Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
  • A61H23/00—Percussion or vibration massage, e.g. using supersonic vibration; Suction-vibration massage; Massage with moving diaphragms
  • A61H23/02—Percussion or vibration massage, e.g. using supersonic vibration; Suction-vibration massage; Massage with moving diaphragms with electric or magnetic drive
  • A61H23/0245—Percussion or vibration massage, e.g. using supersonic vibration; Suction-vibration massage; Massage with moving diaphragms with electric or magnetic drive with ultrasonic transducers, e.g. piezoelectric
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
  • A61H31/00—Artificial respiration or heart stimulation, e.g. heart massage
  • A61H31/004—Heart stimulation
  • A61H31/006—Power driven
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
  • A61N1/00—Electrotherapy; Circuits therefor
  • A61N1/18—Applying electric currents by contact electrodes
  • A61N1/32—Applying electric currents by contact electrodes alternating or intermittent currents
  • A61N1/36—Applying electric currents by contact electrodes alternating or intermittent currents for stimulation
  • A61N1/362—Heart stimulators
  • A61N1/3629—Heart stimulators in combination with non-electric therapy
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
  • A61N1/00—Electrotherapy; Circuits therefor
  • A61N1/18—Applying electric currents by contact electrodes
  • A61N1/32—Applying electric currents by contact electrodes alternating or intermittent currents
  • A61N1/36—Applying electric currents by contact electrodes alternating or intermittent currents for stimulation
  • A61N1/362—Heart stimulators
  • A61N1/3627—Heart stimulators for treating a mechanical deficiency of the heart, e.g. congestive heart failure or cardiomyopathy
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
  • A61N1/00—Electrotherapy; Circuits therefor
  • A61N1/18—Applying electric currents by contact electrodes
  • A61N1/32—Applying electric currents by contact electrodes alternating or intermittent currents
  • A61N1/38—Applying electric currents by contact electrodes alternating or intermittent currents for producing shock effects
  • A61N1/39—Heart defibrillators
  • A61N1/3956—Implantable devices for applying electric shocks to the heart, e.g. for cardioversion
  • A61N1/3962—Implantable devices for applying electric shocks to the heart, e.g. for cardioversion in combination with another heart therapy
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
  • A61N1/00—Electrotherapy; Circuits therefor
  • A61N1/18—Applying electric currents by contact electrodes
  • A61N1/32—Applying electric currents by contact electrodes alternating or intermittent currents
  • A61N1/38—Applying electric currents by contact electrodes alternating or intermittent currents for producing shock effects
  • A61N1/39—Heart defibrillators
  • A61N1/3956—Implantable devices for applying electric shocks to the heart, e.g. for cardioversion
  • A61N1/3962—Implantable devices for applying electric shocks to the heart, e.g. for cardioversion in combination with another heart therapy
  • A61N1/39622—Pacing therapy
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
  • A61N7/00—Ultrasound therapy
  • A61N2007/0004—Applications of ultrasound therapy
  • A61N2007/0021—Neural system treatment
  • A61N2007/0026—Stimulation of nerve tissue
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
  • A61N7/00—Ultrasound therapy

Definitions

• the present invention relates generally to medical devices and treatment methods. More particularly, the present invention relates to methods and apparatus for treating heart failure and conditions related to heart failure with vibrational energy.
• HF Heart failure
• ACC American College of Cardiology
• AHA American Heart Association
• HF generally results from underlying factors such as hypertension, diabetes, valvular disease, cardiomyopathy, coronary artery disease, and structural changes to the heart muscle.
• HF is characterized by reduced ventricular wall motion in systole and/or diastole as well as a low ejection fraction.
• U.S. Patent No. 4,651,716 describes externally applied ultrasonic energy to enhance cardiac contractility.
• Patents describing the treatment of heart conditions using mechanical shock therapy include U.S. Patent Nos. 6,408,205; 6,330,475; 6,110,098; and 5,433,731.
• Other patents of interest include U.S. Patent Nos. 6,539,262; 6,439,236; 6,233,484, 5,800,464; 5,871,506; 5,292,338; 5,165,403; and 4,651,716; and WO 03/070323 and WO 99/061058, which relate to other systems applying treatment for arrhythmias, heart failure, and contractility.
• Medical publications discussing the effects of ultrasound energy and/or mechanical action on the heart and heart failure treatments include:
• Forester GV et al. Ultrasound Intensity and Contractile Characteristics of Rat Isolated Papillary Muscle. Ultrasound in Med. And Biol. 1985;11(4):591-598 Forester GN, Roy OZ, and Mortimer AJ, Enhancement of contractility in rat isolated papillary muscle with therapeutic ultrasound. Mol. Cell Cardiol. 1982; 14(8):475-7.
• the present invention relies on the beneficial and ameliorative effects of vibrational energy to improve cardiac function in patients suffering from or at risk of heart failure.
• Vibrational energy is applied from an implanted or external transducer under a variety of particular protocols, depending on the patient condition and the desired therapy.
• the delivery of vibrational energy to the heart provides at least one of an increase in contractility, vasodilation, tissue perfusion, and/or an increase in cardiac output.
• vibrational energy may be delivered substantially continually in order to promote long-term improvement in cardiac function.
• substantially continually it is meant that vibrational energy will be applied at all times or, more usually, at regular intervals in order to promote a long-term improvement in heart function.
• the vibrational energy may be delivered in response to a manually initiated signal, typically initiated by medical personnel or the patient in response to an acute cardiac episode in order to treat symptoms, or alternatively, in order to assess whether a patient would benefit from vibrational therapy.
• the vibrational energy will be delivered in automatic response to detection of a cardiac event.
• the event will preferably be detected by implanted sensors which are part of or linked to the control circuitry for a vibrational transducer.
• the sensors would be adapted for use to detect changes in blood pressure, O 2 saturation, heart chamber dimensions, changes or patterns in ECG waveform morphology, contractility, or other types of indicators of heart failure conditions.
• the vibrational energy will be delivered following defibrillation, typically by an implanted defibrillator.
• the vibrational energy may be delivered following termination of the defibrillation therapy or, in some cases, may at least partly overlap the defibrillation therapy.
• the vibrational transducer will be configured to apply vibrational energy to at least a portion of the heart, often including at least the ventricular regions of the heart and more typically including all regions of the heart.
• the implantable vibrational transducers may be implanted at least partially over the patient's ribs or sternum, or at least partially within a gap between the patient's ribs, or at least partially under the patient's ribs, or in the abdomen.
• the gap will usually be the natural intercostal space, but in other instances could be a gap resulting from removal of one or more ribs to define the implantation space.
• the implantable vibrational transducers may be either within or outside of the peritoneal cavity.
• Delivery of the vibrational energy for the treatment of HF may comprise activating a single piezo-electric transducer, activating a piezo-composite material, sequentially activating individual vibrational transducer segments, or the like.
• the nature of the vibrational energy is set forth in detail below, but will usually have a frequency in the range from 0.02 to 10 MHz, a burst length less than 5,000 cycles, a burst rate less than 100 kHz, a duty cycle less than 50%, a mechanical index less than 20, and a thermal index less than 4.
• the vibrational energy will be delivered to at least 50% of the heart, preferably at least 75%) of the heart, but alternatively may be less than 50%>, of the heart.
• systems for treating HF comprise a vibrational transducer and control circuitry for detecting the onset of a cardiac event, such as reduced contractility, associated with HF and for activating the vibrational transducer.
• the vibrational transducer is preferably implantable in a patient in the subcutaneous space near the patient's heart, and the control circuitry is adapted to cause the transducer to deliver controlled vibrational energy, usually ultrasonic energy, to the heart under conditions which promote improved cardiac function. Such conditions were described generally above in connection with the methods of the present invention.
• the implantable vibrational transducer and control circuitry will usually be packaged in a common housing, but in some instances may be packaged separately in separate implantable housings, and typically connected by a cable.
• the vibrational transducer may comprise any of the structures described above, and the transducer will operate under the conditions described above.
• the control circuitry may optionally comprise sensors such as ECG elements or other conventional circuitry for detecting cardiac events related to HF, and will usually further comprise a signal generator for the transducer, a power amplifier, and an impedance matching circuit, optionally including multiple such circuits for multi-segmented transducers.
• the ECG elements and circuitry are also useful for synchronizing delivery of the vibrational energy with the heart rhythm.
• the circuitry will further comprise a battery or a remotely rechargeable battery, such as a battery which may be recharged using inductive coupling.
• Figs. 1A and IB are schematic illustrations of a longitudinal vibrational wave traveling through biological tissue.
• Fig. 1 A shows the pulse repetition period (PRP) while Fig. IB shows the details of a single burst or pulse.
• Fig. 2 is a schematic illustration of the effects of frequency (wavelength) on the focal characteristics of an ultrasonic beam.
• Fig. 3 illustrates high frequency beams from convex, flat, and concave apertures which form divergent, mildly focused, and sharply focused beams, respectively.
• Figs. 4A and 4B illustrate the anatomy in which the vibrational transducers of the present invention are to be implanted.
• Figs. 5A-5C illustrate alternative implantation sites for the vibrational transducers and transducer assemblies of the present invention.
• Fig. 6 illustrates a first embodiment of a vibrational transducer assembly constructed in accordance with the principles of the present invention.
• Fig. 7 illustrates a second embodiment of a vibrational transducer assembly constructed in accordance with the principles of the present invention.
• Fig. 8 illustrates a third embodiment of a vibrational transducer assembly constructed in accordance with the principles of the present invention.
• Figs. 9A and 9B illustrate a circuit configuration (Fig. 9A) and serial burst pattern (Fig. 9B) which would be suitable for operating the vibrational transducer assembly of Fig. 8.
• Fig. 10 is a block diagram showing an embodiment of the control circuitry implementation of the present invention.
• Figs. 11 A and B illustrate an implantation site as in Fig. 5C for the vibrational transducers and transducer assemblies of the present invention in the anterior chest.
• Fig. 12 illustrates a system constructed in accordance with the principles of the present invention for chronically treating a patient in order to promote long-term improvement in heart function.
• Fig. 13 illustrates a system constructed in accordance with the principles of the present invention for treating acute cardiac events associated with heart failure.
• Fig. 14 illustrates a system constructed in accordance with the principles of the present invention for permitting the patient or other individual to manually initiate vibrational treatment to improve heart function.
• Fig. 15 illustrates a system constructed in accordance with the principles of the present invention for automatically delivering vibrational energy to improve heart function following treatment with an implantable defibrillator.
• the present invention relies on directing vibrational energy, particularly ultrasound energy, into cardiac tissue in order to improve cardiac function.
• vibrational energy particularly ultrasound energy
• An understanding of the nature of ultrasound energy and biological tissue is of use.
• Ultrasound in biological tissues is virtually exclusively a longitudinal traveling wave, as illustrated in Figures 1A and IB.
• the wave travels at typically 1.5 millimeters per microsecond, in a straight line unless reflected or refracted.
• Ultrasound may be CW (continuous wave), meaning it is on all the time, or burst mode, comprising periods of ON time separated by lengths of OFF time (Fig. 1A).
• the lengths of the ON and OFF periods may be the same or different, and the total of the "on time” and the "off time” is referred to as the pulse repetition period (PRP).
• PRP pulse repetition period
• ultrasound waves do not come up to peak amplitude instantaneously.
• the number of cycles involved in the rise time and the fall time are approximately equal to the Q (quality factor) of the device.
• the period of an ultrasound wave is the time for one complete cycle.
• the reciprocal of period is the frequency. Bursts may occur at any selected frequency.
• the burst rate is defined as the pulse repetition frequency (PRF), which is the reciprocal of the pulse repetition period (1/PRP).
• PRF pulse repetition frequency
• the amplitude of the wave can be defined in terms of pressure. In power applications, the magnitude of peak positive pressure is usually greater than that of the peak negative pressure.
• the waveform is slightly asymmetric due to non-linearities. These non-linearities arise from different velocities of sound in the body as a function of signal strength, and are dependent on the distance of travel through tissue and of course, amplitude.
• the duty cycle is defined as the percent of time the ultrasound is in the ON state. Thus, a continuous wave would have a duty cycle of 100 percent.
• Intensity is the ultrasound power per unit area.
• Ispta intensity, spatial peak temporal average
• Isppa intensity, spatial peak pulse average
• MI Mechanical Index
• TI Thermal Index
• An ultrasound beam is attenuated by the tissues through which it propagates. Tissue motion has no effect on ultrasound attenuation. At frequencies below 5 MHz, attenuation in blood is negligible. Attenuation in myocardium, muscle, fat, and skin is approximately 0.3 dB per MHz per centimeter of propagation path. Consequently, a 1 MHz beam will suffer little attenuation through the body wall and heart. All frequencies of ultrasound do not propagate well through air; it is virtually totally attenuated. The lungs and bowel gas essentially totally obstruct the beam. Attenuation in bone is strongly frequency-dependent. The attenuation at 1 MHz is in excess of 12 dB, rising almost linearly with frequency. At 100 kHz, attenuation is negligible.
• Ultrasonic beams are highly dependent on the aperture of the radiator and the frequency, and whether the beam is continuous wave or burst mode.
• a simple rule is that in the far field, the beam width is given by the wavelength divided by the aperture.
• a low frequency (Low f) beam might be almost isotropic (equal intensity in all directions) while a high frequency (High f) beam will be focused, as illustrated in Figure 2.
• the shape of the aperture will affect the beam.
• Figure 3 depicts high frequency beams from convex, planar, and concave apertures, forming divergent, mildly focused, and sharply focused beams, respectively.
• pulsed and continuous beams have approximately the same profiles, hi the near field, however, continuous beams are characterized by multiple peaks and valleys due to constructive and destructive interference, respectively, of wavefronts from across the aperture. (For short bursts of ultrasound, constructive and destructive interference is limited to emissions from smaller portions of the aperture, and consequently, near field emission profiles are more uniform.)
• the present invention relies on directing ultrasound and other vibrational energy to regions of the heart H in order to stabilize cardiac function and/or treat an acute event associated with HF as generally discussed above.
• the present invention will provide for directing the ultrasonic energy to at least 50% of the heart, preferably at least 75%.
• the vibrational transducer assembly As the heart is located beneath the body wall (BW), ribs R and sternum S, however, the vibrational transducer assembly (as described in greater detail below) must be properly located to deliver the energy. Bone and cartilage significantly attenuate the propagation of high frequency ultrasonic energy, and the lungs L (which are filled with air) will totally obstruct the transmission of such energy.
• a vibrational transducer assembly 10 either over the ribs R and/or sternum, as shown in Fig. 5C, between or in place of the ribs, as shown in Fig. 5B, or perhaps less desirably under the ribs R, as shown in Fig. 5 A.
• the vibrational transducer assembly 10 will usually be placed over or spaced slightly anteriorly from the pericardium. Alternatively, but not shown, the transducer assembly may be implanted in the abdomen, either within or outside of the peritoneal cavity.
• a first exemplary vibrational transducer assembly 10A comprises a quarter wave front surface matched device.
• a half-wave thickness of piezoelectric ceramic 12 is sandwiched between thin layer electrodes 14 having leads 17 and a quarter- wave matching layer 16 disposed over the first surface.
• the piezo- electric ceramic 12 is positioned in a housing 18 with an air cavity 20 at its rear surface, hi this way, the quarter- wave matching layer 16 provides a front surface of the assembly 10A, and the edges and back of the housing need only be strong enough to provide mechanical support.
• the air cavity 20 will typically have a width of about 1 mm, and the thickness of the ceramic and matching layer will vary depending on the desired frequency of operation. Table 1 below shows the operational frequencies and thicknesses of the ceramic layer 12 and matching layer 16.
• the methods of the present invention likely result from the mechanical effects of ultrasound.
• the maximum frequency might be on the order of 1 MHz.
• the device package thickness might be on the order of 30 mm thick, probably the maximum acceptable for an implant. If the device needs to be implanted over the ribs, or placed externally, the low frequencies are preferred. At 0.25 MHz, the attenuation due to bone might be minimal, thus suggesting an operational frequency in the 0.10 to 0.5 MHz range.
• the transducer assembly 10A may be substituted with a 1-3 piezo- composite material instead of the piezo-electric ceramic.
• Piezo-composite material consists of piezo-electric ceramic posts in a polymer matrix. Such materials are thinner than the equivalent pure ceramic material needed to achieve a particular frequency and there is no need to provide a matching layer. Thus, a simple seal providing electrical insulation may be substituted for the matching layer 16 of Fig. 6. Suitable thicknesses for the piezo-composite material are shown in Table 2 below.
• the piezo-composite materials have another significant benefit in that they can be easily curved, potentially to conform to anatomical features or to optimize the transducer beam profile. It must be remembered that any curvature will affect the focal characteristics of the device.
• the transducer assembly 10A may be substituted with recently developed higher strain materials such as single crystal or polymer piezo-electrics instead of the piezo-electric ceramic.
• the single crystal materials would utilize a similar structure as depicted in Figure 6.
• Polymer piezo-electric materials may be backed by a rigid foam material and would utilize a layer of high voltage insulator over the front surface instead of a quarter-wave matching layer.
• the polymer piezo-electric material may be backed with a high impedance material. Both backing techniques facilitate the proj ection of the maximum amount of energy into the patient.
• Driving materials for transducers may also include any other electromechanical material, a specific example being magnetostrictive materials.
• a vibrational transducer assembly 10B may be formed as a variation on a Tonpilz transducer where a piezo drive 30 (shown as a stack of piezo- electric material) induces ultrasonic vibration in a front vibrator 32.
• the package 34 provides the necessary tail mass for operation of the transducer assembly.
• a structure (not shown) for retaining the front surface vibrator 32 against the ceramic stack 30 and housing 34 may be provided. Strong vibrations of the surface vibrator may exceed the tensile strength of the ceramic and/or bonding material.
• Such transducer assemblies are particularly well suited to operation at low frequencies, 0.1 MHz and below.
• the device of the present invention may require an aperture generating a relatively wide acoustic beam in order to deliver ultrasonic or other vibrational energy over a relatively large portion of the heart. Due to biological constraints, the transducer may be in close proximity to the heart, and as such, the heart will be in the near field of the acoustic beam. With typical human heart dimensions of 12 cm in length and 10 cm in width, the ultrasonic or other vibrational energy aperture will typically be circular with a diameter on the order of 10 cm, more preferably elliptical with long and short axes of 12 and 10 cm, respectively, and most preferably elliptical with the ultrasonic or other vibrational energy aperture slightly exceeding the dimensions of the heart to assure maximal coverage of myocardium with therapeutic energy. It is recognized that many different sizes of devices might be required to meet the needs of different sized patients.
• the single crystals may be wired in parallel and be driven by a single signal generator, power amplifier, and impedance matching circuit.
• the single crystals may have individual signal generators, driving amplifiers, and/or impedance matching circuits for parallel or serial operation.
• the single crystals may be driven in a sequential (multiplexed) manner by a single signal generator, power amplifier, and matching circuit.
• All of the alternative devices may be driven with a high voltage and a high current. After appropriate electrical impedance matching, the current drain on the battery may exceed the capability of the same. It is thus proposed to segment the aperture into multiple individual pieces of piezo-electric, as depicted in Figure 8 and as described above.
• each element may be driven by an individual power amplifier, impedance matching circuit, and signal generator (or a signal generator gated to individual amplifiers).
• the single crystals may be driven in a sequential (multiplexed) manner by a single signal generator, power amplifier, and matching circuit. As such then, exposure of the heart would be segmental. If, for example, the aperture consisted of 10 elements, operating with 5 cycles at 1 MHz, each element might be triggered every 50 microseconds, allowing for an effective 10 percent duty cycle. This would reduce the peak current demand on the battery by a factor of 10.
• the ultrasonic transducer may also be structured as a two-dimensional phased array or as an annular array to achieve specific requirements related to the delivery of ultrasonic power uniformly throughout the heart.
• each element would be driven individually such that the combination of elements produces a sharp or broad beam in a particular direction.
• each element may be driven in serial format to generate a roster of individual beams with wider profiles.
• the mosaic of individual pieces may be mounted on a flat coplanar surface, or the devices might be so mounted as to give the front surface of the device either a concave or convex surface for better implantation under the patient's skin.
• Figure 9A and 9B depict one possible circuit configuration for generating serial bursts from the segmented aperture, and further depicts the interlaced output from each of the individual elements within the aperture. It is possible to generate multiple bursts from every element during a small fraction of the cardiac cycle. The myocardium will effectively experience simultaneous ultrasound exposure. Care must be exercised in the implementation of this concept to prevent excessive beam spreading from the smaller elements and loss of far field signal strength. Low frequency devices would be more prone to this problem than high frequency devices.
• the segmented aperture of individual elements of electro mechanical material, or clusters of one to several posts of a piezo composite material may be driven in a phased sequence, so as to create an ultrasound beam in one of several particular directions.
• “Phasing” means that the driving signals applied to all elements or segments of the aperture have such time delays that the wavefronts from each element or segment arrive at a designated tissue mass at the same time (constructive interference). Although the amplitude in this tissue mass will be greater due to the focusing effect of the phased aperture, the beam may no longer cover the entire region of tissue requiring treatment.
• the beam may be directed to multiple tissue masses in the region of treatment, so as to effectively uniformly expose the entire region with ultrasound.
• Circuit configurations for operation in a phased array mode may be quite similar to the circuit configuration depicted in Figure 9A.
• All elements would be operative at the same time, albeit with different time delays.
• the burst generator would provide the different time delays which would be directed to specific amplifiers/elements through the multiplexer (MUX). Multiple sets of time delays would result in beams in multiple directions.
• the aperture maybe comprised of a series of segments or elements in a linear arrangement.
• Such an array of elements may be implanted or fixed externally for directing vibrational energy to the heart from between the ribs.
• a second string of elements could be implemented in similar format, for directing vibrational energy to the heart through another intercostal space, either above or below the first string of elements.
• a string of elements may be implemented over the sternum.
• the single or multiple linear strands of aperture segments or elements can be electrically driven in parallel or in serial format, or driven in a phased format for targeting of a specific region of the heart, or for sweeping the ultrasonic beam across a greater portion of the heart.
• the device of the present invention may not require an aperture for generating a wide acoustic beam since it is not necessary for the acoustic beam to deliver energy to the majority of the heart.
• pacing may be accomplished by delivering vibrational energy from a portion of the transducer aperture using a segmental design, or alternatively, from a separate transducer aperture generating a narrower acoustic beam. If using a separate transducer, the separate transducer may be smaller in size and of a different shape.
• the invention may be comprised of one or more that one transducer assembly, connected by a cable (not illustrated).
• the desired effect is a mechanical effect.
• Operating a transducer in continuous wave mode creates a maximum thermal effect and a minimal mechanical effect.
• Operating in a burst mode with a low duty cycle and a high amplitude minimizes thermal effects and maximizes mechanical effects.
• high burst rates (and short burst lengths) provide the yet further enhancements to a mechanical effect. Consequently, a preferred design will be for shortest possible burst lengths, maximum amplitude, and duty cycle to the thermal limit.
• the overhead on the aperture is expected to be minimal, perhaps adding 5 to 10 mm to the diameter of a device.
• the thickness of the device will be defined by the type and the frequency.
• the electronics package (and battery) can be combined with the transducer or can be separately housed, with a cable between the two units.
• Figure 10 represents a block diagram of a possible electronics package.
• the sensor circuit would be monitoring the heart and the power side of the system would generally remain idle until a specified time interval has elapsed or after a cardiac event has occurred.
• the sensor circuits may be integral with the CPU. Once the time interval has elapsed or the event is detected, the CPU would trigger the burst generator which would generate a preprogrammed series of bursts, for a specified period of time or until sensor monitoring indicates that heart function has returned to an acceptable level.
• the electrical bursts would pass to a power amplifier, an impedance matching circuit, and on to the transducer.
• a battery would supply power for the typically digital circuits in the CPU, telemetry, sensor, and burst generator, the typically analog circuits in the front ends of the sensor and amplifier, and to a voltage converter producing the high voltage for the output stages of the amplifier.
• Monitoring circuitry would provide feedback to the CPU about the actual performance of the power amplifier and transducer(s).
• a battery volume on the order of one or two commercial "D" cells is anticipated.
• the amplifier and impedance matching circuits might require on the order of 25 cubic centimeters of volume, and the digital portions on the order of 5 cubic centimeters. In all, it is reasonable to assume that the package could be implanted into the chest of a human.
• Use of a rechargeable battery system utilizing transcutaneous inductive energy transmission or other charging apparatus may be beneficial.
• the circuitry of Fig. 10 may be adapted to drive the associated vibrational transducer under conditions which will impart vibrational energy to the heart so that HF is abated.
• the vibrational transducer may be operated under the conditions specified in Table 3.
• the device of the present invention may or may not allow for synchronization of the therapeutic ultrasound or vibrational energy burst to the cardiac cycle.
• the system will immediately initiate the preprogrammed therapeutic protocol, irrespective of the time point on the cardiac cycle.
• the system may trigger during any time within specified intervals of the cardiac cycle.
• the system may trigger treatment during a specific portion of the cardiac cycle, for example, during the refractory period.
• the refractory period is defined as that portion of the cardiac cycle in which the heart tissue is not excitable.
• vibrational therapy might be applied for the complete cardiac cycle or a portion thereof. It is further anticipated that the vibrational energy therapy might be repeated for more than one cardiac cycle.
• HF HF
• the vibrational transducers may be adapted for manual control by either the patient or by a doctor or other medical personnel.
• Treatment of HF may be accomplished with implanted vibrational transducers, with both automatically triggered and manually triggered modalities.
• the circuitry for automatic triggering of transducers has been discussed above.
• Manual triggering may be accomplished using an external wand, such as a radio frequency or magnetic controller, in order to initiate operation of the transducer.
• an implantable transducer 120 may be placed subcutaneously in an area of the anterior chest directly over the ribs and/or sternum and preferably over the ventricular region of the heart, as shown in Figs. 11 A and 1 IB.
• the vibrational transducers may be incorporated into external units capable of being applied to the anterior chest. Such units will both provide for acute treatment and enable the determination of patients in whom a subsequent implantable system will be beneficial.
• the patient will usually be reclining on the table, bed, or ground; vibrational transducer attached to an external generator by an attached cord is applied over the patient's chest, preferably using a gel layer to enhance contact.
• the transducer will be placed generally over the heart and the transducer may be configured to direct the energy over a specific region, preferably the ventricular region.
• circuitry for sensing the electrocardiogram will usually be included in order to synchronize the timing of the delivery of the vibrational energy to an appropriate point in the cardiac cycle based on detection of the ventricular QRS .
• vibrational transducer systems described above will be combined with suitable circuitry and other components in order to permit actuation of the transducer(s) under particular conditions and in response to particular events, depending on the desired treatment protocol to be implemented.
• the vibrational transducer systems may function automatically in response to detected conditions or may be activated manually by an external activator, such as a patient "wand" or radiofrequency remote control which permits the patient to initiate function of the transducer whenever desired.
• a system 200 constructed in accordance with the principles of the present invention for allowing chronic treatment of the heart in order to provide long-term benefit is illustrated.
• the system comprises an ultrasound transducer 202, as generally described above.
• the system 200 will include processing circuitry 204 which will control the timing and duration of transducer operation.
• the ultrasound energy may be delivered continuously or under a simple timed program.
• the vibrational energy will be delivered in a manner synchronized with a portion of the cardiac cycle in order to avoid undesirable arrhythmic effects.
• the system includes electrodes 206 implanted to detect heart function, signal processing circuitry 208, waveform and rate analysis circuitry 210, and circuitry 212 for synchronizing operation of the transducer with the detected ECG.
• the system will be adapted to permit external communication in order to reprogram the system, retrieve patient data, and the like.
• System 300 includes transducer 302, output processing circuitry 304, ECG synchronization circuitry 312, electrodes 306, signal processing circuitry 308, and waveform and rate analysis circuitry 310, generally as described above for system 200.
• Data from the physiologic sensor 316 is fed to sensor processing circuitry 318 which in turn is delivered to circuitry 320 which is programmed to detect the cardiac event to be treated.
• the signal is sent to the ECG synchronization circuitry in order to initiate ultrasound function.
• the system 300 will also include a communications link 214 capable of wireless communication in order to reprogram the system, retrieve patient data, and the like.
• the system 400 includes output processing circuitry 404, ECG synchronization circuitry 412, electrodes 406, signal processing circuitry 408, and waveform and rate analysis circuitry 410, as generally described with the prior systems.
• a manual activation sensor 420 is further provided in order to permit the user or other individual to selectively initiate output of the ultrasound transducer whenever desired, typically when the patient senses a cardiac event.
• external circuitry 414 will be provided to permit external reprogramming of the system.
• a system 500 for initiating ultrasound transducer operation after or overlapping with operation of an implantable cardiac defibrillator includes an ultrasound transducer 502, output processing circuitry 504, ECG synchronization circuitry 512, ECG electrodes 506, signal processing circuitry 508, and waveform and rate analysis circuitry 510, as generally described above with the prior systems.
• Implantable circuitry 520 is further provided and coupled to an implantable defibrillator in order to detect operation of the ICD; alternatively, the circuitry 520 would remotely sense the operation of the ICD. The circuitry 520, once defibrillator actuation is detected, will initiate operation of the ultrasound transducer in order to deliver vibrational energy to the heart.
• the vibrational transducer operation will be initiated immediately following discharge of the ICD. It is possible, however, that the ultrasound transducer operation could be initiated to briefly overlap with the firing of the ICD.
• an external link is preferably provided in order to permit external reprogramming of the system.
• the HF systems of the present invention may be combined with an ICD (or other implantable therapeutic and/or diagnostic device) in a common enclosure, optionally sharing a power supply, communications circuitry and/or other common features.

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• 2004
  • 2004-06-15 WO PCT/US2004/018991 patent/WO2004112885A2/en active Application Filing
  • 2004-06-15 EP EP04755327A patent/EP1644078A4/de not_active Withdrawn
  • 2004-06-15 EP EP04755270A patent/EP1641526A4/de not_active Withdrawn
  • 2004-06-15 EP EP04755325A patent/EP1641519A4/de not_active Withdrawn
  • 2004-06-15 JP JP2006517293A patent/JP2007523670A/ja not_active Withdrawn
  • 2004-06-15 WO PCT/US2004/019084 patent/WO2004112887A2/en active Application Filing
  • 2004-06-15 WO PCT/US2004/019082 patent/WO2004112886A2/en active Application Filing
  • 2004-06-15 AT AT04755266T patent/ATE462471T1/de not_active IP Right Cessation
  • 2004-06-15 WO PCT/US2004/018987 patent/WO2004112895A1/en active Application Filing
  • 2004-06-15 DE DE602004026308T patent/DE602004026308D1/de not_active Expired - Lifetime
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