jul 2005 B2
6932771 Whitmore Aug 2005 B2
6932814 Wood Aug 2005 B2
6936044 McDaniel Aug 2005 B2
6936046 Hissong Aug 2005 B2
6945937 Culp et al. Sep 2005 B2
6948843 Laugharn et al. Sep 2005 B2
6953941 Nakano et al. Oct 2005 B2
6958043 Hissong Oct 2005 B2
6971994 Young et al. Dec 2005 B1
6974417 Lockwood Dec 2005 B2
6976492 Ingle Dec 2005 B2
6992305 Maezawa et al. Jan 2006 B2
6997923 Anderson Feb 2006 B2
7006874 Knowlton Feb 2006 B2
7020528 Neev Mar 2006 B2
7022089 Ooba Apr 2006 B2
7058440 Heuscher et al. Jun 2006 B2
7063666 Weng Jun 2006 B2
7070565 Vaezy et al. Jul 2006 B2
7074218 Washington et al. Jul 2006 B2
7094252 Koop Aug 2006 B2
7108663 Talish et al. Sep 2006 B2
7115123 Knowlton Oct 2006 B2
7122029 Koop et al. Oct 2006 B2
7142905 Slayton Nov 2006 B2
7165451 Brooks et al. Jan 2007 B1
7179238 Hissong Feb 2007 B2
7189230 Knowlton Mar 2007 B2
7229411 Slayton Jun 2007 B2
7235592 Muratoglu Jun 2007 B2
7258674 Cribbs Aug 2007 B2
7273459 Desilets Sep 2007 B2
7294125 Phalen et al. Nov 2007 B2
7297117 Trucco Nov 2007 B2
7303555 Makin et al. Dec 2007 B2
7311679 Desilets et al. Dec 2007 B2
7327071 Nishiyama et al. Feb 2008 B2
7331951 Eshel et al. Feb 2008 B2
7332985 Larson et al. Feb 2008 B2
7338434 Haarstad et al. Mar 2008 B1
7347855 Eshel Mar 2008 B2
RE40403 Cho et al. Jun 2008 E
7393325 Barthe Jul 2008 B2
7398116 Edwards Jul 2008 B2
7399279 Abend et al. Jul 2008 B2
7491171 Barthe et al. Feb 2009 B2
7507235 Keogh et al. Mar 2009 B2
7510536 Foley et al. Mar 2009 B2
7517315 Willis Apr 2009 B2
7530356 Slayton May 2009 B2
7530958 Slayton May 2009 B2
7532201 Quistgaard et al. May 2009 B2
7571336 Barthe Aug 2009 B2
7601120 Moilanen et al. Oct 2009 B2
7615015 Coleman Nov 2009 B2
7615016 Barthe Nov 2009 B2
7652411 Crunkilton et al. Jan 2010 B2
7662114 Seip et al. Feb 2010 B2
7674257 Pless et al. Mar 2010 B2
7686763 Vaezy et al. Mar 2010 B2
7713203 Lacoste et al. Mar 2010 B2
7694406 Wildes et al. Apr 2010 B2
7695437 Quistgaard et al. Apr 2010 B2
7727156 Angelsen et al. Jun 2010 B2
7758524 Barthe Jul 2010 B2
7766848 Desilets et al. Aug 2010 B2
7789841 Huckle et al. Sep 2010 B2
7806839 Mast et al. Oct 2010 B2
7815570 Eshel et al. Oct 2010 B2
7819826 Diederich et al. Oct 2010 B2
7828734 Azhari et al. Oct 2010 B2
7824348 Barthe Nov 2010 B2
7833162 Hasegawa et al. Nov 2010 B2
7841984 Cribbs et al. Nov 2010 B2
7846096 Mast et al. Dec 2010 B2
7857773 Desilets et al. Dec 2010 B2
7875023 Eshel et al. Jan 2011 B2
7901359 Mandrusov et al. Mar 2011 B2
7905007 Calisti et al. Mar 2011 B2
7905844 Desilets et al. Mar 2011 B2
7914453 Slayton et al. Mar 2011 B2
7914469 Torbati Mar 2011 B2
7955281 Pedersen et al. Jun 2011 B2
7967764 Lidgren et al. Jun 2011 B2
7967839 Flock et al. Jun 2011 B2
7955262 Rosenberg Jul 2011 B2
7993289 Quistgaard et al. Aug 2011 B2
8057465 Sliwa, Jr. et al. Sep 2011 B2
8057389 Barthe et al. Nov 2011 B2
8066641 Barthe et al. Nov 2011 B2
8123707 Huckle et al. Feb 2012 B2
8128618 Gliklich et al. Mar 2012 B2
8133180 Slayton et al. Mar 2012 B2
8133191 Rosenberg et al. Mar 2012 B2
8142200 Crunkilton et al. Mar 2012 B2
8152904 Slobodzian et al. Apr 2012 B2
8162858 Manna et al. Apr 2012 B2
8166332 Barthe et al. Apr 2012 B2
8182428 Angelsen et al. May 2012 B2
8197409 Foley et al. Jun 2012 B2
8206299 Foley et al. Jun 2012 B2
8208346 Crunkilton Jun 2012 B2
8211017 Foley et al. Jul 2012 B2
8262591 Pedersen et al. Sep 2012 B2
8262650 Zanelli et al. Sep 2012 B2
8264126 Toda et al. Sep 2012 B2
8273037 Kreindel et al. Sep 2012 B2
8282554 Makin et al. Oct 2012 B2
8292835 Cimino Oct 2012 B1
8298163 Cimino Oct 2012 B1
8333700 Barthe et al. Dec 2012 B1
8334637 Crunkilton et al. Dec 2012 B2
8337407 Quistgaard et al. Dec 2012 B2
8343051 Desilets et al. Jan 2013 B2
8454540 Eshel et al. Jan 2013 B2
8366622 Slayton et al. Feb 2013 B2
8398549 Palmeri et al. Mar 2013 B2
8409097 Slayton et al. Apr 2013 B2
8425435 Wing et al. Apr 2013 B2
8388535 Weng et al. May 2013 B2
8444562 Barthe et al. May 2013 B2
8460193 Barthe et al. Jun 2013 B2
8480585 Slayton et al. Jul 2013 B2
8486001 Weyant Jul 2013 B2
8506486 Slayton et al. Aug 2013 B2
8512250 Quistgaard et al. Aug 2013 B2
8523775 Barthe et al. Sep 2013 B2
8523849 Liu et al. Sep 2013 B2
8535228 Slayton et al. Sep 2013 B2
8570837 Toda et al. Oct 2013 B2
8573392 Bennett et al. Nov 2013 B2
8583211 Salomir et al. Nov 2013 B2
8585618 Hunziker et al. Nov 2013 B2
8604672 Toda et al. Dec 2013 B2
8622937 Weng et al. Jan 2014 B2
8636665 Slayton et al. Jan 2014 B2
8641622 Barthe et al. Feb 2014 B2
8663112 Slayton et al. Mar 2014 B2
8672848 Slayton et al. Mar 2014 B2
8690778 Slayton et al. Apr 2014 B2
8690779 Slayton et al. Apr 2014 B2
8690780 Slayton et al. Apr 2014 B2
8708935 Barthe et al. Apr 2014 B2
8715186 Slayton et al. May 2014 B2
8726781 Eckhoff et al. May 2014 B2
8728071 Lischinsky et al. May 2014 B2
8753295 Thierman Jun 2014 B2
8758253 Sano et al. Jun 2014 B2
8836203 Nobles et al. Sep 2014 B2
8857438 Barthe et al. Oct 2014 B2
8858471 Barthe et al. Oct 2014 B2
8915853 Barthe et al. Dec 2014 B2
8915854 Slayton et al. Dec 2014 B2
8915870 Barthe et al. Dec 2014 B2
8920320 Stecco et al. Dec 2014 B2
8920324 Slayton et al. Dec 2014 B2
8926533 Bockenstedt et al. Jan 2015 B2
8932224 Barthe et al. Jan 2015 B2
8932238 Wing et al. Jan 2015 B2
8968205 Zeng et al. Mar 2015 B2
9011336 Slayton et al. Apr 2015 B2
9039617 Slayton et al. May 2015 B2
9039619 Barthe et al. May 2015 B2
9050116 Homer Jun 2015 B2
9095697 Barthe et al. Aug 2015 B2
9107798 Azhari et al. Aug 2015 B2
9114247 Barthe et al. Aug 2015 B2
9180314 Desilets et al. Nov 2015 B2
9216276 Slayton et al. Dec 2015 B2
9220915 Liu et al. Dec 2015 B2
9272162 Slayton et al. Mar 2016 B2
9283409 Slayton et al. Mar 2016 B2
9283410 Slayton et al. Mar 2016 B2
9295607 Rosenberg Mar 2016 B2
9308390 Youngquist Apr 2016 B2
9308391 Liu et al. Apr 2016 B2
9314650 Rosenberg et al. Apr 2016 B2
9320537 Slayton et al. Apr 2016 B2
9345910 Slayton et al. May 2016 B2
9421029 Barthe et al. Aug 2016 B2
9427600 Barthe et al. Aug 2016 B2
9427601 Barthe et al. Aug 2016 B2
9433803 Lin et al. Sep 2016 B2
9440093 Homer Sep 2016 B2
9440096 Barthe et al. Sep 2016 B2
9492645 Zhou et al. Nov 2016 B2
9492686 Da Silva Nov 2016 B2
9498651 Sapozhnikov et al. Nov 2016 B2
9510802 Barthe et al. Dec 2016 B2
9522290 Slayton et al. Dec 2016 B2
9532832 Ron Edoute et al. Jan 2017 B2
9533174 Barthe et al. Jan 2017 B2
9533175 Slayton et al. Jan 2017 B2
9545529 Britva et al. Jan 2017 B2
9566454 Barthe et al. Feb 2017 B2
9623267 Ulric et al. Apr 2017 B2
9694211 Barthe et al. Jul 2017 B2
9694212 Barthe et al. Jul 2017 B2
9700340 Barthe et al. Jul 2017 B2
9707412 Slayton et al. Jul 2017 B2
9710607 Ramdas et al. Jul 2017 B2
9713731 Slayton et al. Jul 2017 B2
9802063 Barthe et al. Oct 2017 B2
9827449 Barthe et al. Nov 2017 B2
9827450 Slayton et al. Nov 2017 B2
9833639 Slayton et al. Dec 2017 B2
9833640 Barthe et al. Dec 2017 B2
9895560 Barthe et al. Feb 2018 B2
9907535 Barthe et al. Mar 2018 B2
9919167 Domankevitz Mar 2018 B2
9974982 Slayton et al. May 2018 B2
9993664 Aviad et al. Jun 2018 B2
10010721 Slayton et al. Jul 2018 B2
10010724 Barthe et al. Jul 2018 B2
10010725 Slayton et al. Jul 2018 B2
10010726 Barthe et al. Jul 2018 B2
10016626 Zovrin et al. Jul 2018 B2
10046181 Barthe et al. Aug 2018 B2
10046182 Barthe et al. Aug 2018 B2
10070883 Barthe et al. Sep 2018 B2
10183183 Burdette Jan 2019 B2
10226645 Barthe Mar 2019 B2
10238894 Slayton et al. Mar 2019 B2
10245450 Slayton et al. Apr 2019 B2
10252086 Barthe et al. Apr 2019 B2
10265550 Barthe et al. Apr 2019 B2
10272272 Lee et al. Apr 2019 B2
10300308 Seip et al. May 2019 B2
10328289 Barthe et al. Jun 2019 B2
10406383 Luebcke Sep 2019 B2
10420960 Emery Sep 2019 B2
10420961 Lacoste Sep 2019 B2
10485573 Clark, III et al. Nov 2019 B2
10492862 Domankevitz Dec 2019 B2
10525288 Slayton et al. Jan 2020 B2
10532230 Barthe et al. Jan 2020 B2
10537304 Barthe et al. Jan 2020 B2
10556123 Altshuler et al. Feb 2020 B2
10583287 Schwarz Mar 2020 B2
10603519 Slayton et al. Mar 2020 B2
10603523 Slayton et al. Mar 2020 B2
10610705 Barthe et al. Apr 2020 B2
10610706 Barthe et al. Apr 2020 B2
10639006 Choi et al. May 2020 B2
10639504 Kim May 2020 B2
10751246 Kaila Aug 2020 B2
10772646 Lu et al. Sep 2020 B2
10780298 Cain et al. Sep 2020 B2
10888716 Slayton et al. Jan 2021 B2
10888717 Slayton et al. Jan 2021 B2
10888718 Barthe et al. Jan 2021 B2
10960236 Slayton et al. Mar 2021 B2
20010009997 Pope Jul 2001 A1
20010009999 Kaufman et al. Jul 2001 A1
20010014780 Martin Aug 2001 A1
20010014819 Ingle Aug 2001 A1
20010031922 Weng Oct 2001 A1
20010039380 Larson et al. Nov 2001 A1
20010041880 Brisken Nov 2001 A1
20020000763 Jones Jan 2002 A1
20020002345 Marlinghaus Jan 2002 A1
20020040199 Klopotek Apr 2002 A1
20020040442 Ishidera Apr 2002 A1
20020055702 Atala May 2002 A1
20020062077 Emmenegger May 2002 A1
20020062142 Knowlton May 2002 A1
20020072691 Thompson et al. Jun 2002 A1
20020082528 Friedman Jun 2002 A1
20020082529 Suorsa et al. Jun 2002 A1
20020082589 Friedman Jun 2002 A1
20020087080 Slayton Jul 2002 A1
20020095143 Key Jul 2002 A1
20020099094 Anderson Jul 2002 A1
20020111569 Rosenschien et al. Aug 2002 A1
20020115917 Honda et al. Aug 2002 A1
20020128639 Pless et al. Aug 2002 A1
20020128648 Weber Sep 2002 A1
20020143252 Dunne et al. Oct 2002 A1
20020156400 Babaev Oct 2002 A1
20020161357 Anderson Oct 2002 A1
20020165529 Danek Nov 2002 A1
20020168049 Schriever Nov 2002 A1
20020169394 Eppstein et al. Nov 2002 A1
20020169442 Neev Nov 2002 A1
20020173721 Grunwald et al. Nov 2002 A1
20020193784 McHale et al. Dec 2002 A1
20020193831 Smith Dec 2002 A1
20030009153 Brisken et al. Jan 2003 A1
20030014039 Barzell et al. Jan 2003 A1
20030018255 Martin Jan 2003 A1
20030018270 Makin et al. Jan 2003 A1
20030023283 McDaniel Jan 2003 A1
20030028111 Vaezy et al. Feb 2003 A1
20030028113 Gilbert et al. Feb 2003 A1
20030032900 Ella Feb 2003 A1
20030036706 Slayton et al. Feb 2003 A1
20030040739 Koop Feb 2003 A1
20030050678 Sierra Mar 2003 A1
20030055308 Friemel et al. Mar 2003 A1
20030055417 Truckai et al. Mar 2003 A1
20030060736 Martin et al. Mar 2003 A1
20030065313 Koop Apr 2003 A1
20030066708 Allison et al. Apr 2003 A1
20030073907 Taylor Apr 2003 A1
20030074023 Kaplan Apr 2003 A1
20030083536 Eshel May 2003 A1
20030092988 Makin May 2003 A1
20030097071 Halmann et al. May 2003 A1
20030099383 Lefebvre May 2003 A1
20030125629 Ustuner Jul 2003 A1
20030135135 Miwa et al. Jul 2003 A1
20030139790 Ingle et al. Jul 2003 A1
20030149366 Stringer et al. Aug 2003 A1
20030153961 Babaev Aug 2003 A1
20030171678 Batten et al. Sep 2003 A1
20030171701 Babaev Sep 2003 A1
20030176790 Slayton Sep 2003 A1
20030191396 Sanghvi Oct 2003 A1
20030199794 Sakurai et al. Oct 2003 A1
20030200481 Stanley Oct 2003 A1
20030212129 Liu et al. Nov 2003 A1
20030212351 Hissong Nov 2003 A1
20030212393 Knowlton Nov 2003 A1
20030216648 Lizzi et al. Nov 2003 A1
20030216795 Harth Nov 2003 A1
20030220536 Hissong Nov 2003 A1
20030220585 Hissong Nov 2003 A1
20030229331 Brisken et al. Dec 2003 A1
20030233085 Giammarusti Dec 2003 A1
20030236487 Knowlton Dec 2003 A1
20040000316 Knowlton Jan 2004 A1
20040001809 Brisken Jan 2004 A1
20040002658 Marian, Jr. Jan 2004 A1
20040002705 Knowlton Jan 2004 A1
20040010222 Nunomura et al. Jan 2004 A1
20040015079 Berger et al. Jan 2004 A1
20040015106 Coleman Jan 2004 A1
20040030227 Littrup Feb 2004 A1
20040030268 Weng et al. Feb 2004 A1
20040039312 Hillstead Feb 2004 A1
20040039418 Elstrom Feb 2004 A1
20040041563 Lewin et al. Mar 2004 A1
20040041880 Ikeda et al. Mar 2004 A1
20040042168 Yang et al. Mar 2004 A1
20040044375 Diederich et al. Mar 2004 A1
20040049134 Tosaya et al. Mar 2004 A1
20040049734 Tosaya et al. Mar 2004 A1
20040059266 Fry Mar 2004 A1
20040068186 Ishida et al. Apr 2004 A1
20040073079 Altshuler et al. Apr 2004 A1
20040073113 Salgo Apr 2004 A1
20040073115 Horzewski et al. Apr 2004 A1
20040073116 Smith Apr 2004 A1
20040073204 Ryan et al. Apr 2004 A1
20040077977 Ella et al. Apr 2004 A1
20040082857 Schonenberger Apr 2004 A1
20040082859 Schaer Apr 2004 A1
20040102697 Evron May 2004 A1
20040105559 Aylward et al. Jun 2004 A1
20040106867 Eshel et al. Jun 2004 A1
20040122323 Vortman et al. Jun 2004 A1
20040122493 Ishibashi et al. Jun 2004 A1
20040143297 Ramsey Jul 2004 A1
20040152982 Hwang et al. Aug 2004 A1
20040158150 Rabiner et al. Aug 2004 A1
20040186535 Knowlton Sep 2004 A1
20040189155 Funakubo Sep 2004 A1
20040206365 Knowlton Oct 2004 A1
20040210214 Knowlton Oct 2004 A1
20040217675 Desilets Nov 2004 A1
20040249318 Tanaka Dec 2004 A1
20040254620 Lacoste Dec 2004 A1
20040267252 Washington et al. Dec 2004 A1
20050007879 Nishida Jan 2005 A1
20050033201 Takahashi Feb 2005 A1
20050033316 Kertz Feb 2005 A1
20050038340 Vaezy et al. Feb 2005 A1
20050055018 Kreindel Mar 2005 A1
20050055073 Weber Mar 2005 A1
20050061834 Garcia et al. Mar 2005 A1
20050070961 Maki Mar 2005 A1
20050074407 Smith Apr 2005 A1
20050080469 Larson Apr 2005 A1
20050085731 Miller et al. Apr 2005 A1
20050091770 Mourad et al. May 2005 A1
20050096542 Weng et al. May 2005 A1
20050104690 Larson et al. May 2005 A1
20050113689 Gritzky May 2005 A1
20050131302 Poland Jun 2005 A1
20050137656 Malak Jun 2005 A1
20050143677 Young et al. Jun 2005 A1
20050154313 Desilets Jul 2005 A1
20050154314 Quistgaard Jul 2005 A1
20050154332 Zanelli Jul 2005 A1
20050154431 Quistgaard Jul 2005 A1
20050187495 Quistgaard Aug 2005 A1
20050191252 Mitsui Sep 2005 A1
20050193451 Quistgaard Sep 2005 A1
20050193820 Sheljaskow et al. Sep 2005 A1
20050197681 Barolet et al. Sep 2005 A1
20050203399 Vaezy Sep 2005 A1
20050228281 Nefos Oct 2005 A1
20050240127 Seip et al. Oct 2005 A1
20050240170 Zhang et al. Oct 2005 A1
20050251120 Anderson et al. Nov 2005 A1
20050251125 Pless et al. Nov 2005 A1
20050256406 Barthe Nov 2005 A1
20050261584 Eshel Nov 2005 A1
20050261585 Makin et al. Nov 2005 A1
20050267454 Hissong Dec 2005 A1
20050288748 Li et al. Dec 2005 A1
20060004306 Altshuler Jan 2006 A1
20060020260 Dover et al. Jan 2006 A1
20060025756 Francischelli Feb 2006 A1
20060042201 Curry Mar 2006 A1
20060058664 Barthe Mar 2006 A1
20060058671 Vitek et al. Mar 2006 A1
20060058707 Barthe Mar 2006 A1
20060058712 Altshuler et al. Mar 2006 A1
20060074309 Bonnefous Apr 2006 A1
20060074313 Slayton et al. Apr 2006 A1
20060074314 Slayton Apr 2006 A1
20060074355 Slayton Apr 2006 A1
20060079816 Barthe Apr 2006 A1
20060079868 Makin Apr 2006 A1
20060084891 Barthe Apr 2006 A1
20060089632 Barthe Apr 2006 A1
20060089688 Panescu Apr 2006 A1
20060094988 Tosaya May 2006 A1
20060106325 Perrier May 2006 A1
20060111744 Makin May 2006 A1
20060116583 Ogasawara et al. Jun 2006 A1
20060116671 Slayton Jun 2006 A1
20060122508 Slayton Jun 2006 A1
20060122509 Desilets Jun 2006 A1
20060161062 Arditi et al. Jul 2006 A1
20060184069 Vaitekunas Aug 2006 A1
20060184071 Klopotek Aug 2006 A1
20060189972 Grossman Aug 2006 A1
20060206105 Chopra Sep 2006 A1
20060224090 Ostrovsky et al. Oct 2006 A1
20060229514 Wiener Oct 2006 A1
20060238068 May et al. Oct 2006 A1
20060241440 Eshel Oct 2006 A1
20060241442 Barthe Oct 2006 A1
20060241470 Novak et al. Oct 2006 A1
20060241576 Diederich et al. Oct 2006 A1
20060250046 Koizumi et al. Nov 2006 A1
20060282691 Barthe Dec 2006 A1
20060291710 Wang et al. Dec 2006 A1
20070016039 Vortman et al. Jan 2007 A1
20070032784 Gilklich et al. Feb 2007 A1
20070035201 Desilets Feb 2007 A1
20070055154 Torbati Mar 2007 A1
20070055155 Owen et al. Mar 2007 A1
20070055156 Desilets et al. Mar 2007 A1
20070065420 Johnson Mar 2007 A1
20070083120 Cain et al. Apr 2007 A1
20070087060 Dietrich Apr 2007 A1
20070088245 Babaev et al. Apr 2007 A1
20070088346 Mirizzi et al. Apr 2007 A1
20070161902 Dan Jul 2007 A1
20070166357 Shaffer et al. Jul 2007 A1
20070167709 Slayton Jul 2007 A1
20070018553 Kennedy Aug 2007 A1
20070208253 Slayton Sep 2007 A1
20070219448 Seip Sep 2007 A1
20070219604 Yaroslavsky et al. Sep 2007 A1
20070219605 Yaroslavsky et al. Sep 2007 A1
20070238994 Stecco et al. Oct 2007 A1
20070239075 Rosenberg Oct 2007 A1
20070239077 Azhari et al. Oct 2007 A1
20070239079 Manstein et al. Oct 2007 A1
20070239142 Altshuler Oct 2007 A1
20080015435 Cribbs et al. Jan 2008 A1
20080027328 Klopotek Jan 2008 A1
20080033458 McLean et al. Feb 2008 A1
20080039724 Seip et al. Feb 2008 A1
20080071255 Barthe Mar 2008 A1
20080086054 Slayton Apr 2008 A1
20080086056 Chang et al. Apr 2008 A1
20080097214 Meyers et al. Apr 2008 A1
20080097253 Pedersen et al. Apr 2008 A1
20080114251 Weymer May 2008 A1
20080139943 Deng et al. Jun 2008 A1
20080139974 Da Silva Jun 2008 A1
20080146970 Litman et al. Jun 2008 A1
20080167556 Thompson Jul 2008 A1
20080183077 Moreau-Gobard et al. Jul 2008 A1
20080183110 Davenport et al. Jul 2008 A1
20080188745 Chen et al. Aug 2008 A1
20080194964 Randall et al. Aug 2008 A1
20080195000 Spooner et al. Aug 2008 A1
20080200810 Buchalter Aug 2008 A1
20080200813 Quistgaard Aug 2008 A1
20080214966 Slayton Sep 2008 A1
20080214988 Altshuler et al. Sep 2008 A1
20080221491 Slayton Sep 2008 A1
20080223379 Stuker et al. Sep 2008 A1
20080242991 Moon et al. Oct 2008 A1
20080243035 Crunkilton Oct 2008 A1
20080269608 Anderson et al. Oct 2008 A1
20080275342 Barthe Nov 2008 A1
20080281206 Bartlett et al. Nov 2008 A1
20080281236 Eshel et al. Nov 2008 A1
20080281237 Slayton Nov 2008 A1
20080281255 Slayton Nov 2008 A1
20080294072 Crutchfield, III Nov 2008 A1
20080294073 Barthe Nov 2008 A1
20080319356 Cain Dec 2008 A1
20090005680 Jones et al. Jan 2009 A1
20090012394 Hobelsberger et al. Jan 2009 A1
20090043198 Milner et al. Feb 2009 A1
20090043293 Pankratov et al. Feb 2009 A1
20090048514 Azhari et al. Feb 2009 A1
20090069677 Chen et al. Mar 2009 A1
20090093737 Chomas et al. Apr 2009 A1
20090156969 Santangelo Jun 2009 A1
20090163807 Sliwa Jun 2009 A1
20090171252 Bockenstedt et al. Jul 2009 A1
20090171266 Harris Jul 2009 A1
20090177122 Peterson Jul 2009 A1
20090177123 Peterson Jul 2009 A1
20090182231 Barthe et al. Jul 2009 A1
20090198157 Babaev et al. Aug 2009 A1
20090216159 Slayton et al. Aug 2009 A1
20090226424 Hsu Sep 2009 A1
20090227910 Pedersen et al. Sep 2009 A1
20090230823 Kushculey et al. Sep 2009 A1
20090253988 Slayton et al. Oct 2009 A1
20090281463 Chapelon et al. Nov 2009 A1
20090312693 Thapliyal et al. Dec 2009 A1
20090318909 Debenedictis et al. Dec 2009 A1
20090326420 Moonen et al. Dec 2009 A1
20100011236 Barthe et al. Jan 2010 A1
20100022919 Peterson Jan 2010 A1
20100022921 Seip et al. Jan 2010 A1
20100022922 Barthe et al. Jan 2010 A1
20100030076 Vortman et al. Feb 2010 A1
20100042020 Ben-Ezra Feb 2010 A1
20100049178 Deem et al. Feb 2010 A1
20100056925 Zhang et al. Mar 2010 A1
20100056962 Vortman et al. Mar 2010 A1
20100100014 Eshel et al. Apr 2010 A1
20100113983 Heckerman et al. May 2010 A1
20100130891 Taggart et al. May 2010 A1
20100160782 Slayton et al. Jun 2010 A1
20100160837 Hunziker et al. Jun 2010 A1
20100168576 Poland et al. Jul 2010 A1
20100191120 Kraus et al. Jul 2010 A1
20100241035 Barthe et al. Sep 2010 A1
20100249602 Buckley et al. Sep 2010 A1
20100249669 Ulric et al. Sep 2010 A1
20100256489 Pedersen et al. Oct 2010 A1
20100274161 Azhari et al. Oct 2010 A1
20100280420 Barthe et al. Nov 2010 A1
20100286518 Lee et al. Nov 2010 A1
20100312150 Douglas et al. Dec 2010 A1
20110040171 Foley et al. Feb 2011 A1
20110040190 Jahnke et al. Feb 2011 A1
20110040213 Dietz et al. Feb 2011 A1
20110040214 Foley et al. Feb 2011 A1
20110066084 Desilets et al. Mar 2011 A1
20110072970 Slobodzian et al. Mar 2011 A1
20110077514 Ulric et al. Mar 2011 A1
20110079083 Yoo Apr 2011 A1
20110087099 Eshel et al. Apr 2011 A1
20110087255 McCormack et al. Apr 2011 A1
20110112405 Barthe et al. May 2011 A1
20110144490 Davis et al. Jun 2011 A1
20110178444 Slayton et al. Jul 2011 A1
20110178541 Azhari Jul 2011 A1
20110190745 Uebelhoer et al. Aug 2011 A1
20110201976 Sanghvi et al. Aug 2011 A1
20110251524 Azhari et al. Oct 2011 A1
20110251527 Kushculey et al. Oct 2011 A1
20110270137 Goren et al. Nov 2011 A1
20110319793 Henrik et al. Dec 2011 A1
20110319794 Gertner Dec 2011 A1
20120004549 Barthe et al. Jan 2012 A1
20120016239 Barthe et al. Jan 2012 A1
20120029353 Slayton et al. Feb 2012 A1
20120035473 Sanghvi et al. Feb 2012 A1
20120035475 Barthe et al. Feb 2012 A1
20120035476 Barthe et al. Feb 2012 A1
20120046547 Barthe et al. Feb 2012 A1
20120053458 Barthe et al. Mar 2012 A1
20120059288 Barthe et al. Mar 2012 A1
20120111339 Barthe et al. May 2012 A1
20120123304 Rybyanets et al. May 2012 A1
20120136280 Rosenberg et al. May 2012 A1
20120136282 Rosenberg et al. May 2012 A1
20120143056 Slayton et al. Jun 2012 A1
20120143100 Jeong et al. Jun 2012 A1
20120165668 Slayton et al. Jun 2012 A1
20120165848 Slayton et al. Jun 2012 A1
20120191019 Desilets et al. Jul 2012 A1
20120191020 Vitek et al. Jul 2012 A1
20120197120 Makin et al. Aug 2012 A1
20120197121 Slayton et al. Aug 2012 A1
20120209150 Zeng et al. Aug 2012 A1
20120215105 Slayton et al. Aug 2012 A1
20120271202 Wisdom Oct 2012 A1
20120271294 Barthe Oct 2012 A1
20120277639 Pollock et al. Nov 2012 A1
20120296240 Azhari et al. Nov 2012 A1
20120302883 Kong et al. Nov 2012 A1
20120316426 Foley et al. Dec 2012 A1
20120330197 Makin et al. Dec 2012 A1
20120330222 Makin et al. Dec 2012 A1
20120330223 Makin et al. Dec 2012 A1
20120330283 Hyde et al. Dec 2012 A1
20120330284 Hyde et al. Dec 2012 A1
20130012755 Slayton Jan 2013 A1
20130012816 Slayton et al. Jan 2013 A1
20130012838 Jaeger et al. Jan 2013 A1
20130012842 Barthe Jan 2013 A1
20130018285 Park et al. Jan 2013 A1
20130018286 Slayton et al. Jan 2013 A1
20130046209 Slayton et al. Feb 2013 A1
20130051178 Rybyanets Feb 2013 A1
20130060170 Lee et al. Mar 2013 A1
20130066208 Barthe et al. Mar 2013 A1
20130066237 Smotrich et al. Mar 2013 A1
20130072826 Slayton et al. Mar 2013 A1
20130073001 Campbell Mar 2013 A1
20130096471 Slayton et al. Apr 2013 A1
20130096596 Schafer Apr 2013 A1
20130190659 Slayton et al. Jul 2013 A1
20130211293 Auboiroux et al. Aug 2013 A1
20130225994 Hsu et al. Aug 2013 A1
20130268032 Neev Oct 2013 A1
20130274603 Barthe et al. Oct 2013 A1
20130278111 Sammoura Oct 2013 A1
20130281853 Slayton et al. Oct 2013 A1
20130281891 Slayton et al. Oct 2013 A1
20130296697 Slayton et al. Nov 2013 A1
20130296700 Slayton et al. Nov 2013 A1
20130296743 Lee et al. Nov 2013 A1
20130303904 Barthe et al. Nov 2013 A1
20130303905 Barthe et al. Nov 2013 A1
20130310714 Eshel et al. Nov 2013 A1
20130310863 Makin et al. Nov 2013 A1
20130345562 Barthe et al. Dec 2013 A1
20140024974 Slayton et al. Jan 2014 A1
20140050054 Toda et al. Feb 2014 A1
20140081300 Melodelima et al. Mar 2014 A1
20140082907 Barthe et al. Mar 2014 A1
20140117814 Toda et al. May 2014 A1
20140142430 Slayton et al. May 2014 A1
20140148834 Barthe et al. May 2014 A1
20140155747 Bennett Jun 2014 A1
20140180174 Slayton et al. Jun 2014 A1
20140187944 Slayton et al. Jul 2014 A1
20140188015 Slayton et al. Jul 2014 A1
20140188145 Slayton et al. Jul 2014 A1
20140194723 Herzog et al. Jul 2014 A1
20140208856 Schmid Jul 2014 A1
20140221823 Keogh et al. Aug 2014 A1
20140236049 Barthe et al. Aug 2014 A1
20140236061 Lee et al. Aug 2014 A1
20140243713 Slayton et al. Aug 2014 A1
20140257145 Emery Sep 2014 A1
20140276055 Barthe et al. Sep 2014 A1
20140330124 Carol Nov 2014 A1
20150000674 Barthe et al. Jan 2015 A1
20150025420 Slayton et al. Jan 2015 A1
20150064165 Perry et al. Mar 2015 A1
20150080723 Barthe et al. Mar 2015 A1
20150080771 Barthe et al. Mar 2015 A1
20150080874 Slayton et al. Mar 2015 A1
20150088182 Slayton et al. Mar 2015 A1
20150141734 Chapelon et al. May 2015 A1
20150164734 Slayton et al. Jun 2015 A1
20150165238 Slayton et al. Jun 2015 A1
20150165243 Slayton et al. Jun 2015 A1
20150174388 Slayton Jun 2015 A1
20150202468 Slayton et al. Jul 2015 A1
20150217141 Barthe et al. Aug 2015 A1
20150224347 Barthe Aug 2015 A1
20150238258 Palero et al. Aug 2015 A1
20150297188 Konofagou Oct 2015 A1
20150321026 Branson et al. Nov 2015 A1
20150360058 Barthe et al. Dec 2015 A1
20150374333 Barthe et al. Dec 2015 A1
20150375014 Slayton et al. Dec 2015 A1
20160001097 Cho et al. Jan 2016 A1
20160016015 Slayton et al. Jan 2016 A1
20160027994 Toda et al. Jan 2016 A1
20160151618 Powers et al. Jun 2016 A1
20160158580 Slayton et al. Jun 2016 A1
20160175619 Lee et al. Jun 2016 A1
20160206335 Slayton Jul 2016 A1
20160206341 Slayton Jul 2016 A1
20160256675 Slayton Sep 2016 A1
20160296769 Barthe et al. Oct 2016 A1
20160310444 Dobak, III Oct 2016 A1
20160361571 Bernabei Dec 2016 A1
20160361572 Slayton Dec 2016 A1
20170028227 Emery et al. Feb 2017 A1
20170043190 Barthe et al. Feb 2017 A1
20170050019 Ron Edoute et al. Feb 2017 A1
20170080257 Paunescu et al. Mar 2017 A1
20170100585 Hall et al. Apr 2017 A1
20170119345 Levien May 2017 A1
20170136263 Reil May 2017 A1
20170209201 Slayton et al. Jul 2017 A1
20170209202 Friedrichs et al. Jul 2017 A1
20170304654 Blanche et al. Oct 2017 A1
20170368574 Sammoura Dec 2017 A1
20180001113 Streeter Jan 2018 A1
20180015308 Reed et al. Jan 2018 A1
20180043147 Slayton Feb 2018 A1
20180099162 Bernabei Apr 2018 A1
20180099163 Bernabei Apr 2018 A1
20180126190 Aviad et al. May 2018 A1
20180154184 Kong et al. Jun 2018 A1
20180207450 Sanchez et al. Jul 2018 A1
20180272156 Slayton et al. Sep 2018 A1
20180272157 Barthe et al. Sep 2018 A1
20180272158 Barthe et al. Sep 2018 A1
20180272159 Slayton et al. Sep 2018 A1
20180317884 Chapelon et al. Nov 2018 A1
20180333595 Barthe et al. Nov 2018 A1
20180360420 Vortman et al. Dec 2018 A1
20190000498 Barthe et al. Jan 2019 A1
20190009110 Gross et al. Jan 2019 A1
20190009111 Myhr et al. Jan 2019 A1
20190022405 Greenbaum et al. Jan 2019 A1
20190038921 Domankevitz Feb 2019 A1
20190060675 Krone et al. Feb 2019 A1
20190091490 Alexander et al. Mar 2019 A1
20190142380 Emery et al. May 2019 A1
20190143148 Slayton May 2019 A1
20190184202 Zereshkian et al. Jun 2019 A1
20190184203 Slayton et al. Jun 2019 A1
20190184205 Slayton et al. Jun 2019 A1
20190184207 Barthe et al. Jun 2019 A1
20190184208 Barthe et al. Jun 2019 A1
20190224501 Burdette Jul 2019 A1
20190262634 Barthe et al. Aug 2019 A1
20190282834 Zawada et al. Sep 2019 A1
20190290939 Watson Sep 2019 A1
20190350562 Slayton et al. Nov 2019 A1
20190366126 Pahk et al. Dec 2019 A1
20190366127 Emery Dec 2019 A1
20190366128 Slayton et al. Dec 2019 A1
20200094083 Slayton et al. Mar 2020 A1
20200100762 Barthe et al. Apr 2020 A1
20200129759 Schwarz Apr 2020 A1
20200171330 Barthe et al. Jun 2020 A1
20200179727 Slayton et al. Jun 2020 A1
20200179729 Slayton et al. Jun 2020 A1
20200188703 Barthe et al. Jun 2020 A1
20200188704 Barthe et al. Jun 2020 A1
20200206072 Capelli et al. Jul 2020 A1
20200222728 Khokhlova et al. Jul 2020 A1
20210038925 Emery Feb 2021 A1
Foreign Referenced Citations (192)
Number Date Country
2460061 Nov 2001 CN
1734284 Dec 2009 CN
104027893 Sep 2014 CN
4029175 Mar 1992 DE
10140064 Mar 2003 DE
10219297 Nov 2003 DE
10219217 Dec 2004 DE
20314479 Dec 2004 DE
0142215 May 1984 EP
0344773 Dec 1989 EP
1479412 Nov 1991 EP
0473553 Apr 1992 EP
670147 Feb 1995 EP
0661029 Jul 1995 EP
724894 Feb 1996 EP
763371 Nov 1996 EP
1044038 Oct 2000 EP
1050322 Nov 2000 EP
1234566 Aug 2002 EP
1262160 Dec 2002 EP
0659387 Apr 2003 EP
1374944 Jan 2004 EP
1028660 Jan 2008 EP
1874241 Jan 2008 EP
1362223 May 2008 EP
1750804 Jul 2008 EP
1283690 Nov 2008 EP
1811901 Apr 2009 EP
1785164 Aug 2009 EP
2230904 Sep 2010 EP
1501331 Jun 2011 EP
2066405 Nov 2011 EP
2474050 Jul 2012 EP
2709726 Nov 2015 EP
1538980 Jan 2017 EP
3124047 Jan 2017 EP
2897547 Nov 2017 EP
2173261 Aug 2018 EP
3417911 Dec 2018 EP
2532851 Sep 1983 FR
2685872 Jan 1992 FR
2672486 Aug 1992 FR
2703254 Mar 1994 FR
2113099 Aug 1983 GB
102516 Jan 1996 IL
112369 Aug 1999 IL
120079 Mar 2001 IL
63036171 Feb 1988 JP
03048299 Mar 1991 JP
3123559 May 1991 JP
03136642 Jun 1991 JP
4089058 Mar 1992 JP
04150847 May 1992 JP
7080087 Mar 1995 JP
07505793 Jun 1995 JP
7184907 Jul 1995 JP
7222782 Aug 1995 JP
09047458 Feb 1997 JP
9108288 Apr 1997 JP
9503926 Apr 1997 JP
3053069 Oct 1998 JP
11123226 May 1999 JP
11505440 May 1999 JP
11506636 Jun 1999 JP
10248850 Sep 1999 JP
2000126310 May 2000 JP
2000166940 Jun 2000 JP
2000233009 Aug 2000 JP
2001-46387 Feb 2001 JP
2001136599 May 2001 JP
2001170068 Jun 2001 JP
2002505596 Feb 2002 JP
2002078764 Mar 2002 JP
2002515786 May 2002 JP
2002537013 May 2002 JP
2002521118 Jul 2002 JP
2002537939 Nov 2002 JP
2003050298 Jul 2003 JP
2003204982 Jul 2003 JP
2004-504898 Feb 2004 JP
2004-507280 Mar 2004 JP
2004154256 Mar 2004 JP
2004-509671 Apr 2004 JP
2004-512856 Apr 2004 JP
2004147719 May 2004 JP
2005503388 Feb 2005 JP
2005527336 Sep 2005 JP
2005323213 Nov 2005 JP
2006520247 Sep 2006 JP
2008515559 May 2008 JP
2009518126 May 2009 JP
2010517695 May 2010 JP
2001-0019317 Mar 2001 KR
1020010024871 Mar 2001 KR
2002-0038547 May 2002 KR
100400870 Oct 2003 KR
20060121267 Nov 2006 KR
1020060113930 Nov 2006 KR
1020070065332 Jun 2007 KR
1020070070161 Jul 2007 KR
1020070098856 Oct 2007 KR
1020070104878 Oct 2007 KR
1020070114105 Nov 2007 KR
1020000059516 Apr 2012 KR
10-2013-0124598 Nov 2013 KR
10-1365946 Feb 2014 KR
386883 Sep 2000 TW
201208734 Mar 2012 TW
WO9312742 Jul 1993 WO
WO9524159 Sep 1995 WO
WO9625888 Aug 1996 WO
WO9634568 Nov 1996 WO
WO9639079 Dec 1996 WO
WO9735518 Oct 1997 WO
WO9832379 Jul 1998 WO
WO9852465 Nov 1998 WO
WO9933520 Jul 1999 WO
WO9939677 Aug 1999 WO
WO9949788 Oct 1999 WO
WO200006032 Feb 2000 WO
WO0015300 Mar 2000 WO
WO0021612 Apr 2000 WO
WO0048518 Aug 2000 WO
WO0053113 Sep 2000 WO
WO200071021 Nov 2000 WO
WO0128623 Apr 2001 WO
WO01045550 Jun 2001 WO
WO0182777 Nov 2001 WO
WO0182778 Nov 2001 WO
WO0187161 Nov 2001 WO
WO01080709 Nov 2001 WO
WO0209812 Feb 2002 WO
WO0209813 Feb 2002 WO
WO02015768 Feb 2002 WO
WO0224050 Mar 2002 WO
WO2002054018 Jul 2002 WO
WO02092168 Nov 2002 WO
WO03053266 Jul 2003 WO
WO03065347 Aug 2003 WO
WO03070105 Aug 2003 WO
WO03077833 Sep 2003 WO
WO03086215 Oct 2003 WO
WO03096883 Nov 2003 WO
WO03099177 Dec 2003 WO
WO03099382 Dec 2003 WO
WO03101530 Dec 2003 WO
WO2004000116 Dec 2003 WO
WO2004080147 Sep 2004 WO
WO2004110558 Dec 2004 WO
WO2005011804 Feb 2005 WO
WO2005065408 Jul 2005 WO
WO2005065409 Jul 2005 WO
WO2005090978 Sep 2005 WO
WO2005113068 Dec 2005 WO
WO2006042163 Apr 2006 WO
WO2006036870 Apr 2006 WO
WO2006042168 Apr 2006 WO
WO2006042201 Apr 2006 WO
WO2006065671 Jun 2006 WO
WO2006082573 Aug 2006 WO
WO2006104568 Oct 2006 WO
WO2007067563 Jun 2007 WO
WO2008036479 Mar 2008 WO
WO2008036622 Mar 2008 WO
WO2008144274 Nov 2008 WO
WO2009013729 Jan 2009 WO
WO2009149390 Oct 2009 WO
WO2012134645 Oct 2012 WO
WO2013048912 Apr 2013 WO
WO2013178830 Dec 2013 WO
WO2014045216 Mar 2014 WO
WO2014055708 Apr 2014 WO
WO2014057388 Apr 2014 WO
WO2014127091 Aug 2014 WO
WO2015160708 Oct 2015 WO
WO2016054155 Apr 2016 WO
WO2016115363 Jul 2016 WO
WO2017127328 Jul 2017 WO
WO2017149506 Sep 2017 WO
WO2017165595 Sep 2017 WO
WO 2017212489 Dec 2017 WO
WO2017212489 Dec 2017 WO
WO2018035012 Feb 2018 WO
WO2018158355 Sep 2018 WO
WO2019008573 Jan 2019 WO
WO 2019147596 Aug 2019 WO
WO2019147596 Aug 2019 WO
WO2019164836 Aug 2019 WO
WO2020009324 Jan 2020 WO
WO2020075906 Apr 2020 WO
WO2020080730 Apr 2020 WO
WO2020121307 Jun 2020 WO
Non-Patent Literature Citations (197)
Entry
US 10,398,895 B2, 09/2019, Schwarz (withdrawn)
PCT/US2017/46703 International Search Report dated Jan. 12, 2018, 32 pages.
Agren, Magnus S. et al., Collagenase in Wound Healing: Effect of Wound Age and Type. The Journal of Investigative Dermatology, vol. 99/No. 6, (Dec. 1992).
Alam, M., “The future of noninvasive procedural dermatology”. Semin Cutan Med Surg. Mar. 2013; 32(1):59-61.
Alam, M., et al., “Ultrasound tightening of facial and neck skin: a rater-blinded prospective cohort study”. J Am Acad Dermatol, 2010. 62(2): p. 262-9.
Alexiades-Armenakas, M., “Ultrasound Technologies for Dermatologic Techniques”. J Drugs Derm. 2014. 12 (11): p. 1305.
Alster, T.S., et. al., “Noninvasive lifting of arm, thigh, and knee skin with transcutaneousintense focused ultrasound”. Dermatol Surg, 2012. 38(5): p. 754-9.
Alster, Tinas S., Tanzi, Elizabeth L., “Cellulite Treatment using a Novel Combination Radiofrequency, Infrared Light, and Mechanical Tissue Manipulation Device,” Journal of Cosmetic & Laser Therapy, Jun. 2005, vol. 7, Issue 2, pp. 81-85.
Arosarena, O., “Options and Challenges for Facial Rejuvenation in Patients With Higher Fitzpatrick Skin Phototypes”. JAMA Facial Plastic Surgery, 2015.
Arthur et al., “Non-invasive estimation of hyperthermia temperatures with ultrasound,” Int. J. Hyperthermia, Sep. 2005, 21(6), pp. 589-600.
Barthe et al., “Ultrasound therapy system and ablation results utilizing miniature imaging/therapy arrays,” Ultrasonics Symposium, 2004 IEEE, Aug. 23, 2004, pp. 1792-1795, vol. 3.
Bozec, Laurent et al., Thermal Denaturation Studies of Collagen by Microthermal Analysis and Atomic Force Microscopy, Biophysical Journal, vol. 101, pp. 228-236. (Jul. 2001).
Brobst, R.W., et al., “Noninvasive Treatment of the Neck”. Facial Plast Surg Clin North Am, 2014. 22(2): p. 191-202.
Brobst, R.W., et., al., “Ulthera: initial and six month results”. Facial Plast Surg Clin North Am, 2012. 20(2): p. 163-76.
Calderhead et al., “One Mechanism Behind LED Photo-Therapy for Wound Healing and Skin Rejuvenation: Key Role of the Mast Cell” Laser Therapy 17.3: 141-148 (2008).
Casabona, G., et al., “Microfocused Ultrasound With Visualization and Fillers for Increased Neocollagenesis: Clinical and Histological Evaluation”. Dermatol Surg 2014;40:S194-S198.
Casabona, G., et al., “Microfocused Ultrasound with Visualization and Calcium Hydroxylapatite for Improving Skin Laxity and Cellulite Appearance”; Plast Reconstr Surg Glob Open. Jul. 25, 2017;5(7):e1388, 8 pages.
Chan, N.P., et al., “Safety study of transcutaneous focused ultrasound for non-invasive skin tightening in Asians”. Lasers Surg Med, 2011. 43(5): p. 366-75.
Chapelon et al., “Effects of Cavitation In The High Intensity Therapeutic Ultrasound”, Ultrasonics Symposium—1357 (1991).
Chapelon, et al., “Thresholds for Tissue Ablation by Focused Ultrasound” (1990).
Chen, L. et al., “Effect of Blood Perfusion on the ablation of liver parenchyma with high intensity focused ultrasound,” Phys. Med. Biol; 38:1661-1673; 1993b.
Coon, Joshua et al., “Protein identification using sequential ion/ion reactions and tandem mass spectrometry” Proceedings of the National Academy of Sciences of the USA, vol. 102, No. 27, Jul. 27, 2005, pp. 9463-9468.
Corry, Peter M., et al., “Human Cancer Treatment with Ultrasound”, IEEE Transactions on Sonics and Ultrasonics, vol. SU-31, No. 5, Sep. 1984, pp. 444, 456.
Damianou et al., “Application of the Thermal Dose Concept for Predicting the Necrosed Tissue Volume During Ultrasound Surgery,” 1993 IEEE Ultrasound Symposium, pp. 1199-1202.
Daum et al., Design and Evaluation of a Feedback Based Phased Array System for Ultrasound Surgery, IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control, vol. 45, No. 2, Mar. 1998, pp. 431-438.
Davis, Brian J., et al., “An Acoustic Phase Shift Technique for the Non-Invasive Measurement of Temperature Changes in Tissues”, 1985 Ultrasonics Symposium, pp. 921-924.
Dayan, S.H., et al., “Prospective, Multi-Center, Pivotal Trial Evaluating the Safety and Effectiveness of Micro-Focused Ultrasound with Visualization (MFU-V) for Improvement in Lines and Wrinkles of the Décolletage”. Plast Reconstr Surg. Oct. 2014; 134(4 Suppl 1):123-4.
Decision of the Korean Intellectual Property Tribunal dated Jun. 28, 2013 regarding Korean Patent No. 10-1142108, which is related to the pending application and/or an application identified in the Table on pp. 1-4 of the Information Disclosure Statement herein (English translation, English translation certification, and Korean decision included).
Delon Martin, C., et al, “Venous Thrombosis Generation By Means of High-Intensity Focused Ultrasound” Ultrasound in Med. & Biol., vol. 21, No. 1, pp. 113-119 (1995).
Dierickx, Christine C., “The Role of Deep Heating for Noninvasive Skin Rejuvenation” Lasers in Surgery and Medicine 38:799-807 (2006).
Dobke, M.K., et al., “Tissue restructuring by energy-based surgical tools”. Clin Plast Surg, 2012. 39(4): p. 399-408.
Dong, Yuan-Lin et al., “Effect of Ibuprofen on the Inflammatory Response To Surgical Wounds” The Journal of Trauma, vol. 35, No. 3. (1993).
Dvivedi, Sanjay, et al. “Effect of Ibuprofen and diclofenac sodium on experimental wound healing” Indian Journal of Experimental Biology, vol. 35, pp. 1243-1245. (Nov. 1997).
Fabi, S.G., “Microfocused Ultrasound With Visualization for Skin Tightening and Lifting: My Experience and a Review of the Literature”. Dermatol Surg. Dec. 2014; 40 Suppl 12:S164-7.
Fabi, S.G., “Noninvasive skin tightening: focus on new ultrasound techniques”. Clin Cosmet Investig Dermatol. Feb. 5, 2015; 8:47-52.
Fabi, S.G., et. al., “A prospective multicenter pilot study of the safety and efficacy of microfocused ultrasound with visualization for improving lines and wrinkles of the décolleté”. Dermatol Surg. Mar. 2015; 41(3):327-35.
Fabi, S.G., et. al., “Evaluation of microfocused ultrasound with visualization for lifting, tightening, and wrinkle reduction of the decolletage”. J Am Acad Dermatol, 2013. 69(6): p. 965-71.
Fabi, S.G., et. al., “Future directions in cutaneous laser surgery”. Dermatol Clin, 2014. 32(1): p. 61-9.
Fabi, S.G., et. al., “Retrospective Evaluation of Micro-focused Ultrasound for Lifting and Tightening the Face and Neck”. Dermatol Surg, 2014.
Friedmann D.P., “Comments on evaluation of microfocused ultrasound system for improving skin laxity and tightening in the lower face”. Aesthet Surg J. Mar. 2015;35(3):NP81-2.
Friedmann, D.P., et. al., “Combination of intense pulsed light, Sculptra, and Ultherapy for treatment of the aging face”. J Cosmet Dermatol, 2014. 13(2): p. 109-18.
Fry, W.J. et al., “Production of Focal Destructive Lesions in the Central Nervous System with Ultrasound,” J. Neurosurg., 11:471-478; 1954.
Fujimoto, et al., “A New Cavitation Suppression Technique for Local Ablation Using High-Intensity Focused Ultrasound” Ultrasonics Symposium—1629 (1995).
Gliklich et al., Clinical Pilot Study of Intense Ultrasound therapy to Deep Dermal Facial Skin and Subcutaneous Tissues, Arch Facial Plastic Surgery, Mar. 1, 2007, vol. 9, No. 1.
Gold, M.H., et. al., “Use of Micro-Focused Ultrasound with Visualization to Lift and Tighten Lax Knee Skin”. J Cosmet Laser Ther, 2014: p. 1-15.
Goldberg, D.J., et. al., “Safety and Efficacy of Microfocused Ultrasound to Lift, Tighten, and Smooth the Buttocks”. Dermatol Surg 2014; 40:1113-1117.
Greene, R.M., et al., “Skin tightening technologies”. Facial Plast Surg. Feb. 2014; 30(1):62-7.
Greenhalgh, David G., “Wound healing and diabetes mellitus” Clinics in Plastic Surgery 30; 37-45. (2003).
Guo, S. et al., “Factors Affecting Wound Healing” Critical Reviews in Oral Biology & Medicine, J Dent Res 89(3), pp. 219-229. (2010).
Haar, G.R et al., “Tissue Destruction with Focused Ultrasound in Vivo,” Eur. Urol. 23 (suppl. 1):8-11; 1993.
Hantash, Basil M. et al., “Bipolar Fractional Radiofrequency Treatment Induces Neoelastogenesis and Neocollagenesis” Lasers in Surgery and Medicine 41:1-9 (2009).
Hantash, Basil M. et al., “In Vivo Histological Evaluation of a Novel Ablative Fractional Resurfacing Device” Lasers in Surgery and Medicine 39:96-107 (2007).
Harris, M.O., “Safety of Microfocused Ultrasound With Visualization in Patients With Fitzpatrick Skin Phototypes III to VI”. JAMA Facial Plast. Surg, 2015.
Hart, et. al., “Current Concepts in the Use of PLLA:Clinical Synergy Noted with Combined Use of Microfocused Ultrasound and Poly-I-Lactic Acid on the Face, Neck, and Décolletage”. Amer. Soc. Plast. Surg. 2015. 136; 180-187S.
Hassan et al., “Structure and Applications of Poly(vinyl alcohol) Hydrogels Produced by Conventional Crosslinking or by Freezing/Thawing Methods,” advanced in Polymer Science, 2000, pp. 37-65, vol. 153.
Hassan et al., “Structure and Morphology of Freeze/Thawed PVA Hydrogels,” Macromolecules, Mar. 11, 2000, pp. 2472-2479, vol. 33, No. 7.
Hexsel et al., “A Validated Photonumeric Cellulite Severity Scale”; J Eur Acad Dermatol Venereol. May 2009; 23(5):523-8, 6 pages.
Hitchcock, T.M. et. al., “Review of the safety profile for microfocused ultrasound with Visualization”. Journal of Cosmetic Dermatology, 13, 329-335. (2014).
Husseini et al, “The Role of Cavitation in Acoustically Activated Drug Delivery,” J. Control Release, Oct. 3, 2005, pp. 253-261, vol. 107(2).
Husseini et al. “Investigating the mechanism of acoustically activated uptake of drugs from Plutonic micelles,” BMD Cancer 2002, 2:20k, Aug. 30, 2002, pp. 1-6.
Hynynen et al., Temperature Distributions During Local Ultrasound Induced Hyperthermia In Vivo, Ultrasonics Symposium—745 (1982).
Jeffers et al., “Evaluation of the Effect of Cavitation Activity on Drug-Ultrasound Synergisms,” 1993 IEEE Ultrasonics Symposium, pp. 925-928.
Jenne, J., et al., “Temperature Mapping for High Energy US-Therapy”, 1994 Ultrasonics Symposium, pp. 1879-1882.
Jeong, K.H., et al., “Neurologic complication associated with intense focused ultrasound”. J Cosmet Laser Ther, 2013.
Johnson, S.A., et al., “Non-Intrusive Measurement of Microwave and Ultrasound-Induced Hyperthermia by Acoustic Temperature Tomography”, Ultrasonics Symposium Proceedings, pp. 977-982. (1977).
Kim, H.J., et al., “Coagulation and ablation patterns of high-intensity focused ultrasound on a tissue mimicking phantom and cadaveric skin”. Laser Med Sci. Sep. 4, 2015.
Kornstein, A.N., “Ulthera for silicone lip correction”. Plast Reconstr Surg, 2012. 129(6): p. 1014e-1015e.
Kornstein, A.N., “Ultherapy shrinks nasal skin after rhinoplasty following failure of conservative measures”. Plast Reconstr Surg, 2013. 131(4): p. 664e-6e.
Krischak, G.D., et al., “The effects of non-steroidal anti-inflammatory drug application on incisional wound healing in rats” Journal of Wound Care, vol. 6, No. 2, (Feb. 2007).
Laubach, H.J., et. al., “Confined Thermal Damage with Intense Ultrasound (IUS)” [abstr.] American Society for Laser Medicine and Surgery Abstracts, p. 15 #43 (Apr. 2006).
Laubach, H.J., et. al., “Intense focused ultrasound: evaluation of a new treatment modality for precise microcoagulation within the skin”. Dermatol Surg, 2008. 34(5): p. 727-34.
Lee, H.J., et. al., “The efficacy and safety of intense focused ultrasound in the treatment of enlarged facial pores in Asian skin”. J Dermatolog Treat, 2014.
Lee, H.S., et. al., “Multiple Pass Ultrasound Tightening of Skin Laxity of the Lower Face and Neck”. Dermatol Surg, 2011.
Lin, Sung-Jan, et al., “Monitoring the thermally induced structural transitions of collagen by use of second-harmonic generation microscopy” Optics Letters, vol. 30, No. 6, (Mar. 15, 2005).
Macgregor J.L., et. al., “Microfocused Ultrasound for Skin Tightening”. Semin Cutan Med Surg 32:18-25. (2013).
Madersbacher, S. et al., “Tissue Ablation in Benign Prostatic Hyperplasia with High Intensity Focused Ultrasound,” Dur. Urol., 23 (suppl. 1):39-43; 1993.
Makin et al, “B-Scan Imaging and Thermal Lesion Monitoring Using Miniaturized Dual-Functionality Ultrasound Arrays,” Ultrasonics Symposium, 2004 IEEE, Aug. 23, 2004, pp. 1788-1791, vol. 3.
Makin et al, “Confirmed Bulk Ablation and Therapy Monitoring Using Intracorporeal Image-Treat Ultrasound Arrays,” 4th International Symposium on Therapeutic Ultrasound, Sep. 19, 2004.
Makin et al., “Miniaturized Ultrasound Arrays for Interstitial Ablation and Imaging,” UltraSound Med. Biol. 2005, Nov. 1, 2005, pp. 1539-1550, vol. 31(11).
Manohar et al, “Photoacoustic mammography laboratory prototype: imaging of breast tissue phantoms,” Journal of Biomedical Optics, Nov./Dec. 2004, pp. 1172-1181, vol. 9, No. 6.
Mast et al, “Bulk Ablation of Soft Tissue with Intense Ultrasound; Modeling and Experiments,” J. Acoust. Soc. Am., Oct. 1, 2005, pp. 2715-2724, vol. 118(4).
Meshkinpour, Azin, et al., “Treatment of Hypertrophic Scars and Keloids With a Radiofrequency Device: A Study of Collagen Effects” Lasers in Surgery and Medicine 37:343-349 (2005).
Minkis, K., et. al., “Ultrasound skin tightening”. Dermatol Clin, 2014. 32(1): p. 71-7.
Mitragotri, S., “Healing sound: the use of ultrasound in drug delivery and other therapeutic applications,” Nature Reviews; Drug Delivery, pp. 255-260, vol. 4 (Mar. 2005).
Mosser, David M. et al., “Exploring the full spectrum of macrophage activation” Nat Rev Immunol; 8(12): 958-969. (Dec. 2008).
Murota, Sei-Itsu, et al., “Stimulatory Effect of Prostaglandins on the Production of Hexosamine-Containing Substances by Cultured Fibroblasts (3) Induction of Hyaluronic Acid Synthetase by Prostaglandin” Department of Pharmacology, Tokyo Metropolitan Institute of Gerontology, Itabashiku, Tokyo-173, Japan. (Nov. 1977, vol. 14, No. 5).
Murota, Sei-Itsu, et al., “The Stimulatory Effect of Prostaglandins on Production of Hexosamine-Containing Substances by Cultured Fibroblasts” Department of Pharmacology, Tokyo Metropolitan Institute of Gerontology, Itabashiku, Tokyo-173, Japan. (Aug. 1976, vol. 12, No. 2).
Nestor, M.S. et. al., “Safety and Efficacy of Micro-focused Ultrasound Plus Visualization for the Treatment of Axillary Hyperhidrosis”. J Clin Aesthet Dermatol, 2014. 7(4): p. 14-21.
Oni, G., et. al. “Response to ‘comments on evaluation of microfocused ultrasound system for improving skin laxity and tightening in the lower face’”. Aesthet Surg J. Mar. 2015;35(3):NP83-4.
Oni, G., et. al., “Evaluation of a Microfocused Ultrasound System for Improving Skin Laxity and Tightening in the Lower Face”. Aesthet Surg J, 2014. 38:861-868.
Pak, C.S., et. al., “Safety and Efficacy of Ulthera in the Rejuvenation of Aging Lower Eyelids: A Pivotal Clinical Trial”. Aesthetic Plast Surg, 2014.
Paradossi et al., “Poly(vinyl alcohol) as versatile biomaterial for potential biomedical applications,” Journal of Materials Science: Materials in Medicine, 2003, pp. 687-691, vol. 14.
Pritzker, R.N., et. al, “Updates in noninvasive and minimally invasive skin tightening”. Semin Cutan Med Surg. Dec. 2014;33(4):182-7.
Pritzker, R.N., et. al., “Comparison of different technologies for noninvasive skin tightening”. Journal of Cosmetic Dermatology, 13, 315-323. (2014).
Rappolee, Daniel A., et al., “Wound Macrophages Express TGF and Other Growth Factors in Vivo: Analysis by mRNA Phenotyping” Science, vol. 241, No. 4866 (Aug. 1988).
Reid, Gavin, et al., “Tandem Mass spectrometry of ribonuclease A and B: N-linked glycosylation site analysis of whole protein ions,” Analytical Chemistry. Feb. 1, 2002, vol. 74, No. 3, pp. 577-583.
Righetti et al, “Elastographic Characterization of HIFU-lnduced Lesions in Canine Livers,” 1999, Ultrasound in Med & Bio, vol. 25, No. 7, pp. 1099-1113.
Rokhsar, C., et. al., “Safety and efficacy of microfocused ultrasound in tightening of lax elbow skin”. Dermatol Surg. 2015; 41(7):821-6.
Rosenberg, Carol S. “Wound Healing in the Patient with Diabetes Mellitus” Nursing Clinics of North America, vol. 25, No. 1, (Mar. 1990).
Saad et al., “Ultrasound-Enhanced Effects of Adriamycin Against Murine Tumors,” Ultrasound in Med. & Biol. vol. 18, No. 8, pp. 715-723 (1992).
Sabet-Peyman, E.J. et. al., “Complications Using Intense Ultrasound Therapy to TreatDeep Dermal Facial Skin and Subcutaneous Tissues”. Dermatol Surg 2014; 40:1108-1112.
Sandulache, Vlad C. et al., “Prostaglandin E2 inhibition of keloid fibroblast migration, contraction, and transforming growth factor (TGF)-B1-induced collagen synthesis” Wound Rep Reg 15 122-133, 2007. (2007).
Sanghvi, N.T., et al., “Transrectal Ablation of Prostate Tissue Using Focused Ultrasound,” 1993 Ultrasonics Symposium, IEEE, pp. 1207-1210.
Sasaki, G.H. et. al., “Clinical Efficacy and Safety of Focused-lmage Ultrasonography: A 2-Year Experience”. Aesthet Surg J, 2012.
Sasaki, G.H. et. al., “Microfocused Ultrasound for Nonablative Skin and Subdermal Tightening to the Periorbitum and Body Sites: Preliminary Report on Eighty-Two Patients”. Journal of Cosmetics, Dermatological Sciences and Applications, 2012, 2, 108-116.
Sassen, Sander, “ATI's R520 architecture, the new king of the hill?” http://www.hardwareanalysis.com/content/article/1813, Sep. 16, 2005, 2 pages.
Seip, Ralf, et al., “Noninvasive Detection of Thermal Effects Due to Highly Focused Ultrasonic Fields,” IEEE Symposium, pp. 1229-1232, vol. 2, Oct. 3-Nov. 1993.
Seip, Ralf, et al., “Noninvasive Estimation of Tissue Temperature Response to Heating Fields Using Diagnostic Ultrasound,” IEEE Transactions on Biomedical Engineering, vol. 42, No. 8, Aug. 1995, pp. 828-839.
Simon et al., “Applications of Lipid-Coated Microbubble Ultrasonic Contrast to Tumor Therapy,” Ultrasound in Med. & Biol. vol. 19, No. 2, pp. 123-125 (1993).
Sklar, L.R., et. al., “Use of transcutaneous ultrasound for lipolysis and skin tightening: a review”. Aesthetic Plast Surg, 2014. 38(2): p. 429-41.
Smith, Nadine Barrie, et al., “Non-invasive In Vivo Temperature Mapping of Ultrasound Heating Using Magnetic Resonance Techniques”, 1994 Ultrasonics Symposium, pp. 1829-1832, vol. 3.
Suh, D.H., et. al., “A intense-focused ultrasound tightening for the treatment of infraorbital laxity”. J Cosmet Laser Ther, 2012. 14(6): p. 290-5.
Suh, D.H., et. al., “Comparative histometric analysis of the effects of high-intensity focused ultrasound and radiofrequency on skin”. J Cosmet Laser Ther. Mar. 24, 2015:1-7.
Suh, D.H., et. al., “Intense Focused Ultrasound Tightening in Asian Skin: Clinical and Pathologic Results” American Society for Dermatologic Surgery, Inc.; 37:1595-1602. (2011).
Surry et al., “Poly(vinyl alcohol) cryogel phantoms for use in ultrasound and MR imaging,” Phys. Med. Biol., Dec. 6, 2004, pp. 5529-5546, vol. 49.
Syka J. E. P. et al., “Peptide and Protein Sequence Analysis by Electron Transfer Dissociation Mass Spectrometry,” Proceedings of the National Academy of Sciences of USA, National Academy of Science, Washington, DC, vol. 101, No. 26, Jun. 29, 2004, pp. 9528-9533.
Talbert, D. G., “An Add-On Modification for Linear Array Real-Time Ultrasound Scanners to Produce 3D Displays,” UTS Int'l 1977 Brighton, England (Jun. 28-30, 1977) pp. 57-67.
Tata et al., “Interaction of Ultrasound and Model Membrane Systems: Analyses and Predictions,” American Chemical Society, Phys. Chem. 1992, 96, pp. 3548-3555.
Ueno, S., et al., “Ultrasound Thermometry in Hyperthermia”, 1990 Ultrasonic Symposium, pp. 1645-1652.
Verhofstad, Michiel H.J. et al., “Collagen Synthesis in rat skin and ileum fibroblasts is affected differently by diabetes-related factors” Int. J. Exp. Path. (1998), 79, 321-328.
Wang, H., et al., “Limits on Focused Ultrasound for Deep Hyperthermia”, 1994 Ultrasonic Symposium, Nov. 1-4, 1994, pp. 1869-1872, vol. 3.
Wasson, Scott, “NVIDIA's GeForce 7800 GTX graphics processor Power MADD,” http://techreport.com/reviews/2005q2/geforce-7800gtx/index.x?pg=1, Jun. 22, 2005, 4 pages.
Weiss, M., “Commentary: noninvasive skin tightening: ultrasound and other technologies: where are we in 2011?” Dermatol Surg, 2012. 38(1): p. 28-30.
White et al. “Selective Creating of Thermal Injury Zones in the Superficial Musculoaponeurotic System Using Intense Ultrasound Therapy,” Arch Facial Plastic Surgery, Jan./Feb. 2007, vol. 9, No. 1 (pp. 22-29).
White, W. M., et al., “Selective Transcutaneous Delivery of Energy to Facial Subdermal Tissues Using the Ultrasound Therapy System” [abstr]. American Society for Laser Medicine and Surgery Abstracts, p. 37 #113 (Apr. 2006).
White, W. Matthew, et al., “Selective Transcutaneous Delivery of Energy to Porcine Soft Tissues Using Intense Ultrasound (IUS)” Lasers in Surgery and Medicine 40:67-75 (2008).
Woodward, J.A., et. al. “Safety and Efficacy of Combining Microfocused Ultrasound With Fractional CO2 Laser Resurfacing for Lifting and Tightening the Face and Neck”. Dermatol Surg, Dec. 2014 40:S190-S193.
Zelickson, Brian D. et al., “Histological and Ultrastructural Evaluation of the Effects of a Radiofrequency-Based Nonablative Dermal Remodeling Device, A Pilot Study” Arch Dermatol, vol. 140, (Feb. 2004).
Ulthera, Inc., Petition for Inter Partes Review filed Jul. 19, 2016 in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 63 pages (Filed Jul. 19, 2016).
ULTHERA Exhibit 1001, U.S. Pat. No. 6,113,559 to Klopotek, filed Jul. 19, 2016 in re IPR2016-01459.
ULTHERA Exhibit 1002, Patent file history of U.S. Pat. No. 6,113,559 Klopotek filed Jul. 19, 2016 in re IPR2016-01459.
ULTHERA Exhibit 1003, Declaration of Expert Witness Mark E. Schafer, Ph.D. filed Jul. 19, 2016 in re IPR2016-01459.
ULTHERA Exhibit 1004, Curriculum Vitae of Mark E. Schafer, Ph.D. filed Jul. 19, 2016 in re IPR2016-01459.
ULTHERA Exhibit 1005, International PCT Publication WO96/34568 Knowlton filed Jul. 19, 2016 in re IPR2016-01459.
ULTHERA Exhibit 1006, French Patent No. 2,672,486, Technomed patent filed Jul. 19, 2016 in re IPR2016-01459.
ULTHERA Exhibit 1007, English translation of French Patent No. 2,672,486, Technomed filed Jul. 19, 2016 in re IPR2016-01459.
ULTHERA Exhibit 1008, International PCT Publication WO93/12742, Technomed PCT filed Jul. 19, 2016 in re IPR2016-01459.
ULTHERA Exhibit 1009, English translation of International PCT Publication WO93/12742, Technomed PCT filed Jul. 19, 2016 in re IPR2016-01459.
ULTHERA Exhibit 1010, U.S. Pat. No. 5,601,526, which claims priority to Technomed PCT filed Jul. 19, 2016 in re IPR2016-01459.
ULTHERA Exhibit 1011, Patent file history for European Patent Application No. 98964890.2, Klopotek filed Jul. 19, 2016 in re IPR2016-01459.
ULTHERA Exhibit 1012, Translator Declaration filed Jul. 19, 2016 in re IPR2016-01459.
ULTHERA Exhibit 1013, U.S. Pat. No. 5,230,334 to Klopotek filed Jul. 19, 2016 in re IPR2016-01459.
ULTHERA Exhibit 1014, U.S. Pat. No. 5,755,753 to Knowlton filed Jul. 19, 2016 in re IPR2016-01459.
ULTHERA Exhibit 1015, Excerpts from The American Medical Association Encyclopedia of Medicine (1989) filed Jul. 19, 2016 in re IPR2016-01459.
ULTHERA Exhibit 1016, The Simultaneous Study of Light Emissions and Shock Waves Produced by Cavitation Bubbles, G. Gimenez, J. Acoust. Soc. Am. 71(4), Apr. 1982, pp. 839-847 (filed Jul. 19, 2016 in re IPR2016-01459).
ULTHERA Exhibit 1017, Excerpts from Gray's Anatomy (1995) (filed Jul. 19, 2016 in re IPR2016-01459).
ULTHERA Exhibit 1018, Anatomy of the Superficial Venous System, Comjen G.M., Dermatol. Surg., 1995; 21:35-45 (filed Jul. 19, 2016 in re IPR2016-01459).
ULTHERA Exhibit 1019, Section 2.6 from Ultrasonics Theory and Application, by G.L. Gooberman (Hart Publishing Co., 1969) (filed Jul. 19, 2016 in re IPR2016-01459).
ULTHERA Exhibit 1020, Deep Local Hyperthermia for Cancer Therapy: External Electromagnetic and Ultrasound Techniques, A.Y. Cheung and A. Neyzari, Cancer Research (Suppl.), vol. 44, pp. 4736-4744 (1984) (filed Jul. 19, 2016 in re IPR2016-01459).
Decision on Institution of Inter Partes Review in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 20 pages [011] (Dated Jan. 23, 2017).
DERMAFOCUS Response to Institution of Inter Partes Review in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 73 pages [018] (Dated Apr. 26, 2017).
DERMAFOCUS Exhibit List in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 5 pages [019] (Dated Apr. 26, 2017).
DERMAFOCUS Exhibit 2002, Declaration of Mark Palmeri, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 136 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2003, Deposition of Dr. Mark Schafer, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 327 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2004, Amendment No. 4 to Ulthera Form S-1, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 308 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2005, Excerpt from Churchill Livingstone, Gray's Anatomy (38th ed. 1995), in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 7 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2006, Bo Eklof et al., “Revision of the CEAP Classification for Chronic Venous Disorders: Consensus Statement,” ACTA FAC MED NAISS, vol. 25, No. 1 (2008), 3-10 in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 7 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2007, WebMD, “Varicose Veins and Spider Veins” downloaded from http://www.webmd.com/skin-problems-andtreatments/guide/varicose-spider-veins#1 in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 3 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2008, John M. Porter et al, “Reporting Standards in Venous Disease: An Update,” Journal of Vascular Surgery, vol. 21, No. 4 (1995), 635-645 in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 11 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2009, Kullervo Hynynen, “Review of Ultrasound Therapy,” 1997 Ultrasonics Symposium (1997), 1305-1313, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 9 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2010, A.G. Visioli et al, “Prelimiary Results of a Phase I Dose Escalation Clinical Trial Using Focused Ultrasound in the Treatment of Localised Tumours,” European Journal of Ultrasound, vol. 9 (1999), 11-18, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 8 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2011, U.S. Pat. No. 5,143,063, issued on Sep. 1, 1992, Fellner, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 6 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2012, Hugh G. Beebe et al, “Consensus Statement: Classification and Grading of Chronic Venous Disease in the Lower Limbs,” European Journal of Vascular and Endovascular Surgery, vol. 12 (1996), 487-492, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 6 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2013, Excerpt from Mosby's Medical Dictionary (3rd ed. 1990), in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 4 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2014, Excerpt from Miller-Keane Encyclopedia & Dictionary of Medicine, Nursing, & Allied Health (5th ed. 1992), in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 6 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2015, David J. Tibbs et al, Varicose Veins, Venous Disorders, and Lymphatic Problems in the Lower Limbs (1997), Chapter 4: Clinical Patterns of Venous Disorder I, 47-67, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 24 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2016, Mitchel P. Goldman et al, Varicose Veins and Telangiectasias (2nd ed. 1999), Chapter 22: Treatment of Leg Telangiectasias with Laser and High-Intensity Pulsed Light, 470-497, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 31 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2017, Email from Anderson to Klopotek dated May 25, 2004, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 1 page (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2018, List of Klopotek Patents, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 411 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2019, Declaration of Peter Klopotek Civil Action 15-cv-654-SLR, dated Nov. 2, 2016, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 1 page (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2020, “Our Technology,” downloaded from http://jobs.ulthera.com/about on Apr. 10, 2017, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 4 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2021, C. Damianou and K. Hynynen, “Focal Spacing and Near-Field Heating During Pulsed High Temperature Ultrasound Therapy,” Ultrasound in Medicine & Biology, vol. 19, No. 9 (1993), 777-787, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 11 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2022, Excerpt from Mosby's Medical Dictionary (5th ed. 1997), in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 5 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2023, Excerpt from Miller-Keane Encyclopedia & Dictionary of Medicine, Nursing, & Allied Health (6th ed. 1997), in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 7 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2024, Excerpt from Stedman's Concise Medical Dictionary (3 rd ed. 1997), in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 4 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2025, Excerpt from Taber's Cyclopedic Medical Dictionary (18th ed. 1997), in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 9 pages (Filed Apr. 26, 2017).
DERMAFOCUS Exhibit 2026, Bo Eklof et al, “Revision of the CEAP Classification for Chronic Venous Disorders: Consensus Statement,” Journal ofVascular Surgery, vol. 40, No. 6 (2004), 1248-1252.el, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 6 pages (Filed Apr. 26, 2017).
Ulthera, Inc., Reply in Support of Petition for Inter Partes Review in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 33 pages (Filed Aug. 2, 2017).
ULTHERA Exhibit 1022, Use of the Argon and Carbon Dioxide Lasers for Treatment of Superficial Venous Varicosities of the Lower Extremity, D. Apfelberg et al., Lasers in Surgery and Medicine, vol. 4.3, pp. 221-231 (1984) (filed Aug. 2, 2017 in re IPR2016-01459).
ULTHERA Exhibit 1023, 532-Nanometer Green Laser Beam Treatment of Superficial Varicosities of the Lower Extremities, T. Smith et al., Lasers in Surgery and Medicine, vol. 8.2, pp. 130-134 (1988) (filed Aug. 2, 2017 in re IPR2016-01459).
ULTHERA Exhibit 1024, Deposition Transcript of Dr. Mark Palmeri on Jul. 11, 2017 (filed Aug. 2, 2017 in re IPR2016-01459).
ULTHERA Exhibit 1025, Ulthera Oral Proceeding Demonstrative Slides (filed Oct. 2, 2017 in re IPR2016-01459).
DERMAFOCUS Exhibit 2027, DermaFocus Oral Proceeding Demonstrative Slides (filed Oct. 2, 2017 in re IPR2016-01459).
PTAB Record of Oral Hearing held Oct. 4, 2017 in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 67 pages (PTAB Document sent to Ulthera on Nov. 1, 2017).
Final Written Decision of Inter Partes Review in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 37 pages [030] (Entered Jan. 19, 2018).
Adams et al., “High Intensity Focused Ultrasound Ablation of Rabbit Kidney Tumors” Sonablate High-Intensity Focused Ultrasound device; Journal of Endourology vol. 10, No. 1, (Feb. 1996).
Brown J A et al: “Fabrication and performance of 40-60 MHz annular arrays”, 2003 IEEE Ultrasonics Symposium Proceedings. Honolulu, Hawaii, Oct. 5-8, 2003; [IEEE Ultrasonics Symposium Proceedings], New York, NY : IEEE, US, vol. 1, Oct. 5, 2003 (Oct. 5, 2003), pp. 869-872.
Carruthers et al., “Consensus Recommendations for Combined Aesthetic Interventions in the Face Using Botulinum Toxin, Fillers,and Energy-Based Devices” Dermatol Surg 2016 (pp. 1-12).
Driller et al., “Therapeutic Applications of Ultrasound: A Review” IEEE Engineering in Medicine and Biology; (Dec. 1987) pp. 33-40.
Ketterling J. A. et al.: “Design and fabrication of a 40-MHz annular array transducer”, IEEE Transactions On Ultrasonics, Ferroelectrics And Frequency Control, IEEE, US, vol. 52, No. 4, Apr. 1, 2005 (Apr. 1, 2005), pp. 672-681.
MICROCHIP microID 125 kHz EFID System Design Guide, Microchip Technology Inc. (2004).
Sonocare, Inc. Therapeutic Ultrasound System Model CST-100 Instruction Manual (1985).
Webster et al. “The role of ultrasound-induced cavitation in the ‘in vitro’ stimulation of collagen synthesis in human fibroblasts”; Ultrasonics pp. 33-37(Jan. 1980).
Ulthera, Inc., Petitioner Notice of Appeal to Federal Circuit 2018-1542 re: IPR2016-01459; 4 pages from [001] (no appendices) (Filed Feb. 9, 2018).
Federal Circuit Order Granting Ulthera Motion to Remand, re: 2018-1542; 4 pages [022] (Dated May 25, 2018).
Ulthera Brief (Corrected), Fed. Cir. Appeal Case 19-1006 from re: IPR2016-01459; 136 pages [030] (Dated Apr. 3, 2019).
DermaFocus Brief (Corrected), Fed. Cir. Appeal Case 19-1006 from re: IPR2016-01459; 73 pages [032] (Dated Apr. 4, 2019).
Related Publications (1)
Number Date Country
20190142380 A1 May 2019 US
Provisional Applications (4)
Number Date Country
62375607 Aug 2016 US
62482440 Apr 2017 US
62482476 Apr 2017 US
62520055 Jun 2017 US