Abstract: A device configured for implanting beneath a patient's skin for the purpose of tissue, e.g., nerve or muscle, stimulation and/or parameter monitoring and/or data communication. Devices in accordance with the invention are comprised of a sealed housing, typically having an axial dimension of less than 60 mm and a lateral dimension of less than 6 mm, containing a power source for powering electronic circuitry within including a controller, an address storage means, a data signal receiver and an input/output transducer. When used as a stimulator, such a device is useful in a wide variety of applications to stimulate nerves and associated neural pathways, e.g., to decrease or relieve pain, stimulate specific muscles or organs to better carry out a body function (e.g., to exercise weak or unconditioned muscles or to control urinary incontinence), and the like.

Abstract: A programmable output current source for use within an implantable tissue or nerve stimulator, e.g., an implantable cochlear stimulator or spinal cord stimulator, includes parallel-connected P-FET current source sets connected between a positive voltage rail and an electrode node, and parallel-connected N-FET current source sets connected between the electrode node and a negative voltage rail. The N-FET current source sets include n N-FET current sources, where n is an integer 0, 1, 2, 3, 4, . . . , and wherein each N-FET current source, when enabled, respectively sinks a current 2nI from the electrode node to the negative rail, where I is a selectable fixed current. Similarly, the P-FET current source sets include n P-FET current sources, where n=0, 1, 2, 3, . . . n, and wherein each P-FET current source, when enabled, respectively sources a current 2nI from the positive voltage rail to the electrode node.

Abstract: A system for monitoring and/or affecting parameters of a patient's body and more particularly to such a system comprised of a system control unit (SCU) and one or more other devices, preferably battery-powered, implanted in the patient's body, i.e., within the envelope defined by the patient's skin. Each such implanted device is configured to be monitored and/or controlled by the SCU via a wireless communication channel. In accordance with the invention, the SCU comprises a programmable unit capable of (1) transmitting commands to at least some of a plurality of implanted devices and (2) receiving data signal from at least some of those implanted devices. In accordance with a preferred embodiment, the system operates in closed loop fashion whereby the commands transmitted by the SCU are dependent, in part, on the content of the data signals received by the SCU.

Abstract: An implantable living tissue stimulator avoids the use of conventional coupling capacitors in its output stage, yet still prevents an average dc current flow from flowing through living tissue in electrical contact with the stimulator. The output stage generates and applies a biphasic stimulating current pulse to selected paired output terminals. The terminals, in turn, are electrically connected to respective electrodes which are positioned so as to contact the living tissue to be stimulated. In one embodiment, special circuitry is employed within the output stage to block dc current flow through the living tissue and to balance the electrical charge that is delivered to the living tissue. In another embodiment, the electrodes themselves are made from a material that allows them to function as a capacitor. In yet an additional embodiment, the coupling capacitors are integrated into the leads that connect the output terminals of the output stage with the electrodes.

Abstract: A low power switched rectifier circuit is realized using P-MOS and N-MOS FET switches that are turned ON/OFF at just the right time by a detector and inverter circuit (which form an integral part of the rectifier circuit) to rectify an incoming ac signal in a highly efficient manner. Parasitic diodes and transistors that form an integral part of the FET circuitry respond to and rectify the incoming signal during start up, i.e., when no supply voltage is yet present, thereby providing sufficient operating voltage for the FET switches to begin to perform their intended rectifying function. In the absence of an incoming ac signal, i.e., during the time between biphasic pulses, the rectifier circuit is biased with an extremely small static bias current; but in the presence of an incoming ac signal, at a time when the positive and negative phases of the incoming signal are to be connected to positive and negative supply lines, a much larger dynamic bias current is automatically triggered.

Abstract: An implantable sensor/stimulator is connectable to a controller using just two conductors, which two conductors carry both operating power and data (data commands and/or measured data) between the sensor/stimulator and control circuit. Each sensor/stimulator may be serially connected to another sensor/stimulator, again using only two conductors, thereby allowing a "daisy chain" of such sensors/stimulators to be formed. Each sensor/stimulator in the daisy chain is individually addressable by the control circuit. Input data is sent to the sensors over the two conductors using a phase-modulated biphasic modulation scheme, which scheme also provides operating power for each sensor/stimulator connected to the two conductors. Output data is sent from the sensors to the controller over the same two conductors using a pulse-position presence/absence modulation scheme. The data transmission schemes provide a very high signal-to-noise ratio.

Abstract: A cochlea stimulation system includes a patient wearable system comprising an externally wearable signal processor (WP) and a headpiece in electronic communication with an implanted cochlear stimulator (ICS). The ICS comprises eight output stages each having two electrically isolated capacitor-coupled electrodes, designated "A" and "B", circuits for monitoring the voltages on these electrodes, and circuits for both transmitting status information to and receiving control information from the WP. Based upon information received from the WP, a processor within the ICS can control both the frequency and the widths of the output stimulation pulses applied to the electrodes and may select which electrodes to monitor. The ICS receives power and data signals telemetrically through the skin from the WP. To save power, the ICS may be "powered down" by the WP based upon the absence of audio information or "powered up" if audio is present.

Abstract: A low power current-to-frequency converter circuit provides an output frequency signal F.sub.OUT having a frequency that varies as a function of a low level analog input current signal. The analog input current signal is typically generated by an implantable sensor element, designed to sense a particular substance or parameter within body tissue or fluids to which the sensor is exposed, with the magnitude of the analog signal providing a measure of the sensed substance or parameter. Conversion of the low level analog current to the output frequency signal facilitates transmission of the data signal over a shared data bus and other digital processing of the data signal.

Abstract: A power control loop is established between an external control device and an implantable device so that only the amount of power needed by the implant device to sustain its present operating conditions is transmitted across a transcutaneous transmission link, thereby reducing the amount of power expended by the external control device. In one embodiment, the power control loop is used with a cochlea stimulating system that includes an externally wearable signal receiver and processor (WP) and an implanted cochlear stimulator (ICS). The power control loop is provided between the ICS and the WP such that power delivered to the ICS is precisely controlled in a closed loop manner, with a variable amount of RF energy (power) being transmitted across the transcutaneous link between the WP and ICS. The transmitted RF energy is received by the ICS and is converted to a voltage that is used as a power source within the ICS for stimulating electrode contacts of the ICS.

Abstract: An implantable cochlear stimulator (ICS) has eight output stages (212), each having a current source (212B) connected to a pair of electrodes, designated "A" and "B", through respective output coupling capacitors and an electrode switching matrix (212C). An indifferent electrode is connected to each output stage by way of an indifferent electrode switch (212D). The current source generates a precise stimulation current as a function of an analog control voltage. The analog control voltage, in turn, is generated by a logarithmic D/A converter. The D/A converter serially converts data words, received in a data frame from an external source, to respective analog control voltages that are applied sequentially to the current sources of each output stage. An output mode register (208) controls the switching matrix of each stage, as well as the indifferent electrode switch, to configure the electrodes for a desired stimulation configuration, e.g.

Abstract: A physician's tester provides for physician monitoring and control of an implantable human tissue stimulator system, such as an implantable cochlear stimulator (ICS) system. During normal operation, the tissue stimulator system includes an implantable stimulator and a wearable processor (WP). The physician's tester is designed around a microprocessor, and is basically a modification of the WP. The tester provides control over the selection of voltages and currents to be measured and the presetting of parameters in the implantable stimulator during testing of the implanted stimulator and/or a patient's response to data transmitted by the WP/tester to the implanted stimulator. The physician's testor is portable and utilizes telemetry coupling with the implanted stimulator to provide communication between the tester and stimulator for the monitoring, control and measurement of the stimulator parameters. The tester resides in a portable housing having a control panel and a visual display.

Abstract: A tissue stimulating system including an external transmitter for transmitting data to an implanted stimulator including a processor for generating stimulation signals for application to a plurality of tissue stimulating electrodes. The processor selectively monitors the electrodes and/or voltages generated in the stimulator and generates stimulator status indicating signals for transmission to the external transmitter. The external processor receives and processes such status indicating signals.

Abstract: An external wearable processor (WP) of a cochlear stimulating system transmits a data signal to an implanted cochlear stimulator (ICS). The ICS is controlled through the data signal so that cochlear stimulation is provided by the ICS only after a determination is made that the WP is in proper signal contact therewith, and that the ICS is functioning properly. The ICS extracts a raw power signal from the data signal and generates different operating voltages from the extracted raw power signal. A detector generates a power bad signal whenever one of the operating voltages is less than a reference voltage. The ICS also detects and generates a carrier detect signal when the data signal is being received. Clock signals are generated within the ICS, and a phase locked loop (PLL) lock signal is generated when the clock signals are phase locked to the data signal. ICS circuitry further checks the parity of the incoming data signal and generates a parity alarm signal whenever a parity error is detected.

Abstract: An implantable cochlear stimulator (ICS) has eight output stages (212), each having a programmable current source (212B) connected to a pair of electrodes, designated "A" and "B", through respective output coupling capacitors and an electrode switching matrix (212C). An indifferent electrode is connected to each output stage by way of an indifferent electrode switch (212D). An output mode register (208) controls the switching matrix of each stage, as well as the indifferent electrode switch, to configure the electrodes for: (1) bipolar stimulation (current flow between the pair of electrodes of the output stage), (2) monopolar A stimulation (current flow between the "A" electrode of the output stage and the indifferent electrode), (3) monopolar B stimulation (current flow between the "B" electrode of the output stage and the indifferent electrode), or (4) multipolar stimulation (current flow between the "A" or "B" electrode of one output stage and the "A" or "B" electrode of another output stage).

Abstract: A tissue stimulating system includes an external transmitter for transmitting a data signal to an implanted stimulator. The implanted stimulator includes a processor for generating stimulation signals for application to a plurality of tissue stimulating electrodes through respective isolated output channels. The implanted stimulator also includes a power supply that extracts a raw power signal from the data signal. A voltage downconverter generates at least four separate voltages from the extracted raw power signal by alternately connecting at least four capacitors in series across the raw power signal, thereby providing at least four output voltages, and then connecting the capacitors in parallel to transfer the charge stored thereon to a storage capacitor, which serves as the power source for portions of the stimulator.

Abstract: An implantable microstimulator has a structure which is manufactured to be substantially encapsulated within a hermetically-sealed housing inert to body fluids, and of a size and shape capable of implantation in a living body. The internal structure of the microstimulator comprises a coil adapted to function as the secondary winding of a transformer and receive power and control information. Circuit means, including control electronics, a capacitor and electrodes are provided. The electrodes, which may be made one of iridium and the other of tantalum and placed on opposite ends of the microstimulator, or alternatively, an iridium electrode at each end of the microstimulator, are at least partially exposed and provide electrical, stimulating pulses to the body.

Abstract: An addressable, implantable microstimulator is substantially encapsulated within a hermetically-sealed housing inert to body fluids, and of a size and shape capable of implantation in a living body, by expulsion through a hypodermic needle. Power and information for operating the microstimulator is received through a modulated, alternating magnetic field in which a coil is adapted to function as the secondary winding of a transformer. Electrical energy is stored in capacitor means and is released into the living body by controlled, stimulating pulses which pass through body fluids and tissue between the exposed electrodes of the microstimulator. Detection and decoding means within the microstimulator are provided for controlling the stimulating pulses in accordance with the modulation of the received, alternating magnetic field. Means for controllably recharging the capacitor is provided.

Abstract: An addressable, implantable microstimulator is substantially encapsulated within a hermetically-sealed housing inert to body fluids, and of a size and shape capable of implantation in a living body, by expulsion through a hypodermic needle. Power and information for operating the microstimulator is received through a modulated, alternating magnetic field in which a coil is adapted to function as the secondary winding of a transformer. Electrical energy is stored in capacitor means and is released into the living body by controlled, stimulating pulses which pass through body fluids and tissue between the exposed electrodes of the microstimulator. Detection and decoding means within the microstimulator are provided for controlling the stimulating pulses in accordance with the modulation of the received, alternating magnetic field. Means for controllably recharging the capacitor is provided.

Abstract: An implantable microstimulator has a structure which is manufactured to be substantially encapsulated within a hermetically-sealed housing inert to body fluids, and of a size and shape capable of implantation in a living body, by expulsion through a hypodermic needle. The internal structure of the microstimulator comprises a coil adapted to function as the secondary winding of a transformer and receive power and control information. Circuit means, including control electronics, a capacitor and electrodes are provided. The electrodes, which may be made one of iridium and the other of tantalum and placed on opposite ends of the microstimulator, or alternatively, an iridium electrode at each end of the microstimulator, are at least partially exposed and provide electrical, stimulating pulses to the body.

Abstract: A floating current source comprising two identically sized field effect transistors, one defining a reference transistor and the other defining a floating output transistor. The reference transistor has its gate connected to a reference voltage and its source connected to receive an input current from an input current source and to generate a gate-to-source voltage which when applied as a gate-to-source voltage of the floating output transistor will generate an output current in the output transistor equal to the input current. Circuit means are included for applying between the gate and source of the output transistor a voltage equal to the gate-to-source drain voltage of the reference transistor.