The present invention relates to a urinary incontinence treatment apparatus comprising an operable restriction device implantable in a patient, who suffers from urinary incontinence, for engaging the urethra or urine bladder, to form a restricted urine passageway in the urethra or urine bladder. The restriction device is operable to change the restriction of the urine passageway, i.e. to close and enlarge the urine passageway. The term “patient” includes an animal or a human being.
Urine incontinence is a widespread problem. Many people are helped through training of the muscles in the pelvic floor but too many have severe problems with urine leakage. Many different solutions to this problem have been tried. For example, there is a prior manually operated urine incontinence treatment apparatus having an artificial hydraulic sphincter device engaging the urethra and connected to an elastic reservoir implanted in the scrotum or in the region of the labia major. A disadvantage of this prior apparatus is that over time hard fibrosis is developed around the reservoir, which may cause malfunction of pumping components. Furthermore, it is a rather complicated task to manually squeeze the elastic implanted reservoir to pump hydraulic fluid to open the sphincter device when the patient needs to urinate. In particular women can get their fingers wet. The created fibrosis will sooner or later become a hard fibroid layer, which may make it even more difficult to pump the reservoir. Yet a further disadvantage is that the use of hydraulic fluid always entails a risk of fluid leaking from implanted hydraulic components.
A prior hydraulic apparatus designed to compress the urethra is disclosed in U.S. Pat. No. 5,520,606. A prosthetic sphincter with an inflatable cuff, which surrounds the urethra or encloses it on two sides, is disclosed in for example U.S. Pat. Nos. 4,571,749 and 4,222,377. U.S. Pat. No. 4,969,474 discloses a hydraulic method for treating both men and women with urinary incontinence problems in the same way. The apparatus of U.S. Pat. No. 4,969,474 includes a reservoir containing fluid and an inflatable compression means designed to compress urethra without risking tissue loss or necrosis to occur. An artificial hydraulically operated urethra sphincter employing an external magnet to achieve closure of the urethra cuff is disclosed in U.S. Pat. No. 5,562,598.
A prior mechanical prosthetic sphincter disclosed in U.S. Pat. No. 4,619,245 comprises a manually controllable actuating component for implanting at a convenient location in the patient's body.
The object of the present invention is to provide a new convenient urinary incontinence treatment apparatus, the performance of which may be affected by the patient at any time after operation, in particular when various needs arise over the course of a day, so that the patient substantially always is satisfied or comfortable.
This object is achieved by a urinary incontinence treatment apparatus of the kind stated initially characterised by an energy transmission device for wireless transmission of energy from outside the patient's body to inside the patient's body for use in connection with the operation of the restriction device including enlarging or restricting the urine passageway, when the restriction device is implanted.
As a result, the advantage is achieved that the urinary incontinence treatment apparatus of the invention provides simple and effective energy transmission that ensures long reliable function of the apparatus, possibly for the rest of the patient's life.
Generally, the apparatus comprises an energy transforming device implantable in the patient for transforming the energy wirelessly transmitted by the energy transmission device from a first form into a second form, preferably different than the first form.
The energy transforming device may comprise at least one semiconductor type of component or a circuitry of such semiconductor components. The semiconductor component may comprise a transistor or microchip or similar electronic components. However, the semiconductor component may not comprise rectifying diodes.
In accordance with a main embodiment of the invention, the energy transforming device comprises at least one element having a positive region and a negative region and adapted to create an energy field between the positive and negative regions when exposed to the energy of the first form transmitted by the energy transmission device, so that the energy field provides the energy of the second form. Typically, the above-mentioned semiconductor component may include such an element.
In accordance with a preferred embodiment of the invention, the element comprises an electrical junction element capable of inducing an electric field between the positive and negative regions when exposed to the energy of the first form transmitted by the energy transmission device, whereby the energy of the second form comprises electric energy.
Consequently, the restriction device suitably is electrically operated, whereby the positive and negative regions of the electrical junction element supply electric energy for the operation of the restriction device. The apparatus suitably comprises implantable electric conductors connected to the positive and negative regions of the electrical junction element, whereby the electrical junction element is capable of supplying an electric current, such as a direct current, a pulsating direct current, a combination of a direct and pulsating direct current, an alternating current or a combination of a direct and alternating current, via the conductors. Furthermore, the electrical junction element may be capable of supplying a frequency, amplitude, or frequency and amplitude modulated analog, digital, or a combination of analog and digital signal, which is used in connection with control of the restriction device.
The element, preferably in the form of an electrical semiconductor junction element, should be designed to generate an output current exceeding 1 μA when exposed to the energy of the first form transmitted by the energy transmission device. Suitably the electrical junction element forms a flat and thin sheet and has a volume of less than 2000 cm3 to be suited for subcutaneous implantation, so that the electrical junction element can be located just behind the skin of the patient. Alternatively, it would be possible to implant the element in the thorax or cephalic region of the patient, or in an orifice of the patient's body and under the mucosa or intraluminar outside the mucosa of the orifice. Of course, all the components of the energy transforming device including the electrical junction element in contact with the patient's body should be of biocompatible material.
For in vitro appliances, a particular type of an electrical semiconductor junction element has been commonly used, namely a so-called p-n (positive/negative) junction element, typically in the form of solar cells. A solar cell transfers solar energy in the form of visible light into electric energy in the form of direct current. For example, a p-n junction element may comprise two layers of semiconductor, one p-type (positive) and the other n-type (negative), sandwiched together to form a “p-n junction”. This p-n junction induces an electric field across the element when absorbing quanta of light (photons).
To be more precise, the quanta of light transfer their energy to some of the semiconductor's electrons, which are then able to move about through the material. For each such negatively charged electron, a corresponding positive charge—a “hole”—is created. In an ordinary semiconductor, these electrons and holes recombine after a short time and their energy is wasted as heat. However, when the electrons and holes are swept across the p-n junction in opposite directions by the action of the electric field, the separation of charge induces a voltage across the p-n junction element. By connecting the p-n junction element to an external circuit, the electrons are able to flow thereby creating a current.
Surprisingly, it has been proved that although both the skin and subcutis absorb energy from an external light beam directed against the skin portion behind which a properly designed p-n junction element is located, the light energy transmitted through the skin can induce a current from the p-n junction element strong enough (minimum 1 μA) to enable the operation of the electrically operated restriction device. Thus, such a p-n junction element is now for the first time used for in vivo applications.
The apparatus may comprise an implantable pulse generator for generating electrical pulses from the energy of the second form produced by the energy field.
Generally, the energy transforming device is adapted to transform the energy of the first form directly or indirectly into the energy of the second form.
In accordance with a preferred embodiment of the invention, the energy of the second form comprises electric energy and the energy transforming device comprises a capacitor, which may be adapted to produce electric pulses from the transformed electric energy. Preferably, the capacitor may be adapted to produce the pulses as the energy transforming device transforms the energy of the first form transmitted by the energy transmission device into the electric energy of the second form. The capacitor should be small to facilitate implantation thereof; i.e. its capacity may not be more than 0.1 μF.
The apparatus may comprise an implantable stabiliser for stabilising the energy of the second form. Where the energy of the second form comprises electric current the stabiliser may comprise at least one capacitor of the type described above.
In most embodiments of the invention, the apparatus comprises implantable electrical components. Where the electrical components include a capacitor of the type described above or an accumulator, at least one, preferably a single, voltage level guard may advantageously be provided, wherein the charge and discharge of the capacitor or accumulator is controlled by use of the voltage level guard. As a result, there is no need for any implanted current detector and/or charge level detector for the control of the capacitor, which makes the apparatus simple and reliable.
In a particular embodiment of the invention, the wireless energy of the first form comprises sound waves and the energy of the second form comprises electric energy, wherein the energy transforming device is adapted to directly transform the sound waves into electric energy.
The apparatus may comprise an implantable motor or pump for operating the restriction device, wherein the motor or pump is powered by the transformed energy.
In accordance with a main aspect of the invention, the energy transmission device may be adapted to transmit wireless energy for direct use in connection with the operation of the restriction device, as the wireless energy is being transmitted. The advantage of directly using energy as it is transmitted is that the apparatus can be of a very simple design and the few components involved makes the apparatus extremely reliable. For example, the energy transmission device may be adapted to directly power the motor or pump with wireless energy. The wireless energy may comprise a magnetic field or electromagnetic waves, suitably in the form of a signal, for direct power of the motor or pump. All the various functions of the motor and associated components described in the present specification may be used where applicable.
As an alternative to the above-noted main aspect of the invention, the energy transforming device may be adapted to supply the energy of the second form for direct use in connection with the operation of the restriction device, as the energy of the first form is being transformed into the energy of the second form. Consequently, the energy transforming device may be adapted to directly power the motor or pump with the energy of the second form.
Generally, the energy transforming device directly operates the restriction device with the energy of the second form in a non-magnetic, non-thermal or non-mechanical manner.
Where the apparatus comprises a motor, which may be adapted to directly or intermittently operate the restriction device, the energy transforming device may power the motor with the energy of the second form. Suitably, the restriction device is operable to perform a reversible function and the motor is capable of reversing said function.
In accordance with another embodiment of the invention, the restriction device comprises a hydraulic restriction device, and the apparatus comprises an implantable pump for operating the hydraulic restriction device, wherein the energy transforming device supplies the energy of the second form for driving the pump. Preferably, the pump is not a plunger type of pump, but may comprise a peristaltic or membrane pump.
The energy transforming device preferably is capable of generating as the energy of the second form a current exceeding 1 μA, when transferring the energy of the first form transmitted by the energy transmission device.
The apparatus may comprise an implantable adjustment device for adjusting the restriction device to change the restriction of the urine passageway. In accordance with a first alternative the adjustment device is adapted to mechanically adjust the restriction device. In accordance with a second alternative the adjustment device is adapted to hydraulically adjust the restriction device by using implanted hydraulic means. Such hydraulic means may not use hydraulic fluid of the kind having a viscosity that substantially increases when exposed to heat or a magnetic field.
The apparatus of the present invention is not limited to the use of visible light for the wireless transmission of energy. Thus, in accordance with a broad aspect of the invention, the energy transmission device transmits energy by at least one wireless signal, preferably containing radiant energy.
The wireless signal may comprises a wave signal, for example an electromagnetic wave signal, such as an infrared light signal, a visible light signal, an ultra violet light signal, a laser signal, a micro wave signal, a radio wave signal, an x-ray radiation signal, and a gamma radiation signal. Where applicable, one or more of the above signals may be combined. Alternatively, the wave signal may comprise a sound wave signal, such as an ultrasonic signal. Generally, the wireless signal may comprise a digital, analog or a digital and analog signal.
The energy of the first form transmitted by the energy transmission device may comprise an electric or magnetic field transmitted in pulses, for example digital pulses. Furthermore, the energy transforming device may transform the energy of the first form, which may comprise polarised energy, into a direct current, pulsating direct current, a combination of a direct and pulsating direct current, an alternating current or a combination of a direct and alternating current. Alternatively, the energy of the first form may comprise kinetic energy.
The energy of the second form may comprise a frequency, amplitude or frequency and amplitude modulated analog, digital or combined analog and digital signal.
The restriction device may be non-inflatable, i.e. with no hydraulic fluid involved for the adjustments of the restriction device. This eliminates problems with fluid leaking from the restriction device.
The apparatus suitably comprises implantable electric conductors connected to the energy transforming device, whereby the energy transforming device is capable of supplying an electric current, such as direct current, a pulsating direct current, a combination of a direct and pulsating direct current, an alternating current or a combination of a direct and alternating current, via the conductors. Furthermore, the energy transforming device may be capable of supplying a frequency, amplitude, or frequency and amplitude modulated analog, digital, or a combination of analog and digital signal, which is used in connection with control of the restriction device.
In accordance with a main embodiment of the invention, the apparatus comprises an implantable operation device for operating the restriction device and a control device for controlling the operation device, wherein the energy transforming device powers the operation device with the energy of the second form. The operation device preferably comprises a motor, for example an electric linear motor or an electric rotary motor that is controlled by the control device to rotate a desired number of revolutions. Optionally, an implantable gearing may be connected to the motor. The electric motor may have electrically conductive parts made of plastics. Alternatively, the motor may comprise a hydraulic or pneumatic fluid motor, wherein the control device controls the fluid flow through the fluid motor. Motors currently available on the market are getting smaller and smaller. Furthermore, there is a great variety of control methods and miniaturised control equipment available. For example, the number of revolutions of a rotary motor may be analysed by a Hall-element just a few mm in size.
In accordance with another embodiment of the invention, the restriction device comprises hydraulic means and the operation device is adapted to conduct a hydraulic fluid in the hydraulic means. The operation device comprises a fluid conduit connected to the hydraulic means of the restriction device, and a reservoir for fluid, wherein the reservoir forms part of the conduit. The reservoir may form a fluid chamber with a variable volume, and the operation device may be adapted to distribute fluid from the chamber to the hydraulic means of the restriction device by reduction of the volume of the chamber and to withdraw fluid from the hydraulic means to the chamber by expansion of the volume of the chamber. The operation device suitably comprises an implantable motor used for reducing and expanding the volume of the chamber. Also, the operation device may comprise a pump for pumping the hydraulic fluid in the hydraulic means of the restriction device. All of the hydraulic components involved are preferably devoid of any non-return valve. This is of great advantage, because with valves involved there is always a risk of malfunction due to improperly working valves, especially when long time periods passes between valve operations.
The control device may be adapted to reverse the operation device by shifting polarity of the energy of the second form. Where the operation device comprises an electric motor the energy of the second form suitably comprises electric energy.
In accordance with yet another embodiment of the invention, the restriction device is operable to perform a reversible function, such as enlarging and restricting the urine passageway, and there is a reversing device implanted in the patient for reversing the function performed by the restriction device. Such a reversing function preferably involves enlarging and restricting the urine passageway by the restriction device, suitably in a stepless manner. In this connection, the control device suitably controls the reversing device, which may include a switch, to reverse the function performed by the restriction device. The reversing device may comprise hydraulic means including a valve for shifting the flow direction of a fluid in the hydraulic means. Alternatively, the reversing device may comprise a mechanical reversing device, such as a switch or a gearbox.
Where the reversing device comprises a switch it may be operable by the energy of the second form. In this case, the control device suitably controls the operation of the switch by shifting polarity of the energy of the second form supplied to the switch. The switch may comprise an electric switch and the source of energy may supply electric energy for the operation of the switch.
In accordance with an advantageous embodiment of the invention, the apparatus further comprises an energy storage device implanted in the patient for storing the energy of the second form and for supplying energy in connection with the operation of the restriction device. The implanted energy storage device preferably comprises an electric source of energy, such as an accumulator, a rechargeable battery or a combination of an accumulator and rechargeable battery.
The apparatus may further comprise a switch implantable in the patient for switching the operation of the restriction device and a source of energy implantable in the patient. This embodiment is particularly suited for applications where the energy transmission efficiency of the apparatus is insufficient, i.e. where the implanted restriction device is to perform more advanced operations. Such a source of energy preferably is a battery. Alternatively, the source of energy is an accumulator that also may store the energy of the second form.
In accordance with a first alternative, the switch is operated by the energy of the second form supplied by the energy storage device to switch from an off mode, in which the source of energy is not in use, to an on mode, in which the source of energy supplies energy for the operation of the restriction device. In this case, the implanted source of energy may comprise a battery, preferably having a lifetime of at least 10 years, or an accumulator. However, other kinds of sources are also conceivable, such as a nuclear source of energy or a chemical source of energy (fuel cells).
In accordance with a second alternative, the apparatus further comprises a remote control for controlling the supply of energy of the implanted source of energy, wherein the switch is operated by the energy of the second form supplied by the energy storage device to switch from an off mode, in which the remote control is prevented from controlling the source of energy and the source of energy is not in use, to a standby mode, in which the remote control is permitted to control the source of energy to supply energy for the operation of the restriction device.
In accordance with a third alternative, the energy storage device is omitted, wherein the switch is operated by the energy of the second form supplied by the energy transforming device to switch from an off mode, in which the remote control is prevented from controlling the source of energy and the source of energy is not in use, to a standby mode, in which the remote control is permitted to control the source of energy to supply energy for the operation of the restriction device.
In accordance with a fourth alternative, also the remote control is omitted, wherein the switch is operated by the energy of the second form supplied by the energy transforming device to switch from an off mode, in which the source of energy is not in use, to an on mode, in which the source of energy supplies energy for the operation of the restriction device. Where applicable, in the described embodiments the switch may switch when the energy transmission device is transmitting wireless energy, preferably while the transferred energy of the second form is stabilised by an implanted capacitor, which may temporarily (for a few seconds) store the energy of the second form.
In the above noted third and fourth alternatives, the energy transmission device may be substituted for the energy transforming device, whereby the switch is operated by the energy of the first form.
The switch mentioned above may comprise an electronic switch or, where applicable, a mechanical switch.
The advantage of using a switch above all is increased control safety; i.e. interfering signals in the patient's surroundings cannot affect the implanted restriction device. Furthermore, the lifetime of the implanted source of energy will be significantly prolonged, since the energy consumption of the apparatus will be reduced to a minimum. During the above-mentioned standby mode, the remote control uses energy from the implanted source of energy. By means of the energy transmission device energy may be transmitted to activate the switch to connect the implanted source of energy only when energy is required in connection with the operation of the restriction device.
All of the above embodiments may be combined with at least one implantable sensor for sensing at least one physical parameter of the patient, wherein the control device may control the restriction device in response to signals from the sensor. For example, the sensor may comprise a pressure sensor for directly or indirectly sensing the pressure against the restriction device, human tissue or in the urine passageway, or the pressure against the urethra or the lower part of the urine bladder. The control device may comprise an internal control unit implanted in the patient for, preferably directly, controlling the restriction device in response to signals from the sensor. In response to signals from the sensor, for example pressure, the patient's position or any other important physical parameter, the internal control unit may send information thereon to outside the patient's body. The control unit may also automatically control the restriction device in response to signals from the sensor. For example, the control unit may control the restriction device to further restrict the urine passageway in response to the sensor sensing that the patient is lying, or enlarge the urine passageway in response to the sensor sensing an abnormally high pressure against the restriction device.
Alternatively, the control device may comprise an external control unit outside the patient's body for, suitably directly, controlling the restriction device in response to signals from the sensor. The external control unit may store information on the physical parameter sensed by the sensor and may be manually operated to control the restriction device based on the stored information. In addition, there may be at least one implantable sender for sending information on the physical parameter sensed by the sensor.
An external data communicator may be provided outside the patient's body and an internal data communicator may be implanted in the patient for communicating with the external communicator. The internal communicator may feed data related to the patient, or related to the restriction device, back to the external communicator. Alternatively or in combination, the external communicator may feed data to the internal communicator. The internal communicator may suitably feed data related to at least one physical signal of the patient.
The apparatus may further comprise an implantable programmable control unit for controlling the restriction device, preferably over time in accordance with an activity schedule program. This will advance the apparatus and make possible an adaptation of the apparatus to the individual patients.
Many of the above embodiments are suitably remote controlled. Thus, the apparatus advantageously comprises a wireless remote control transmitting at least one wireless control signal for controlling the restriction device. With such a remote control it will be possible to adapt the function of the apparatus to the patient's need in a daily basis, which is beneficial with respect to the treatment of the patient. The control signal may comprise a frequency, amplitude or frequency or amplitude modulated signal. Furthermore, the control signal may comprise an analog or a digital signal, or a combination of an analog and digital signal.
The wireless remote control may be capable of obtaining information on the condition of the implanted restriction device and of controlling the restriction device in response to the information. Also, the remote control may be capable of sending information related to the restriction device from inside the patient's body to the outside thereof.
In a particular embodiment of the invention, the wireless remote control comprises at least one external signal transmitter or transceiver and at least one internal signal receiver or transceiver implantable in the patient. In another particular embodiment of the invention, the wireless remote control comprises at least one external signal receiver or transceiver and at least one internal signal transmitter or transceiver implantable in the patient.
The wireless remote control may transmit a carrier signal for carrying the control signal, wherein the carrier signal is frequency, amplitude or frequency and amplitude modulated. The carrier signal may also comprise digital, analog or a combination of digital and analog signals. Such signals may comprise wave signals. Also the control signal used with the carrier signal may be frequency, amplitude or frequency and amplitude modulated, and be digital, analog or combined digital and analog.
The control signal may comprise a wave signal, for example, a sound wave signal, such as an ultrasound wave signal, an electromagnetic wave signal, such as an infrared light signal, a visible light signal, an ultra violet light signal, a laser signal, a micro wave signal, a radio wave signal, an x-ray radiation signal, or a gamma radiation signal. Where applicable, two or more of the above signals may be combined.
The control signal may be digital or analog, and may comprise an electric or magnetic field. Suitably, the wireless remote control may transmit an electromagnetic carrier wave signal for carrying the digital or analog control signal. For example, use of an analog carrier wave signal carrying a digital control signal would give safe communication. The control signal may be transmitted in pulses by the wireless remote control.
The energy transmission device may function different from or similar to the energy transforming device. For example, the energy transmission and transforming devices function differently when the energy transmission device comprises a coil used for transmitting the energy of the first form and the energy transforming device comprises an electrical junction element for transforming the transmitted energy into the energy of the second form. The energy transmission and transforming devices function similar to each other when the energy transmission device comprises a coil used for transmitting the energy of the first form and the energy transforming device also comprises a coil for transforming the transmitted energy into the energy of the second form.
In accordance with an alternative embodiment of the invention, the apparatus comprises an activatable source of energy implantable in the patient, wherein the source of energy is activated by wireless energy transmitted by the energy transmission device, to supply energy which is used in connection with the operation of the restriction device.
The implantable restriction device suitably is embedded in a soft or gel-like material. For example, a silicone material having hardness less than 20 Shore.
All the above described various components, such as the motor, pump and capacitor, may be combined in the different embodiments where applicable. Also the various functions described in connection with the above embodiments of the invention may be used in different applications, where applicable.
All the various ways of transferring, transforming and controlling energy presented in the present specification may be practised by using all of the various components and solutions described.
The present invention also provides an implanting method, comprising the steps of providing a urinary incontinence treatment apparatus described above, cutting an opening in a patient's mucosa in an orifice of the patient's body, and implanting the energy transforming device in the patient's body through the opening.
There is also provided a laparascopical implanting method, in accordance with a first alternative, comprising the steps of providing a urinary incontinence treatment apparatus as described above, placing at least two laparascopic cannula within a patient's body, and implanting the energy transforming device in the patient's body by using the at least two laparascopic cannula.
In accordance with a second alternative there is provided a laparoscopic surgical method of implanting a urinary incontinence treatment apparatus, comprising the steps of laparascopically placing a restriction device of the apparatus through the abdomen or thorax of a patient, placing at least two laparoscopic trocars within the patient's body, using at least one dissecting tool inserted through the laparoscopic trocar, introducing the restriction device through the trocar, and placing the restriction device in engagement with the urethra or urine bladder to create a restricted urine passageway.
The method may further comprise implanting an energy transforming device of the apparatus, for example subcutaneously, in the abdomen, thorax or cephalic region, or other locations in the patient's body.
The method may further comprise postoperatively adjusting the restricted urine passageway in a non-invasive procedure.
The present invention also provides a method of treating a human or animal having chronic urinary incontinence comprising:
(a) Surgically implanting in the human or animal a restriction device engaging the human's or animal's urine bladder or urethra, to form a restricted passageway in the urethra or urine bladder.
(b) Surgically implanting in the human or animal an operation device, which can adjust the restricted passageway in response to supplied energy. And, (c) in a non-invasive post-operative procedure, from time to time, supplying energy to the operation device so as to enlarge the restricted passageway to allow urine to readily pass through. In the method (c) may be practised several times (e.g. 2-10) a day.
The invention is described in more detail in the following with reference to the accompanying drawings, in which
Referring to the drawing figures, like reference numerals designate identical or corresponding elements throughout the several figures.
The apparatus of
In accordance with one alternative, the capacitor 40 in the embodiment of
Alternatively, the switch 52 may be operated by energy supplied by the accumulator 38 to switch from an off mode, in which the wireless remote control is prevented from controlling the battery 50 to supply electric energy and is not in use, to a standby mode, in which the wireless remote control is permitted to control the battery 50 to supply electric energy for the operation of the restriction device 4.
A sensor 56 may be implanted in the patient for sensing a physical parameter of the patient, such as the pressure in the urine passageway. The implanted control unit 36, or alternatively the external wireless remote control of the energy transmission device 10, may control the restriction device 4 in response to signals from the sensor 56. A transceiver may be combined with the sensor 56 for sending information on the sensed physical parameter to the external wireless remote control. The wireless remote control may comprise a signal transmitter or transceiver and the implanted control unit 36 may comprise a signal receiver or transceiver. Alternatively, the wireless remote control may comprise a signal receiver or transceiver and the implanted control unit 36 may comprise a signal transmitter or transceiver. The above transceivers, transmitters and receivers may be used for sending information or data related to the restriction device 4 from inside the patient's body to the outside thereof.
Where the motor/pump unit 18 and battery 50 for powering the motor/pump unit 18 are implanted, the battery 50 may be equipped with a transceiver for sending information on the condition of the battery 50.
Those skilled in the art will realise that the above various embodiments according to
I=I0(exp.(qV/kT)−1)
where
I is the external current flow,
I0 is the reverse saturation current,
q is the fundamental electronic charge of 1.602×10-19 coulombs,
V is the applied voltage,
k is the Boltzmann constant, and
T is the absolute temperature.
Under large negative applied voltage (reverse bias), the exponential term becomes negligible compared to 1.0, and I is approximately −I0. I0 is strongly dependent on the temperature of the junction and hence on the intrinsic-carrier concentration. I0 is larger for materials with smaller bandgaps than for those with larger bandgaps. The rectifier action of the diode—that is, its restriction of current flow to only one direction—is in this particular embodiment the key to the operation of the p-n junction element 58.
An alternative way to design a p-n junction element is to deposit a thin layer of semiconductor onto a supporting material which does not absorb the kind of energy utilised in the respective embodiments. For use with wirelessly transmitted energy in terms of light waves, glass could be a suitable material. Various materials may be used in the semiconductor layers such as but not limited to cadmium telluride, copper-indium-diselenide and silicon. It is also possible to use a multilayer structure with several layers of p and n-type materials to improve efficiency.
The electric energy generated by the p-n junction element 58 could be of the same type as generated by solar cells, in which the negative and positive fields create a direct current. Alternatively, the negative and positive semiconductor layers may change polarity following the transmitted waves, thereby generating an alternating current.
The p-n junction element 58 is designed to make it suited for implantation. Thus, all the external surfaces of the element 58 in contact with the human body are made of a biocompatible material. The p-n junction semiconductors are designed to operate optimally at a body temperature of 37° C. because the current output, which should be more than 1 μA, is significantly depending on temperature as shown above. Since both the skin and subcutis absorb energy, the relation between the sensitivity or working area of the element 58 and the intensity or strength of the wireless energy transmission is considered. The p-n junction element 58 preferably is designed flat and small. Alternatively, if the element 58 is made in larger sizes it should be flexible, in order to adapt to the patient's body movements. The volume of the element 58 should be kept less than 2000 cm3.
Wireless energy carried by a signal transmitted by a wireless remote control of an external energy transmission device 10 at least partly penetrates the patient's skin and hits the element 6. The energy thus hitting the element 6 is transformed into energy of a different form that is suited for powering the operation device 68. For example, where the operation device 68 is an electric motor the element 6 comprises an electric p-n junction element that transforms the wireless energy into an electric current for powering the electric motor. Where the operation device 68 comprises a pump, the element 6 may transform the wireless energy into kinetic energy for powering the pump.
The transformed energy may be utilised for directly operating the restriction device 4 or, where the restriction device 4 is electrically operated, for storage in a capacitor and/or an accumulator for later or parallel use. Preferably (but not necessarily) the element 6 is controlled by a microprocessor. The wireless remote control of the external energy transmission device 10 is used to control the utilisation of the transmitted energy and any function or command to/from the implanted restriction device 4.
An external signal transmitting antenna 132 is to be positioned close to a signal receiving antenna 134 implanted close to the skin 130. As an alternative, the receiving antenna 134 may be placed for example inside the abdomen of the patient. The receiving antenna 134 comprises a coil, approximately 1-100 mm, preferably 25 mm in diameter, wound with a very thin wire and tuned with a capacitor to a specific high frequency. A small coil is chosen if it is to be implanted under the skin of the patient and a large coil is chosen if it is to be implanted in the abdomen of the patient. The transmitting antenna 132 comprises a coil having about the same size as the coil of the receiving antenna 134 but wound with a thick wire that can handle the larger currents that is necessary. The coil of the transmitting antenna 132 is tuned to the same specific high frequency as the coil of the receiving antenna 134.
An external control unit 136 comprises a microprocessor, a high frequency electromagnetic wave signal generator and a power amplifier. The microprocessor of the control unit 136 is adapted to switch the generator on/off and to modulate signals generated by the generator to send digital information via the power amplifier and the antennas 132,134 to an implanted control unit 138. To avoid that accidental random high frequency fields trigger control commands, digital signal codes are used. A conventional keypad placed on the external control unit 136 is connected to the microprocessor thereof. The keypad is used to order the microprocessor to send digital signals to either contract or enlarge the restriction device. The microprocessor starts a command by applying a high frequency signal on the antenna 132. After a short time, when the signal has energised the implanted parts of the control system, commands are sent to contract or enlarge the restriction device in predefined steps. The commands are sent as digital packets in the form illustrated below.
The commands are sent continuously during a rather long time period (e.g. about 30 seconds or more). When a new contract or enlarge step is desired the Count byte is increased by one to allow the implanted control unit 138 to decode and understand that another step is demanded by the external control unit 136. If any part of the digital packet is erroneous, its content is simply ignored.
Through a line 140, an implanted energiser unit 126 draws energy from the high frequency electromagnetic wave signals received by the receiving antenna 134. The energiser unit 126 stores the energy in an energy storage device, such as a large capacitor, powers the control unit 138 and powers the electric motor 128 via a line 142.
The control unit 138 comprises a demodulator and a microprocessor. The demodulator demodulates digital signals sent from the external control unit 136. The microprocessor of the control unit 138 receives, the digital packet, decodes it and, provided that the power supply of the energiser unit 126 has sufficient energy stored, sends a signal via a signal line 144 to the motor 128 to either contract or enlarge the restriction device depending on the received command code.
Alternatively, the energy stored in the energy storage device of the energiser unit may only be used for powering a switch, and the energy for powering the motor 128 may be obtained from another implanted energy source of relatively high capacity, for example a battery. In this case the switch is adapted to connect said battery to the control unit 138 in an on mode when said switch is powered by the energy storage device and to keep the battery disconnected from the control unit in a standby mode when the switch is not powered.
With reference to
The implanted signal receiving antenna coil 134 forms together with a capacitor 154 a resonant circuit that is tuned to the same frequency as the transmitting antenna 132. The signal receiving antenna coil 134 induces a current from the received high frequency electromagnetic waves and a rectifying diode 160 rectifies the induced current, which charges a storage capacitor 158. A coil 156 connected between the antenna coil 134 and the diode 160 prevents the capacitor 158 and the diode 160 from loading the circuit of the signal receiving antenna 134 at higher frequencies. Thus, the coil 156 makes it possible to charge the capacitor 158 and to transmit digital information using amplitude modulation.
A capacitor 162 and a resistor 164 connected in parallel and a diode 166 forms a detector used to detect amplitude modulated digital information. A filter circuit is formed by a resistor 168 connected in series with a resistor 170 connected in series with a capacitor 172 connected in series with the resistor 168 via ground, and a capacitor 174, one terminal of which is connected between the resistors 168,170 and the other terminal of which is connected between the diode 166 and the circuit formed by the capacitor 162 and resistor 164. The filter circuit is used to filter out undesired low and high frequencies. The detected and filtered signals are fed to an implanted microprocessor 176 that decodes the digital information and controls the motor 128 via an H-bridge 178 comprising transistors 180, 182, 184 and 186. The motor 128 can be driven in two opposite directions by the H-bridge 178.
The microprocessor 176 also monitors the amount of stored energy in the storage capacitor 158. Before sending signals to activate the motor 128, the microprocessor 176 checks whether the energy stored in the storage capacitor 158 is enough. If the stored energy is not enough to perform the requested operation, the microprocessor 176 waits for the received signals to charge the storage capacitor 158 before activating the motor 128.
This application is a continuation of application Ser. No. 10/203,189, filed Oct. 22, 2002 now U.S. Pat. No. 7,621,863, which is the U.S. national phase of International Application No. PCT/SE01/00270, filed Feb. 9, 2001, which designated the U.S., and which claims the benefit of U.S. Provisional Application Nos. 60/181,469, filed Feb. 10, 2000 and 60/181,550, filed Feb. 10, 2000, the entire contents of which are hereby incorporated by reference in this application.
Number | Name | Date | Kind |
---|---|---|---|
2060913 | Weaver | Nov 1936 | A |
2795641 | Ross | Jun 1957 | A |
3209081 | Ducote et al. | Sep 1965 | A |
3598287 | De Man | Aug 1971 | A |
3692027 | Ellinwood, Jr. | Sep 1972 | A |
3731679 | Wilhelmson et al. | May 1973 | A |
3731681 | Blackshear et al. | May 1973 | A |
3750194 | Summers | Aug 1973 | A |
3817237 | Bolduc | Jun 1974 | A |
3855122 | Bourganel | Dec 1974 | A |
3875928 | Angelchik | Apr 1975 | A |
3923060 | Ellinwood, Jr. | Dec 1975 | A |
3954102 | Buuck | May 1976 | A |
4003379 | Ellinwood, Jr. | Jan 1977 | A |
4004379 | Castagna | Jan 1977 | A |
4009711 | Uson | Mar 1977 | A |
4026305 | Brownlee et al. | May 1977 | A |
4044401 | Guiset | Aug 1977 | A |
4201202 | Finney et al. | May 1980 | A |
4221219 | Tucker | Sep 1980 | A |
4235222 | Ionescu | Nov 1980 | A |
4243306 | Bononi | Jan 1981 | A |
4246893 | Berson | Jan 1981 | A |
4265241 | Portner et al. | May 1981 | A |
4271827 | Angelchik | Jun 1981 | A |
4274407 | Scarlett | Jun 1981 | A |
4303225 | Freeman | Dec 1981 | A |
4304225 | Freeman | Dec 1981 | A |
4318396 | Finney | Mar 1982 | A |
4342308 | Trick | Aug 1982 | A |
4369771 | Trick | Jan 1983 | A |
4400169 | Stephen | Aug 1983 | A |
4412530 | Burton | Nov 1983 | A |
4424807 | Evans, Sr. | Jan 1984 | A |
4426893 | Miller | Jan 1984 | A |
4456175 | Mamrosov et al. | Jun 1984 | A |
4464628 | Nozawa | Aug 1984 | A |
4491461 | Hoekstra | Jan 1985 | A |
4505710 | Collins | Mar 1985 | A |
4509947 | Lattin | Apr 1985 | A |
4542753 | Brenman et al. | Sep 1985 | A |
4550720 | Trick | Nov 1985 | A |
4556050 | Hodgson et al. | Dec 1985 | A |
4559930 | Cobiski | Dec 1985 | A |
4559939 | Levine et al. | Dec 1985 | A |
4563175 | LaFond | Jan 1986 | A |
4583523 | Kleinke et al. | Apr 1986 | A |
4584994 | Bamberger et al. | Apr 1986 | A |
4592339 | Kuzmak et al. | Jun 1986 | A |
4592355 | Antebi | Jun 1986 | A |
4599081 | Cohen | Jul 1986 | A |
4602621 | Hakky | Jul 1986 | A |
4610658 | Buchwald et al. | Sep 1986 | A |
4623350 | Lapeyre et al. | Nov 1986 | A |
4628928 | Lowell | Dec 1986 | A |
4664100 | Rudloff | May 1987 | A |
4677534 | Okochi | Jun 1987 | A |
4679560 | Galbraith | Jul 1987 | A |
4696288 | Kuzmak et al. | Sep 1987 | A |
4711231 | Finegold et al. | Dec 1987 | A |
4723538 | Stewart et al. | Feb 1988 | A |
4756949 | Spence et al. | Jul 1988 | A |
4771780 | Sholder | Sep 1988 | A |
4828544 | Lane et al. | May 1989 | A |
4828990 | Higashi et al. | May 1989 | A |
4829990 | Thuroff et al. | May 1989 | A |
4846794 | Hertzer | Jul 1989 | A |
4902279 | Schmidtz et al. | Feb 1990 | A |
4925443 | Heilman et al. | May 1990 | A |
4941461 | Fischell | Jul 1990 | A |
4942668 | Franklin | Jul 1990 | A |
4958630 | Rosenbluth et al. | Sep 1990 | A |
4979955 | Smith | Dec 1990 | A |
4982731 | Lue et al. | Jan 1991 | A |
5006106 | Angelchik | Apr 1991 | A |
5012822 | Schwarz | May 1991 | A |
5042084 | Daly | Aug 1991 | A |
5048511 | Rosenbluth et al. | Sep 1991 | A |
5057075 | Moncrief et al. | Oct 1991 | A |
5062416 | Stucks | Nov 1991 | A |
5074868 | Kuzmak | Dec 1991 | A |
5098369 | Heilman et al. | Mar 1992 | A |
5112202 | Oshima et al. | May 1992 | A |
5123428 | Schwarz | Jun 1992 | A |
5160338 | Vincent | Nov 1992 | A |
5226429 | Kuzmak | Jul 1993 | A |
5250020 | Bley | Oct 1993 | A |
5297536 | Wilk | Mar 1994 | A |
5304206 | Baker, Jr. et al. | Apr 1994 | A |
5316543 | Eberbach | May 1994 | A |
5358474 | Kaldany | Oct 1994 | A |
5415660 | Campbell et al. | May 1995 | A |
5437605 | Helmy | Aug 1995 | A |
5449368 | Kuzmak | Sep 1995 | A |
5453079 | Schwaninger | Sep 1995 | A |
5454840 | Krakovsky et al. | Oct 1995 | A |
5501703 | Holsheimer et al. | Mar 1996 | A |
5505733 | Justin et al. | Apr 1996 | A |
5509888 | Miller | Apr 1996 | A |
5518504 | Polyak | May 1996 | A |
5540731 | Testerman | Jul 1996 | A |
5569187 | Kaiser | Oct 1996 | A |
5578069 | Miner, II | Nov 1996 | A |
5582580 | Buckman, Jr. et al. | Dec 1996 | A |
5665065 | Colman et al. | Sep 1997 | A |
5676674 | Bolanos et al. | Oct 1997 | A |
5690108 | Chakeres | Nov 1997 | A |
5702431 | Wang et al. | Dec 1997 | A |
5704893 | Timm | Jan 1998 | A |
5735887 | Barreras, Sr. et al. | Apr 1998 | A |
5749909 | Schroeppel et al. | May 1998 | A |
5769877 | Barreras, Sr. | Jun 1998 | A |
5771903 | Jakobsson | Jun 1998 | A |
5814020 | Gross | Sep 1998 | A |
5823991 | Shim | Oct 1998 | A |
5827286 | Incavo et al. | Oct 1998 | A |
5848962 | Feindt et al. | Dec 1998 | A |
5858001 | Tsals et al. | Jan 1999 | A |
5876425 | Gord et al. | Mar 1999 | A |
5900909 | Parulski et al. | May 1999 | A |
5902336 | Mishkin | May 1999 | A |
5910149 | Kuzmak | Jun 1999 | A |
5928195 | Malamud et al. | Jul 1999 | A |
5938584 | Ardito et al. | Aug 1999 | A |
5938669 | Klaiber et al. | Aug 1999 | A |
5978712 | Suda et al. | Nov 1999 | A |
5995874 | Borza | Nov 1999 | A |
5997501 | Gross et al. | Dec 1999 | A |
6003736 | Ljunggren | Dec 1999 | A |
6067991 | Forsell | May 2000 | A |
6074341 | Anderson et al. | Jun 2000 | A |
6077215 | Leysieffer | Jun 2000 | A |
6095968 | Snyders | Aug 2000 | A |
6102887 | Altman | Aug 2000 | A |
6102922 | Jakobsson et al. | Aug 2000 | A |
6113574 | Spinello | Sep 2000 | A |
6117067 | Gil-Vernet | Sep 2000 | A |
6134470 | Hartlaub | Oct 2000 | A |
6135945 | Sultan | Oct 2000 | A |
6162238 | Kaplan et al. | Dec 2000 | A |
6185452 | Schulman et al. | Feb 2001 | B1 |
6197055 | Matthews | Mar 2001 | B1 |
6210347 | Forsell | Apr 2001 | B1 |
6221060 | Willard | Apr 2001 | B1 |
6233474 | Lemelson | May 2001 | B1 |
6275737 | Mann | Aug 2001 | B1 |
6319191 | Sayet et al. | Nov 2001 | B1 |
6346099 | Altman | Feb 2002 | B1 |
6436054 | Viola et al. | Aug 2002 | B1 |
6450173 | Forsell | Sep 2002 | B1 |
6450946 | Forsell | Sep 2002 | B1 |
6453907 | Forsell | Sep 2002 | B1 |
6454698 | Forsell | Sep 2002 | B1 |
6454699 | Forsell | Sep 2002 | B1 |
6454700 | Forsell | Sep 2002 | B1 |
6454701 | Forsell | Sep 2002 | B1 |
6456883 | Torgerson et al. | Sep 2002 | B1 |
6460543 | Forsell | Oct 2002 | B1 |
6461292 | Forsell | Oct 2002 | B1 |
6461293 | Forsell | Oct 2002 | B1 |
6463935 | Forsell | Oct 2002 | B1 |
6464628 | Forsell | Oct 2002 | B1 |
6470892 | Forsell | Oct 2002 | B1 |
6471635 | Forsell | Oct 2002 | B1 |
6475136 | Forsell | Nov 2002 | B1 |
6482145 | Forsell | Nov 2002 | B1 |
6503189 | Forsell | Jan 2003 | B1 |
6572585 | Choi | Jun 2003 | B2 |
6589229 | Connelly et al. | Jul 2003 | B1 |
6638208 | Natarajan et al. | Oct 2003 | B1 |
6638303 | Campbell | Oct 2003 | B1 |
6659936 | Furness et al. | Dec 2003 | B1 |
6678561 | Forsell | Jan 2004 | B2 |
6689085 | Rubenstein et al. | Feb 2004 | B1 |
6709385 | Forsell | Mar 2004 | B2 |
6740075 | Lebel et al. | May 2004 | B2 |
6772011 | Dolgin | Aug 2004 | B2 |
6895280 | Meadows et al. | May 2005 | B2 |
6911002 | Fierro | Jun 2005 | B2 |
6915165 | Forsell | Jul 2005 | B2 |
6929625 | Bierman | Aug 2005 | B2 |
6948918 | Hansen | Sep 2005 | B2 |
6953429 | Forsell | Oct 2005 | B2 |
6960233 | Berg et al. | Nov 2005 | B1 |
6979351 | Forsell et al. | Dec 2005 | B2 |
7011624 | Forsell | Mar 2006 | B2 |
7017583 | Forsell | Mar 2006 | B2 |
7043295 | Starkebaum | May 2006 | B2 |
7066922 | Angel et al. | Jun 2006 | B2 |
7108686 | Burke et al. | Sep 2006 | B2 |
7207936 | Forsell | Apr 2007 | B2 |
7235044 | Forsell | Jun 2007 | B2 |
7238165 | Vincent et al. | Jul 2007 | B2 |
7250037 | Shermer et al. | Jul 2007 | B2 |
7311690 | Burnett | Dec 2007 | B2 |
7338437 | Forsell | Mar 2008 | B2 |
7367938 | Forsell | May 2008 | B2 |
7371208 | Forsell | May 2008 | B2 |
7395822 | Burton et al. | Jul 2008 | B1 |
7407479 | Forsell | Aug 2008 | B2 |
7407481 | Forsell | Aug 2008 | B2 |
7442165 | Forsell | Oct 2008 | B2 |
7455663 | Bikovsky | Nov 2008 | B2 |
7569050 | Moberg et al. | Aug 2009 | B2 |
7621863 | Forsell | Nov 2009 | B2 |
7648455 | Forsell | Jan 2010 | B2 |
7666132 | Forsell | Feb 2010 | B2 |
20010011543 | Forsell | Aug 2001 | A1 |
20020022759 | Forsell | Feb 2002 | A1 |
20020028980 | Thierfelder et al. | Mar 2002 | A1 |
20020040208 | Flaherty et al. | Apr 2002 | A1 |
20020055711 | Lavi et al. | May 2002 | A1 |
20020095139 | Keogh et al. | Jul 2002 | A1 |
20020095164 | Andreas et al. | Jul 2002 | A1 |
20020151922 | Hogendijk et al. | Oct 2002 | A1 |
20020165575 | Saleh | Nov 2002 | A1 |
20020183588 | Fierro | Dec 2002 | A1 |
20030009221 | Forsell | Jan 2003 | A1 |
20030014010 | Carpenter et al. | Jan 2003 | A1 |
20030014086 | Sharma | Jan 2003 | A1 |
20030021822 | Lloyd | Jan 2003 | A1 |
20030032855 | Shahinpoor | Feb 2003 | A1 |
20030032857 | Forsell | Feb 2003 | A1 |
20030050591 | Patrick McHale | Mar 2003 | A1 |
20030055442 | Laufer et al. | Mar 2003 | A1 |
20030060893 | Forsell | Mar 2003 | A1 |
20030066536 | Forsell | Apr 2003 | A1 |
20030069547 | Gonon | Apr 2003 | A1 |
20030088148 | Forsell | May 2003 | A1 |
20030092962 | Forsell | May 2003 | A1 |
20030100929 | Forsell | May 2003 | A1 |
20030105385 | Forsell | Jun 2003 | A1 |
20030109771 | Forsell | Jun 2003 | A1 |
20030125605 | Forsell | Jul 2003 | A1 |
20030125768 | Forsell | Jul 2003 | A1 |
20030144648 | Forsell | Jul 2003 | A1 |
20030163029 | Sonnenschein et al. | Aug 2003 | A1 |
20030208247 | Spinelli et al. | Nov 2003 | A1 |
20030233143 | Gharib et al. | Dec 2003 | A1 |
20040034275 | Forsell | Feb 2004 | A1 |
20040068299 | Laske et al. | Apr 2004 | A1 |
20040089313 | Utley et al. | May 2004 | A1 |
20040102804 | Chin | May 2004 | A1 |
20040122526 | Imran | Jun 2004 | A1 |
20040122527 | Imran | Jun 2004 | A1 |
20040147871 | Burnett | Jul 2004 | A1 |
20040162568 | Saadat et al. | Aug 2004 | A1 |
20040177918 | Murata et al. | Sep 2004 | A1 |
20040249451 | Lu et al. | Dec 2004 | A1 |
20040260316 | Knudson et al. | Dec 2004 | A1 |
20050038484 | Knudson et al. | Feb 2005 | A1 |
20050055025 | Zacouto et al. | Mar 2005 | A1 |
20050075697 | Olson et al. | Apr 2005 | A1 |
20050240229 | Whitehurst et al. | Oct 2005 | A1 |
20050245957 | Starkebaum et al. | Nov 2005 | A1 |
20050261712 | Balbierz et al. | Nov 2005 | A1 |
20050266042 | Tseng | Dec 2005 | A1 |
20050267405 | Shah | Dec 2005 | A1 |
20050267596 | Chen et al. | Dec 2005 | A1 |
20060069414 | Imran et al. | Mar 2006 | A1 |
20060127246 | Forsell | Jun 2006 | A1 |
20060142635 | Forsell | Jun 2006 | A1 |
20060149124 | Forsell | Jul 2006 | A1 |
20060167539 | Mcewan | Jul 2006 | A1 |
20060224177 | Finitsis | Oct 2006 | A1 |
20060229688 | McClure et al. | Oct 2006 | A1 |
20060235482 | Forsell | Oct 2006 | A1 |
20060257446 | Tropsha et al. | Nov 2006 | A1 |
20070015959 | Forsell | Jan 2007 | A1 |
20070038232 | Kraemer | Feb 2007 | A1 |
20070049790 | Wagner et al. | Mar 2007 | A1 |
20070073099 | Forsell | Mar 2007 | A1 |
20070092862 | Gerber | Apr 2007 | A1 |
20070156204 | Denker et al. | Jul 2007 | A1 |
20070167670 | Coleman et al. | Jul 2007 | A1 |
20070193632 | Shu | Aug 2007 | A1 |
20070225802 | Forsell | Sep 2007 | A1 |
20070232848 | Forsell | Oct 2007 | A1 |
20070233019 | Forsell | Oct 2007 | A1 |
20070250020 | Kim et al. | Oct 2007 | A1 |
20070265675 | Lund et al. | Nov 2007 | A1 |
20080004487 | Haverfield | Jan 2008 | A1 |
20080045783 | Forsell | Feb 2008 | A1 |
20080051718 | Kavazov et al. | Feb 2008 | A1 |
20080086179 | Sharma | Apr 2008 | A1 |
20080103544 | Weiner | May 2008 | A1 |
20080200753 | Forsell | Aug 2008 | A1 |
20080214888 | Shalom | Sep 2008 | A1 |
20080269548 | Vecchiotti et al. | Oct 2008 | A1 |
20080275296 | Forsell | Nov 2008 | A1 |
20090018388 | Forsell | Jan 2009 | A1 |
20090054725 | Forsell | Feb 2009 | A1 |
20090240100 | Forsell | Sep 2009 | A1 |
20090240294 | Forsell | Sep 2009 | A1 |
20090247817 | Forsell | Oct 2009 | A1 |
20090247818 | Forsell | Oct 2009 | A1 |
20090248033 | Forsell | Oct 2009 | A1 |
20090250068 | Forsell | Oct 2009 | A1 |
20090254106 | Forsell | Oct 2009 | A1 |
20100145138 | Forsell | Jun 2010 | A1 |
20100145139 | Forsell | Jun 2010 | A1 |
20100217067 | Forsell | Aug 2010 | A1 |
20100312047 | Forsell | Dec 2010 | A1 |
20100312048 | Forsell | Dec 2010 | A1 |
20100312049 | Forsell | Dec 2010 | A1 |
20100312050 | Forsell | Dec 2010 | A1 |
20100312163 | Forsell | Dec 2010 | A1 |
20100312164 | Forsell | Dec 2010 | A1 |
20100312356 | Forsell | Dec 2010 | A1 |
20100318116 | Forsell | Dec 2010 | A1 |
20100318117 | Forsell | Dec 2010 | A1 |
20100318118 | Forsell | Dec 2010 | A1 |
20100324360 | Forsell | Dec 2010 | A1 |
20100324361 | Forsell | Dec 2010 | A1 |
20100324362 | Forsell | Dec 2010 | A1 |
20100324591 | Forsell | Dec 2010 | A1 |
20100331614 | Forsell | Dec 2010 | A1 |
20100331615 | Forsell | Dec 2010 | A1 |
20100331616 | Forsell | Dec 2010 | A1 |
20100331617 | Forsell | Dec 2010 | A1 |
20100331945 | Forsell | Dec 2010 | A1 |
20100332000 | Forsell | Dec 2010 | A1 |
20110009894 | Forsell | Jan 2011 | A1 |
20110009896 | Forsell | Jan 2011 | A1 |
20110009897 | Forsell | Jan 2011 | A1 |
20110015473 | Forsell | Jan 2011 | A1 |
20110015474 | Forsell | Jan 2011 | A1 |
20110040143 | Forsell | Feb 2011 | A1 |
Number | Date | Country |
---|---|---|
19511998 | Oct 1996 | DE |
0102548 | Mar 1984 | EP |
01 343 40 | Mar 1985 | EP |
0 200 286 | Nov 1986 | EP |
0 300 552 | Jan 1989 | EP |
0378251 | Jul 1990 | EP |
0412191 | Feb 1991 | EP |
0 583 012 | Feb 1994 | EP |
0611561 | Sep 1994 | EP |
0626154 | Nov 1994 | EP |
0876808 | Nov 1998 | EP |
1 004 330 | May 2000 | EP |
1 033 142 | Sep 2000 | EP |
1 072 238 | Jan 2001 | EP |
1072238 | Jan 2001 | EP |
1 514 526 | Mar 2005 | EP |
1563814 | Aug 2005 | EP |
1563886 | Aug 2005 | EP |
1 586 283 | Oct 2005 | EP |
1598030 | Nov 2005 | EP |
1 681 041 | Jul 2006 | EP |
1 878 452 | Jan 2008 | EP |
1 913 880 | Apr 2008 | EP |
2688693 | Sep 1993 | FR |
2688693 | Sep 1993 | FR |
2692777 | Dec 1993 | FR |
2692777 | Dec 1993 | FR |
2756485 | Jun 1998 | FR |
27565485 | Jun 1998 | FR |
2797181 | Feb 2001 | FR |
8 856 74 | Dec 1961 | GB |
1194358 | Jun 1970 | GB |
WO 8401282 | Apr 1984 | WO |
WO 9427504 | Dec 1994 | WO |
WO 9601597 | Jan 1996 | WO |
WO 9611036 | Apr 1996 | WO |
WO 9639932 | Dec 1996 | WO |
WO 9741799 | Nov 1997 | WO |
WO 9850099 | Nov 1998 | WO |
WO 9918885 | Apr 1999 | WO |
WO 0009048 | Feb 2000 | WO |
WO 0015158 | Mar 2000 | WO |
WO 0016686 | Mar 2000 | WO |
WO 0112078 | Aug 2000 | WO |
WO 0112108 | Feb 2001 | WO |
WO 0145487 | Jun 2001 | WO |
WO 0145590 | Jun 2001 | WO |
WO 0147434 | Jul 2001 | WO |
WO 0147575 | Jul 2001 | WO |
WO 0147439 | Jul 2001 | WO |
WO 0158391 | Aug 2001 | WO |
WO 0154615 | Aug 2001 | WO |
WO 0167964 | Sep 2001 | WO |
WO 0238217 | May 2002 | WO |
WO 0240083 | May 2002 | WO |
WO 02053210 | Jul 2002 | WO |
WO 02058563 | Aug 2002 | WO |
WO 02087657 | Nov 2002 | WO |
WO 02100481 | Dec 2002 | WO |
WO 03002192 | Jan 2003 | WO |
WO 03033054 | Apr 2003 | WO |
WO 2004012806 | Feb 2004 | WO |
WO 2004018037 | Mar 2004 | WO |
WO 2004019765 | Mar 2004 | WO |
WO 2004060171 | Jul 2004 | WO |
WO 2004071684 | Aug 2004 | WO |
WO 2004101029 | Nov 2004 | WO |
WO 9806358 | Feb 2005 | WO |
WO 2005072169 | Aug 2005 | WO |
WO 2005105003 | Nov 2005 | WO |
WO 2006122285 | Nov 2006 | WO |
WO 2006134106 | Dec 2006 | WO |
WO 2007017880 | Feb 2007 | WO |
WO 0147435 | Apr 2007 | WO |
WO 2007041795 | Apr 2007 | WO |
WO 2007051563 | May 2007 | WO |
WO 2007109759 | Sep 2007 | WO |
WO 2007137026 | Nov 2007 | WO |
WO 2007149555 | Dec 2007 | WO |
WO 2008135988 | Nov 2008 | WO |
WO 2009010799 | Jan 2009 | WO |
WO 2009 096854 | Aug 2009 | WO |
WO 2009096865 | Aug 2009 | WO |
WO 2009096868 | Aug 2009 | WO |
WO 2009115645 | Sep 2009 | WO |
Number | Date | Country | |
---|---|---|---|
20100145138 A1 | Jun 2010 | US |
Number | Date | Country | |
---|---|---|---|
60181469 | Feb 2000 | US | |
60181550 | Feb 2000 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 10203189 | US | |
Child | 12591434 | US |