Abstract: A neurostimulation paddle lead, method of neurostimulation, and neurostimulation system are provided. The neurostimulation paddle lead carries a plurality of electrodes comprising at least four columns of electrodes having a spacing between two inner electrode columns less than a spacing between the inner electrode columns and adjacent outer electrode columns. The inner electrode columns may also be longitudinally offset from the outer electrode columns. The methods and neurostimulation systems steer current between the electrodes to modify a medial-lateral electrical field created adjacent spinal cord tissue.

Abstract: The invention relates to a multi-electrode array comprising a plurality of electrodes, the electrodes being spaced apart from each other by spacer means, the electrodes being secured to the spacer means, the spacer means being encapsulated within a housing. The invention also relates to an implantable device comprising a multi-electrode array of the invention, a method of manufacturing electrodes for use in an array of the invention and a method for manufacturing a multi-electrode array of the invention. The invention also relates to a method for monitoring the effect of a test substance on a biological tissue using a multi-electrode array of the invention.

Abstract: An electrical stimulation device and method for the treatment of dysphagia is disclosed. In a preferred embodiment, the electrical stimulation device includes one or more channels of electrodes each of which includes a first electrode positioned in electrical contact with tissue of a target region of a patient and a second electrode positioned in electrical contact with tissue of a posterior neck region or a posterior thoracic region of the patient. A series of electrical pulses are then applied to the patient through the one or more channels of electrodes in accordance with a procedure for treating dysphagia.

Abstract: In some embodiments, a paddle lead is implanted within a patient such that the electrodes are positioned within the cervical or thoracic spinal levels. An electrode combination on a first row of electrodes can be determined that is effective for a first pain location with minimal effects on other regions of the body. The first pain location can be addressed by stimulating a first dorsal column fiber due to the relatively fine electrical field resolution achievable by the multiple columns. Then, another electrode combination on a second row of electrodes can be determined for a second pain location with minimal effects on other regions. The second pain location could be addressed by stimulating a second dorsal column fiber. After the determination of the appropriate electrodes for stimulation, the patient's IPG can be programmed to deliver pulses using the first and second rows according to the determined electrode combinations.

Abstract: A system or appliance to treat heart failure (HF) conditions. The appliance includes a structural support or cardiac constraint to limit further distension of weakened heart tissue. The appliance also includes an implantable stimulation pulse generator and controller such that the appliance can automatically monitor cardiac activity and provide therapeutic stimulations for detected arrhythmias. The appliance can also include one or more surface electrodes. The surface electrodes can be arranged on opposite sides of the heart to apply relatively spatially uniform stimulation potentials across the heart with reduced shunting around the target tissue. A surface electrode can also be arranged to wrap substantially about a periphery of the patient's heart and used with an internal electrode to apply a relatively homogeneous shock while facilitating lower voltage and smaller shocking capacitors.

Abstract: A static electric therapy apparatus is disclosed which does not leave a user discomfort. The static electric therapy apparatus comprises an electric potential generator connected to an alternating power supply, and an output terminal which provides a human body with electric potential by touching the human body, which output terminal is connected to the electric potential generator; and the static electric therapy apparatus is characterized in that it further comprises a ground wire connected to the output terminal; a direct-current power supply applying negative voltage to the output terminal, which is connected to the output terminal in series; and a transfer switch which switches the case where the output terminal is connected to the potential generator and the case where the output terminal is connected to the ground wire, the switch being connected to the output terminal.

Abstract: An electrical epidermal stimulation device for treating skin ailments having a power supply configured to provide power to the electrical epidermal stimulator, a first and second electrode configured to provide an electrical stimulus to an area of application, a wake up module configured to wake up a control module when a current flows from the first electrode to the second electrode, a voltage step generator module configured to generate a voltage, and an output drive module configured to control a direction of the voltage step to the first and second electrodes. In one embodiment, the electrical epidermal stimulation device comprises an indicator module for notifying a user that the device is functioning. In another embodiment, the voltage step generator module provides a voltage that increases and decreases in predetermined amounts to create a voltage step. In another embodiment, the direction of voltage application switches between the first and second electrodes.

Abstract: A multi-element probe array suitable for sensing or stimulating is disclosed. In one embodiment, the multi-element probe array includes a plurality of microfibers extending longitudinally and oriented substantially parallel to form a bundle. Probe elements are defined by a first subset of the microfibers displaced in a forward direction along the longitudinal axis relative to spacer elements defined by a second subset of the microfibers. Interface elements and communication elements are disposed on the probe elements.

Abstract: A lead assembly includes a lead body and at least one cables at least partially disposed within the lead body. The cable has a non-electrode portion and an electrode portion, where the non-electrode portion extends within the lead body, and the electrode portion is external to the lead body.

Abstract: A minimally invasive intraluminal electrode assembly that includes a cannulated tube and a plurality of wires disposed within the cannulated tube. Each of the plurality of wires has one of a plurality of electrical contacts on a distal end thereof. The distal portion of the plurality of wires assumes a radially constrained configuration within the cannulated tube in a retracted position and a radially extended position outward of the cannulated tube in a deployed position. The electrode assembly further comprises a spring electrode connecting the plurality of electrical contacts to collectively form a substantially circular configuration in a deployed position.

Abstract: A method and apparatus for making a connection with a part of a body to transfer an electromagnetic signal for a predetermined purpose, the apparatus including: a garment including one or more electrode capable of passing the signal to or from the part of the body; and a controller for controlling the nature of or processing the signal dependant on one or more parameters in order to vary the nature of the signal dependant on the purpose; wherein at least one parameter of the one or more parameters is stored on a data storage device included in the garment.

Abstract: The invention provides an implant, system and method for electrically stimulating a target tissue to either activate or block neural impulses. The implant provides a conductive pathway for a portion of electrical current flowing between surface electrodes positioned on the skin and transmits that current to the target tissue. The implant has a passive electrical conductor of sufficient length to extend from subcutaneous tissue located below a surface cathodic electrode to the target tissue. The conductor has a pick-up end which forms an electrical termination having a sufficient surface area to allow a sufficient portion of the electrical current to flow through the conductor, in preference to flowing through body tissue between the surface electrodes, such that the target tissue is stimulated to either activate or block neural impulses. The conductor also has a stimulating end which forms an electrical termination for delivering the current to the target body tissue.

Abstract: Optimizing cardiac preload based on measured pulmonary artery pressure involves varying, for each repetition of an acute burst protocol, a parameter of pacing applied to a patient's heart during the acute burst protocol. Pulmonary artery pressure is measured during the repetitions of the acute burst protocol. An optimum ventricular preload is determined based on the measured pulmonary artery pressure. Pacing therapy is provided using a value of the parameter that is selected based on the determination of optimum ventricular preload.

Abstract: The invention is a method of automatically adjusting an electrode array to the neural characteristics of an individual patient. By recording neural response to a predetermined input stimulus, one can alter that input stimulus to the needs of an individual patient. A minimum input stimulus is applied to a patient, followed by recording neural response in the vicinity of the input stimulus. By alternating stimulation and recording at gradually increasing levels, one can determine the minimum input that creates a neural response, thereby identifying the threshold stimulation level. One can further determine a maximum level by increasing stimulus until a predetermined maximum neural response is obtained.

Abstract: A method of treating a wound or preventing injury to a region susceptible to injury comprising the steps of placing a pair of electrodes placed spaced apart in the region of a wound and applying a predetermined sequence of current waveforms across the electrodes. The sequence of current waveforms comprises a first waveform comprising a series of current pulses having an amplitude in a range of from 80 to 300 ?A, having a frequency in a range from 0.5 to 1.5 pulses per second and a pulse width in a range from 333 to 1000 ms, a second waveform comprising a series of current pulses having an amplitude in a range of from 20 to 60 ?A, having a frequency in a range from 2 to 4 pulses per second and a pulse width in a range from 125 to 250 ms and a third waveform comprising a series of current pulses having an amplitude in a range of from 250 to 640 ?A, having a frequency in a range of from 80 to 120 pulses per second and a pulse width in a range from 4 to 6 ms.

Abstract: A medical electrical lead includes a lead body and a connector terminal. A conductor extends from the lead body to the connector terminal along a helical path through a transition zone.

Abstract: An electric stimulator for alpha-wave derivation is characterized in that frequency selected from a range of 1 Hz to 50 Hz, preferably, 7 Hz to 14 Hz, and an output voltage are applied to auricle of a patient's ears to derive alpha-waves, and that cycle and intensity of stimulation are varied depending upon body temperature and blood sugar. Prompt reaction may be obtained by directly applying the voltage to the ears, and the reaction may continue when stimulation is extended. In addition, it is suitable to treat various diseases having common cause due to stress or arousal reaction in the human body.

Abstract: A method for applying variable electro-muscle stimulation (EMS) to an exercising person includes a belt having a plurality of electrodes placed around the abdomen at the rectus abdominis and obliques. The person then gets into an exercise apparatus which has a rotatable component. Attached to the rotatable component is a transducer that senses the position of the component. An EMS generator is connected to the belt through the transducer. As the user exercises in a first direction, increasing stimulation is applied to the subject muscles. As the user moves the rotatable component in the opposite direction, decreasing stimulation is applied to the user. In an alternative embodiment, the belt has at least one pair of electrodes connected to a common adjustment control so that as the voltage increases to one of the electrodes, it decreases to the other electrode of the pair, and vice versa. A toggle switch makes possible the selection of a particular pair.

Abstract: This document discusses, among other things, brain stimulation models, systems, devices, and methods, such as for deep brain stimulation (DBS) or other electrical stimulation. A model computes a volume of influence region for a simulated electrical stimulation using certain stimulation parameters, such as amplitude, pulsewidth, frequency, pulse morphology, electrode contact selection or location, return path electrode selection, pulse polarity, etc. The model uses a non-uniform tissue conductivity. This accurately represents brain tissue, which has highly directionally conductive neuron pathways yielding a non-homogeneous and anisotropic tissue medium. In one example, the non-uniform tissue conductivity is obtained from diffusion tensor imaging (DTI) data. In one example, a second difference of an electric potential distribution is used to define a volume of activation (VOA) or similar volume of influence.

Abstract: An implantable medical device (IMD) includes one or more semiconductor switches and one or more switch driver circuits. The semiconductor switches, in response to one or more switch-on and switch-off commands that each have a voltage magnitude, switch between a conductive state and a non-conductive state, respectively, to thereby selectively supply one or more therapy pulses using electrical energy from an electrical energy source. The switch driver circuits, in response to drive commands, selectively supply the switch-on and switch-off commands to the semiconductor switches. The switch driver circuits, using a portion of the supplied therapy pulses, increase the voltage magnitudes of the switch-on and switch-off commands to a magnitude that maintains the switch in the conductive state or the non-conductive state, respectively, while the therapy pulses are being supplied.

Abstract: In general, the invention is directed to a technique for selection of parameter configurations for a neurostimulator using genetic algorithms. The technique may be employed by a programming device to allow a clinician to select parameter configurations, and then program an implantable neurostimulator to deliver therapy using the selected parameter configurations. In operation, the programming device executes an electrode configuration search algorithm to guide the clinician in the selection of electrode configurations. The search algorithm relies on a genetic algorithms to identify potential optimum electrode configurations within an electrode set. The genetic algorithms provide guidance in the electrode configuration selections process, interactively guiding the clinician by suggesting the configurations that are most likely to be efficacious given the results of tests already performed during an evaluation session.

Abstract: An article of clothing for use in water includes an electroactive material integrated into the clothing, at least one electrode integrated into the clothing and wherein the electroactive material is adapted to release electrical impulses into the water. A method of generating electrical energy on a person includes wearing clothing with an integrated electroactive material that produces electrical charges upon movement of the person and harvesting electrical energy from the electroactive material for use with an electrical load. An article of clothing includes an electroactive material integrated into the clothing, at least one electrode integrated into the clothing, and wherein the electroactive material is adapted to generate an electrical field around the clothing.

Abstract: A device for applying a therapeutic electrical field to a user's body includes an electroactive material shaped for application to a user body to provide a therapeutic electric field in response to pressure applied to the electroactive material and one or more electrodes integrated into the electroactive material and disposed along an inner surface of the electroactive material for delivering the therapeutic electric field to the user's body.

Abstract: Methods, apparatus, and systems are provided to stimulate multiple sites in a heart. A controller senses electrical activity associated with sinus rhythm of the heart. A signal generator is configured to generate an electrical signal for stimulating the heart. Based on the electrical signal, a distributor circuit then distributes the stimulating signals, such as pacing pulses, to a heart. The distributor circuit may vary the delay time between stimulating signals, inhibit a stimulating signal, trigger application of a stimulating signal, or vary the characteristics, such as the pulse width and amplitude, of a stimulating signal.

Abstract: Electrodes designed in accordance with the present invention may selectively employ arc shaped contacts; variations in contact number, positioning, spacing, and/or distribution; variations in contact area, size, or periphery; and/or on-electrode conductive links or interconnections between particular contacts to provide enhanced efficiency neural stimulation, and/or increased electrode reliability.

Abstract: A method and apparatus for speeding the healing process of soft tissues, bone fractures, cancerous tissue, nerve pathways and other body tissues wherein a portable base comprising a plurality of cells is applied with the cells facing or encircling the wound. The cells generate electro-magnetic radiations, radio frequencies, magnetic fields, current-voltage signals or combinations thereof via a field generator coil or electrodes. Each cell is powered and controlled individually via self-contained controls or remote controls. The type, frequency, pulse characteristics, repetition rate and signal density of the energy are varied according to the size and type of wound to be treated and according to the proximity of each cell to the wounded tissue.

Abstract: A device and method for cardiac rhythm management in which a heart chamber is paced in accordance with sense signals from the opposite chamber or other distant cardiac site. The method is particularly useful in delivering cardiac resynchronization therapy.

Abstract: Multi-phase RF ablation employing a two-dimensional or three-dimensional electrode array produces a multitude of currents paths on the surface of the ablation zone. This results in a uniform lesion with a size defined by the span of the electrode array. An orthogonal electrode catheter array suitable for cardiac ablation is used in conjunction with a two-phase RF power source to produce uniform square-shaped lesions of size 1.2 cm2. Lesions of larger size are created by successive adjacent placement of the square-shaped lesions. A temperature sensor at the electrode tip allows monitoring of ablation temperature and regulation of thereof to minimize the electrode tips from being fouled by coagulum. In another embodiment, an external auxiliary electrode is used in combination with the catheter electrodes. This also produces lesions of greater depth. In yet another embodiment, ablation is performed with a sequence of elementary electrode-electrical configurations.

Abstract: A multi-purpose, functional electrical stimulation (FES) system 10 includes an implantable stimulator unit 12 for stimulating a plurality of different sites in a patient's body 14. A transmitter 20 is arranged externally of the patient's body 14 for supplying signals transcutaneously to the stimulator unit 12. A controller 16 is in communication with the transmitter 20. At least one implantable switching node 26 has an input terminal 30 in electrical communication with the stimulator unit 12 and a plurality of output terminals to each of which one of a further switching node 26 and a stimulating element 24 is connected. The switching node 26 including addressing circuitry 44 for switching at least one output terminal into electrical connection with the input terminal 30 of the switching node 26 in response to a control signal received from the controller 16 via the stimulator unit 12.

Abstract: A system for delivering a substance into a body at a treatment site that includes an alternating current source and a plurality of electrodes. Circuitry is connected between the alternating current source and the electrodes for supplying current to the electrodes when the electrodes are in electrical contact with said body so that a uni-directional current flow for delivering the substance into the body is maintained at the treatment site and a bi-directional current flow is maintained throughout the body. At least one of the electrodes is divided into sub-electrodes to, for example, reduce hazards associated with current concentration. These and other systems and methods are adaptable for large treatment areas and/or use a convenient and low-cost arrangement of electronics.

Abstract: The electrical signal sensing and/or signal application device for sensing electrical signals on a surface and/or for applying electrical signals to a surface, particularly of human or animal skin or other organs or tissues, comprises a substrate (12) having first and second major surfaces (14), and a plurality of electrodes (16) arranged on the first major surface (14) of the substrate (12) and projecting therefrom, each of the electrodes (16) comprising a pointed contact end (36) facing away from the substrate (12) for contacting the surface, and a base end (26) facing towards the substrate (12). On the first or second or both major surfaces (14) of the substrate (12) there is arranged a plurality of first contact pads (22) for electrical connection to contact elements of an evaluation and/or driving means for evaluating the sensed electric signals and/or applying signals to the electrodes (16), the first contact pads (22) being electrically connected to the electrodes (16).

Abstract: An improved medical implant device is provided which has a plurality of micro-electrodes. The use of a plurality of micro-electrodes allows a clinically effective electrical stimulation pathway to be selected once the implant is positioned within or adjacent to the tissue to be treated even if the implant is not optimally placed or located. Thus, in cases where the implant is not optimally placed, it is not necessary to remove the implant and then reposition it within or adjacent to the tissue to be treated, thereby reducing stress to the patient caused by additional surgery. Moreover, using the micro-electrodes of this invention, directional electrostimulation can be provided to the tissue to be treated. Implant devices with a plurality of micro-electrodes are provided which are especially adapted for use in reducing the frequency and/or severity of neurological tremors.

Abstract: Pathological conditions are alleviated by bone conduction practiced by the application of sinusoidal electric waves at frequencies of between 4,200 and 6,500 hertz at less than 200 microamperes current.

Abstract: Medical electrode arrangements are provided for electrotherapy and monitoring applications. In one embodiment, each electrode arrangement includes a smaller electrode that is releasably attached to the back of a larger electrode. For adult applications, the larger electrode is applied to the patient. For pediatric applications, the larger electrode is preferably removed, and the smaller electrode is applied to the patient. Face-to-face and back-to-back electrode arrangement configurations are also provided. In a further embodiment, an electrode arrangement is comprised of first and second conductive regions of a common substrate that are separable by a division line in the substrate. For adult applications, stored energy is conducted through both conductive regions. For pediatric applications, the second region of the substrate is removed along the division line. A sensing mechanism is also provided to detect whether the electrode arrangement has been placed in an adult or pediatric configuration.

Abstract: A device, which is preferably disc shaped, has two primary layers. A first layer has one side, which is the lower side in use, for adhering to a patient's skin surface, a second, upper layer on the underside of which electrical circuitry is printed or affixed so that the electrical circuitry is sandwiched between the layers. The device can be made in several sizes to accommodate patient size and location of the acupuncture point to be stimulated. Two distinct forms of the device are presented: a single use and a reusable device for. In the single use device, the first, lower layer is preferably a foam with non-conductive adhesive on both sides: the bottom side for adhering to the skin and the top side for adhering to the upper polyester disc. The holes through this lower foam layer include, preferably, eight holes spaced concentrically about one central hole in the middle of the lower foam layer.

Abstract: This invention is an improved acupuncture device comprising of several cartridges (including a control circuit, a power supply unit, and a power switch in each cartridge) and leads among cartridges. Each cartridge has a conductive clip, which can lock a picking onto the cartridge. Open the power switch to power on the control circuit, and the current will flow to the picking through the clip. Stamp the picking onto an acupoint to excite it with the low frequency current generated by the control circuit. In this way, the device can result in the same effect as needle therapy. Furthermore, due to the flexibility of the leads, the device can be applied on multi acupoints.

Abstract: Medical electrode arrangements are provided for electrotherapy and monitoring applications. In one embodiment, each electrode arrangement includes a smaller electrode that is releasably attached to the back of a larger electrode. For adult applications, the larger electrode is applied to the patient. For pediatric applications, the larger electrode is preferably removed, and the smaller electrode is applied to the patient. Face-to-face and back-to-back electrode arrangement configurations are also provided. In another embodiment, an electrode arrangement is comprised of first and second conductive regions that are separable from each other. In yet further embodiments, an electrode arrangement is comprised of two or more electrodes that are not physically or electrically connected to each other. At least one electrode from each electrode arrangement is placed on the patient. A sensor is also provided to sense which electrodes in each electrode arrangement have been placed on the patient.

Abstract: An implantable pulse generator includes a current steering capability that allows a clinician or patient to quickly determine a desired electrode stimulation pattern, including which electrodes of a group of electrodes within an electrode array should receive a stimulation current, including the amplitude, width and pulse repetition rate of such current. Movement of the selected group of electrodes is facilitated through the use of remotely generated directional signals, generated by a pointing device, such as a joystick. As movement of the selected group of electrodes occurs, current redistribution amongst the various electrode contacts takes place. The redistribution of stimulus amplitudes utilizes re-normalization of amplitudes so that the perceptual level remains fairly constant. This prevents the resulting paresthesia from falling below the perceptual threshold or above the comfort threshold.

Abstract: A device for attaching at least three electrodes to a subject for stimulating abdominal muscles of the subject. The device comprises an attachment mechanism for extending around the torso of the subject and a main locating element on the attachment mechanism for locating a central electrode of the at least three electrodes adjacent the umbilicus of the subject. Two secondary locating elements are also provided on the attachment mechanism disposed on respective opposite sides of the main locating element for locating two corresponding side electrodes of the at least three electrodes spaced apart from the central electrode in a general direction towards a corresponding one of the right and left mid-axillary lines of the torso intermediate the rib cage and corresponding right and left iliac crests. By applying at least one pulsed signal to the subject through the respective central and side electrodes, abdominal muscles of the subject are stimulated.

Abstract: A method for applying variable electro-muscle stimulation (EMS) to an exercising person includes a belt having a plurality of electrodes placed around the abdomen at the rectus abdominis and obliques. The person then gets into an exercise apparatus which has a rotatable component. Attached to the rotatable component is a transducer that senses the position of the component. An EMS generator is connected to the belt through the transducer. As the user exercises in a first direction, increasing stimulation is applied to the subject muscles. As the user moves the rotatable component in the opposite direction, decreasing stimulation is applied to the user. In an alternative embodiment, the belt has at least one pair of electrodes connected to a common adjustment control so that as the voltage increases to one of the electrodes, it decreases to the other electrode of the pair, and vice versa. A toggle switch makes possible the selection of a particular pair.

Abstract: The method and apparatus for balancing the electric potential of a human body takes advantage of pressing to arouse the force and latent power of self-treatment by electric current of the human body. The method mainly is done by pressing the abdomen and the buttocks to make the human body generate regular respiration whereby positive and negative ions in the nature are absorbed and delivered by the blood and the nerve system for circulation to make complement and get a balanced effect with the positive and negative ions in the cell tissues in the nerve system of the human body. The apparatus is provided mainly on a base with massage mechanisms, by pressing the vital points on the abdomen and the buttocks periodically for predetermined times with the massage mechanisms, and by the images shown, the user can totally pay attention to the area where the electric current flows through to promote balancing of the positive and negative ions to get the effect of removing diseases and making good health.

Abstract: The electrical signal sensing and/or signal application device for sensing electrical signals on a surface and/or for applying electrical signals to a surface, particularly of human or animal skin or other organs or tissues, comprises a substrate (12) having first and second major surfaces (14), and a plurality of electrodes (16) arranged on the first major surface (14) of the substrate (12) and projecting therefrom, each of the electrodes (16) comprising a pointed contact end (36) facing away from the substrate (12) for contacting the surface, and a base end (26) facing towards the substrate (12). On the first or second or both major surfaces (14) of the substrate (12) there is arranged a plurality of first contact pads (22) for electrical connection to contact elements of an evaluation and/or driving means for evaluating the sensed electric signals and/or applying signals to the electrodes (16), the first contact pads (22) being electrically connected to the electrodes (16).

Abstract: An electrical stimulation device method provides for exact repeatable positioning of stimulation pads onto a body part. The device includes a flexible member for contacting a body part and hook/loop members for tightly supporting the flexible member against the body part. At least one electrical bus is provided which may include a connector for enabling connection of the bus to an electrical lead wire and an electrical contact disposed on the inside of the flexible member. A conductive pad is provided which has dimensions substantially smaller than the dimensions of the flexible member and includes a cover adhesive layer for removably adhering the conductive pad to the flexible member inside with a first side of the cover layer covering the bus contact and an electrical communication therewith. A current controlling media is adhered to a second side of the cover layer and a base layer disposed on the current controlling media is provided for removably adhering the conductive pad to the body part.

Abstract: An electrical stimulation device method provides for exact repeatable positioning of stimulation pads onto a body part. The device includes a flexible member for contacting a body part and hook/loop members for tightly supporting the flexible member against the body part. At least one electrical bus is provided which may include a connector for enabling connection of the bus to an electrical lead wire and an electrical contact disposed on the inside of the flexible member. A conductive pad is provided which has dimensions substantially smaller than the dimensions of the flexible member and includes a cover adhesive layer for removably adhering the conductive pad to the flexible member inside with a first side of the cover layer covering the bus contact and an electrical communication therewith. A current controlling media is adhered to a second side of the cover layer and a base layer disposed on the current controlling media is provided for removably adhering the conductive pad to the body part.

Abstract: A joint protector includes a band surrounding a human body and having an inner side and an outer side. A power supplier is securely attached to the outer side of the band. A flexible heating pad is attached to the inner side of the band and electrically connected to the power supplier. The flexible heating pad provides heat energy to warm the user's skin and reduce pain due to the electric resistance of the flexible heating pad. An inner layer is securely adhered on the inner side of the band for covering the flexible heating pad.

Abstract: A device for attaching at least three electrodes to a subject for stimulating abdominal muscles of the subject. The device comprises an attachment mechanism that further comprises a main locating element for locating a central electrode of the at least three electrodes, and two secondary locating elements disposed on respective opposite sides of the main locating element for locating two corresponding side electrodes of the at least three electrodes spaced apart from the central electrode. A receiver is also provided for receiving a signal generated by a signal generator for generating at least one pulsed signal. A selector is also provided for selecting one or more of the electrodes through which a pulsed signal is to be applied.

Abstract: A device, which is preferably disc shaped, has two primary layers. A first layer has one side, which is the lower side in use, for adhering to a patient's skin surface, a second, upper layer on the underside of which electrical circuitry is printed or affixed so that the electrical circuitry is sandwiched between the layers. The device can be made in several sizes to accommodate patient size and location of the acupuncture point to be stimulated. Two distinct forms of the device are presented: a single use and a reusable device for. In the single use device, the first, lower layer is preferably a foam with non-conductive adhesive on both sides: the bottom side for adhering to the skin and the top side for adhering to the upper polyester disc. The holes through this lower foam layer include, preferably, eight holes spaced concentrically about one central hole in the middle of the lower foam layer.

Abstract: A method for stimulating abdominal muscles of a subject, comprising the steps of providing at least three electrodes, one of the at least three electrodes being a central electrode and the other two of the at least three electrodes being side electrodes located on the subject spaced apart from the central electrode on respective sides thereof, and passing at least one pulsed signal subcutaneously through the subject between selected electrodes of the at least three electrodes.

Abstract: An apparatus and method for treatment of congestive heart failure from the right side of the heart. An implantable cardiac stimulation system with a multi-electrode lead having three or more selectable electrodes, together with apparatus for identifying an optimal subset of electrodes, apparatus for shaping a propagating wave front, and apparatus for modifying the intrinsic ventricular cardiac activation sequence, or generating simultaneous or near simultaneous pacing pulses to the septum or right ventricular outflow tract during ventricular systole in order to improve left ventricular cardiac efficiency and reduce mitral regurgitation in patients with dilated cardiomyopathy. A three dimensional map of electrode placement may be calculated. A sub set of the available electrodes in the right side of the heart is selected for stimulation such that septal motion during systole is reduced or the mitral valve area is stiffened to reduce mitral regurgitation.

Abstract: An implantable medical device (IMD) is disclosed that is formed on a substrate composed of liquid crystal polymer (LCP). In one embodiment, the IMD can be an interconnection module for interconnecting an electrode array to an equipment module. The interconnecting module includes conductors disposed on the LCP substrate and coupled to the electrode array, and wherein the conductors are encapsulated using a silicone or LCP encapsulant. In another embodiment, the IMD is an electrode array and interconnect module disposed on an integral LCP substrate. An equipment module can be coupled to the interconnect module. Alternatively, a hybrid electronic circuit can be coupled to the interconnect module for signal processing and conditioning signals received from the electrode array or for providing stimulus signals to the electrode array. In this embodiment, all of the conductors and at least a portion of the electrodes in the electrode array are encapsulated using a silicone or LCP encapsulant.